检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:许圣淳(综述) 张晓良(审校)[1] XU Shengchun;ZHANG Xiaoliang(Institute of Nephrology,Southeast University School of Medicine,Zhongda Hospital,Nanjing 210009,China)
机构地区:[1]东南大学附属中大医院肾内科,南京210009
出 处:《肾脏病与透析肾移植杂志》2024年第2期177-181,共5页Chinese Journal of Nephrology,Dialysis & Transplantation
摘 要:sKlotho是由“抗衰老”因子α-Klotho生成的可溶性蛋白,在体内发挥多效性作用。慢性肾脏病(CKD)是一种sKlotho缺乏性疾病,在CKD基础上发生的心脏重塑称为尿毒症心肌病(UC),以左心室肥厚和心肌纤维化为特征性表现,临床危害大,是CKD患者最主要的死亡原因。近年来研究发现,sKlotho可以保护心脏,通过靶向多种信号通路调控心肌肥厚、纤维化及心脏电生理。本文就sKlotho对UC的保护作用及其机制作一综述。sKlotho,a soluble form of the anti-aging proteinα-Klotho,exerts multifaceted biological effects.Chronic kidney disease(CKD),marked by a deficiency in sKlotho,leads to the development of uremic cardiomyopathy(UC).UC,characterized by left ventricular hypertrophy and myocardial fibrosis,is a detrimental condition and a leading cause of mortality in patients undergoing dialysis.Emerging research has highlighted the cardioprotective potential of sKlotho,particularly in modulating signaling pathways associated with myocardial hypertrophy,fibrosis,and cardiac electrophysiology.This article comprehensively reviews the protective roles and mechanisms of sKlotho in the context of uremic cardiomyopathy,offering insights into novel therapeutic avenues.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.49