Atractyloside

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Atractyloside skeletal.svg

Atractyloside

Atractyloside is a toxic natural compound found in certain plants, particularly in the genera Atractylis and Kochia. It is known for its potent inhibitory effects on mitochondrial function, specifically targeting the enzyme adenine nucleotide translocase. This disruption of mitochondrial function can lead to severe cellular damage and toxicity.

Chemical Structure[edit | edit source]

Atractyloside is a diterpenoid glycoside with the chemical formula C15H24O8. It consists of a tricyclic diterpene core attached to a sugar moiety. The compound is highly water-soluble and is often extracted from plant sources for research purposes.

Mechanism of Action[edit | edit source]

Atractyloside exerts its toxic effects by binding to adenine nucleotide translocase, a protein located in the inner mitochondrial membrane. By inhibiting this protein, atractyloside disrupts the transport of ADP and ATP across the mitochondrial membrane, leading to a collapse of the mitochondrial membrane potential and inhibition of ATP synthesis. This disruption ultimately results in mitochondrial dysfunction and cell death.

Toxicity[edit | edit source]

Exposure to atractyloside can have severe toxic effects on various organs, particularly the liver and kidneys. The compound is known to induce mitochondrial swelling, oxidative stress, and cell death in affected tissues. Ingestion or inhalation of atractyloside can lead to symptoms such as abdominal pain, nausea, vomiting, and organ failure.

Treatment[edit | edit source]

There is no specific antidote for atractyloside poisoning. Treatment is primarily supportive and focuses on managing symptoms and providing supportive care to prevent further organ damage. In severe cases, interventions such as hemodialysis may be necessary to remove the toxin from the bloodstream.

Research and Applications[edit | edit source]

Despite its toxicity, atractyloside has been used in research settings to study mitochondrial function and the mechanisms of cell death. Its ability to selectively target adenine nucleotide translocase has made it a valuable tool for investigating mitochondrial pathways and developing potential therapeutic strategies for conditions involving mitochondrial dysfunction.


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Contributors: Prab R. Tumpati, MD