已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Evolocumab prevents atrial fibrillation in rheumatoid arthritis rats through restraint of PCSK9 induced atrial remodeling

医学 类风湿性关节炎 PCSK9 心房颤动 心脏病学 Evolocumab公司 内科学 胆固醇 低密度脂蛋白受体 载脂蛋白B 脂蛋白 载脂蛋白A1
作者
Xuejie Han,Yunzhen Gao,Meijiao He,Yingchun Luo,Wei Ying,Yu Duan,Song Zhang,Hui Yu,Jiuxu Kan,Tianlan Hou,Yun Zhang,Yue Li
出处
期刊:Journal of Advanced Research [Elsevier BV]
被引量:3
标识
DOI:10.1016/j.jare.2023.09.007
摘要

Proprotein convertase subtilisin/kexin type 9 (PCSK9) is implicated in the pathogenesis and progression of autoimmune disease. Patients with rheumatoid arthritis (RA) are at high risk of developing atrial fibrillation (AF), while whether PCSK9 is involved in the onset of AF among RA patients remains unclear.To explore the role of PCSK9 in the occurrence of AF in RA patients and decipher the underlying mechanism.We established a rat model of collagen-induced arthritis (CIA) by immunization with type II collagen in Freund's incomplete adjuvant. Atrial electrophysiological test was used to evaluate AF susceptibility. We performed a clinical study to examine the correlation between PCSK9 level and AF, which recruited healthy control, RA patients and RA patients complicated with AF. Evolocumab (a monoclonal antibody of PCSK9) is administered via intraperitoneal injection in CIA rats to assess the role of PCSK9 in RA-related AF. LPS-RS (LPS inhibitor), clodronate liposomes (depletion of macrophages), and cell co-culture model were used to dissect the mechanism underlying PCSK9 promotes AF.AF inducibility and duration were higher in CIA rats, accompanied by elevated plasma and atrial PCSK9. Interestingly, compared with healthy control subjects, patients with RA showed an increase in PCSK9, and the PCSK9 is much higher in RA patients complicated with AF. The level of PCSK9 was independently associated with AF risk in RA patients. In the in vivo experiment, evolocumab reduced AF susceptibility, and ameliorated atrial structural remodeling of CIA rats. Mechanistically, augmented LPS in CIA rats led to an increase in PCSK9, which exacerbated fibrosis of cardiac fibroblasts and apoptosis of cardiac myocytes by enhancement of M1 macrophages polarization and inflammation, thereby contributing to AF.This study suggests that elevated PCSK9 causes atrial structural remodeling by enhancement of M1 macrophages polarization in atria, and evolocumab can effectively protects CIA rats from AF.
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
1秒前
橘色天际线完成签到,获得积分10
1秒前
泌外科研发布了新的文献求助10
1秒前
alexyusheng发布了新的文献求助10
1秒前
2秒前
123发布了新的文献求助10
7秒前
8秒前
xuhanghang完成签到,获得积分10
11秒前
赘婿应助zx2025采纳,获得10
11秒前
12秒前
12秒前
知了发布了新的文献求助10
13秒前
萧一江完成签到,获得积分10
15秒前
15秒前
爱笑雨双发布了新的文献求助10
16秒前
YingxueRen完成签到,获得积分10
17秒前
李健的粉丝团团长应助123采纳,获得10
18秒前
20秒前
20秒前
斯人如机完成签到 ,获得积分10
20秒前
冯乌完成签到,获得积分10
21秒前
火华发布了新的文献求助10
23秒前
24秒前
加油完成签到 ,获得积分10
25秒前
852应助爱小妍采纳,获得10
27秒前
杰尼龟006发布了新的文献求助10
29秒前
111完成签到 ,获得积分10
30秒前
大渣饼完成签到 ,获得积分10
34秒前
尊敬秋双完成签到 ,获得积分10
34秒前
大个应助LLXY采纳,获得10
37秒前
37秒前
爱学习爱劳动完成签到,获得积分10
39秒前
Orange应助王老裂采纳,获得10
39秒前
43秒前
Igniting发布了新的文献求助10
44秒前
可爱的函函应助知了采纳,获得10
44秒前
44秒前
lixiaorui发布了新的文献求助10
44秒前
思源应助笑点低南霜采纳,获得10
45秒前
标致的朝雪关注了科研通微信公众号
46秒前
高分求助中
Encyclopedia of Mathematical Physics 2nd edition 888
Technologies supporting mass customization of apparel: A pilot project 600
Introduction to Strong Mixing Conditions Volumes 1-3 500
Tip60 complex regulates eggshell formation and oviposition in the white-backed planthopper, providing effective targets for pest control 400
Optical and electric properties of monocrystalline synthetic diamond irradiated by neutrons 320
共融服務學習指南 300
Essentials of Pharmacoeconomics: Health Economics and Outcomes Research 3rd Edition. by Karen Rascati 300
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 3803841
求助须知:如何正确求助?哪些是违规求助? 3348632
关于积分的说明 10339665
捐赠科研通 3064787
什么是DOI,文献DOI怎么找? 1682776
邀请新用户注册赠送积分活动 808429
科研通“疑难数据库(出版商)”最低求助积分说明 764096