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Antihypertensive, antioxidant, and renal protective impact of integrated GJD with captopril in spontaneously hypertensive rats
被引:5
|作者:
Mohammed, Shadi A. D.
[1
,4
]
Liu, Hanxing
[1
]
Baldi, Salem
[2
]
Wang, Yu
[3
]
Chen, Pingping
[3
]
Lu, Fang
[3
]
Liu, Shumin
[3
]
机构:
[1] Heilongjiang Univ Chinese Med, Grad Sch, Harbin 150040, Heilongjiang, Peoples R China
[2] Axbio Biotechnol Shenzhen Co Ltd, Res Ctr Mol Diagnost & Sequencing, Shenzhen 518057, Guangdong, Peoples R China
[3] Heilongjiang Univ Chinese Med, Inst Tradit Chinese Med, Harbin 150040, Heilongjiang, Peoples R China
[4] Lebanese Int Univ, Sch Pharm, Sanaa 18644, Yemen
关键词:
RENIN-ANGIOTENSIN SYSTEM;
OXIDATIVE STRESS;
NITRIC-OXIDE;
BLOOD-PRESSURE;
NADPH OXIDASE;
PATHOPHYSIOLOGY;
DYSFUNCTION;
EXPRESSION;
PHYSIOLOGY;
MECHANISM;
D O I:
10.1038/s41598-023-38020-0
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Hypertension is the most prevalent chronic disease World-wide, and the leading preventable risk factor for cardiovascular disease (CVD). Few patients accomplish the objective of decreasing blood pressure and avoiding hypertensive target organ damage after treatments with antihypertensive agents which opens the door for other treatments, such as herbal-and antihypertensive combination therapy. Captopril (CAP), as a-pril which inhibits angiotensin converting enzyme has long been used in the management of hypertension and CVD. Gedan Jiangya Decoction (GJD) is known for antihypertensive effects in prior studies. The research is aimed to determine whether GJD in combination with captopril has antihypertensive, kidney protective, antioxidant, and vasoactive effects in spontaneously hypertensive rats (SHR). Regular measurements of systolic and diastolic blood pressure (SBP and DBP), and body weight were monitored weekly. H & E staining was utilized to examine histopathology. The combined effects were studied using ELISA, immunohistochemistry, and qRT-PCR. Significant reductions in SBP, DBP, aortic wall thickness, and improvement in renal tissue were observed following GJD + CAP treatment, with increased serum levels of NO, SOD, GSH-Px, and CAT and decreases in Ang II, ET-1, and MDA. Similarly, GJD + CAP treatment of SHR's significantly decreased ET-1 and AGTR1 mRNA and protein expression while increasing eNOS mRNA and protein expression in thoracic aorta and kidney tissue. In conclusion, the present investigation found that GJD + CAP treatment decreases SHR blood pressure, improves aorta remodeling and renal protection, and that this effect could be attributable, in part, due to antioxidant and vascular tone improvement.
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页数:14
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