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Related Concept Videos

Sedatives and Hypnotics Drugs: Barbiturates01:20

Sedatives and Hypnotics Drugs: Barbiturates

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...
Sedatives and Hypnotics Drugs: Miscellaneous Agents01:17

Sedatives and Hypnotics Drugs: Miscellaneous Agents

Sedatives and hypnotics encompass a wide range of substances, each with its unique mechanism of action, uses, and potential adverse effects.
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Sedatives and Hypnotics Drugs: Benzodiazepines01:19

Sedatives and Hypnotics Drugs: Benzodiazepines

Benzodiazepines have both sedative and hypnotic properties. They include compounds such as diazepam (Valium) and alprazolam (Xanax). Structurally, their cores are similar, consisting of the fusion of a benzene ring and a diazepine ring, but they share a common mechanism of action in the central nervous system (CNS).
Benzodiazepines work by enhancing the effects of the inhibitory neurotransmitter GABA. They bind to the GABAA receptor, increasing its affinity for GABA, which opens chloride...
Anxiolytic Drugs: Benzodiazepines and Buspirone01:29

Anxiolytic Drugs: Benzodiazepines and Buspirone

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...
Synthesis and Regulation of Thyroid Hormones01:20

Synthesis and Regulation of Thyroid Hormones

Low blood levels of the thyroid hormones — triiodothyronine (T3) and thyroxine (T4) — signal the hypothalamus to release the thyrotropin-releasing hormone (TRH). TRH then reaches the pituitary gland and stimulates the release of thyroid-stimulating hormone(TSH) into the bloodstream.
Upon reaching the thyroid gland, TSH stimulates the follicular cells' active uptake of iodide ions from the blood. The ions diffuse to the apical surface of the cells and are oxidized to iodine. The iodine is then...
Sedatives and Hypnotics: Overview01:23

Sedatives and Hypnotics: Overview

Sedatives are drugs that alleviate anxiety, while hypnotics induce sleep. Both classes of medication suppress neuronal activity, leading to a calming effect for sedatives and facilitating sleep for hypnotics.
Sedative-hypnotics are categorized into barbiturates, benzodiazepines (BZDs), and non-benzodiazepines or Z-drugs. These drugs work by suppressing central nervous system activity, and this suppression is dose-dependent. Older sedative medications, like barbiturates, follow a linear curve in...

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Related Experiment Video

Updated: Jul 2, 2026

In vivo Characterization of Endocrine Disrupting Chemical Effects via Thyroid Hormone Action Indicator Mouse
04:14

In vivo Characterization of Endocrine Disrupting Chemical Effects via Thyroid Hormone Action Indicator Mouse

Published on: October 6, 2023

Benzofuran derivatives and the thyroid.

T S Han1, G R Williams, M P J Vanderpump

  • 1Department of Endocrinology, Royal Free and University College Medical School, Royal Free Hospital, Hampstead, London NW3 2QG, UK.

Clinical Endocrinology
|August 30, 2008
PubMed
Summary

Amiodarone, a common anti-arrhythmic drug, can cause thyroid dysfunction due to its iodine content. Dronedarone, a related drug, offers similar anti-arrhythmic benefits with fewer thyroid-related side effects.

Related Experiment Videos

Last Updated: Jul 2, 2026

In vivo Characterization of Endocrine Disrupting Chemical Effects via Thyroid Hormone Action Indicator Mouse
04:14

In vivo Characterization of Endocrine Disrupting Chemical Effects via Thyroid Hormone Action Indicator Mouse

Published on: October 6, 2023

Area of Science:

  • Pharmacology
  • Endocrinology
  • Biochemistry

Background:

  • Amiodarone is a widely used anti-arrhythmic medication with significant thyroid-related adverse effects.
  • Thyroid dysfunction is a common and challenging complication of amiodarone therapy.
  • Benzofuran derivatives, like amiodarone and dronedarone, are key in treating tachyarrhythmias.

Purpose of the Study:

  • To review the biochemistry and pharmacology of benzofuran derivatives, focusing on their effects on thyroid function.
  • To discuss the mechanisms underlying amiodarone-induced thyroid disorders.
  • To suggest management strategies for amiodarone-induced hypothyroidism and thyrotoxicosis.

Main Methods:

  • Literature review of benzofuran derivatives, amiodarone, and dronedarone.
  • Analysis of pharmacological and biochemical mechanisms of action.
  • Evaluation of clinical data on thyroid dysfunction associated with these drugs.

Main Results:

  • Amiodarone's high iodine content and inherent drug effects contribute to thyroid dysfunction.
  • Dronedarone, a non-iodinated analog, exhibits anti-arrhythmic properties with a lower risk of thyroid toxicity.
  • Recommendations for managing amiodarone-induced thyroid disorders are provided.

Conclusions:

  • Dronedarone may serve as a safer alternative to amiodarone for patients at risk of thyroid dysfunction.
  • While less potent, dronedarone's reduced thyroid toxicity makes it a viable option in specific patient populations.
  • Further research is needed to fully elucidate the long-term comparative efficacy and safety of these agents.