Aloe-emodin prevents nerve injury and neuroinflammation caused by ischemic stroke via the PI3K/AKT/mTOR and NF-κB pathway

神经炎症 PI3K/AKT/mTOR通路 蛋白激酶B 药理学 芦荟大黄素 体内 炎症 免疫印迹 氧化应激 脂多糖 大黄素 医学 化学 细胞凋亡 内科学 生物 生物化学 生物技术 基因
作者
Minghua Xian,Jiale Cai,Kening Zheng,Qu Liu,Yali Liu,Huiting Lin,Shengwang Liang,Shumei Wang
出处
期刊:Food & Function [Royal Society of Chemistry]
卷期号:12 (17): 8056-8067 被引量:88
标识
DOI:10.1039/d1fo01144h
摘要

Ischemic stroke (IS) caused by cerebral arterial occlusion is the leading cause of global morbidity and mortality. Cellular oxidative stress and inflammation play a vital role in the pathological process of neural damage in IS. It is necessary to develop functional food or drugs, which target neuroinflammation and oxidation mechanisms against IS. The molecule compound aloe-emodin (AE) is derived from aloe and rhubarb. However, the exact mechanism of the pharmacological action of AE on IS remains unclear. Here, for aiming to demonstrate the mechanism of AE, our study explored the middle cerebral occlusion reperfusion (MCAO/R) rats in vivo, oxygen and glucose deprivation reperfusion (OGD/R), and lipopolysaccharide (LPS)-stimulated cells in vitro. We found that AE significantly improved the infarct size and behavioral score of MCAO/R rats, decreased the expression of TNF-α, MDA, LDH, Caspase 3, and increased the expression of SOD, Bcl-2/Bax. Liquid chromatography-mass spectrometry (LC/MS) results showed that AE could penetrate the blood-brain barrier in the sham group and MCAO/R group. In vitro, AE significantly protected SH-SY5Y cells from the insult of OGD/R and reduced the production of inflammatory cytokines in BV2 cells stimulated by LPS. In vivo and in vitro, western blot analysis results showed that AE significantly increased the expression of PI3K, AKT and mTOR proteins. In addition, AE significantly decreased NF-κB protein expression in BV2 cells. The use of AKT-specific inhibitor MK-2206 2HCL to inhibit AKT expression can block the protective effect of AE on SH-SY5Y cells subjected to OGD/R insults. Overall, our study suggests that AE protected against cerebral ischemia-reperfusion injury probably via the PI3K/AKT/mTOR and NF-κB signaling pathways. Thus, these results indicated that AE could be a promising first-line therapy for preventing and treating ischemic stroke and can be used as functional food.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
叶叶叶完成签到,获得积分10
1秒前
Lucas应助Domagin采纳,获得10
2秒前
Li完成签到 ,获得积分10
3秒前
莫友安完成签到 ,获得积分10
5秒前
赘婿应助Saluzi采纳,获得10
5秒前
量子星尘发布了新的文献求助10
7秒前
冷酷的蘑菇完成签到,获得积分10
7秒前
英姑应助qiwei采纳,获得10
8秒前
朴实雨珍完成签到,获得积分10
9秒前
欧大大完成签到,获得积分10
10秒前
xiaozhang完成签到 ,获得积分10
11秒前
量子星尘发布了新的文献求助10
11秒前
13秒前
凌壬靖完成签到 ,获得积分10
14秒前
凶狠的洋葱完成签到,获得积分10
14秒前
14秒前
熊熊出击完成签到 ,获得积分10
15秒前
科研通AI5应助周周采纳,获得30
15秒前
明亮的绫完成签到 ,获得积分10
16秒前
jijun完成签到,获得积分10
17秒前
量子星尘发布了新的文献求助10
18秒前
CipherSage应助z'x采纳,获得10
18秒前
Saluzi发布了新的文献求助10
19秒前
心楠完成签到 ,获得积分10
19秒前
科研通AI5应助秋水采纳,获得10
20秒前
mmd完成签到 ,获得积分10
20秒前
21秒前
21秒前
22秒前
22秒前
粥粥完成签到 ,获得积分10
22秒前
23秒前
qiwei发布了新的文献求助10
24秒前
sally完成签到 ,获得积分10
25秒前
25秒前
25秒前
ttldhbds完成签到,获得积分20
26秒前
26秒前
王永吉完成签到,获得积分10
26秒前
27秒前
高分求助中
Production Logging: Theoretical and Interpretive Elements 2700
Neuromuscular and Electrodiagnostic Medicine Board Review 1000
Statistical Methods for the Social Sciences, Global Edition, 6th edition 600
こんなに痛いのにどうして「なんでもない」と医者にいわれてしまうのでしょうか 510
The Insulin Resistance Epidemic: Uncovering the Root Cause of Chronic Disease  500
Walter Gilbert: Selected Works 500
An Annotated Checklist of Dinosaur Species by Continent 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3662487
求助须知:如何正确求助?哪些是违规求助? 3223261
关于积分的说明 9750825
捐赠科研通 2933130
什么是DOI,文献DOI怎么找? 1605938
邀请新用户注册赠送积分活动 758208
科研通“疑难数据库(出版商)”最低求助积分说明 734743