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Physiology and Pathophysiology of the Intrarenal Renin-Angiotensin System: An Update
被引:176
|作者:
Yang, Tianxin
[1
,2
]
Xu, Chuanming
[2
]
机构:
[1] Univ Utah, Vet Affairs Med Ctr, Internal Med, Salt Lake City, UT USA
[2] Sun Yat sen Univ, Sch Med, Inst Hypertens, Guangzhou, Peoples R China
来源:
基金:
美国国家卫生研究院;
中国国家自然科学基金;
关键词:
II-INDUCED HYPERTENSION;
LIVER X RECEPTOR;
CHRONIC KIDNEY-DISEASE;
VACUOLAR H+-ATPASE;
SOLUBLE (PRO)RENIN RECEPTOR;
RENAL INTERSTITIAL FIBROSIS;
CARDIOVASCULAR RISK-FACTORS;
VITAMIN-D SUPPLEMENTATION;
BLOOD-PRESSURE REGULATION;
PROXIMAL TUBULE CELLS;
D O I:
10.1681/ASN.2016070734
中图分类号:
R5 [内科学];
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号:
1002 ;
100201 ;
摘要:
The renin-angiotensin system (RAS) has a pivotal role in the maintenance of extra cellular volume homeostasis and blood pressure through complex mechanisms. Apart from the well known systemic RAS, occurrence of a local RAS has been documented in multiple tissues, including the kidney. A large body of recent evidence from pharmacologic and genetic studies, particularly those using various transgenic approaches to manipulate intrarenal levels of RAS components, has established the important role of intrarenal RAS in hypertension. Recent studies have also begun to unravel the molecular mechanisms that govern intrarenal RAS activity. This local system is under the control of complex regulatory networks consisting of positive regulators of (pro)renin receptor, Wnt/p-catenin signaling, and PG E-2/PG E-2 receptor EP4 subtype, and negative regulators of Klotho, vitamin D receptor, and liver X receptors. This review highlights recent advances in defining the regulation and function of intrarenal RAS as a unique entity separate from systemic angiotensin II generation.
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页码:1040 / 1049
页数:10
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