| Literature DB >> 30291731 |
Xiaoyu Qu1, Huan Gao1, Lina Tao1, Yueming Zhang1, Jinghui Zhai1, Yanqing Song1, Sixi Zhang1.
Abstract
The nucleotide-binding oligomerization domain-like receptor family, pyrin domain containing 3 (NLRP3) inflammasome has a key role in the inflammatory response. We found that cisplatin (7.5, 15 mg/kg, IV) could induce acute injury to the liver and kidneys of rats. Western blot and immunohistochemical analyses showed that expression of NLRP3, caspase-1 and interleukin-1β was upregulated significantly in a dose-dependent manner after cisplatin exposure. Autophagy could inhibit NLRP3 expression and assembly of the NLRP3 inflammasome. Expression of light chain 3 II/I and p62 suggested that autophagy was inhibited during injury to the liver and kidneys. These data suggested that cisplatin might activate NLRP3 by inhibiting autophagy in the liver and kidneys of rats.Entities:
Keywords: NLRP3; autophagy; cisplatin; kidney injury; liver injury
Year: 2018 PMID: 30291731 DOI: 10.1002/jbt.22228
Source DB: PubMed Journal: J Biochem Mol Toxicol ISSN: 1095-6670 Impact factor: 3.642