Endothelial and vascular smooth muscle dysfunction in hypertension

被引:25
作者
de Oliveira, Mariana Gonsalves [1 ]
Nadruz Jr, Wilson [2 ]
Monica, Fabiola Zakia [1 ,3 ]
机构
[1] Univ Estadual Campinas, Fac Med Sci, Dept Translat Med Pharmacol, Campinas, SP, Brazil
[2] Univ Estadual Campinas, Fac Med Sci, Dept Internal Med, Campinas, SP, Brazil
[3] Univ Campinas Unicamp, Fac Med Sci, Dept Translat Med Pharmacol, Alexander Fleming St, BR-13083881 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Vascular function; Hypertension; NO-cGMP; Endothelin antagonist; SGLT2; inhibitors; RAAS inhibitors; SOLUBLE GUANYLATE-CYCLASE; ANGIOTENSIN-II RECEPTOR; CYCLIC GUANOSINE-MONOPHOSPHATE; NITRIC-OXIDE SYNTHASE; OXIDATIVE STRESS; BLOOD-PRESSURE; NADPH OXIDASE; MINERALOCORTICOID RECEPTOR; DOUBLE-BLIND; BAY; 41-2272;
D O I
10.1016/j.bcp.2022.115263
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The development of essential hypertension involves several factors. Vascular dysfunction, characterized by endothelial dysfunction, low-grade inflammation and structural remodeling, plays an important role in the initiation and maintenance of essential hypertension. Although the mechanistic pathways by which essential hypertension develops are poorly understood, several pharmacological classes available on the clinical settings improve blood pressure by interfering in the cardiac output and/or vascular function. This review is divided in two major sections. The first section depicts the major molecular pathways as renin angiotensin aldosterone system (RAAS), endothelin, nitric oxide signalling pathway and oxidative stress in the development of vascular dysfunction. The second section describes the role of some pharmacological classes such as i) RAAS inhibitors, ii) dual angiotensin receptor-neprilysin inhibitors, iii) endothelin-1 receptor antagonists, iv) soluble guanylate cyclase modulators, v) phosphodiesterase type 5 inhibitors and vi) sodium-glucose cotransporter 2 inhibitors in the context of hypertension. Some classes are already approved in the treatment of hypertension, but others are not yet approved. However, due to their potential benefits these classes were included.
引用
收藏
页数:16
相关论文
共 215 条
[1]   The biochemical pharmacology of renin inhibitors: Implications for translational medicine in hypertension, diabetic nephropathy and heart failure: Expectations and reality [J].
Abassi, Zaid ;
Winaver, Joseph ;
Feuerstein, Giora Z. .
BIOCHEMICAL PHARMACOLOGY, 2009, 78 (08) :933-940
[2]   Collecting duct-specific knockout of endothelia-1 causes hypertension and sodium retention [J].
Ahn, D ;
Ge, YQ ;
Stricklett, PK ;
Gill, P ;
Taylor, D ;
Hughes, AK ;
Yanagisawa, M ;
Miller, L ;
Nelson, RD ;
Kohan, DE .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (04) :504-511
[3]   Subcellular Reactive Oxygen Species (ROS) in Cardiovascular Pathophysiology [J].
Aldosari, Sarah ;
Awad, Maan ;
Harrington, Elizabeth O. ;
Sellke, Frank W. ;
Abid, M. Ruhul .
ANTIOXIDANTS, 2018, 7 (01)
[4]   Aliskiren ? A promising antioxidant agent beyond hypertension reduction [J].
Alshahrani, Saeed .
CHEMICO-BIOLOGICAL INTERACTIONS, 2020, 326
[5]   Effects of the selective chymase inhibitor TEI-F00806 on the intrarenal renin-angiotensin system in salt-treated angiotensin I-infused hypertensive mice [J].
Ansary, Tuba M. ;
Urushihara, Maki ;
Fujisawa, Yoshihide ;
Nagata, Sayaka ;
Urata, Hidenori ;
Nakano, Daisuke ;
Hirofumi, Hitomi ;
Kitamura, Kazuo ;
Kagami, Shoji ;
Nishiyama, Akira .
EXPERIMENTAL PHYSIOLOGY, 2018, 103 (11) :1524-1531
[6]   CLONING AND EXPRESSION OF A CDNA-ENCODING AN ENDOTHELIN RECEPTOR [J].
ARAI, H ;
HORI, S ;
ARAMORI, I ;
OHKUBO, H ;
NAKANISHI, S .
NATURE, 1990, 348 (6303) :730-732
[7]   Vericiguat in Patients with Heart Failure and Reduced Ejection Fraction [J].
Armstrong, Paul W. ;
Pieske, Burkert ;
Anstrom, Kevin J. ;
Ezekowitz, Justin ;
Hernandez, Adrian F. ;
Butler, Javed ;
Lam, Carolyn S. P. ;
Ponikowski, Piotr ;
Voors, Adriaan A. ;
Jia, Gang ;
McNulty, Steven E. ;
Patel, Mahesh J. ;
Roessig, Lothar ;
Koglin, Joerg ;
O'Connor, Christopher M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 382 (20) :1883-1893
[8]   NITRIC-OXIDE ACTIVATES GUANYLATE CYCLASE AND INCREASES GUANOSINE 3'-5'-CYCLIC MONOPHOSPHATE LEVELS IN VARIOUS TISSUE PREPARATIONS [J].
ARNOLD, WP ;
MITTAL, CK ;
KATSUKI, S ;
MURAD, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (08) :3203-3207
[9]   A new look at the renin-angiotensin system-Focusing on the vascular system [J].
Aurelie Nguyen Dinh Cat ;
Touyz, Rhian M. .
PEPTIDES, 2011, 32 (10) :2141-2150
[10]   Clinical and Molecular Genetics of the Phosphodiesterases (PDEs) [J].
Azevedo, Monalisa F. ;
Faucz, Fabio R. ;
Bimpaki, Eirini ;
Horvath, Anelia ;
Levy, Isaac ;
de Alexandre, Rodrigo B. ;
Ahmad, Faiyaz ;
Manganiello, Vincent ;
Stratakis, Constantine A. .
ENDOCRINE REVIEWS, 2014, 35 (02) :195-233