Pentobarbital is a short acting barbiturate that is available as both a free acid and a sodium salt, the former of which is only slightly soluble in water and ethanol. One trade name for this drug is Nembutal®, coined by Dr. John S. Lundy, who started using it in 1930, from the structural formula of the sodium salt—Na (sodium) + ethyl + methyl + butyl + al (common suffix for barbiturates).[ | url = https://www.aana.com/archives/imagine/1997/08imagine97.asp}}]
Uses
Approved
Pentobarbital's
FDA approved human uses include treatment of
seizures
and preoperative (and other)
sedation; it is also approved as a short-term
hypnotic.
In France, it is used in the treatment of insomnia, and as a preanesthetic.
Unapproved/Investigational/Off-Label
Off-label uses of pentobarbital include reduction of intracranial pressure in
Reye's syndrome, traumatic brain injury
and induction of coma in cerebral
ischemia patients.
Veterinary medicine
In
veterinary medicine sodium pentobarbital—traded under names such as
Sagatal—is used as an
anaesthetic.
Pentobarbital is an ingredient in
Equithesin.
Veterinary Euthanasia
It is used by itself, or more often in combination with complementary agents such as
phenytoin, in commercial
animal euthanasia injectable solutions. Trade names include
Euthasol,
Euthatal,
Beuthanasia-D and
Fatal Plus.
Metabolism
Pentobarbital undergoes
first-pass metabolism in the liver and possibly the intestines.
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Drug Interactions
Administration of
alcohol,
opioids,
antihistamines, other
sedative-hypnotics, and other
central nervous system depressants will additively increase the sedation caused by pentobarbital.
The S-
isomers of
fluoxetine and its active
metabolite, norfluoxetine, reverse the
down-regulation of
allopregnanolone by pentobarbital, thus reversing the loss of
righting reflex, at doses 10-50 times lower than that required for serotonin reuptake.
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Tricyclic antidepressants decrease serum levels of pentobarbital.
References and End Notes
Anticonvulsants | barbiturates
Pentobarbital | ペントバルビタール | Pentobarbital