Picrotoxinin (left) and picrotin (right)
Clinical data
ATC code none
CAS Number 124-87-8 YesY
PubChem (CID) 5360688
DrugBank DB00466 YesY
ChemSpider 16736444 YesY
KEGG C09529 N
ECHA InfoCard 100.004.288
Chemical and physical data
3D model (Jmol) Interactive image
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Picrotoxin, also known as cocculin, is a poisonous crystalline plant compound, first isolated by the French pharmacist and chemist Pierre François Guillaume Boullay (1777–1869) in 1812.[1] The name "picrotoxin" is a combination of the Greek words "picros" (bitter) and "toxicon" (poison).[2]

Found primarily in the fruit of the climbing plant Anamirta cocculus, it has a strong physiological action. It acts as a non-competitive channel blocker for the GABAA receptor chloride channels.[3] It is therefore a channel blocker rather than a receptor antagonist.

On the other hand, evidence exists that picrotoxin acts as a competitive antagonist, and not as a channel blocker. For example, Newland and Cull-Candy (1992) found that when recording GABA-activated currents in neurons, picrotoxin "did not alter the amplitude of the main conductance state. However, picrotoxin did reduce the frequency of channel openings." They concluded, "Our data are consistent with a mechanism whereby picrotoxin binds preferentially to an agonist bound form of the receptor and stabilizes an agonist-bound shut state. This could, for example, mean that picrotoxin enhances the occurrence of a desensitized state or an allosterically blocked state." [4]

As GABA itself is an inhibitory neurotransmitter, infusion of picrotoxin has stimulant and convulsant effects. As such, picrotoxin can be used to counter barbiturate poisoning, that can occur during general anesthesia or during a large intake outside of the hospital.[5]

Chemical structure

Picrotoxin is an equimolar mixture of two compounds, picrotoxinin (C15H16O6; CAS# 17617-45-7) and picrotin (C15H18O7; CAS# 21416-53-5).[6]

Other uses

Picrotoxin is classified as an illegal performance-enhancing "Class 1 substance" by the American Quarter Horse Association.


  1. Boullay, P. F. G. (1812). "Analyse chimique de la Coque du Levant, Menispermum cocculus". Bulletin de Pharmacie (in French). 4: 5–34. (Note: "Menispermum cocculus" has been renamed "Anamirta cocculus".)
  2. (Boullay, 1812), p. 31.
  3. Rho, J. M.; Donevan, S. D.; Rogawski, M. A. (1996). "Direct activation of GABA-A receptors by barbiturates in cultured rat hippocampal neurons". Journal of Physiology. 497 (2): 509–522. doi:10.1113/jphysiol.1996.sp021784. PMC 1161000Freely accessible. PMID 8961191.
  4. Newland, C. F.; Cull-Candy, S. G. (1992). "On the mechanism of action of picrotoxin on GABA receptor channels in dissociated sympathetic neurones of the rat". Journal of Physiology. 447 (1): 191–213. doi:10.1113/jphysiol.1992.sp018998. PMC 1176032Freely accessible. PMID 1317428.
  5. Nilsson, E.; Eyrich, B. (1950). "On Treatment of Barbiturate Poisoning". Acta Medica Scandinavica. 137 (6): 381–389. doi:10.1111/j.0954-6820.1950.tb12129.x. PMID 15432128.
  6. "Picrotoxin". Catalog. Sigma Aldrich.
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