A selective adrenergic alpha-1 antagonist used in the treatment of HEART FAILURE; HYPERTENSION; PHEOCHROMOCYTOMA; RAYNAUD DISEASE; PROSTATIC HYPERTROPHY; and URINARY RETENTION.
Drugs that bind to but do not activate alpha-adrenergic receptors thereby blocking the actions of endogenous or exogenous adrenergic agonists. Adrenergic alpha-antagonists are used in the treatment of hypertension, vasospasm, peripheral vascular disease, shock, and pheochromocytoma.
Drugs that bind to and block the activation of ADRENERGIC ALPHA-1 RECEPTORS.
One of the two major pharmacological subdivisions of adrenergic receptors that were originally defined by the relative potencies of various adrenergic compounds. The alpha receptors were initially described as excitatory receptors that post-junctionally stimulate SMOOTH MUSCLE contraction. However, further analysis has revealed a more complex picture involving several alpha receptor subtypes and their involvement in feedback regulation.
A subclass of alpha-adrenergic receptors that mediate contraction of SMOOTH MUSCLE in a variety of tissues such as ARTERIOLES; VEINS; and the UTERUS. They are usually found on postsynaptic membranes and signal through GQ-G11 G-PROTEINS.
A plant alkaloid with alpha-2-adrenergic blocking activity. Yohimbine has been used as a mydriatic and in the treatment of ERECTILE DYSFUNCTION.
Drugs that selectively bind to and activate alpha adrenergic receptors.
An imidazoline sympatholytic agent that stimulates ALPHA-2 ADRENERGIC RECEPTORS and central IMIDAZOLINE RECEPTORS. It is commonly used in the management of HYPERTENSION.
1,4-Diethylene dioxides. Industrial solvents. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), dioxane itself may "reasonably be anticipated to be a carcinogen." (Merck Index, 11th ed)
Precursor of epinephrine that is secreted by the adrenal medulla and is a widespread central and autonomic neurotransmitter. Norepinephrine is the principal transmitter of most postganglionic sympathetic fibers and of the diffuse projection system in the brain arising from the locus ceruleus. It is also found in plants and is used pharmacologically as a sympathomimetic.
The effects, both local and systemic, caused by the bite of SCORPIONS.
An alpha-1 adrenergic agonist used as a mydriatic, nasal decongestant, and cardiotonic agent.
Compounds that bind to and activate ADRENERGIC ALPHA-1 RECEPTORS.
Drugs that bind to but do not activate ADRENERGIC RECEPTORS. Adrenergic antagonists block the actions of the endogenous adrenergic transmitters EPINEPHRINE and NOREPINEPHRINE.
Cell-surface proteins that bind epinephrine and/or norepinephrine with high affinity and trigger intracellular changes. The two major classes of adrenergic receptors, alpha and beta, were originally discriminated based on their cellular actions but now are distinguished by their relative affinity for characteristic synthetic ligands. Adrenergic receptors may also be classified according to the subtypes of G-proteins with which they bind; this scheme does not respect the alpha-beta distinction.
Drugs that bind to and block the activation of ADRENERGIC ALPHA-2 RECEPTORS.
A nonselective alpha-adrenergic antagonist. It is used in the treatment of hypertension and hypertensive emergencies, pheochromocytoma, vasospasm of RAYNAUD DISEASE and frostbite, clonidine withdrawal syndrome, impotence, and peripheral vascular disease.
A benzodioxane-linked imidazole that has alpha-2 adrenoceptor antagonist activity.
A prazosin-related compound that is a selective alpha-1-adrenergic blocker.
An alpha-1 adrenergic agonist that causes prolonged peripheral VASOCONSTRICTION.
A direct acting sympathomimetic used as a vasoconstrictor to relieve nasal congestion. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1251)
An alpha-adrenergic antagonist with long duration of action. It has been used to treat hypertension and as a peripheral vasodilator.
A subclass of alpha-adrenergic receptors found on both presynaptic and postsynaptic membranes where they signal through Gi-Go G-PROTEINS. While postsynaptic alpha-2 receptors play a traditional role in mediating the effects of ADRENERGIC AGONISTS, the subset of alpha-2 receptors found on presynaptic membranes signal the feedback inhibition of NEUROTRANSMITTER release.
Dibenzoquinolines derived in plants from (S)-reticuline (BENZYLISOQUINOLINES).
A widely used non-cardioselective beta-adrenergic antagonist. Propranolol has been used for MYOCARDIAL INFARCTION; ARRHYTHMIA; ANGINA PECTORIS; HYPERTENSION; HYPERTHYROIDISM; MIGRAINE; PHEOCHROMOCYTOMA; and ANXIETY but adverse effects instigate replacement by newer drugs.
The physiological narrowing of BLOOD VESSELS by contraction of the VASCULAR SMOOTH MUSCLE.
Quantitative determination of receptor (binding) proteins in body fluids or tissue using radioactively labeled binding reagents (e.g., antibodies, intracellular receptors, plasma binders).
Compounds that bind to and activate ADRENERGIC ALPHA-2 RECEPTORS.
A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments.
Arthropods of the order Scorpiones, of which 1500 to 2000 species have been described. The most common live in tropical or subtropical areas. They are nocturnal and feed principally on insects and other arthropods. They are large arachnids but do not attack man spontaneously. They have a venomous sting. Their medical significance varies considerably and is dependent on their habits and venom potency rather than on their size. At most, the sting is equivalent to that of a hornet but certain species possess a highly toxic venom potentially fatal to humans. (From Dorland, 27th ed; Smith, Insects and Other Arthropods of Medical Importance, 1973, p417; Barnes, Invertebrate Zoology, 5th ed, p503)
Use of electric potential or currents to elicit biological responses.
Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding.
Drugs that bind to but do not activate beta-adrenergic receptors thereby blocking the actions of beta-adrenergic agonists. Adrenergic beta-antagonists are used for treatment of hypertension, cardiac arrhythmias, angina pectoris, glaucoma, migraine headaches, and anxiety.
Antisera used to counteract poisoning by animal VENOMS, especially SNAKE VENOMS.
A tricyclic dibenzazepine compound that potentiates neurotransmission. Desipramine selectively blocks reuptake of norepinephrine from the neural synapse, and also appears to impair serotonin transport. This compound also possesses minor anticholinergic activity, through its affinity to muscarinic receptors.
The relationship between the dose of an administered drug and the response of the organism to the drug.
Compounds in which a methyl group is attached to the cyano moiety.
The nonstriated involuntary muscle tissue of blood vessels.
The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
Drugs that act on adrenergic receptors or affect the life cycle of adrenergic transmitters. Included here are adrenergic agonists and antagonists and agents that affect the synthesis, storage, uptake, metabolism, or release of adrenergic transmitters.
The interaction of two or more substrates or ligands with the same binding site. The displacement of one by the other is used in quantitative and selective affinity measurements.
PRESSURE of the BLOOD on the ARTERIES and other BLOOD VESSELS.
An alpha-2 adrenergic agonist that has both central and peripheral nervous system effects. Its primary clinical use is as an antihypertensive agent.
The domestic dog, Canis familiaris, comprising about 400 breeds, of the carnivore family CANIDAE. They are worldwide in distribution and live in association with people. (Walker's Mammals of the World, 5th ed, p1065)
An alkaloid found in the roots of Rauwolfia serpentina and R. vomitoria. Reserpine inhibits the uptake of norepinephrine into storage vesicles resulting in depletion of catecholamines and serotonin from central and peripheral axon terminals. It has been used as an antihypertensive and an antipsychotic as well as a research tool, but its adverse effects limit its clinical use.
An act which constitutes the termination of a given instinctive behavior pattern or sequence.
A strain of albino rat developed at the Wistar Institute that has spread widely at other institutions. This has markedly diluted the original strain.
Arteries which arise from the abdominal aorta and distribute to most of the intestines.
A 9,10alpha-dihydro derivative of ERGOTAMINE. It is used as a vasoconstrictor, specifically for the therapy of MIGRAINE DISORDERS.
An adrenergic alpha-2 agonist used as a sedative, analgesic and centrally acting muscle relaxant in VETERINARY MEDICINE.
A direct-acting vasodilator that is used as an antihypertensive agent.
Drugs that inhibit the actions of the sympathetic nervous system by any mechanism. The most common of these are the ADRENERGIC ANTAGONISTS and drugs that deplete norepinephrine or reduce the release of transmitters from adrenergic postganglionic terminals (see ADRENERGIC AGENTS). Drugs that act in the central nervous system to reduce sympathetic activity (e.g., centrally acting alpha-2 adrenergic agonists, see ADRENERGIC ALPHA-AGONISTS) are included here.
One of two major pharmacologically defined classes of adrenergic receptors. The beta adrenergic receptors play an important role in regulating CARDIAC MUSCLE contraction, SMOOTH MUSCLE relaxation, and GLYCOGENOLYSIS.
A mixture of three different hydrogenated derivatives of ERGOTAMINE: DIHYDROERGOCORNINE; DIHYDROERGOCRISTINE; and DIHYDROERGOCRYPTINE. Dihydroergotoxine has been proposed to be a neuroprotective agent and a nootropic agent. The mechanism of its therapeutic actions is not clear, but it can act as an alpha-adrenergic antagonist and a dopamine agonist. The methanesulfonate salts of this mixture of alkaloids are called ERGOLOID MESYLATES.
The species Oryctolagus cuniculus, in the family Leporidae, order LAGOMORPHA. Rabbits are born in burrows, furless, and with eyes and ears closed. In contrast with HARES, rabbits have 22 chromosome pairs.
Drugs that block the transport of adrenergic transmitters into axon terminals or into storage vesicles within terminals. The tricyclic antidepressants (ANTIDEPRESSIVE AGENTS, TRICYCLIC) and amphetamines are among the therapeutically important drugs that may act via inhibition of adrenergic transport. Many of these drugs also block transport of serotonin.
A strain of albino rat used widely for experimental purposes because of its calmness and ease of handling. It was developed by the Sprague-Dawley Animal Company.
Seven membered heterocyclic rings containing a NITROGEN atom.
A potent vasodilator agent with calcium antagonistic action. It is a useful anti-anginal agent that also lowers blood pressure.

alpha1-adrenergic receptor subtypes in human peripheral blood lymphocytes. (1/1153)

We investigated the expression of alpha1-adrenergic receptor subtypes in intact human peripheral blood lymphocytes using reverse transcription-polymerase chain reaction (RT-PCR) and radioligand binding assay techniques combined with antibodies against the three subtypes of alpha1-adrenergic receptors (alpha1A, alpha1B, and alpha1D). RT-PCR amplified in peripheral blood lymphocytes a 348-bp alpha1A-adrenergic receptor fragment, a 689-bp alpha1B-adrenergic receptor fragment, and a 540-bp alpha1D-adrenergic receptor fragment. Radioligand binding assay with [3H]prazosin as radioligand revealed a high-affinity binding with a dissociation constant value of 0. 65+/-0.05 nmol/L and a maximum density of binding sites of 175. 3+/-20.5 fmol/10(6) cells. The pharmacological profile of [3H]prazosin binding to human peripheral blood lymphocytes was consistent with the labeling of alpha1-adrenergic receptors. Antibodies against alpha1A-, alpha1B-, and alpha1D-receptor subtypes decreased [3H]prazosin binding to a different extent. This indicates that human peripheral blood lymphocytes express the three alpha1-adrenergic receptor subtypes. Of the three different alpha1-adrenergic receptor subtypes, the alpha1B is the most represented and the alpha1D, the least. Future studies should clarify the functional relevance of alpha1-adrenergic receptors expressed by peripheral blood lymphocytes. The identification of these sites may represent a step for evaluating whether they represent a marker of alpha1-adrenergic receptors in cardiovascular disorders or for assessing responses to drug treatment on these receptors.  (+info)

Neural modulation of cephalexin intestinal absorption through the di- and tripeptide brush border transporter of rat jejunum in vivo. (2/1153)

Intestinal absorption of beta-lactamine antibiotics (e.g., cefixime and cephalexin) has been shown to proceed through the dipeptide carrier system. In a previous study, nifedipine (NFP), an L-type calcium channel blocker, enhanced the absorption of cefixime in vivo but not in vitro, and it was suggested that neural mechanisms might be involved in the effect of NFP. The aim of the present study was to assess the involvement of the nervous system on the intestinal absorption of cephalexin (CFX). To investigate this, we used a single-pass jejunal perfusion technique in rats. NFP and diltiazem enhanced approximately 2-fold the plasma levels of CFX in treated rats versus untreated controls. NFP also increased approximately 2-fold the CFX level in portal plasma and increased urinary excretion of CFX, thus indicating that CFX did effectively increase CFX intestinal absorption. Perfusing high concentrations of dipeptides in the jejunal lumen competitively reduced CFX absorption and inhibited the enhancement of CFX absorption produced by NFP. Hexamethonium and lidocaine inhibited the effect of NFP, whereas atropine, capsaicin, clonidine, and isoproterenol enhanced CFX absorption by the same order of magnitude as NFP. Thus, complex neural networks can modulate the function of the intestinal di- and tripeptide transporter. Sympathetic noradrenergic fibers, intestinal sensory neurons, and nicotinic synapses are involved in the increase of CFX absorption produced by NFP.  (+info)

Transcriptional regulation of alpha1-adrenoceptor gene in the rat liver during different phases of sepsis. (3/1153)

Changes in alpha1-adrenoceptor (alpha1AR) gene expression in the rat liver during different phases of sepsis were studied. Sepsis was induced by cecal ligation and puncture (CLP). Septic rats exhibit two metabolically distinct phases: an initial hyperglycemic phase (9 h after CLP, early sepsis) followed by a hypoglycemic phase (18 h after CLP; late sepsis). The [3H]prazosin binding studies show that the density of alpha1AR was increased by 30% during the early phase while it was decreased by 24% during the late phase of sepsis. Western blot analyses reveal that alpha1AR protein level was elevated by 48% during early sepsis but was decreased by 55% during late sepsis. Northern blot analyses depict that the steady-state level of alpha1bAR mRNA was enhanced by 21% during the early phase but was declined by 29% during the late phase of sepsis. Nuclear run-off assays show that the transcription rate of alpha1bAR gene transcript was increased by 76% during early sepsis while it was decreased by 29% during late sepsis. The actinomycin D pulse-chase studies indicate that the half-life of alpha1bAR mRNA remained unaffected during the early and the late phases of sepsis. These findings demonstrate that during the early phase of sepsis, the increase in the rate of transcription of alpha1bAR gene paralleled with the elevations in the alpha1bAR mRNA abundance and alpha1AR protein level, while during the late phase of sepsis, the decrease in the rate of transcription of alpha1bAR gene coincided with the declines in the alpha1bAR mRNA abundance and the alpha1AR protein level in the rat liver. These observations indicate that the altered expression of alpha1AR genes in the rat liver during the progression of sepsis was regulated transcriptionally.  (+info)

Effects of heptanol on the neurogenic and myogenic contractions of the guinea-pig vas deferens. (4/1153)

1. The effects of the putative gap junction uncoupler, 1-heptanol, on the neurogenic and myogenic contractile responses of guinea-pig vas deferens were studied in vitro. 2. Superfusion of 2.0 mM heptanol for 20-30 min produced the following reversible changes in the biphasic neurogenic contractile response (8 trials): (i) suppression of both phases; (ii) delayed development of both the first as well as the second phase, accompanied by complete temporal separation of the two phases; (iii) prominent oscillations of force during the second (noradrenergic) phase only. 3. To eliminate prejunctional effects of heptanol, myogenic contractions were evoked by field stimulation of the vas in the presence of suramin (200 microM) and prazosin (1 microM). Heptanol (2.0 mM) abolished these contractions reversibly. 4. These results show that (i) heptanol inhibits both excitatory junction potential (EJP)-dependent and non EJP-dependent contractions of the vas; (ii) a postjunctional site of action of heptanol, probably intercellular uncoupling of smooth muscle cells, contributes to the inhibition of contraction.  (+info)

Spread of vasodilatation and vasoconstriction along feed arteries and arterioles of hamster skeletal muscle. (5/1153)

1. In arterioles of the hamster cheek pouch, vasodilatation and vasoconstriction can spread via the conduction of electrical signals through gap junctions between cells that comprise the vessel wall. However, conduction in resistance networks supplying other tissues has received relatively little attention. In anaesthetized hamsters, we have investigated the spread of dilatation and constriction along feed arteries and arterioles of the retractor muscle, which is contiguous with the cheek pouch. 2. When released from a micropipette, acetylcholine (ACh) triggered vasodilatation that spread rapidly along feed arteries external to the muscle and arterioles within the muscle. Responses were independent of changes in wall shear rate, perivascular nerve activity, or release of nitric oxide, indicating cell-to-cell conduction. 3. Vasodilatation conducted without decrement along unbranched feed arteries, yet decayed markedly in arteriolar networks. Thus, branching of the conduction pathway dissipated the vasodilatation. 4. Noradrenaline (NA) or a depolarizing KCl stimulus evoked constriction of arterioles and feed arteries of the retractor muscle that was constrained to the vicinity of the micropipette. This behaviour contrasts sharply with the conduction of vasodilatation in these microvessels and with the conduction of vasoconstriction elicited by NA and KCl in cheek pouch arterioles. 5. Focal electrical stimulation produced constriction that spread rapidly along feed arteries and arterioles. These responses were inhibited by tetrodotoxin or prazosin, confirming the release of NA along perivascular sympathetic nerves, which are absent from arterioles studied in the cheek pouch. Thus, sympathetic nerve activity co-ordinated the contraction of smooth muscle cells as effectively as the conduction of vasodilatation co-ordinated their relaxation. 6. In the light of previous findings in the cheek pouch, the properties of vasoconstriction and vasodilatation in feed arteries and arterioles of the retractor muscle indicate that substantive differences can exist in the nature of signal transmission along microvessels of tissues that differ in structure and function.  (+info)

Nitric oxide mediates sympathetic vasoconstriction at supraspinal, spinal, and synaptic levels. (6/1153)

The purposes of this study were to investigate the level of the sympathetic nervous system in which nitric oxide (NO) mediates regional sympathetic vasoconstriction and to determine whether neural mechanisms are involved in vasoconstriction after NO inhibition. Ganglionic blockade (hexamethonium), alpha1-receptor blockade (prazosin), and spinal section at T1 were used to study sympathetic involvement. NO was blocked with Nomega-nitro-L-arginine methyl ester (L-NAME). Regional blood flow in the mesenteric and renal arteries and terminal aorta was monitored by electromagnetic flowmetry in conscious rats. L-NAME (3-5 mg/kg iv) increased arterial pressure and peripheral resistance. Ganglionic blockade (25 mg/kg iv) significantly reduced the increase in resistance in the mesentery and kidney in intact and spinal-sectioned rats. Ganglionic blockade significantly decreased hindquarter resistance in intact rats but not in spinal-sectioned rats. Prazosin (200 micrograms/kg iv) significantly reduced the increased hindquarter resistance. We concluded that NO suppresses sympathetic vasoconstriction in the mesentery and kidney at the spinal level, whereas hindquarter tone is mediated at supraspinal and synaptic levels.  (+info)

Differential vascular alpha1-adrenoceptor antagonism by tamsulosin and terazosin. (7/1153)

AIMS: In patients with lower urinary tract symptoms suggestive of benign prostatic obstruction the alpha1-adrenoceptor antagonist terazosin lowers blood pressure whereas only very small if any alterations were reported with the alpha1-adrenoceptor antagonist tamsulosin. Therefore, we have compared the vascular alpha1-adrenoceptor antagonism of tamsulosin and terazosin directly. METHODS: Ten healthy subjects were investigated in a randomized, single-blind, three-way cross-over design and received a single dose of 0.4 mg tamsulosin, 5 mg terazosin or placebo on 3 study days at least 1 week apart. Before and 1, 3, 5, 7, 10 and 23.5 h after drug intake, alterations of diastolic blood pressure and other haemodynamic parameters in response to a graded infusion of the alpha1-adrenoceptor agonist phenylephrine were determined non-invasively. RESULTS: At most time points tamsulosin inhibited phenylephrine-induced diastolic blood pressure elevations significantly less than terazosin (5 h time point: median difference in inhibition 35%, 95% CI: 18.7-50.3%). On the other hand, phenylephrine-induced changes of cardiac output, heart rate and stroke volume were similar during both active treatments. CONCLUSIONS: In doses equi-effective for treatment of lower urinary tract symptoms tamsulosin causes less inhibition of vasoconstriction than terazosin.  (+info)

Characterization of alpha1-adrenoceptor subtypes mediating vasoconstriction in human umbilical vein. (8/1153)

1. The present study attempted to characterize pharmacologically the subtypes of alpha-adrenoceptors mediating contractions in human umbilical vein (HUV). 2. HUV rings were mounted in isolated organ baths and cumulative concentration-response curves were constructed for the alpha-adrenoceptor agonists phenylephrine and adrenaline. Adrenaline was more potent than phenylephrine (pD2=7.29 and 6.04 respectively). 3. Isoproterenol exhibited no agonism on KCl pre-contracted HUV rings. Propranolol (1 microM) and rauwolscine (0.1 microM) did not affect the concentration-response curves to adrenaline. These results demonstrate the lack of involvement of functional beta-or alpha2-adrenoceptors in adrenaline-induced vasoconstriction. 4. The non subtype selective alpha1-adrenoceptor antagonist prazosin was evaluated on phenylephrine and adrenaline concentration-response curves. The effects of the competitive alpha1A and alpha1D-adrenoceptor antagonists, 5-methyl urapidil and BMY 7378 and the irreversible alpha1B selective compound chloroethylclonidine (CEC) were also evaluated on adrenaline concentration-response curves. 5. The potencies of prazosin against responses mediated by adrenaline (pA2= 10.87) and phenylephrine (pA2= 10.70) indicate the involvement of prazosin-sensitive functional alpha1-adrenoceptor subtype in vasoconstriction of the HUV. 6. The potencies of 5-methyl urapidil (pA2 = 6.70) and BMY 7378 (pA2= 7.34) were not consistent with the activation of an alpha1A- or alpha1D-adrenoceptor population. 7. Exposure to a relatively low CEC concentration (3 microM) abolished the maximum response to adrenaline suggesting that this response was mediated by an alpha1B-adrenoceptor subtype. 8. We conclude that HUV express a prazosin-sensitive functional alpha1-adrenoceptor resembling the alpha1B-subtype according with the low pA2 values for both 5-methyl urapidil and BMY 7378 and the high sensitivity to CEC.  (+info)

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To test the hypothesis that the hypotensive action of urapidil is in part related to a direct action on the brain, the central (intracerebroventricular) and peripheral (intravenous) effects of urapidil were studied and compared with those obtained with clonidine and prazosin. All studies were conducted in conscious, chronically instrumented stroke-prone spontaneously hypertensive rats (SHRSP). Efferent sympathetic nervous system activity was estimated by means of a bipolar electrode implanted on the splanchnic nerve. Only clonidine, administered intracerebroventricularly and intravenously, decreased sympathetic nerve activity. Urapidil and prazosin either did not affect sympathetic nerve activity after central administration or increased it after peripheral administration at low and high doses, respectively. Centrally administered urapidil and prazosin lowered blood pressure but also blocked the response to intravenously administered phenylephrine; this result suggests a peripheral effect. ...
The exact mechanism of the hypotensive action of prazosin is unknown. Prazosin causes a decrease in total peripheral resistance and was originally thought to have a direct relaxant action on vascular smooth muscle. Recent animal studies, however, have suggested that the vasodilator effect of prazosin is also related to blockade of postsynaptic alpha-adrenoceptors. The results of dog forelimb experiments demonstrate that the peripheral vasodilator effect of prazosin is confined mainly to the level of the resistance vessels (arterioles). Unlike conventional alpha-blockers, the antihypertensive action of prazosin is usually not accompanied by a reflex tachycardia. Tolerance has not been observed to develop in long term therapy.. Hemodynamic studies have been carried out in man following acute single dose administration and during the course of long term maintenance therapy. The results confirm that the therapeutic effect is a fall in blood pressure unaccompanied by a clinically significant change ...
Tell your doctor about all other medications you use, especially other blood pressure medications including diuretics (water pills).. Prazosin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.. FDA pregnancy category C. It is not known whether prazosin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Prazosin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. ...
Tell your doctor about all other medications you use, especially other blood pressure medications including diuretics (water pills).. Prazosin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.. FDA pregnancy category C. It is not known whether prazosin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Prazosin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. ...
Tell your doctor about all other medications you use, especially other blood pressure medications including diuretics (water pills).. Prazosin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.. FDA pregnancy category C. It is not known whether prazosin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Prazosin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. ...
Tell your doctor about all other medications you use, especially other blood pressure medications including diuretics (water pills).. Prazosin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.. FDA pregnancy category C. It is not known whether prazosin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Prazosin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. ...
Tell your doctor about all other medications you use, especially other blood pressure medications including diuretics (water pills).. Prazosin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.. FDA pregnancy category C. It is not known whether prazosin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Prazosin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. ...
Tell your doctor about all other medications you use, especially other blood pressure medications including diuretics (water pills).. Prazosin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.. FDA pregnancy category C. It is not known whether prazosin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Prazosin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. ...
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We have used the subtype-selective radioligands [3H]prazosin (an alpha 1-adrenergic antagonist) and [3H]yohimbine (an alpha 2-adrenergic antagonist) to examine alpha-adrenergic receptors in rat renal cortical membranes. Under the conditions used in this study, [3H]prazosin bound only to alpha 1-adrenergic receptors, whereas [3H]yohimbine bound only to alpha 2-adrenergic receptors; the two radioligands were completely selective and did not bind to a common site. The ratio of alpha 2- to alpha 1-adrenergic receptors was about 3:1. Guanyl nucleotides decreased the affinity of epinephrine at both receptor subtypes, but this effect was greater at the alpha 2-receptor and, according to computer analysis, occurred through different mechanisms at the two receptor subtypes. NaCl decreased the affinity of epinephrine at both alpha-receptor subtypes; this effect was more Na+-selective at alpha 2- than at alpha 1-receptors. Guanyl nucleotides and NaCl were additive in decreasing the affinity of epinephrine ...
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Prazosin, 1-(4-amino-6,7-dimetoksi-2-hinazolinil)-4-(2-furoil)-piperazin, se sintetiše iz 2-amino-4,5-dimetoksibenzoinske kiseline, koji nakon reakcije sa natrijum cijanatom podleže heterociklizaciji do 2,4-dihidroksi-6,7-dimetoksihinazolina. Supstituisanje hidroksilnih grupa ovog jedinjenja atomima hlora reakcijom sa tionil hloridom, ili smešom fosfor oksihlorida sa fosfor pentahloridom daje 2,4-dihloro-6,7-dimetoksihinazolin. Naknadnom reakcijom sa amonijakom, atom hlora u C4 poziciji pirimidinskog prstena se zamenjuje amino grupom, što dovodi do formiranja 4-amino-2-hloro-6,7-dimetoksihinazolina. Njegovim uvođenjem u reakciju sa 1-(2-furoil)piperazinom formira se prazosin.[3][4][5][6][7][8][9][10][11][12]. ...
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After depletion of intracellular calcium stores sensitive to noradrenaline, a spontaneous increase in the resting tone (IRT) when incubated in Ca2+-containing solution was observed in isolated rat aorta, but not in tail artery. This IRT does not depend on agonist activation of α1-adrenoceptors but it is inhibited by prazosin. A close relationship was found between the inhibitory potencies of prazosin (pIC50 = 9.833), BMY 7378 (pIC50 = 8.924), and 5-methylurapidil (pIC50 = 7.883) against IRT and their affinities for cloned α1D-adrenoceptors. Chloroethylclonidine (100 μmol · l−1) did not inhibit the IRT. After depletion of internal calcium stores by noradrenaline in absence of the agonist, loading in Ca2+-containing solution also brings about an increase in the inositol phosphate (IP) levels in rat aorta (not seen in tail artery) that is inhibited by prazosin (1 μmol · l−1), BMY 7378 (10 μmol · l−1), and 5-methylurapidil (10 μmol · l−1), thus confirming the results obtained in ...
This case discusses α1-adrenergic blockade by prazosin and PDE 5-mediated hypotension by tadalafil in the presence of local anesthetic-induced sympathectomy
Minipress is classified as an alpha-adrenergic blocker. The active ingredient of the medication, Prazosin, stimulates an inevitable action relaxing the arteries and veins. This way, the treatment produces easier blood circulation in the body.
By W. Dan. Saint Andrews Presbyterian College.. A blinded study withholding modern drugs from one group ofmatched patients is not possible. Also, theelevated toe plate cannot be moved once it is molded into place. Stress is an abstract concept, the components of which must bededuced from measurements of load, or from measurements of strain and elastic constants In addition,stress is dened based solely on its effects. Adrenergic receptors in man: direct identication, physiologic regula-tion and clinical alterations. This worksheetis also very helpful when writing a letter of medical need (see algorithms). Alternatively, ligament behavioris modied so that the need to specify an initial conguration where all ligaments are simultaneously attheir relaxed state is no longer necessary. EMBO J;:ж Lipsky PE, van der Heijde DM, St Clair EW et al. The physician then takes the responsibilityfor the administration and safety of the prescribed treatment, as is the case with any othermedical treatment. These ...
Learn about Minipress (Prazosin HCl) may treat, uses, dosage, side effects, drug interactions, warnings, patient labeling, reviews, and related medications.
Terazosin with NDC 50268-767 is a a human prescription drug product labeled by Avpak. The generic name of Terazosin is terazosin hydrochloride.
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Minipress used for treatment of high blood pressure alone or concomitantly with diuretics or beta-adrenergic blocking medications.
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Terazosin should be taken in the form of capsules orally . The dosage can be two capsules per day, or one capsule per day before bedtime.. Your doctor may decide to gradually increase the initial prescription dosage.. ...
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It has been previously shown that beta-adrenergic agonists stimulate growth hormone (GH) release from perifused rat anterior pituitary cell aggregates cultured in serum-free defined medium for 5-6 days. The present data show that the natural beta-agonist epinephrine (EPI) stimulates GH release through an additional alpha-adrenergic mechanism. The involvement of this mechanism was suggested by the following findings. The intrinsic activity of EPI, at concentrations greater than 10 nM, was significantly higher than that of isoproterenol (ISO) in stimulating GH release. Phenylephrine (PHE), a specific agonist of alpha 1-adrenergic receptors, provoked a significant rise of GH release. The effect was concentration dependent between 100 nM and 10 microM. The stimulatory effect of EPI and PHE was lowered, respectively blocked, by low concentrations of the potent alpha 1-adrenergic antagonist prazosin. The EPI-induced GH release could be totally blocked only by administration of both alpha- and ...
Headaches following combat-related post-concussive injury are common, and in some patients can increase in frequency and severity to become very debilitating. Posttraumatic headaches (PTHAs), particularly those following blast-related head injury, can be resistant to standard headache therapies. The objective of this study is to evaluate the effectiveness of the medication prazosin as a prophylactic (preventive) agent in treating combat-related PTHAs. Prazosin is a generic drug originally marketed over 30 years ago as a treatment for high blood pressure. It has subsequently been found to be safe and effective for treating other problems, including most recently posttraumatic stress disorder (PTSD) and disrupted sleep in active duty Iraq/Afghanistan Service Members and Veterans. In preliminary studies, prazosin has also been found to substantially reduce the intensity and frequency of PTHAs in this population. This finding is the motivation behind this study.. The investigators hypotheses are ...
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Background: Some α1-adrenoceptor antagonists possess anti-cancer actions that are independent of α1-adrenoceptors and the aim of these studies was to assess the relative cytotoxic potencies of α1-adrenoceptor antagonists and the mechanisms involved in these actions. Methods: PC-3 and LNCap human prostate cancer cells were exposed to α1-adrenoceptor antagonists (0.01-100μM) and cell survival assessed after 24-72hr. The levels of apoptosis, autophagy and stress related proteins were also determined. Results: The relative cytotoxic potency order was prazosin=doxazosin|terazosin=silodosin=alfuzosin|tamsulosin on both cell types, but LNCaP cells were significantly more sensitive to these effects than PC-3 cells. Prazosin and doxazosin increased levels of apoptotsis and autophagy in both cell lines, and activated EphA2 receptors in PC-3 cells. Autophagy contributed to survival of LNCaP, but promoted cell death in PC-3 cells. Treatment with prazosin (30μM) altered the expression of several cell stress
In animals, terazosin causes a decrease in blood pressure by decreasing total peripheral vascular resistance. The vasodilatory hypotensive action of terazosin appears to be produced mainly by blockade of alpha-1 adrenoceptors. Terazosin decreases blood pressure gradually within 15 minutes following oral administration.. Patients in clinical trials of terazosin were administered once daily (the great majority) and twice daily regimens with total doses usually in the range of 5 to 20 mg/day, and had mild (about 77%, diastolic pressure 95 to 105 mmHg) or moderate (23%, diastolic pressure 105 to 115 mmHg) hypertension. Because terazosin, like all alpha antagonists, can cause unusually large falls in blood pressure after the first dose or first few doses, the initial dose was 1 mg in virtually all trials, with subsequent titration to a specified fixed dose or titration to some specified blood pressure end point (usually a supine diastolic pressure of 90 mmHg).. Blood pressure responses were measured ...
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Diltiazem works well to lower blood pressure and prevent chest pain, but you have to be okay with avoiding alcohol. You cant miss doses, and you might get persistent swelling. Prazosin is used mostly to make urination easier for men with an enlarged prostate, but it can cause dizziness.
Prazosin: Belongs to the class of alpha-adrenoreceptor antagonists, peripherally-acting antiadrenergic agents. Used in the treatment of hypertension.,
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BACKGROUND AND PURPOSE: In mouse tail arteries, selective alpha(2)-adrenoceptor antagonism with rauwolscine caused powerful dilation during constriction to the alpha(1)-adrenoceptor agonist phenylephrine. This study therefore assessed phenylephrines selectivity at vascular alpha-adrenoceptors and the mechanism(s) underlying dilation to rauwolscine. EXPERIMENTAL APPROACH: Mouse isolated tail arter
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TERAZOSIN HYDROCHLORIDE ANHYDROUS, INDICATIONS AND USAGE Terazosin capsules are indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH). There is a rapid response, with approximately 70% of patients experiencing a
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Earlier nonselective alpha 1-adrenergic blocking drugs such as phentolamine and phenoxybenzamine are now restricted to the pharmacological management of alpha 1-adrenergic crisis and phaeochromocytoma. Prazosin, the first selective alpha 1-blocker approved for the treatment of hypertension, became a …
Prazosin. Prazosin, an alpha-1 adrenergic antagonist, has been used in veterans with PTSD to reduce nightmares. Studies show ... Green, Ben (July 2014). "Prazosin in the Treatment of PTSD". Journal of Psychiatric Practice. 20 (4): 253-259. doi:10.1097/01. ... prazosin, propranolol, guanfacine, clonidine, quetiapine, olanzapine, valproate, gabapentin).[4][186][187] ... "Efficacy of Prazosin in Posttraumatic Stress Disorder: A Systematic Review and Meta-Analysis". The Primary Care Companion for ...
First selective alpha-1 blocker that was approved to treat hypertension was prazosin. Prazosin was synthesized in 1974 when ... As of 2018, prazosin is the only alpha-1 blocker known to act as an inverse agonist at all alpha-1 adrenergic receptor subtypes ... Prazosin is commonly used as an anti-hypertensive, but because alpha-1 adrenergic activity has been connected to fear and ... Prazosin has been established as an effective and safe centrally active alpha-1 adrenergic receptor antagonist. It can be used ...
First generation alpha-1 blockers, like prazosin are not recommended to treat lower urinary tract symptoms because of their ... Stanaszek, W. F.; Kellerman, D.; Brogden, R. N.; Romankiewicz, J. A. (April 1983). "Prazosin update. A review of its ...
Prazosin is an α1-blocker that acts as an inverse agonist at alpha-1 adrenergic receptors. Raskind and colleagues studied the ... "Prazosin: Biological activity". IUPHAR. International Union of Basic and Clinical Pharmacology. Retrieved 3 June 2016. Murray A ... Patients who were taking prazosin had a robust improvement in overall sleep quality (effect size, 1.6) and recurrent ... February 2003). "Reduction of Nightmares and Other PTSD Symptoms in Combat Veterans by Prazosin: A Placebo-Controlled Study". ...
"Prazosin-Related Compounds. Effect of Transforming the Piperazinylquinazoline Moiety into an Aminomethyltetrahydroacridine ...
The alpha blocker prazosin (Minipress) is most notorious for producing a first dose phenomenon. Other drugs of the same family ... For this reason, treatment with prazosin (Minipress) should always be initiated with a low dose and should be taken at bedtime ... "Minipress (Prazosin HCl) drug warnings and precautions - prescription drugs and medications at RxList". Archived from the ... First pass effect Graham RM, Thornell IR, Gain JM, Bagnoli C, Oates HF, Stokes GS (1976). "Prazosin: the first-dose phenomenon ...
Graham RM, Thornell IR, Gain JM, Bagnoli C, Oates HF, Stokes GS (November 1976). "Prazosin: the first-dose phenomenon". British ... prazosin, terazosin) is the preferred agent. However, the patient should be warned about the potential side-effect known as " ...
Green B (July 2014). "Prazosin in the treatment of PTSD". Journal of Psychiatric Practice. 20 (4): 253-9. doi:10.1097/01.pra. ...
Prazosin Ketanserin David J. Triggle (1996). Dictionary of Pharmacological Agents. Boca Raton: Chapman & Hall/CRC. ISBN 0-412- ...
Adverse effects of prazosin to treat PTSD nightmares include dizziness, First Dose Effect (a sudden loss of consciousness), ... Green, Ben (2014). "Prazosin in the Treatment of PTSD". Journal of Psychiatric Practice. 20 (4): 253-259. doi:10.1097/01.pra. ... Prazosin, doxazosin, and terazosin have been particularly useful for patients with BPH, especially in patients with ... High doses of the α1 blocker, prazosin, have been efficacious in treating patients with PTSD induced nightmares due to its ...
A comparison of prazosin and moxisylyte". J. Auton. Nerv. Syst. 79 (2-3): 191-5. doi:10.1016/S0165-1838(99)00105-8. PMID ...
Prazosin (of MT3). *S-20928. *S-22153. *S-24601. *S-25567 ...
"Prazosin Relieves Nightmares and Sleep Disturbance in PTSD". Hoehn-Saric, Rudolf; Merchant, A. F.; Keyser, M. L.; Smith, V. K ... The alpha1 antagonist prazosin could be effective for PTSD The Alpha-2 adrenergic receptor agonists clonidine and guanfacine ... Koola, M. M.; Varghese, S. P.; Fawcett, J. A. (2013). "High-dose prazosin for the treatment of post-traumatic stress disorder ...
Usually, the drug Prazosin is recommended for H. tamulus stings. The drug can reduce the increasing blood pressure. Tamapin ... prazosin in the management of severe Mesobuthus tamulus (Indian red scorpion) envenoming at rural settings" (PDF). Journal of ... Scorpion antivenom has little effect in clinical treatment but application of prazosin reduces the mortality rate to less than ...
Kjaergaard N, Kjaergaard B, Lauritsen JG (June 1988). "Prazosin, an adrenergic blocking agent inadequate as male contraceptive ...
Prazosin in the management of cardiovascular manifestations of scorpion sting. Lancet. 1986;i:510-11.PubMed 9. Mills EJ, Ford N ...
February 2018). "Trial of Prazosin for Post-Traumatic Stress Disorder in Military Veterans". The New England Journal of ... Prazosin, an alpha-adrenoceptor antagonist, is also widely prescribed, particularly for sleep-related symptoms. Early studies ... prazosin, propranolol, guanfacine, clonidine, quetiapine, olanzapine, valproate, gabapentin). Glucocorticoids may be useful for ... though a recent relatively large trial failed to show a statistically significant difference between prazosin and placebo. ...
This characteristic immobility could be counteracted by the pre-administration of prazosin. Subsequent experiments using the ... prazosin (standard α1 ligand); against [3H]-yohimbine (standard α2 ligand), l-synephrine showed a pIC50 = 5.01, and d- ... with prazosin being the more potent antagonist (pA2 = 9.38, vs pA2 = 8.23 for ketanserin). Synephrine constrictions were also ... This constriction was found to be competitively antagonized by prazosin (a standard α1 antagonist) and ketanserin, ...
Medications like prazosin are sometimes used to treat nightmares in people with PTSD. Therapy usually helps to deal with the ... Prazosin would significantly decrease the number of PTSD related nightmares and would therefore improve sleep quality. However ... The most efficient is an alpha-blocker, named Prazosin, which reduce tone during sleep by blocking noradrenergic receptors. ... Reduction of Nightmares and Other PTSD Symptoms in Combat Veterans by Prazosin: A Placebo-Controlled Study, American Journal of ...
Prazosin) • Agoniști alfa-2 (ex. Clonidină, Dexmedetomidină, Guanfacină) • Beta-blocante (ex. Propranolol) ...
... and prazosin. Sublingual nifedipine is not recommended in hypertensive urgencies. This is because nifedipine can cause rapid ...
Prazosin (Minipress) for nightmares: prazosin is approved for the use of hypertension. A 2012 systematic review showed a small ... Other non-FDA-approved uses for prazosin include the treatment of Raynaud's disease and poisoning due to scorpion venom. ...
Ellingsen Ø, Kjekshus J. Prazosin ved anstrengelsesutløst angina pectoris (Prazosin in exercise induced angina pectoris). ...
Waldo R (March 1979). "Prazosin relieves Raynaud's vasospasm". JAMA. 241 (10): 1037. doi:10.1001/jama.241.10.1037. PMID 762741. ... Elsevier Saunergic blockers such as prazosin can be used to control Raynaud's vasospasms under supervision of a health care ... Sympatholytic agents, such as the alpha-adrenergic blocker prazosin, may provide temporary relief to secondary Raynaud's ... "Prazosin for Raynaud's phenomenon in progressive systemic sclerosis". Cochrane Database of Systematic Reviews. doi:10.1002/ ...
Prazosin (koristi se za hipertenziju). *Silodosin. *Tamsulosin (koristi se za benignu prostatičnu hiperplaziju) ...
... prazosin, nifedipine, nitroprusside, and electrical stimulation". Neurourology and Urodynamics. 14 (2): 153-68. doi:10.1002/nau ...
1997). "Effects of acepromazine maleate, isoxsuprine hydrochloride and prazosin hydrochloride on laminar blood flow in healthy ...
Patients with hypertension on admission are given a single dose of 5 mg sublingual nifedipine and oral prazosin. The blood ... oral prazosin, and oxygen by mask. Galvez, A; Gimenez-Gallego, G; Reuben, JP; Roy-Contancin, L; Feigenbaum, P; Kaczorowski, GJ ...
Prazosin: learn about side effects, dosage, special precautions, and more on MedlinePlus ... Prazosin controls high blood pressure but does not cure it. Continue to take prazosin even if you feel well. Do not stop taking ... Prazosin is used alone or in combination with other medications to treat high blood pressure. Prazosin is in a class of ... Before taking prazosin,. *tell your doctor and pharmacist if you are allergic to prazosin, alfuzosin (Uroxatral), doxazosin ( ...
Professional guide for Prazosin. Includes: pharmacology, pharmacokinetics, contraindications, interactions, adverse reactions ... Prazosin crosses the placenta and its pharmacokinetics may be slightly altered during pregnancy (Bourget 1995; Rubin 1983). ... Prazosin Hydrochloride. Dosage Forms. Excipient information presented when available (limited, particularly for generics); ... Data from a meta-analysis of six randomized-controlled trials, supports the use of prazosin in reducing trauma nightmares and ...
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This case discusses α1-adrenergic blockade by prazosin and PDE 5-mediated hypotension by tadalafil in the presence of local ... Pharmacodynamic Prazosin Tadalafil Lidocaine Hypotension Local anesthetic Epidural Sympathectomy α1-adrenergic blockade Anti- ... Prazosin for the treatment of post traumatic stress disorder sleep disturbances. Pharmacotherapy. 2008;28(5):656-66.PubMed ... Gustin A.N., Bishop M.J. (2015) Prazosin and the PTSD Paratrooper. In: Marcucci C. et al. (eds) A Case Approach to ...
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Prazosin is marketed by Pfizer and was initially approved by the FDA in 1988 . It belongs to the class of drugs known as alpha- ... Prazosin, also known as Minipress, is a drug used to treat hypertension. ... Prazosin, also known as Minipress, is a drug used to treat hypertension. Prazosin is marketed by Pfizer and was initially ... Prazosin hydrochloride (2 mg/1) + Polythiazide (0.5 mg/1). Capsule. Oral. Pfizer Labs. 2006-10-05. Not applicable. US. ...
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Effect of Prazosin on the Peripheral Vasculature during Rest Low, Mild, and Heavy Exercise Workloads.: 878June 1 1:00 PM - 1:15 ... Effect of Prazosin on the Peripheral Vasculature during Rest Low, Mild, and Heavy Exercise Workloads.: 878June 1 1:00 PM - 1:15 ... Home , May 2007 - Volume 39 - Issue 5 , Effect of Prazosin on the Peripheral Vasculature during Rest... ... RESULTS: Prazosin resulted in significant increases FVC at rest when compared to the control protocol (+68 ± 6%). During ...
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Also Known As: Minipress; Douglas Brand of Prazosin Hydrochloride; Pfizer Brand of Prazosin Hydrochloride; Pratsiol; Prazosin ... Key Diseases for which Prazosin is Relevant. * Hypertension (High Blood Pressure) : 34 outcomes 77 studies in 431 results ... Prazosin (Minipress) Summary Description: A selective adrenergic alpha-1 antagonist used in the treatment of HEART FAILURE; ...
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A study recently published in The American Journal of Psychiatry found that the alpha-1 adrenergic receptor antagonist prazosin ... A study recently published in The American Journal of Psychiatry found that the alpha-1 adrenergic receptor antagonist prazosin ...
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Prazosin: Belongs to the class of alpha-adrenoreceptor antagonists, peripherally-acting antiadrenergic agents. Used in the ... Prazosin. Source: National Center for Biotechnology Information. PubChem Database. Prazosin, CID=4893, https://pubchem.ncbi.nlm ... Description: Prazosin is an alpha blocker that competitively inhibits postsynaptic alpha1-adrenoreceptors in vascular smooth ... C02CA01 - prazosin ; Belongs to the class of alpha-adrenoreceptor antagonists, peripherally-acting antiadrenergic agents. Used ...
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  • Prazosin hydrochloride, USP a quinazoline derivative, is the first of a new chemical class of antihypertensives. (nih.gov)
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  • In clinical studies to date, prazosin hydrochloride has not increased plasma renin activity. (nih.gov)
  • Animal studies indicate that prazosin hydrochloride is extensively metabolized, primarily by demethylation and conjugation, and excreted mainly via bile and feces. (nih.gov)
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  • Take prazosin exactly as directed. (medlineplus.gov)
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  • How should I take prazosin? (cardiosmart.org)
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  • APO-Prazosin tablets 2mg contain prazosin, an alpha-blocker used to treat hypertension, benign prostatic hyperplasia (BPH), congestive heart failure and Raynaud's disease and phenomenon. (inhousepharmacy.vu)
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  • Osim njegove alfa blokatorske aktivnosti, prazosin je antagonist MT 3 receptora (koji nije prisutan kod ljudi). (wikipedia.org)
  • The purpose of this study is to evaluate the centrally acting alpha-1 adrenoreceptor (AR) antagonist drug prazosin as a prophylactic treatment for chronic posttraumatic headaches (PTHAs). (clinicaltrials.gov)
  • This double-blind placebo controlled crossover pilot trial will test the hypothesis that prazosin, an alpha-1 adrenergic receptor antagonist, reduces craving for their drug of choice in cocaine-dependent and alcohol-dependent veterans. (clinicaltrials.gov)
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  • In this article, we reanalyze and extend previously reported findings of the effect of prazosin, an α1-adrenergic receptor antagonist, on the extinction of a cocaine-induced conditioned place preference in rats, using a median split of performance during the initial test for preference. (ovid.com)
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  • Prazosin has been established as an effective and safe centrally active alpha-1 adrenergic receptor antagonist. (wikipedia.org)
  • Your doctor will probably start you on a low dose of prazosin and gradually increase your dose. (medlineplus.gov)
  • A single post-test administration of a lower dose of prazosin, 0.3 mg/kg intraperitoneally, impaired extinction in rats that showed a below-median preference during initial testing, but had no effect on extinction in rats that showed an above-median preference during initial testing. (ovid.com)
  • Consistent with other studies of fear and drug conditioning, these results suggest the involvement of the α1-adrenergic receptor in the formation of extinction memories, but also indicate a potentially important differential effect on extinction on the basis of the dose of prazosin and the strength of the initial learning. (ovid.com)
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  • A very rare side effect of prazosin is priapism. (wikipedia.org)
  • Recent animal studies, however, have suggested that the vasodilator effect of prazosin is also related to blockade of postsynaptic alpha-adrenoceptors. (nih.gov)
  • The results of dog forelimb experiments demonstrate that the peripheral vasodilator effect of prazosin is confined mainly to the level of the resistance vessels (arterioles). (nih.gov)
  • Specific Aim 1: To determine the effect of prazosin compared to placebo on headache frequency, headache severity and duration, use of abortive/analgesic medications, and headache-related disability. (clinicaltrials.gov)
  • Specific Aim 2: To determine the effect of prazosin on sleep disturbance, PTSD symptoms, depressive symptoms, alcohol consumption, global cognitive function, health-related quality of life, and global clinical status. (clinicaltrials.gov)
  • Effect of Prazosin on the Peripheral Vasculature during Rest. (lww.com)
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  • You must avoid using prescription drugs if you are allergic to prazosin or similar medicines including alfuzosin (Uroxatral), doxazosin (Cardura), silodosin (Rapaflo), tamsulosin (Flomax), or terazosin (Hytrin). (availablemeds.top)
  • Prazosin is also useful in treating urinary hesitancy associated with benign prostatic hyperplasia, blocking alpha-1 adrenergic receptors, which control constriction of both the prostate and urethra. (wikipedia.org)
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  • Prazosin is used for treating high blood pressure and benign prostatic hyperplasia (BPH). (northern-pharmacy.com)
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  • One phenomenon associated with prazosin is known as the "first dose response", in which the side effects of the drug - specifically orthostatic hypotension, dizziness, and drowsiness - are especially pronounced in the first dose. (wikipedia.org)
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  • Unlike conventional alpha-blockers, the antihypertensive action of prazosin is usually not accompanied by a reflex tachycardia. (nih.gov)
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  • Prazosin is an alpha blocker that competitively inhibits postsynaptic alpha 1 -adrenoreceptors in vascular smooth muscles, resulting to vasodilation, and decrease in total peripheral resistance and blood pressure. (mims.com)
  • These results indicate that in the rat prazosin inhibits vascular postsynaptic α-adrenoceptors and lacks the direct vascular smooth muscle relaxant activity possessed by dihydralazine. (ovid.com)
  • Prazosin differed from phentolamine in that it inhibited the pressor responses to endogenous and exogenous norepinephrine similarly and interfered neither with cardiac presynaptic α-adrenoceptors nor with vascular postsynaptic 5-hydroxytryptamine receptors. (ovid.com)
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  • During cataract surgery, a condition called Intraoperative Floppy Iris Syndrome (IFIS) can happen if you take or have taken prazosin. (rxwiki.com)
  • It is suggested that the alpha receptor blocking action of prazosin is selective for arterioles and this may explain the minor incidence of postural hypotension during clinical use. (aspetjournals.org)
  • Method: A systematic search of English and French clinical studies on any CBTs and Prazosin treatments for PTNMs published from 1980 to 2012 was conducted in PsycINFO, MedLine, PILOTS,and ProQuest Dissertations and Theses. (intechopen.com)
  • Clinical studies show prazosin might offer other therapeutic benefits to PTSD patients, but the results are mixed. (verywellhealth.com)
  • Because of availability of longer-acting, once-daily selective agents, however, the clinical utility of prazosin for BPH has been reduced. (medscape.com)
  • In white prazosin for sale matter https://nityamyoga.com/2019/08/27/buy-ipratropium-bromide-albuterol-sulfate-cheap-online volume correctly inferred as single neurons notably, chen ch, extended matching. (anakovacspsicologia.com)
  • Prazosin has also been used in conjunction with cardiac glycosides and diuretics in the management of severe congestive heart failure. (hmdb.ca)
  • The antihypertensive characteristics of prazosin make it a second-line choice for the treatment of high blood pressure. (wikipedia.org)
  • Concomitant diuretics or other antihypertensives: When adding a diuretic or other antihypertensive, decrease prazosin dose to 1 or 2 mg 3 times daily and retitrate. (drugs.com)
  • Physiologic evaluation of a new antihypertensive agent: prazosin HCl. (ahajournals.org)
  • Urapidil and prazosin either did not affect sympathetic nerve activity after central administration or increased it after peripheral administration at low and high doses, respectively. (ahajournals.org)
  • Intravenous infusions of urapidil and prazosin in sufficient doses to lower blood pressure in spontaneously hypertensive rats by 50 mm Hg completely blocked the actions of phenylephrine. (ahajournals.org)
  • The papers, being among the cause margin doses of zinc, are called upon from radical to case to remove from the steamship casts which have gained life through the brain, or which have been formed in the poisoning, either through submaxillary chain or difficult prazosin online canada mastercard, now in the high organs. (meditationiseasy.com)
  • Fig. 3 Enduring Reinstatement of Deficits on the Beam Walk Task by Multiple Doses of Prazosin. (mcmaster.ca)
  • Review of: McCall W et al, J Clin Psychopharmacol 2018;38(6):618-621 Study Type: Randomized single-blind controlled trial (pilot study) Prazosin has become a mainstay in the pharmacologic treatment of PTSD. (thecarlatreport.com)
  • PHILADELPHIA-Prazosin, an alpha-blocker commonly used to manage acute lower urinary tract symptoms (LUTS) among men receiving radiation therapy for prostate cancer (PCa), may decrease the likelihood of recurrent cancer, according to new study findings presented at the International Continence Society's 2018 annual meeting. (renalandurologynews.com)
  • Prazosin is marketed by Pfizer and was initially approved by the FDA in 1988 16 . (drugbank.ca)
  • Prazosin causes a decrease in total peripheral resistance and was originally thought to have a direct relaxant action on vascular smooth muscle. (nih.gov)
  • Many of the above effects are due to vasodilation of blood vessels caused by prazosin, resulting in decreased peripheral resistance 7 , Label . (drugbank.ca)
  • To test the hypothesis that the hypotensive action of urapidil is in part related to a direct action on the brain, the central (intracerebroventricular) and peripheral (intravenous) effects of urapidil were studied and compared with those obtained with clonidine and prazosin. (ahajournals.org)
  • Thus, our findings suggest that peripheral prazosin injection in REMSD would not bring the body temperature to normal, rather might become counterproductive. (ias.ac.in)
  • Prazosin as an α-adrenergic blocking drug has both an expanding effect both on the arteries and veins, a little more on voluminous venous vessels, which leads to a decrease in the venous influx to the heart and facilitating the work of the heart muscle due to a decrease in peripheral resistance. (buy-clomid-cheap-price-free-shipping.com)
  • Prazosin is an alpha-1 blocker medication primarily used to treat high blood pressure, symptoms of an enlarged prostate, and posttraumatic stress disorder (PTSD). (wikipedia.org)
  • Based on the American Psychiatric Association practice guidelines for the treatment of acute stress disorder and posttraumatic stress disorder , prazosin appears effective for the management of trauma-related nightmares and sleep disruption associated with PTSD. (drugs.com)
  • Some people who have posttraumatic stress disorder (PTSD) and have been taking prazosin for their medical conditions or who have taken it in research studies have said they have fewer headaches. (clinicaltrials.gov)
  • The impetus for this study comes from a large open-label case series in Iraq and Afghanistan Veterans with mTBI and PTHAs and data from a placebo-controlled trial evaluating use of prazosin for posttraumatic stress disorder (PTSD) in active-duty Servicemembers (SMs). (clinicaltrials.gov)
  • Prazosin is used alone or in combination with other medications to treat high blood pressure. (medlineplus.gov)
  • Prazosin controls high blood pressure but does not cure it. (medlineplus.gov)
  • When prazosin is started, however, heart rate and contractility can increase in order to maintain the pre-treatment blood pressures because the body has reached homeostasis at its abnormally high blood pressure. (wikipedia.org)
  • When use to treat high blood pressure or heart failure, prazosin is often used together with other medicines. (news-medical.net)
  • The Food and Drug Administration (FDA) has approved prazosin for treating people with high blood pressure. (clinicaltrials.gov)
  • Prazosin treats high blood pressure. (rxwiki.com)
  • Prazosin is in a class of medications called alpha-blockers. (medlineplus.gov)
  • Prazosin is in a group of drugs called alpha-adrenergic (AL-fa ad-ren-ER-jik) blockers. (cardiosmart.org)
  • Prazosin belongs to the family of medications called antihypertensives, specifically the group known as alpha 1-blockers . (medbroadcast.com)
  • Some evidence shows that some alpha-blockers, such as prazosin, decrease PCa incidence and increase apoptosis in the prostate. (renalandurologynews.com)
  • Prazosin belongs to a group of drugs called alpha-blockers. (rxwiki.com)
  • alpha blockers and diuretics prazosin polythiazide minizide ace inhibitors and diuretics benazepril hctz lotensin hct captopril hctz. (scotlandinstitute.com)
  • Prazosin is a small grouping of drugs called alpha-adrenergic (AL-fa ad-ren-ER-jik) blockers. (availablemeds.top)
  • The advantage of prazosin over nonselective alpha-adrenergic blockers includes a lower incidence of adverse effects. (medscape.com)
  • First generation alpha-1 blockers, like prazosin are not recommended to treat lower urinary tract symptoms because of their blood-pressure-lowering effect. (wikipedia.org)
  • Mathe et al (1996) Prazosin inhibits MK-801-induced hyperlocomotion and DA release in the nucleus accumbens. (tocris.com)
  • The exact mechanism of the hypotensive action of prazosin is unknown. (nih.gov)
  • Awan NA, Miller RR, Maxwell K, Mason DT (1977) Effects of prazosin on forearm resistance and capacitance vessels. (springer.com)
  • Cavero I, Lefevre F, Roach AG (1977) Differential effects of prazosin on the pre- and post-synaptic adrenoceptors in the rat and dog. (springer.com)
  • Non-P-glycoprotein-specific effects of prazosin on membrane fluidity and permeability were excluded. (nih.gov)
  • Effects of sodium nitroprusside, isosorbide dinitrate, isoproterenol, phentolamine and prazosin on hepatic venous responses to sympathetic nerve stimulation in the cat. (aspetjournals.org)
  • Prazosin can be given alone or given with other blood pressure-lowering drugs, including diuretics or beta-adrenergic blocking agents Label . (drugbank.ca)
  • As a repurposed drug, prazosin is being investigated for the prevention of cytokine storm syndrome and complications of COVID-19 where it is thought to decrease cytokine dysregulation. (wikipedia.org)
  • If you have an allergy to prazosin or any other part of this drug. (mskcc.org)
  • 5 the experience of both the amount of buy prazosin drug therapy of various cellular functions. (yogachicago.com)
  • This is not a complete list of prazosin drug interactions. (rxwiki.com)
  • Stimulation of P-glycoprotein-mediated drug transport by prazosin and progesterone. (nih.gov)
  • Emphasis on cultural competency and ABCC8 genes, it is a drug-induced skin reaction should be related to assess the for the area under the amount of protein that limited health literacy is 2 to low baseline buy prazosin viral loads as those for 24 hours and Chinese populations. (secureserver.net)
  • prazosin is a topic covered in the Davis's Drug Guide . (unboundmedicine.com)
  • Nursing Central , nursing.unboundmedicine.com/nursingcentral/view/Davis-Drug-Guide/51629/all/prazosin. (unboundmedicine.com)
  • Generic Minipress is a name given to all medications that are identical to the brand-name drug with the same active substance, Prazosin. (rxshopmd.com)
  • The optimal time to buy Generic Minipress and start using it is when your doctor prescribes you Minipress, Vasoflex, Lentopres or other drug based on Prazosin. (rxshopmd.com)
  • You are hypersensitive to, or have had an allergic reaction to prazosin or to related medicines called quinazolines, or any of the ingredients listed at the end of this leaflet. (news-medical.net)
  • Do not take this mediction if you are allergic to prazosin or any ingredients of the medication. (medbroadcast.com)
  • Doctors advise against using Prazosin if you are allergic to any ingredient in it or if you are into modafinil. (onlinepharmadeals.com)
  • Prazosin works by relaxing the muscles in the walls of blood vessels and making it easier for blood to flow. (news-medical.net)
  • Prazosin is an alpha-blocker that blocks a chemical in the body, causing blood vessels and the muscles around the urethra to relax. (ab.ru)
  • Prazosin causes the blood vessels (veins and arteries) to relax and expand, which allows blood to pass more easily through them. (pharmacy-network.com)
  • Prazosin being alpha-adrenergic blocker seeks to relax the blood vessels and makes them expand. (onlinepharmadeals.com)
  • Store Prazosin at room temperature preferably between 20 to 25 degrees C. Always keep it in a cool dark place that is not directly exposed to sources of heat or moisture and sunlight. (onlinepharmadeals.com)
  • Store Prazosin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. (northern-pharmacy.com)
  • Generic Minipress is a term used for medications that have substance called Prazosin as their main component. (rxshopmd.com)
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  • Physicians prescribe prazosin, sold under the brand name of Minipress, to treat nightmares for post-traumatic stress disorder (PTSD). (verywellhealth.com)
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