褪黑素
SIRT3
医学
缺血
麻醉
标记法
药理学
锡尔图因
细胞凋亡
再灌注损伤
氧化应激
内分泌学
内科学
化学
免疫组织化学
生物化学
乙酰化
基因
作者
Lili Liu,Hongping Chen,Jing Jin,Zhanbin Tang,Pengqi Yin,Di Zhong,Guozhong Li
出处
期刊:Life Sciences
[Elsevier BV]
日期:2019-11-04
卷期号:239: 117036-117036
被引量:64
标识
DOI:10.1016/j.lfs.2019.117036
摘要
Previous literature has shown that melatonin plays a critical role in protecting against cerebral ischemia/reperfusion (I/R) injury. Sirtuin3(SIRT3), as one member of the sirtuin family, protects against oxidative stress-related diseases. However, the association between melatonin and SIRT3 in cerebral I/R injury is not well understood. Our experiment was planned to investigate whether melatonin protects against cerebral I/R injury through SIRT3 activation.We selected transient middle cerebral artery occlusion (tMCAO) mice as the model of cerebral I/R injury. Male C57/BL6 mice were pre-treated with or without a selective SIRT3 inhibitor and then subjected to tMCAO surgery. Melatonin (20 mg/kg) was given to mice by intraperitoneal injection after ischemia and before reperfusion. Then, we observed the changes in the SIRT3 and downstream relative proteins, infarction volume, neurological score, Nissl, H&E and TUNEL staining, and the expression of apoptosis proteins after tMCAO.Melatonin upregulated the expression of SIRT3 after tMCAO, and alleviated the neurological dysfunction and cell apoptosis through SIRT3 activation.Our research proved that melatonin promoted SIRT3 expression after tMCAO and alleviated cerebral I/R injury by activating the SIRT3 signaling pathway. This study provides novel therapeutic targets and mechanisms for the treatment of ischemic stroke in the clinic, especially during cerebrovascular reperfusion.
科研通智能强力驱动
Strongly Powered by AbleSci AI