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Related Concept Videos

CNS Depressants: Barbiturates and Benzodiazepines01:14

CNS Depressants: Barbiturates and Benzodiazepines

CNS depressants include drugs from the category of barbiturates and benzodiazepines. They are valuable medications for managing anxiety disorders and insomnia. Barbiturates, once used to induce and maintain sleep, have been replaced mainly by benzodiazepines due to barbiturate's toxicity, tolerance, and overdose risks. They interact with GABAA receptors, leading to sedation at low doses and potentially coma and death at higher doses. Phenobarbital, a long-acting barbiturate, possesses...
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Medications are typically administered to achieve therapeutic effects. Some drugs can modify an individual's mood and perception, frequently resulting in various enjoyable experiences. However, this can result in drug dependency, a condition marked by continuous drug use despite potential negative consequences. Drug dependency primarily falls into two categories: psychological and physical dependence. Psychological dependence occurs when the pleasurable feelings induced by the drug...
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Sedatives and hypnotics encompass a drug class that acts on the central nervous system (CNS) to alleviate anxiety, promote relaxation and induce sleep.These drugs function by amplifying the actions of the neurotransmitter γ-aminobutyric acid (GABA), resulting in reduced neuronal activity. Barbiturates, a subset of sedatives and hypnotics first synthesized in the late 1800s, are categorized into ultra-short, short, intermediate, and long-acting groups based on their duration of effect. A key...
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Drug dependence, abuse, and addiction are complex phenomena that can precipitate various abnormal states. Physical dependence refers to a state of pharmacological adaptation to a drug. This adaptation often results in tolerance—a reduced response to the drug after repeated administrations. When the drug use is abruptly stopped, withdrawal symptoms occur due to the body's need to readjust from the pharmacologically induced imbalance. However, tolerance and withdrawal symptoms do not necessarily...
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Ethanol, a clear colorless alcohol, has been consumed by humans for millennia, but its effects on the body are far from benign. At lower doses, it induces decreased inhibitions and loquaciousness, leading to its social appeal. However, it can cause severe consequences at higher doses, such as coma and respiratory depression, due to its zero-order elimination kinetics. Chronic ethanol abuse wreaks havoc on multiple organ systems, particularly the CNS and the liver. Abrupt cessation of ethanol...
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Benzodiazepines are a class of anxiolytic drugs known for their rapid efficacy and high therapeutic-to-lethal dose ratio, but with a potential risk of drug dependence. These drugs are lipophilic, allowing for rapid absorption after oral administration, eventually reaching the central nervous system (CNS). Once in the CNS, benzodiazepines bind to the allosteric site of the GABAA receptor. This binding enhances the inhibitory effects of the neurotransmitter GABA. By doing so, they prevent...

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Related Experiment Video

Updated: May 14, 2026

Chronic Intermittent Ethanol Vapor Exposure Paired with Two-Bottle Choice to Model Alcohol Use Disorder
05:12

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Published on: June 23, 2023

Phenibut dependence.

Andriy V Samokhvalov1, C Lindsay Paton-Gay, Kam Balchand

  • 1Centre for Addiction and Mental Health, Toronto, Ontario, Canada.

BMJ Case Reports
|February 9, 2013
PubMed
Summary
This summary is machine-generated.

Phenibut, a GABA agonist, can cause dependence and withdrawal symptoms when used for anxiety. A 9-week treatment substituting phenibut with baclofen successfully managed withdrawal and dependence.

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Area of Science:

  • Neuroscience
  • Psychiatry
  • Pharmacology

Background:

  • Phenibut, a gamma-aminobutyric acid (GABA) agonist, is used as an anxiolytic in Russia but is available as a supplement in Western countries.
  • It is increasingly used for self-medication of anxiety, insomnia, and alcohol cravings.

Observation:

  • A patient self-medicating with phenibut developed tolerance and significant withdrawal symptoms within 3-4 hours of last use.
  • The patient experienced functional impairment at work and home due to phenibut dependence.

Findings:

  • A 9-week treatment protocol gradually substituted phenibut with baclofen, a GABA agonist with similar properties.
  • This substitution and subsequent tapering of baclofen successfully managed the patient's phenibut dependence and withdrawal.

Implications:

  • This case highlights the potential for phenibut dependence and the challenges in managing withdrawal.
  • Baclofen can be an effective substitute for phenibut, facilitating a gradual taper and treatment of dependence.