Barbiturate: Difference between revisions

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#REDIRECT [[Barbiturates]]
{{short description|Class of drugs derived from barbituric acid}}


{{stub}}
[[File:Barbituric-acid-structural.svg|thumb|right|Structural formula of barbituric acid, the core structure of barbiturates.]]
[[Category:Barbiturates| ]]
 
[[Category:AMPA receptor antagonists]]
'''Barbiturates''' are a class of [[sedative]] and [[hypnotic]] medications that are derived from [[barbituric acid]]. They were first synthesized in the late 19th century and have been used in medicine for their [[anxiolytic]], [[anticonvulsant]], and [[anesthetic]] properties. However, due to their potential for [[addiction]] and [[overdose]], their use has declined in favor of safer alternatives such as [[benzodiazepines]].
[[Category:Anticonvulsants]]
 
[[Category:Anxiolytics]]
==History==
[[Category:Calcium channel blockers]]
The first barbiturate, [[barbital]], was synthesized in 1903 by German chemists [[Emil Fischer]] and [[Joseph von Mering]]. It was marketed under the trade name Veronal and was used as a [[sleeping aid]]. Over the following decades, numerous barbiturates were developed, each with varying durations of action and potency.
[[Category:Chemical classes of psychoactive drugs]]
 
[[Category:GABAA receptor positive allosteric modulators]]
==Pharmacology==
[[Category:German inventions|Barbiturates]]
Barbiturates act as central nervous system [[depressants]]. They enhance the action of the [[neurotransmitter]] [[gamma-aminobutyric acid]] (GABA) by binding to the [[GABA_A receptor]], leading to increased [[chloride]] ion influx and hyperpolarization of neurons. This results in a sedative effect, reducing [[anxiety]] and inducing [[sleep]].
[[Category:Glycine receptor agonists]]
 
===Classification===
Barbiturates are classified based on their duration of action:
* '''Ultra-short-acting''': Used for [[anesthesia]] induction (e.g., [[thiopental]]).
* '''Short-acting''': Used for [[insomnia]] and [[preoperative sedation]] (e.g., [[pentobarbital]]).
* '''Intermediate-acting''': Used for [[anxiety]] and [[insomnia]] (e.g., [[amobarbital]]).
* '''Long-acting''': Used for [[epilepsy]] and [[seizure]] control (e.g., [[phenobarbital]]).
 
==Medical Uses==
Barbiturates have been used in the treatment of various conditions, including:
* [[Seizure disorders]]: Long-acting barbiturates like phenobarbital are used to control seizures.
* [[Anesthesia]]: Ultra-short-acting barbiturates are used to induce anesthesia.
* [[Insomnia]]: Short-acting barbiturates were historically used as sleep aids.
 
==Risks and Side Effects==
[[File:Rational_harm_assessment_of_drugs_radar_plot.svg|thumb|left|Radar plot showing the harm assessment of various drugs, including barbiturates.]]
Barbiturates have a narrow [[therapeutic index]], meaning the difference between a therapeutic dose and a toxic dose is small. Overdose can lead to [[respiratory depression]], [[coma]], and [[death]]. Chronic use can result in [[tolerance]], [[dependence]], and [[withdrawal syndrome]].
 
==Legal Status==
Due to their potential for abuse and addiction, barbiturates are classified as [[controlled substances]] in many countries. Their medical use is now limited, and they are often replaced by safer alternatives.
 
==Related Pages==
* [[Benzodiazepine]]
* [[Sedative]]
* [[Hypnotic]]
* [[Anxiolytic]]
 
[[File:Barbiturates_generic_numbered.svg|thumb|right|Generic structure of barbiturates, showing the barbituric acid core.]]
 
==See Also==
* [[Central nervous system depressant]]
* [[Drug overdose]]
* [[Substance dependence]]
 
[[Category:Barbiturates]]
[[Category:Sedatives]]
[[Category:Hypnotics]]
[[Category:Hypnotics]]
[[Category:Kainate receptor antagonists]]
[[Category:Nicotinic antagonists]]
<gallery>
File:Barbituric-acid-structural.svg|Barbituric Acid Structure
File:Rational harm assessment of drugs radar plot.svg|Rational Harm Assessment of Drugs
File:Barbiturates generic numbered.svg|Barbiturates Generic Numbered
</gallery>

Latest revision as of 21:25, 4 March 2025

Class of drugs derived from barbituric acid


Structural formula of barbituric acid, the core structure of barbiturates.

Barbiturates are a class of sedative and hypnotic medications that are derived from barbituric acid. They were first synthesized in the late 19th century and have been used in medicine for their anxiolytic, anticonvulsant, and anesthetic properties. However, due to their potential for addiction and overdose, their use has declined in favor of safer alternatives such as benzodiazepines.

History[edit]

The first barbiturate, barbital, was synthesized in 1903 by German chemists Emil Fischer and Joseph von Mering. It was marketed under the trade name Veronal and was used as a sleeping aid. Over the following decades, numerous barbiturates were developed, each with varying durations of action and potency.

Pharmacology[edit]

Barbiturates act as central nervous system depressants. They enhance the action of the neurotransmitter gamma-aminobutyric acid (GABA) by binding to the GABA_A receptor, leading to increased chloride ion influx and hyperpolarization of neurons. This results in a sedative effect, reducing anxiety and inducing sleep.

Classification[edit]

Barbiturates are classified based on their duration of action:

Medical Uses[edit]

Barbiturates have been used in the treatment of various conditions, including:

  • Seizure disorders: Long-acting barbiturates like phenobarbital are used to control seizures.
  • Anesthesia: Ultra-short-acting barbiturates are used to induce anesthesia.
  • Insomnia: Short-acting barbiturates were historically used as sleep aids.

Risks and Side Effects[edit]

Radar plot showing the harm assessment of various drugs, including barbiturates.

Barbiturates have a narrow therapeutic index, meaning the difference between a therapeutic dose and a toxic dose is small. Overdose can lead to respiratory depression, coma, and death. Chronic use can result in tolerance, dependence, and withdrawal syndrome.

Legal Status[edit]

Due to their potential for abuse and addiction, barbiturates are classified as controlled substances in many countries. Their medical use is now limited, and they are often replaced by safer alternatives.

Related Pages[edit]

Generic structure of barbiturates, showing the barbituric acid core.

See Also[edit]