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Receptors, Thyrotropin-Releasing Hormone
Signal transduction and hormone-dependent internalization of the thyrotropin-releasing hormone receptor in cells lacking Gq and G11. (1/143)
The thyrotropin-releasing hormone (TRH) receptor was expressed in embryonic fibroblasts from mice lacking the alpha subunits of Gq and G11 (Fq/11 cells) to determine whether G protein coupling is necessary for agonist-dependent receptor internalization. Neither TRH nor agonists acting on endogenous receptors increased intracellular calcium unless the cells were co-transfected with the alpha subunit of Gq. In contrast, temperature-dependent internalization of [3H]MeTRH in Fq/11 cells was the same whether Gqalpha was expressed or not. A rhodamine-labeled TRH analog and fluorescein-labeled transferrin co-localized in endocytic vesicles in Fq/11 cells, indicating that endocytosis took place via the normal clathrin pathway. Cotransfection with beta-arrestin or V53D beta-arrestin increased TRH-dependent receptor sequestration. Fq/11 cells were co-transfected with the TRH receptor and a green fluorescent protein (GFP)-beta-arrestin conjugate. GFP-beta-arrestin was uniformly distributed in the cytoplasm of untreated cells and quickly translocated to the periphery of the cells when TRH was added. A truncated TRH receptor that lacks potential phosphorylation sites in the cytoplasmic carboxyl terminus signaled but did not internalize or cause membrane localization of GFP-beta-arrestin. These results prove that calcium signaling by the TRH receptor requires coupling to a G protein in the Gq family, but TRH-dependent binding of beta-arrestin and sequestration do not. (+info)Role of the dorsomedial hypothalamus in mediating the response to benzodiazepines on trial 2 in the elevated plus-maze test of anxiety. (2/143)
Trial 2 in the elevated plus-maze provides an animal model of specific phobia (fear of heights). On this trial, rats no longer respond to benzodiazepines. The present experiment examined the role of the dorsomedial hypothalamus in mediating insensitivity to chlordiazepoxide on trial 2. Rats received a 5 min exposure to the maze, undrugged. Forty-eight hours later, rats injected with control infusions into the dorsomedial hypothalamus showed the usual lack of response to chlordiazepoxide (5 mg/kg, i.p.). However, those receiving lidocaine injections (40 micrograms/microliter in a volume of 0.2 microliter) in the dorsomedial hypothalamus (producing functional inactivation), immediately before trial 2, responded with an anxiolytic response to chlordiazepoxide, characterised by an increased percentage of time on the open arms and by an increased number of entries into, and time spent on, the distal portions of the open arms. Since the lidocaine injections were without anxiolytic effects, our results suggest that this region of the hypothalamus regulates the functional state of benzodiazepine receptors in other brain regions. (+info)Drug discrimination under a concurrent fixed-ratio fixed-ratio schedule. (3/143)
Pigeons were trained to discriminate 5.0 mg/kg pentobarbital from saline under a two-key concurrent fixed-ratio 10 fixed-ratio 40 schedule of food presentation, in which the fixed-ratio component with the lower response requirement was programmed to reinforce responding on one key after drug administration (pentobarbital-biased key) and on the other key after saline administration (saline-biased key). After responding stabilized, pigeons averaged 98% of their responses on the pentobarbital-biased key during training sessions preceded by pentobarbital, and they averaged 90% of their responses on the saline-biased key during training sessions preceded by saline. In test sessions preceded by doses of pentobarbital, chlordiazepoxide, or ethanol, pigeons switched from responding on the saline-biased key at low doses to responding on the pentobarbital-biased key at higher doses (the dose-response curve was quantal). High doses of phencyclidine produced responding on both keys, whereas pigeons responded almost exclusively on the saline-biased key after all doses of methamphetamine. These and previous experiments using concurrent reinforcement schedules to study drug discrimination illustrate that the schedule of reinforcement is an important determinant of the shape of dose-effect curves in drug-discrimination experiments. (+info)Outpatient detoxification of the addicted or alcoholic patient. (4/143)
Outpatient detoxification of patients with alcohol or other drug addiction is being increasingly undertaken. This type of management is appropriate for patients in stage I or stage II of withdrawal who have no significant comorbid conditions and have a support person willing to monitor their progress. Adequate dosages of appropriate substitute medications are important for successful detoxification. In addition, comorbid psychiatric, personality and medical disorders must be managed, and social and environmental concerns need to be addressed. By providing supportive, nonjudgmental, yet assertive care, the family physician can facilitate the best possible chance for a patient's successful recovery. (+info)The effect of dexamethasone pretreatment on chlordiazepoxide and oxazepam levels in rat plasma. (5/143)
The effect of dexamethasone pretreatment on the level of chlordiazepoxide and oxazepam was examined in the plasma of rats administered with 80 mg/kg of chlorodiazepoxide per os. The concentration of free chlordiazepoxide and unconjugated oxazepam was determined by HPLC method after solid-phase extraction. Pretreatment with dexamethasone significantly increased chlordiazepoxide plasma level 3, 6 and 12 hrs after ingestion, however increase of oxazepam concentration was not statistically significant. AUC 1-24 h after dexamethasone was elevated, for chlordiazepoxide and for oxazepam. (+info)Marijuana smoking and reduced pressure in human eyes: drug action or epiphenomenon? (6/143)
Normal pressure within the human eye was reduced after smoking a socially relevant dose of marijuana (12 mg. delta9-9-tetrahydrocannabinol), but only for light to moderate users who experienced a substantial "high" and a state of peaceful relaxation from the experimental dose. Analysis suggests an indirect effect of the drug associated with relaxation-a psychophysiologic state that can be produced by drug and nondrug means. (+info)Pregabalin may represent a novel class of anxiolytic agents with a broad spectrum of activity. (7/143)
The present study examines the effect of pregabalin (previously S-Isobutylgaba and CI-1008) in two distinct rat models of anxiety. Pregabalin binds with high affinity and selectivity to the alpha(2)delta subunit of voltage dependent calcium channels (VDCC). Its corresponding R-enantiomer (R-isobutylgaba) is approximately 10 fold weaker. Pregabalin dose-dependently induced anxiolytic-like effects in both the rat conflict test and elevated X-maze with respective minimum effective doses (MED) of 3 and 10 mg kg(-1). In contrast, R-isobutylgaba only showed activity at the highest dose of 100 mg kg(-1) in the conflict test. These data indicate that pregabalin may possess clinical utility as a novel anxiolytic agent and demonstrates the importance of the alpha(2)delta subunit of VDCC in the mediation of anxiety related behaviours. (+info)Repeated acquisition of response sequences: stimulus control and drugs. (8/143)
Pigeons obtained food by making four responses on three keys in a specified sequence, e.g., left, right, center, right. Under the "tandem-learning" condition, all three keys were the same color throughout the response sequence, and the sequence was changed from session to session. After total errors per session (overall accuracy) and within-session error reduction (learning) had stabilized, the effects of varying doses phenobarbital and chlordiazepoxide were assessed. For comparison, the drug tests were also conducted under a "tandem-performance" condition, in which the response sequence was the same from session to session, and under corresponding "chain-learning" and "chain-performance" conditions, where different colored keylights were associated with the response sequence. Under all four baseline conditions, the largest dose of each drug impaired overall accuracy. Under the two learning conditions, the error rate decreased across trials within each session, but the degree of negative acceleration was less in the drug sessions than in the control sessions. In contrast, under the two performance conditions, the error rate was relatively constant across trials, but was higher in the drug sessions than in the control sessions. Of the four baselines, the chain-learning condition was the most sensitive to the drug effects. (+info)The exact cause of alcohol withdrawal delirium is not fully understood, but it is thought to be related to changes in the levels of certain neurotransmitters in the brain, such as gamma-aminobutyric acid (GABA) and glutamate, which play a role in regulating the activity of nerve cells.
Alcohol withdrawal delirium can be diagnosed through a combination of physical examination, medical history, and laboratory tests such as bloodwork and imaging studies. Treatment typically involves supportive care, such as fluids, electrolytes, and oxygen, as well as medications to help manage symptoms and prevent complications. In severe cases, hospitalization may be necessary to ensure the person's safety.
Some of the most common signs and symptoms of alcohol withdrawal delirium include:
* Confusion and disorientation
* Agitation and aggression
* Hallucinations (visual or auditory)
* Seizures
* Changes in mental status, such as dementia or delusions
* Fever
* Tremors
* Sweating
* Nausea and vomiting
* Headache
* Muscle aches and pains
Alcohol withdrawal delirium can be a serious condition that requires prompt medical attention. It is important to seek medical help right away if you or someone you know is experiencing these symptoms, especially if they are severe or worsening over time.
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Amitriptyline / chlordiazepoxide Use During Pregnancy | Drugs.com
DailyMed - CHLORDIAZEPOXIDE HYDROCHLORIDE capsule
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Chlordiazepoxide: MedlinePlus Drug Information
MedlinePlus - Search Results for: Chlordiazepoxide
Chlordiazepoxide (Librium) - Uses, dosage, and side effects
Chlordiazepoxide - PubMed
Amitriptyline And Chlordiazepoxide (Limbitrol) - Side Effects, Interactions, Uses, Dosage, Warnings
Chlordiazepoxide HCl | API Products | Cambrex
chlordiazepoxide - PubChem Substance - NCBI
Getting Treatment for a Chlordiazepoxide Addiction - Project Know
Effects of dizocilpine, chlordiazepoxide, and scopolamine alone and in combination on a multiple-component, repeated...
Chlordiazepoxide Archives - Singapore Drugs Database
Sedative, Hypnotic, Anxiolytic Use Disorders Medication: Benzodiazepines, Benzodiazepine antagonist, Barbiturates,...
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Carbamazepine, Clonidine, Chlordiazepoxide의 알콜 금단 증상 치료효과 - 학지사ㆍ교보문고 스콜라
Etd | The effects of chlordiazepoxide and RO15-4513 on cocaine self-administration. | ID: m900nt552 | Hyrax
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Chapter 16: Functional Intestinal Disorders - NIDDK
What are benzos? - Caron Treatment Centers
Dissertation Archive | Department of Psychological and Brain Sciences | UMass Amherst
Librium1
- Depressants generally cause people to become sleepy, while relaxing their minds and bodies.The first and most common branded iteration of chlordiazepoxide is Librium. (projectknow.com)
Librax1
- The information above for Librax (Clidinium/Chlordiazepoxide) was provided to DoctorSolve.com by third parties. (doctorsolve.com)
Benzodiazepines4
- The use of benzodiazepines, including chlordiazepoxide hydrochloride capsules, exposes users to risks of abuse, misuse, and addiction, which can lead to overdose or death. (nih.gov)
- The continued use of benzodiazepines, including chlordiazepoxide hydrochloride capsules, may lead to clinically significant physical dependence. (nih.gov)
- Chlordiazepoxide is in a class of medications called benzodiazepines. (medlineplus.gov)
- As with other benzodiazepines, chlordiazepoxide is not associated with serum aminotransferase or alkaline phosphatase elevations during therapy, and clinically apparent liver injury from chlordiazepoxide has been reported but is rare. (nih.gov)
Hydrochloride14
- Before prescribing chlordiazepoxide hydrochloride capsules and throughout treatment, assess each patient's risk for abuse, misuse, and addiction (see WARNINGS ). (nih.gov)
- Abrupt discontinuation or rapid dosage reduction of chlordiazepoxide hydrochloride capsules after continued use may precipitate acute withdrawal reactions, which can be life-threatening. (nih.gov)
- To reduce the risk of withdrawal reactions, use a gradual taper to discontinue chlordiazepoxide hydrochloride capsules or reduce the dosage (see DOSAGE AND ADMINISTRATION and WARNINGS ). (nih.gov)
- Chlordiazepoxide hydrochloride, USP is the prototype for the benzodiazepine compounds. (nih.gov)
- Chlordiazepoxide hydrochloride, USP is among the safer of the effective psychopharmacologic compounds available, as demonstrated by extensive clinical evidence. (nih.gov)
- Chlordiazepoxide hydrochloride, USP is 7-chloro-2-(methylamino)-5-phenyl-3 H -1,4-benzodiazepine 4-oxide hydrochloride. (nih.gov)
- Chlordiazepoxide HCl/Clidinium Bromide combines in a single capsule formulation the antianxiety action of chlordiazepoxide hydrochloride and the anticholinergic/spasmolytic effects of clidinium bromide, both exclusive developments of Roche research. (nih.gov)
- Each Chlordiazepoxide HCl/Clidinium Bromide capsule contains 5 mg chlordiazepoxide hydrochloride and 2.5 mg clidinium bromide. (nih.gov)
- Chlordiazepoxide hydrochloride is a versatile, therapeutic agent of proven value for the relief of anxiety and tension. (nih.gov)
- Chlordiazepoxide hydrochloride has been studied extensively in many species of animals and these studies are suggestive of action on the limbic system of the brain, which recent evidence indicates is involved in emotional responses. (nih.gov)
- Chlordiazepoxide hydrochloride revealed a "taming" action with the elimination of fear and aggression. (nih.gov)
- The taming effect of chlordiazepoxide hydrochloride was further demonstrated in rats made vicious by lesions in the septal area of the brain. (nih.gov)
- The oral LD of single doses of chlordiazepoxide hydrochloride, calculated according to the method of Miller and Tainter, is 720 ± 51 mg/kg as determined in mice observed over a period of 5 days following dosage. (nih.gov)
- Reproduction studies in rats fed chlordiazepoxide hydrochloride, 10, 20 and 80 mg/kg daily, and bred through one or two matings showed no congenital anomalies, nor were there adverse effects on lactation of the dams or growth of the newborn. (nih.gov)
Benzodiazepine2
- Chlordiazepoxide is an orally available benzodiazepine used for therapy of anxiety disorders and alcohol withdrawal syndromes. (nih.gov)
- Chlordiazepoxide is a benzodiazepine (ben-zoe-dye-AZE-eh-peen). (everydayhealth.com)
Amitriptyline9
- Animal studies with the combination amitriptyline-chlordiazepoxide have not been reported. (drugs.com)
- Amitriptyline-Chlordiazepoxide (amitriptyline-chlordiazepoxide). (drugs.com)
- Amitriptyline and chlordiazepoxide is a combination medicine used to treat moderate to severe depression and anxiety. (everydayhealth.com)
- Amitriptyline and chlordiazepoxide may also be used for purposes not listed in this medication guide. (everydayhealth.com)
- What is Amitriptyline And Chlordiazepoxide (Limbitrol) used for? (everydayhealth.com)
- Do not use amitriptyline and chlordiazepoxide if you have used an MAO inhibitor in the past 14 days. (everydayhealth.com)
- Amitriptyline and chlordiazepoxide may harm an unborn baby. (everydayhealth.com)
- If you use amitriptyline and chlordiazepoxide while you are pregnant, your baby could become dependent on the drug. (everydayhealth.com)
- Amitriptyline and chlordiazepoxide can slow or stop your breathing, especially if you have recently used an opioid medication, alcohol, or other drugs that can slow your breathing. (everydayhealth.com)
Doses3
- Animal studies with chlordiazepoxide have revealed evidence of decreased viability and body weight at maternally toxic doses. (drugs.com)
- Chlordiazepoxide may cause a physical dependence (a condition in which unpleasant physical symptoms occur if a medication is suddenly stopped or taken in smaller doses), especially if you take it for several days to several weeks. (medlineplus.gov)
- Furthermore, low doses of chlordiazepoxide when given together with dizocilpine (0.1 mg/kg) blocked the detrimental effects typically caused by that dizocilpine dose. (uncg.edu)
Anxiety4
- Chlordiazepoxide is used to relieve anxiety and to control agitation caused by alcohol withdrawal. (medlineplus.gov)
- Chlordiazepoxide is a prescription medicine used to treat certain anxiety disorders and symptoms of alcohol withdrawal. (nih.gov)
- Chlordiazepoxide is a depressant that is primarily prescribed for the short-term treatment of severe anxiety and to ease the withdrawal symptoms of alcoholics in detox. (projectknow.com)
- Chlordiazepoxide is only recommended for treatment of anxiety over the course of two to four weeks, so it is not a solution for long-term treatment of the disorder. (projectknow.com)
Withdrawal2
- Stopping chlordiazepoxide suddenly can worsen your condition and cause withdrawal symptoms that may last for several weeks to more than 12 months. (medlineplus.gov)
- Supervised withdrawal through a chlordiazepoxide detox program may be necessary to safely discontinue the use of the drug. (projectknow.com)
Drugs5
- Drinking alcohol or using street drugs during your treatment with chlordiazepoxide also increases the risk that you will experience these serious, life-threatening side effects. (medlineplus.gov)
- Even though the effects of chlordiazepoxide addiction are not as physically debilitating as the effects of other drugs in this class, many people on chlordiazepoxide will benefit from professional help to address the root causes of addictive behavior. (projectknow.com)
- Chlordiazepoxide is one of the least potent drugs in its class, so adults abusing the drug do not typically take it in isolation. (projectknow.com)
- Many adults combine chlordiazepoxide with other drugs to amplify or prolong certain intoxicating effects or alleviate the negative side effects of more potent drugs. (projectknow.com)
- It can also easily lead to the abuse of other drugs when the chlordiazepoxide user develops a tolerance for the high the drug produces. (projectknow.com)
Meprobamate1
- An increased risk of congenital malformations associated with theuse of minor tranquilizers (meprobamate, chlordiazepoxide anddiazepam) during the first trimester of pregnancy has beensuggested in several studies. (nih.gov)
Antianxiety1
- Chlordiazepoxide HCl has antianxiety, sedative, appetite-stimulating and weak analgesic actions. (nih.gov)
Overdose1
- Unfortunately, chlordiazepoxide abuse can easily lead to addiction and overdose, particularly in the young. (projectknow.com)
Metabolites2
GABA1
- The present study investigated the effects of the NMDA receptor antagonist, dizocilpine, the GABA agonist, chlordiazepoxide, and ACh antagonist, scopolamine, given alone and in dizocilpine-chlordiazepoxide and scopolamine-chlordiazepoxide combinations, using a within-subject, repeatedacquisition and performance procedure adapted to the Morris Swim Task. (uncg.edu)
Capsule1
- Chlordiazepoxide comes as a tablet and capsule to take by mouth. (medlineplus.gov)
Sedation2
- Chlordiazepoxide may increase the risk of serious or life-threatening breathing problems, sedation, or coma if used along with certain medications. (medlineplus.gov)
- If chlordiazepoxide is used, monitor the infant for sedation, poor feeding and poor weight gain. (nih.gov)
Dosage1
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Rats1
- 18. Corticotropin-releasing factor potentiates acoustic startle in rats: blockade by chlordiazepoxide. (nih.gov)
Medication1
- Author Comprar LIV 52 Generico En Farmacia: denis31r Inactive User .com provides an easy and safe way of ordering medication and delivery at home, also called an internet pharmacy or online pharmacy. (terminally-incoherent.com)
Medications1
- If you take chlordiazepoxide with any of these medications and you develop any of the following symptoms, call your doctor immediately or seek emergency medical care immediately: unusual dizziness, lightheadedness, extreme sleepiness, slowed or difficult breathing, or unresponsiveness. (medlineplus.gov)
Habit3
- Chlordiazepoxide may be habit forming. (medlineplus.gov)
- Chlordiazepoxide addiction treatment can help a person who has been abusing the drug kick the habit and live a healthy, sober life . (projectknow.com)
- Chlordiazepoxide addiction can be a particularly hard habit to kick, because there are often other addictions that the person is grappling with simultaneously. (projectknow.com)
Treat2
- Chlordiazepoxide is also used to treat irritable bowel syndrome. (medlineplus.gov)
- Young people often treat chlordiazepoxide as a manageable introduction to the illicit drug scene. (projectknow.com)
Treatment2
- Studies have shown that relatively few people with a legitimate prescription for chlordiazepoxide abuse the drug in the ordinary course of treatment. (projectknow.com)
- Chlordiazepoxide addiction treatment tends to focus on those people who have become addicted to the drug through illicit use. (projectknow.com)
Drug2
- An individual can develop a physical dependency on chlordiazepoxide, however, even when the drug is used in the short-term and as prescribed. (projectknow.com)
- Chlordiazepoxide is regulated in the United States as a Schedule IV drug under the Controlled Substances Act. (projectknow.com)
Prescription1
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Physical1
- Any abuse of chlordiazepoxide for recreational purposes can also result in physical dependency, tolerance , and addiction. (projectknow.com)