Epibatidine

From WikiMD's Food, Medicine & Wellness Encyclopedia

Epibatidine is a potent alkaloid and analgesic drug that was first discovered in the skin of the Anthony's poison arrow frog (Epipedobates anthonyi). It has a unique structure and mode of action that has made it the subject of much scientific interest.

History[edit | edit source]

Epibatidine was first isolated in 1974 by John W. Daly, a chemist at the National Institutes of Health (NIH). Daly was studying the chemical defenses of poison dart frogs, and he discovered that the skin of E. anthonyi contained a substance that was more potent than morphine as a painkiller, but without the addictive properties.

Structure and Properties[edit | edit source]

Epibatidine is a heterocyclic compound with a structure that includes a pyridine ring and a [[azabicyclo[2.2.1]heptane]] ring. It is a chiral molecule, meaning it has two possible stereoisomers. The naturally occurring form of the molecule is the (−)-isomer.

Pharmacology[edit | edit source]

Epibatidine acts as an agonist at nicotinic acetylcholine receptors (nAChRs). It has a high affinity for these receptors, and it can stimulate them to a greater degree than the body's natural neurotransmitter, acetylcholine. This results in a powerful analgesic effect.

However, epibatidine also has a high toxicity. It can cause severe side effects, including hypertension, respiratory failure, and death. For this reason, it is not used clinically. Instead, it is studied as a tool to understand the function of nAChRs and to develop new drugs.

Research and Potential Uses[edit | edit source]

Despite its toxicity, epibatidine has been the subject of much research due to its unique properties. Scientists have used it as a tool to study the function of nAChRs, and it has helped to advance our understanding of these important receptors.

In addition, researchers have sought to develop derivatives of epibatidine that retain its analgesic properties but without the toxic side effects. Some of these derivatives have shown promise in preclinical studies, but none have yet reached the market.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD