亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Cardiovascular toxicities by calcineurin inhibitors: Cellular mechanisms behind clinical manifestations

钙调神经磷酸酶 医学 药理学 纤维化 氧化应激 炎症 移植 内科学
作者
Tanawat Attachaipanich,Siriporn C. Chattipakorn,Nipon Chattipakorn
出处
期刊:Acta Physiologica [Wiley]
卷期号:240 (9): e14199-e14199 被引量:12
标识
DOI:10.1111/apha.14199
摘要

Abstract Calcineurin inhibitors (CNI), including cyclosporine A (CsA) and tacrolimus (TAC), are cornerstones of immunosuppressive therapy in solid organ transplant recipients. While extensively recognized for their capacity to induce nephrotoxicity, hypertension, and dyslipidemia, emerging reports suggest potential direct cardiovascular toxicities associated with CNI. Evidence from both in vitro and in vivo studies has demonstrated direct cardiotoxic impact of CNI, manifesting itself as induction of cardiomyocyte apoptosis, enhanced oxidative stress, inflammatory cell infiltration, and cardiac fibrosis. CNI enhances cellular apoptosis through CaSR via activation of the p38 MAPK pathway and deactivation of the ERK pathway, and enhancement of miR‐377 axis. Although CNI could attenuate cardiac hypertrophy in certain animal models, CNI concurrently impaired systolic function, enhanced cardiac fibrosis, and increased the risk of heart failure. Evidence from in vivo studies demonstrated that CNI prolong the duration of action potentials through a decrease in potassium current. CNI also exerted direct effects on endothelial cell injury, inducing apoptosis and enhancing oxidative stress. CNI may induce vascular inflammation through TLR4 via MyD88 and TRIF pathways. In addition, CNI affects vascular function by impairing endothelial‐dependent vasodilation and promoting vasoconstriction. Clinical studies in transplant patients also revealed an increased incidence of cardiac remodeling. However, the evidence is constrained by the limited number of participants and potential confounding factors. Several studies indicate differing cardiovascular toxicity profiles between CsA and TAC, and these could be potentially due to their different interactions with calcineurin subunits and calcineurin‐independent effects. Further studies are needed to clarify these mechanisms to improve cardiovascular outcomes for transplant patients with CNI.
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
liuliu发布了新的文献求助10
7秒前
lovelife完成签到,获得积分10
13秒前
liuliu完成签到,获得积分10
15秒前
ceeray23应助科研通管家采纳,获得10
15秒前
ceeray23应助科研通管家采纳,获得10
15秒前
Criminology34应助科研通管家采纳,获得10
15秒前
ceeray23应助科研通管家采纳,获得10
15秒前
fukase完成签到,获得积分10
33秒前
renhuizhi完成签到,获得积分10
46秒前
xxx发布了新的文献求助10
1分钟前
zpli完成签到 ,获得积分10
1分钟前
1分钟前
1分钟前
小雨发布了新的文献求助10
1分钟前
1分钟前
1分钟前
2分钟前
默默善愁发布了新的文献求助10
2分钟前
Criminology34应助科研通管家采纳,获得10
2分钟前
斯文败类应助科研通管家采纳,获得10
2分钟前
ceeray23应助科研通管家采纳,获得10
2分钟前
我是老大应助默默善愁采纳,获得30
2分钟前
2分钟前
犬来八荒发布了新的文献求助10
2分钟前
2分钟前
Migue发布了新的文献求助50
2分钟前
cy完成签到 ,获得积分10
3分钟前
3分钟前
cccttt发布了新的文献求助10
3分钟前
可爱的函函应助cccttt采纳,获得10
3分钟前
3分钟前
3分钟前
笨蛋美女完成签到 ,获得积分10
3分钟前
完美世界应助666采纳,获得10
3分钟前
朱羊羊发布了新的文献求助10
3分钟前
赤恩完成签到,获得积分10
4分钟前
ceeray23应助科研通管家采纳,获得10
4分钟前
ceeray23应助科研通管家采纳,获得10
4分钟前
科研通AI2S应助科研通管家采纳,获得10
4分钟前
朱羊羊完成签到,获得积分10
4分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Basic And Clinical Science Course 2025-2026 3000
《药学类医疗服务价格项目立项指南(征求意见稿)》 880
花の香りの秘密―遺伝子情報から機能性まで 800
Stop Talking About Wellbeing: A Pragmatic Approach to Teacher Workload 500
Terminologia Embryologica 500
Silicon in Organic, Organometallic, and Polymer Chemistry 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5617127
求助须知:如何正确求助?哪些是违规求助? 4701470
关于积分的说明 14913716
捐赠科研通 4749642
什么是DOI,文献DOI怎么找? 2549305
邀请新用户注册赠送积分活动 1512345
关于科研通互助平台的介绍 1474091