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血管紧张素转换酶抑制剂及其与参与代谢的系统和分子的相互作用。

ACE inhibitors and their interaction with systems and molecules involved in metabolism.

作者信息

Silva-Velasco Diana L, Cervantes-Pérez Luz G, Sánchez-Mendoza Alicia

机构信息

Departamento de Farmacobiología, CINVESTAV-Coapa, Mexico City, Mexico.

Departamento de Farmacología, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.

出版信息

Heliyon. 2024 Jan 14;10(2):e24655. doi: 10.1016/j.heliyon.2024.e24655. eCollection 2024 Jan 30.

Abstract

The main function of the renin-angiotensin-aldosterone system (RAAS) is the regulation of blood pressure; therefore, researchers have focused on its study to treat cardiovascular and renal diseases. One of the most widely used treatments derived from the study of RAAS, is the use of angiotensin-converting enzyme inhibitors (ACEi). Since it was discovered, the main target of ACEi has been the cardiovascular and renal systems. However, being the RAAS expressed locally in several specialized tissues and cells such as pneumocytes, hepatocytes, spleenocytes, enterocytes, adipocytes, and neurons the effect of inhibitors has expanded, because it is expected that RAAS has a role in the specific function of those cells. Many chronic degenerative diseases compromise the correct function of those organs, and in most of them, the RAAS is overactivated. Therefore, the use of ACEi must exert a benefit on an impaired system. Accordingly, the objective of this review is to present a brief overview of the cardiovascular and renal actions of ACEi and its effects in organs that are not the classic targets of ACEi that carry on glucose and lipid metabolism.

摘要

肾素-血管紧张素-醛固酮系统(RAAS)的主要功能是调节血压;因此,研究人员一直专注于对其进行研究以治疗心血管和肾脏疾病。源于对RAAS研究的最广泛使用的治疗方法之一是使用血管紧张素转换酶抑制剂(ACEi)。自被发现以来,ACEi的主要靶点一直是心血管和肾脏系统。然而,由于RAAS在多种特殊组织和细胞(如肺细胞、肝细胞、脾细胞、肠细胞、脂肪细胞和神经元)中局部表达,抑制剂的作用范围有所扩大,因为预计RAAS在这些细胞的特定功能中发挥作用。许多慢性退行性疾病会损害这些器官的正常功能,并且在大多数此类疾病中,RAAS被过度激活。因此,使用ACEi必定会对受损系统产生益处。相应地,本综述的目的是简要概述ACEi的心血管和肾脏作用及其在并非ACEi传统靶点但参与葡萄糖和脂质代谢的器官中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe4/10828069/69d4ad27a1be/gr1.jpg

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