The L-Isomer of bunolol.
A beta-adrenergic antagonist effective for both beta-1 and beta-2 receptors. It is used as an antiarrhythmic, antihypertensive, and antiglaucoma agent.
A cardioselective beta-1-adrenergic antagonist with no partial agonist activity.
A beta-adrenergic antagonist similar in action to PROPRANOLOL. The levo-isomer is the more active. Timolol has been proposed as an antihypertensive, antiarrhythmic, antiangina, and antiglaucoma agent. It is also used in the treatment of MIGRAINE DISORDERS and tremor.
A condition in which the intraocular pressure is elevated above normal and which may lead to glaucoma.
The pressure of the fluids in the eye.
Inflammation of the eyelids.
Works containing information articles on subjects in every field of knowledge, usually arranged in alphabetical order, or a similar work limited to a special field or subject. (From The ALA Glossary of Library and Information Science, 1983)
Conjunctivitis is an inflammation or infection of the conjunctiva, the transparent membrane that lines the inner surface of the eyelids and covers the white part of the eye, resulting in symptoms such as redness, swelling, itching, burning, discharge, and increased sensitivity to light.
Abnormally low BLOOD PRESSURE that can result in inadequate blood flow to the brain and other vital organs. Common symptom is DIZZINESS but greater negative impacts on the body occur when there is prolonged depravation of oxygen and nutrients.
A significant drop in BLOOD PRESSURE after assuming a standing position. Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. Symptoms generally include DIZZINESS, blurred vision, and SYNCOPE.
A tubular duct that conveys TEARS from the LACRIMAL GLAND to the nose.

Betaxolol, a beta(1)-adrenoceptor antagonist, reduces Na(+) influx into cortical synaptosomes by direct interaction with Na(+) channels: comparison with other beta-adrenoceptor antagonists. (1/15)

Betaxolol, a beta(1)-adrenoceptor antagonist used for the treatment of glaucoma, is known to be neuroprotective in paradigms of ischaemia/excitotoxicity. In this study, we examined whether betaxolol and other beta-adrenoceptor antagonists interact directly with neurotoxin binding to sites 1 and 2 of the voltage-sensitive sodium channel (Na(+) channel) in rat cerebrocortical synaptosomes. Betaxolol inhibited specific [(3)H]-batrachotoxinin-A 20-alpha-benzoate ([(3)H]-BTX-B) binding to neurotoxin site 2 in a concentration-dependent manner with an IC(50) value of 9.8 microM. Comparison of all the beta-adrenoceptor antagonists tested revealed a potency order of propranolol>betaxolol approximately levobetaxolol>levobunolol approximately carteolol>/=timolol>atenolol. None of the drugs caused a significant inhibition of [(3)H]-saxitoxin binding to neurotoxin receptor site 1, even at concentrations as high as 250 microM. Saturation experiments showed that betaxolol increased the K(D) of [(3)H]-BTX-B binding but had no effect on the B(max). The association kinetics of [(3)H]-BTX-B were unaffected by betaxolol, but the drug significantly accelerated the dissociation rate of the radioligand. These findings argue for a competitive, indirect, allosteric mode of inhibition of [(3)H]-BTX-B binding by betaxolol. Betaxolol inhibited veratridine-stimulated Na(+) influx in rat cortical synaptosomes with an IC(50) value of 28. 3 microM. Carteolol, levobunolol, timolol and atenolol were significantly less effective than betaxolol at reducing veratridine-evoked Na(+) influx. The ability of betaxolol to interact with neurotoxin site 2 of the Na(+) channel and inhibit Na(+) influx may have a role in its neuroprotective action in paradigms of excitotoxicity/ischaemia and in its therapeutic effect in glaucoma.  (+info)

Noninvasive assessment of aqueous humor turnover in the mouse eye. (2/15)

PURPOSE: To develop a noninvasive test for monitoring changes in aqueous humor turnover in the mouse eye. METHODS: After topical instillation of fluorescein, the rate of decay of fluorescence from aqueous humor and cornea was monitored in Black Swiss, C57 Bl6, and DBA 2J mice with a microscope equipped with epifluorescence and a charge-coupled device (CCD) camera. RESULTS: The rate of decay of fluorescence was identical in right and left eyes over an approximately 70-minute measurement period. The rate of decay was similar in normal mice aged 2 and 18 months. Pilocarpine and latanoprost, known to enhance aqueous humor outflow in humans, accelerated the decay of fluorescence. Levobunolol, known to inhibit aqueous humor inflow in humans, slowed decay. Dimethylamiloride, an inhibitor of the Na(+),H(+) exchanger that is known to act on cultured cells of both the ciliary epithelium and trabecular meshwork and to lower mouse intraocular pressure (IOP), enhanced decay. DBA 2J mice, in which secondary glaucoma develops, displayed a slower decay of fluorescence at 18 months of age than age-matched unaffected animals. CONCLUSIONS: Monitoring decay of fluorescence provides a noninvasive index of aqueous humor dynamics in the mouse eye that facilitates study of ocular hypotensive drugs and mouse models of glaucoma. Coupled with knowledge of IOP, it permits semiquantitative conclusions about the relative roles of aqueous humor inflow and outflow in conditions with altered IOP. Based on this approach, dimethylamiloride appears to lower mouse IOP primarily by enhancing outflow of aqueous humor.  (+info)

Effects of timolol, betaxolol, and levobunolol on human tenon's fibroblasts in tissue culture. (3/15)

Evidence has been found suggesting that long-term therapy with topical antiglaucoma medications may decrease the success of glaucoma filtering surgery. To investigate this question further, the antiproliferative effects of the preservative benzalkonium chloride and three pure and commercially available beta-adrenergic antagonist preparations (timolol, betaxolol, and levobunolol) were studied on tissue cultures of human Tenon's capsule fibroblasts. Each drug preparation was tested on three different cell lines. Fibroblast growth was measured with tritiated thymidine uptake and hexosaminidase assays. Trypan blue uptake was used to assess cell viability microscopically. The commercially available preparations containing benzalkonium chloride and those of betaxolol and levobunolol without the preservative had similar inhibitory doses for 50% of cells. The timolol preparation without preservative was significantly less toxic than its commercially available one. The three tested beta-adrenergic blockers did not stimulate fibroblast proliferation directly in this in vitro model. Even when the cultures were washed free of the drugs, growth continued to be suppressed, suggesting that the inhibition was not reversible. An increase in fibroblasts and inflammatory cells after long-term antiglaucoma medical therapy thus may be caused not by a direct stimulation of cell proliferation but by chronic inflammation from the irritating effects of antiglaucoma medications and/or their preservatives.  (+info)

A comparative study of the effects of OPC-1085 and propranolol on isolated guinea pig atrium. (4/15)

Effects of a newly synthesized beta-blocker, 5-(3-tert-butylamino-2-hydroxy) propoxy-3,4-dihydrocarbostyril (OPC-1085) were compared with those of propranolol. OPC-1085 had a potency about 3 times greater than that of propranolol in blocking the positive inotropic and chronotropic effects of isoprenaline on the isolated guinea pig atrium. At a concentration of over 3 X 10(-5) M OPC-1085 produced negative inotropic and chronotropic effects. However, these effects were about 10 times weaker than those of propranolol. Suppressing effects on the rate of rise and on the maximum driving frequency of action potentials were also more than 10 times less than those of propranolol. There was almost no change in the action potential of vagus nerve after a 10 min treatment with OPC-1085 (10(-5) M), while the action potential was reduced to 60-70% with propranolol (10(-5) M).  (+info)

Effects of anti-glaucoma drugs on resistive index of the medial long posterior ciliary artery using color Doppler imaging in Beagle dogs. (5/15)

Color Doppler imaging (CDI) was carried out to evaluate the effects of anti-glaucoma drugs on ophthalmic circulation using CDI-derived resistive index (RI) values. CDI was performed on nine Beagle dogs, and RI values were calculated for the medial long posterior ciliary artery before and after the administration of anti-glaucoma drugs. A significant increase in RI values was found after topical administration of levobunolol (p < 0.05) or dipivefrin (p < 0.05). Pilocarpine showed no effects on RI values after topical administration. The results suggest that some anti-glaucoma drugs could affect ophthalmic blood flow.  (+info)

Effect of a beta-blocker on altered body position: induced ocular hypertension. (6/15)

The intraocular pressures (IOP) were measured in both eyes of 25 healthy volunteers in various body positions. One eye was pretreated with levobunolol 0.5% or placebo applied in a masked, randomised fashion, while the other served as control. IOP changes in response to levobunolol and to changes in position were significant (p less than 0.0001). However, pressure rises relative to position were not significantly different in eyes treated with drug vs placebo. Levobunolol did not alter relative changes in IOP from changes in body position. However, the overall lowering effect may offer some protection to patients with glaucoma.  (+info)

Levobunolol and metipranolol: comparative ocular hypotensive efficacy, safety, and comfort. (7/15)

Topical levobunolol 0.5% was compared with topical metipranolol 0.6% for efficacy, safety, and comfort in 46 patients with open angle glaucoma or ocular hypertension. The study was of parallel design, randomised, double-masked, and of three months' duration. After a washout interval the study medications were instilled twice daily in both eyes. The overall mean decrease in intraocular pressure (IOP) was approximately 7 mmHg in both groups. More than 90% of patients in both groups successfully completed the study. Both agents caused slight decreases in heart rate and blood pressure. More complaints of burning and stinging were reported in the metipranolol group than in the levobunolol group. This three-month, 46-patient study showed levobunolol 0.5% and metipranolol 0.6% to be similarly effective ocular hypotensive agents.  (+info)

Levobunolol compared with timolol: a four-year study. (8/15)

Fifty-one patients with raised intraocular pressure (IOP) were treated for up to four years with one of three ophthalmic solutions: 0.5% levobunolol, 1% levobunolol, or 0.5% timolol. The study was conducted as a double-masked, randomised trial in which medications were administered twice daily to both eyes. Levobunolol and timolol were equally effective in reducing overall mean IOP; reductions were greater than 8.8 mmHg in all three treatment groups. The study showed levobunolol to be as safe and effective as timolol in the long-term control of raised IOP.  (+info)

Levobunolol is a non-selective beta blocker used in the treatment of glaucoma and high blood pressure. It works by reducing the production of aqueous humor within the eye, thereby decreasing intraocular pressure (IOP). Levobunolol is available as an ophthalmic solution for topical application.

The medical definition of Levobunolol is:

A synthetic, non-selective beta-adrenergic antagonist with membrane-stabilizing activity and a vasodilating effect. It is used in the form of its hydrochloride salt as an ophthalmic solution for the treatment of glaucoma, reducing intraocular pressure by decreasing aqueous humor production. The drug has a prolonged action due to its poor solubility and slow absorption through the cornea.

Metipranolol is a non-selective beta blocker, which is a type of medication that works by blocking the effects of certain hormones like adrenaline (epinephrine) on the heart and blood vessels. This results in a slower heart rate, decreased force of heart contractions, and reduced blood vessel contraction, leading to lower blood pressure and improved oxygen supply to the heart.

Metipranolol is primarily used to treat open-angle glaucoma and ocular hypertension by reducing the production of fluid within the eye, thereby decreasing intraocular pressure. It is available as an ophthalmic solution for topical application.

It's important to note that systemic absorption of metipranolol can occur after ophthalmic use, and it may cause systemic side effects such as bradycardia (slow heart rate), hypotension (low blood pressure), and bronchospasm (narrowing of the airways) in some individuals. Therefore, patients should be monitored for potential systemic side effects during treatment with metipranolol.

Betaxolol is a selective beta-1 adrenergic receptor blocker, which is primarily used in the treatment of glaucoma. It works by reducing the production of aqueous humor inside the eye, thereby decreasing the intraocular pressure (IOP). This can help prevent optic nerve damage and vision loss associated with glaucoma.

Betaxolol ophthalmic solution is usually administered as eyedrops, one or two times per day. Common side effects of betaxolol may include stinging or burning in the eyes, blurred vision, headache, and a bitter taste in the mouth. Serious side effects are rare but can include allergic reactions, slow heart rate, and difficulty breathing.

It is important to note that betaxolol should not be used by people with certain medical conditions, such as severe heart block, uncontrolled heart failure, or asthma. Additionally, it may interact with other medications, so it is essential to inform your healthcare provider about all the drugs you are taking before starting treatment with betaxolol.

Timolol is a non-selective beta blocker drug that is primarily used to treat hypertension, angina pectoris, and glaucoma. It works by blocking the action of certain hormones such as epinephrine (adrenaline) on the heart and blood vessels, which helps to lower heart rate, reduce the force of heart muscle contraction, and decrease blood vessel constriction. These effects can help to lower blood pressure, reduce the workload on the heart, and improve oxygen supply to the heart muscle. In glaucoma treatment, timolol reduces the production of aqueous humor in the eye, thereby decreasing intraocular pressure.

The medical definition of Timolol is:

Timolol (tim-oh-lol) is a beta-adrenergic receptor antagonist used to treat hypertension, angina pectoris, and glaucoma. It works by blocking the action of epinephrine on the heart and blood vessels, which results in decreased heart rate, reduced force of heart muscle contraction, and decreased blood vessel constriction. In glaucoma treatment, timolol reduces aqueous humor production, thereby decreasing intraocular pressure. Timolol is available as an oral tablet, solution for injection, and ophthalmic solution.

Ocular hypertension is a medical condition characterized by elevated pressure within the eye (intraocular pressure or IOP), which is higher than normal but not necessarily high enough to cause any visible damage to the optic nerve or visual field loss. It serves as a significant risk factor for developing glaucoma, a sight-threatening disease.

The normal range of intraocular pressure is typically between 10-21 mmHg (millimeters of mercury). Ocular hypertension is often defined as an IOP consistently above 21 mmHg, although some studies suggest that even pressures between 22-30 mmHg may not cause damage in all individuals. Regular monitoring and follow-up with an ophthalmologist are essential for people diagnosed with ocular hypertension to ensure early detection and management of any potential glaucomatous changes. Treatment options include medications, laser therapy, or surgery to lower the IOP and reduce the risk of glaucoma onset.

Intraocular pressure (IOP) is the fluid pressure within the eye, specifically within the anterior chamber, which is the space between the cornea and the iris. It is measured in millimeters of mercury (mmHg). The aqueous humor, a clear fluid that fills the anterior chamber, is constantly produced and drained, maintaining a balance that determines the IOP. Normal IOP ranges from 10-21 mmHg, with average values around 15-16 mmHg. Elevated IOP is a key risk factor for glaucoma, a group of eye conditions that can lead to optic nerve damage and vision loss if not treated promptly and effectively. Regular monitoring of IOP is essential in diagnosing and managing glaucoma and other ocular health issues.

Blepharitis is a common inflammatory condition that affects the eyelids, specifically the eyelash follicles and the edges of the eyelids (called the "eyelid margins"). It can cause symptoms such as redness, swelling, itching, burning, and a crusty or flaky buildup on the lashes. Blepharitis can be caused by a variety of factors, including bacterial infection, skin disorders like seborrheic dermatitis or rosacea, and meibomian gland dysfunction. It is often a chronic condition that requires ongoing treatment to manage symptoms and prevent recurrence.

An encyclopedia is a comprehensive reference work containing articles on various topics, usually arranged in alphabetical order. In the context of medicine, a medical encyclopedia is a collection of articles that provide information about a wide range of medical topics, including diseases and conditions, treatments, tests, procedures, and anatomy and physiology. Medical encyclopedias may be published in print or electronic formats and are often used as a starting point for researching medical topics. They can provide reliable and accurate information on medical subjects, making them useful resources for healthcare professionals, students, and patients alike. Some well-known examples of medical encyclopedias include the Merck Manual and the Stedman's Medical Dictionary.

Conjunctivitis is an inflammation or infection of the conjunctiva, a thin, clear membrane that covers the inner surface of the eyelids and the outer surface of the eye. The condition can cause redness, itching, burning, tearing, discomfort, and a gritty feeling in the eyes. It can also result in a discharge that can be clear, yellow, or greenish.

Conjunctivitis can have various causes, including bacterial or viral infections, allergies, irritants (such as smoke, chlorine, or contact lens solutions), and underlying medical conditions (like dry eye or autoimmune disorders). Treatment depends on the cause of the condition but may include antibiotics, antihistamines, anti-inflammatory medications, or warm compresses.

It is essential to maintain good hygiene practices, like washing hands frequently and avoiding touching or rubbing the eyes, to prevent spreading conjunctivitis to others. If you suspect you have conjunctivitis, it's recommended that you consult an eye care professional for a proper diagnosis and treatment plan.

Hypotension is a medical term that refers to abnormally low blood pressure, usually defined as a systolic blood pressure less than 90 millimeters of mercury (mm Hg) or a diastolic blood pressure less than 60 mm Hg. Blood pressure is the force exerted by the blood against the walls of the blood vessels as the heart pumps blood.

Hypotension can cause symptoms such as dizziness, lightheadedness, weakness, and fainting, especially when standing up suddenly. In severe cases, hypotension can lead to shock, which is a life-threatening condition characterized by multiple organ failure due to inadequate blood flow.

Hypotension can be caused by various factors, including certain medications, medical conditions such as heart disease, endocrine disorders, and dehydration. It is important to seek medical attention if you experience symptoms of hypotension, as it can indicate an underlying health issue that requires treatment.

Orthostatic hypotension is a type of low blood pressure that occurs when you stand up from a sitting or lying position. The drop in blood pressure causes a brief period of lightheadedness or dizziness, and can even cause fainting in some cases. This condition is also known as postural hypotension.

Orthostatic hypotension is caused by a rapid decrease in blood pressure when you stand up, which reduces the amount of blood that reaches your brain. Normally, when you stand up, your body compensates for this by increasing your heart rate and constricting blood vessels to maintain blood pressure. However, if these mechanisms fail or are impaired, orthostatic hypotension can occur.

Orthostatic hypotension is more common in older adults, but it can also affect younger people who have certain medical conditions or take certain medications. Some of the risk factors for orthostatic hypotension include dehydration, prolonged bed rest, pregnancy, diabetes, heart disease, Parkinson's disease, and certain neurological disorders.

If you experience symptoms of orthostatic hypotension, it is important to seek medical attention. Your healthcare provider can perform tests to determine the underlying cause of your symptoms and recommend appropriate treatment options. Treatment may include lifestyle changes, such as increasing fluid intake, avoiding alcohol and caffeine, and gradually changing positions from lying down or sitting to standing up. In some cases, medication may be necessary to manage orthostatic hypotension.

The nasolacrimal duct is a medical term that refers to the passageway responsible for draining tears from the eye into the nasal cavity. This narrow tube, which is about 12 millimeters long, begins at the inner corner of the eyelid (near the nose) and ends in the inferior meatus of the nasal cavity, close to the inferior turbinate.

The nasolacrimal duct is part of the nasolacrimal system, which includes the puncta (small openings at the inner corner of the eyelids), canaliculi (tiny channels that connect the puncta to the nasolacrimal sac), and the nasolacrimal sac (a small pouch-like structure located between the eye and the nose).

The primary function of the nasolacrimal duct is to help maintain a healthy ocular surface by draining tears, which contain waste products, debris, and pathogens accumulated on the surface of the eye. The continuous flow of tears through the nasolacrimal duct also helps prevent bacterial growth and potential infections.

In some cases, the nasolacrimal duct can become obstructed due to various factors such as age-related changes, inflammation, or congenital abnormalities. This condition, known as nasolacrimal duct obstruction (NLDO), may result in watery eyes, discomfort, and an increased risk of eye infections. In severe cases, medical intervention or surgical procedures might be necessary to restore proper tear drainage.

Levobunolol is the pure L-enantiomer of bunolol and has more than 60 times the pharmacological activity of D-bunolol. It is ... Levobunolol is not useful for the treatment of closed-angle glaucoma. The most common side effect is eye irritation felt as ... Levobunolol is a non-cardioselective beta blocker, that is, it blocks beta-1 receptors as well as beta-2 receptors. The latter ... Levobunolol (trade names AKBeta, Betagan, Vistagan, among others) is a non-selective beta blocker. It is used topically in the ...
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Levobunolol belongs to the class of medications known as beta-blockers. Levobunolol is used to control intraocular (eye) ... The recommended dose of levobunolol eye drops is 1 drop of levobunolol 0.5% once or twice a day in the affected eye(s). Doses ... Levobunolol belongs to the class of medications known as beta-blockers. Levobunolol is used to control intraocular (eye) ... Levobunolol is no longer being manufactured for sale in Canada and is no longer available under any brand names. This article ...
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Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.. Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.. ...
Detailed drug Information for Acnex Topical. Includes common brand names, drug descriptions, warnings, side effects and dosing information.
Using this medicine while you are pregnant can harm your unborn baby. Use an effective form of birth control to keep from getting pregnant. If you think you have become pregnant while using the medicine, tell your doctor right away. Do not use this medicine if you are also taking any of the following medicines: boceprevir (Victrelis®), cobicistat-containing products (Stribild®), cyclosporine (Gengraf®, Neoral®, Sandimmune®), danazol (Danocrine®), gemfibrozil (Lopid®), nefazodone (Serzone®), telaprevir (Incivek®), certain antibiotics (such as clarithromycin, erythromycin, itraconazole, ketoconazole, posaconazole, telithromycin, voriconazole, Nizoral®), or medicines to treat HIV/AIDS (such as atazanavir, indinavir, nelfinavir, ritonavir, saquinavir, tipranavir, Crixivan®, Kaletra®, Lexiva®, Norvir®, Prezista®, Reyataz®). Using these medicines together with sitagliptin and simvastatin combination may increase your risk of muscle injury and could result in kidney problems. Chinese ...
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Generic drug name: levobunolol (lev o BEWN o lole) Brand name(s): BETAGAN GENERIC: available FAMILIES: Drugs for Glaucoma, Beta ... Levobunolol and timolol can decrease lung function by 30 percent, an adverse effect not seen as much with use of betaxolol.[3] ... Betaxolol (BETOPTIC, BETOPTIC S), levobunolol (BETAGAN) and timolol (TIMOPTIC) belong to the beta-blocker family of drugs. When ... Betaxolol (BETOPTIC, BETOPTIC S), levobunolol (BETAGAN) and timolol (TIMOPTIC) belong to the beta-blocker family of drugs. When ...
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In motor sport as in other sports, anti-doping is essential. And in a sense, it is perhaps even more crucial in our sport, in that it is not only a matter of equity, ethics and health, but also a question of safety. By using any substance that can alter judgment and reactions, a driver may indeed put his/her life and the lives of others in danger.. This is why the FIA is committed to such great efforts in preventing and fighting doping, and also why it became a Signatory to the World Anti-Doping Code in December 2010, thus joining the family of the major international sporting federations.. Education and prevention is our priority. The Race True e-learning programme (click here to access), including a course and a quiz, was launched in 2012 and is available in 7 languages (soon more). The success of this awareness-raising campaign relies on our National Federations who are actively participating in ever-growing numbers.. Testing, and when necessary sanctioning, do, nevertheless, remain key ...
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