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耐甲氧西林金黄色葡萄球菌感染对小鼠肾细胞色素P450s表达及活性的影响。

Effects of infection of MRSA on the expression and activity of renal cytochrome P450s in mice.

作者信息

Long Nana, Tang Huaqiao, Lin Lin, Li Jianlong, Guo Lijuan, Sun Fenghui, Dai Min

机构信息

School of Laboratory Medicine, Chengdu Medical College, China.

Sichuan Provincial Engineering Laboratory for Prevention and Control Technology of Veterinary Drug Residue in Animal-origin Food, Chengdu Medical College, China.

出版信息

J Toxicol Sci. 2019;44(4):299-307. doi: 10.2131/jts.44.299.

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) leads to serious infections, but it is not known whether it changes the expression of kidney drug metabolizing enzymes during infection. The mice were infected with different doses of MRSA and the oxidative stress and inflammation levels in the kidney were examined. The mRNA expression and activity of cytochrome P450 enzyme was analysed. Mice infected with high levels of MRSA showed a decrease in renal antioxidant capability and an elevated level of oxidative metabolites, which was accompanied by the release of inflammatory cytokines. The levels of interleukin 1β, tumour necrosis factor alpha, and macrophage inflammatory protein-1α were significantly increased along with the levels of nitric oxide and malondialdehyde. On day 7, mRNA expression of Cyp1a2, 2d22, and 3a11 were decreased by the high level of MRSA, but the low level of MRSA increased their expressions. Cyp2e1 mRNA expression was increased by MRSA in the kidney of mice. High dose of MRSA infection increased the oxidative stress and inflammatory response in mouse kidney, leading to the decrease in the expression of renal drug-metabolizing enzymes and no recovery within 7 days.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)会引发严重感染,但在感染期间它是否会改变肾脏药物代谢酶的表达尚不清楚。用不同剂量的MRSA感染小鼠,并检测肾脏中的氧化应激和炎症水平。分析细胞色素P450酶的mRNA表达和活性。感染高水平MRSA的小鼠肾脏抗氧化能力下降,氧化代谢产物水平升高,同时伴有炎性细胞因子的释放。白细胞介素1β、肿瘤坏死因子α和巨噬细胞炎性蛋白-1α的水平以及一氧化氮和丙二醛的水平均显著升高。在第7天,高水平的MRSA使Cyp1a2、2d22和3a11的mRNA表达下降,但低水平的MRSA则使其表达增加。MRSA使小鼠肾脏中的Cyp2e1 mRNA表达增加。高剂量的MRSA感染增加了小鼠肾脏中的氧化应激和炎症反应,导致肾脏药物代谢酶的表达下降,且在7天内未恢复。

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