钙调神经磷酸酶
药理学
癫痫
化学
天然产物
体内
AMPA受体
NMDA受体
生物化学
神经科学
受体
生物
医学
内科学
遗传学
移植
作者
Qing‐Tong Han,Wanqi Yang,Caixia Zang,Linchao Zhou,Chong‐Jing Zhang,Xiu‐Qi Bao,Jie Cai,Fangfei Li,Qinyan Shi,Xiaoliang Wang,Jing Qu,Dan Zhang,Shi‐Shan Yu
标识
DOI:10.1038/s41392-023-01312-y
摘要
Abstract Tutin, an established toxic natural product that causes epilepsy in rodents, is often used as a tool to develop animal model of acute epileptic seizures. However, the molecular target and toxic mechanism of tutin were unclear. In this study, for the first time, we conducted experiments to clarify the targets in tutin-induced epilepsy using thermal proteome profiling. Our studies showed that calcineurin (CN) was a target of tutin, and that tutin activated CN, leading to seizures. Binding site studies further established that tutin bound within the active site of CN catalytic subunit. CN inhibitor and calcineurin A (CNA) knockdown experiments in vivo proved that tutin induced epilepsy by activating CN, and produced obvious nerve damage. Together, these findings revealed that tutin caused epileptic seizures by activating CN. Moreover, further mechanism studies found that N -methyl- D -aspartate (NMDA) receptors, gamma-aminobutyric acid (GABA) receptors and voltage- and Ca 2+ - activated K + (BK) channels might be involved in related signaling pathways. Our study fully explains the convulsive mechanism of tutin, which provides new ideas for epilepsy treatment and drug development.
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