医学
自噬
PI3K/AKT/mTOR通路
胆固醇
内科学
优势比
免疫印迹
内分泌学
脑出血
信号转导
生物
细胞凋亡
细胞生物学
生物化学
基因
蛛网膜下腔出血
作者
Zixuan Tian,Min Liu,Ziying Zhang,Tao Yan,Shuyi Guo,Miao Yu,Jingyu Wang,Ru Zhang,Yanqing Bi,Nan Zhang,Xingguang Zhang
标识
DOI:10.1016/j.ijcard.2023.131134
摘要
An association between cholesterol and intracerebral hemorrhage (ICH) has been reported, but the mechanism is unclear.In this cross-sectional study, participants aged 50-75 years were selected using multistage stratified cluster sampling. All samples completed a questionnaire (age, gender, medication, etc.) and were examined (blood lipid, height, blood pressure, etc.) for risk factors. Multivariable logistic regression was used to analyze the association between cholesterol levels and ICH risk, after adjusting for age, smoking, hypertension, and other factors. We cultured rat cerebral artery smooth muscle cells at different cholesterol concentrations. The autophagy pathway was identified by transcriptome sequencing. The results were then validated using real-time polymerase chain reaction and western blot.We included 39,595 patients, among whom 286 had ICH. The study showed that a low level of low-density lipoprotein cholesterol (LDL-C) was a risk factor of ICH (odds ratio 2.912, 95% confidence interval 1.460-5.806; P = 0.002). Cell experiments showed that lower cholesterol levels could significantly induce rat cerebral artery smooth muscle cell necrosis. In low-cholesterol groups, expression of the autophagy marker LC3 protein was significantly decreased and p62 protein was significantly increased. In western blot and comparison with the control group, the low cholesterol PI3K/Akt/mTOR signaling pathway was significantly activated in the autophagy pathway, resulting in its inhibition, which in turn led to smooth muscle cell death.Low cholesterol levels may inhibit autophagy through PI3K/Akt/mTOR signaling and induce arterial smooth muscle cell necrosis, thereby increasing the risk of ICH.
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