The association of SPARC with hypertension and its function in endothelial-dependent relaxation

内皮功能障碍 血压 内科学 医学 内皮 体内 内分泌学 骨结合蛋白 临床意义 离体 内皮干细胞 心脏病学 化学 生物 生物化学 体外 生物技术 碱性磷酸酶 骨钙素
作者
Xinwei Li,Wen Zhao,Xinxin Li,Xueying Chen,Yu Li,Jianxun He,Yanwen Qin,Linghai Li,Huina Zhang
出处
期刊:Atherosclerosis [Elsevier]
卷期号:388: 117390-117390
标识
DOI:10.1016/j.atherosclerosis.2023.117390
摘要

Background and aims Secreted protein acidic and rich in cysteine (SPARC) is involved in the pathological processes of many metabolic diseases. However, studies on the relevance of SPARC to hypertension and its involvement in endothelial function are scarce. In this study, we aim to explore the relevance of SPARC to hypertension and investigate its role in endothelium-dependent relaxation (EDR). Methods 110 patients who met the criteria were recruited as participants. Serum SPARC concentrations were determined by Luminex assay. The correlation between SPARC levels and hypertension was analyzed. After treatment with SPARC ex vivo or in vivo, endothelial-dependent relaxation (EDR) was measured by wire myography. Western blotting was performed to detect the expression of proteins relevant to endothelial function. Results Our results showed that serum SPARC levels were significantly higher in the hypertensive group and were positively associated with systolic blood pressure (SBP) and diastolic blood pressure (DBP). Functional results demonstrated that SPARC dramatically impaired EDR and induced the excess production of reactive oxygen species (ROS) in endothelial cells. Further experimental results confirmed that SPARC reduced angiotensin-converting enzyme 2 (ACE2) expression and ACE2 overexpression or activation completely abolished the impairing effect of SPARC on endothelial function. Conclusions The present study reveals the correlation between elevated SPARC and hypertension and confirms its adverse effect on endothelial function, helping establish a comprehensive understanding of hypertension-related endothelial dysfunction in a new scope.
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
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
玛卡巴卡呼噜呼噜完成签到 ,获得积分10
1秒前
子勋发布了新的文献求助10
1秒前
glanceofwind完成签到 ,获得积分10
2秒前
3秒前
DullElm发布了新的文献求助10
5秒前
七七又怪怪完成签到 ,获得积分10
8秒前
歪比巴卜发布了新的文献求助10
11秒前
11秒前
bkagyin应助科研通管家采纳,获得10
19秒前
wanci应助科研通管家采纳,获得10
19秒前
JamesPei应助科研通管家采纳,获得10
19秒前
脑洞疼应助科研通管家采纳,获得10
19秒前
迷你的从蕾完成签到 ,获得积分10
19秒前
Jasper应助科研通管家采纳,获得30
19秒前
夏来应助科研通管家采纳,获得10
19秒前
19秒前
大个应助科研通管家采纳,获得10
19秒前
充电宝应助科研通管家采纳,获得10
19秒前
深情安青应助科研通管家采纳,获得10
19秒前
NexusExplorer应助科研通管家采纳,获得10
19秒前
20秒前
小胡完成签到,获得积分10
23秒前
24秒前
呜呼啦呼发布了新的文献求助30
27秒前
28秒前
JamesPei应助月牙采纳,获得20
30秒前
书雪发布了新的文献求助10
30秒前
左丘不评完成签到 ,获得积分0
35秒前
35秒前
浅蓝色候鸟完成签到 ,获得积分10
39秒前
40秒前
skyyy完成签到 ,获得积分10
42秒前
NexusExplorer应助追寻太阳采纳,获得10
43秒前
lizhiqian2024发布了新的文献求助10
45秒前
Derik发布了新的文献求助10
47秒前
动听靖完成签到 ,获得积分10
53秒前
Lewis完成签到,获得积分10
53秒前
hjh发布了新的文献求助10
54秒前
57秒前
沉静WT完成签到 ,获得积分10
59秒前
高分求助中
LNG地下式貯槽指針(JGA指-107-19)(Recommended practice for LNG inground storage) 1000
Second Language Writing (2nd Edition) by Ken Hyland, 2019 1000
Generalized Linear Mixed Models 第二版 1000
rhetoric, logic and argumentation: a guide to student writers 1000
QMS18Ed2 | process management. 2nd ed 1000
Operative Techniques in Pediatric Orthopaedic Surgery 510
A High Efficiency Grating Coupler Based on Hybrid Si-Lithium Niobate on Insulator Platform 500
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 免疫学 细胞生物学 电极
热门帖子
关注 科研通微信公众号,转发送积分 2922755
求助须知:如何正确求助?哪些是违规求助? 2567257
关于积分的说明 6939383
捐赠科研通 2222931
什么是DOI,文献DOI怎么找? 1181523
版权声明 588937
科研通“疑难数据库(出版商)”最低求助积分说明 578144