小檗碱
马兜铃酸
药理学
肾毒性
肾
化学
生物化学
有机化学
生物
毒性
遗传学
内分泌学
作者
Penglong Wang,Wenbo Guo,Guangrui Huang,Jianhua Zhen,Yini Li,Tong Li,Lu Zhao,Kai Yuan,Xuehao Tian,Xuemei Huang,Yanyan Feng,Haimin Lei,Anlong Xu
标识
DOI:10.1021/acsami.1c06968
摘要
systematic toxicological experiments performed in zebrafish and mice showed that the supramolecule self-assembly formed by Ber and AA significantly reduced the toxicity of AA and attenuated AA-induced acute kidney injury. Ber and AA can self-assemble into linear heterogenous supramolecules (A-B) via electrostatic attraction and π-π stacking, with the hydrophobic groups outside and the hydrophilic groups inside during the drug combination practice. This self-assembly strategy may block the toxic site of AA and hinder its metabolism. Meanwhile, A-B linear supramolecules did not disrupt the homeostasis of gut microflora as AA did. RNA-sequence analysis, immunostaining, and western blot of the mice kidney also showed that A-B supramolecules almost abolished the acute nephrotoxicity of AA in the activation of the immune system and tumorigenesis-related pathways.
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