Details

Autor(en) / Beteiligte

• Nielson, Jason R
• Nath, Anjali K
• Doane, Kim P
• Shi, Xu
• Lee, Jangwoen
• Tippetts, Emily G
• Saha, Kusumika
• Morningstar, Jordan
• Hicks, Kevin G
• Chan, Adriano
• Zhao, Yanbin
• Kelly, Amy
• Hendry-Hofer, Tara B
• Witeof, Alyssa
• Sips, Patrick Y
• Mahon, Sari
• Bebarta, Vikhyat S
• Davisson, Vincent Jo
• Boss, Gerry R
• Rutter, Jared
• MacRae, Calum A
• Brenner, Matthew
• Gerszten, Robert E
• Peterson, Randall T

Titel

Glyoxylate protects against cyanide toxicity through metabolic modulation

Ist Teil von

• Scientific reports, 2022-03, Vol.12 (1), p.4982-16, Article 4982

Ort / Verlag

England: Nature Publishing Group

Erscheinungsjahr

2022

Quelle

MEDLINE

Beschreibungen/Notizen

• Although cyanide's biological effects are pleiotropic, its most obvious effects are as a metabolic poison. Cyanide potently inhibits cytochrome c oxidase and potentially other metabolic enzymes, thereby unleashing a cascade of metabolic perturbations that are believed to cause lethality. From systematic screens of human metabolites using a zebrafish model of cyanide toxicity, we have identified the TCA-derived small molecule glyoxylate as a potential cyanide countermeasure. Following cyanide exposure, treatment with glyoxylate in both mammalian and non-mammalian animal models confers resistance to cyanide toxicity with greater efficacy and faster kinetics than known cyanide scavengers. Glyoxylate-mediated cyanide resistance is accompanied by rapid pyruvate consumption without an accompanying increase in lactate concentration. Lactate dehydrogenase is required for this effect which distinguishes the mechanism of glyoxylate rescue as distinct from countermeasures based solely on chemical cyanide scavenging. Our metabolic data together support the hypothesis that glyoxylate confers survival at least in part by reversing the cyanide-induced redox imbalances in the cytosol and mitochondria. The data presented herein represent the identification of a potential cyanide countermeasure operating through a novel mechanism of metabolic modulation.