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Astragalus Polysaccharide Reduces Blood Pressure, Renal Damage, and Dysfunction Through the TGF- β 1-ILK Pathway.

Authors :
Zheng W
Huang T
Tang QZ
Li S
Qin J
Chen F
Source :
Frontiers in pharmacology [Front Pharmacol] 2021 Oct 06; Vol. 12, pp. 706617. Date of Electronic Publication: 2021 Oct 06 (Print Publication: 2021).
Publication Year :
2021

Abstract

Background: Astragalus polysaccharide extract (APS) has been shown to exhibit antioxidant and anti-inflammatory potential in the treatment of several diseases. However, whether APS could protect against renal damage in hypertensive mice is unknown. Methods: Hematoxylin and eosin staining, immunohistochemistry, real-time polymerase chain reaction, and Western blotting were used to investigate the effect of APS on the renal damage in deoxycorticosterone acetate- (DOCA) salt- and angiotensin II- (Ang II-) induced hypertensive mice and to elucidate the underlying mechanisms. Results: Our data demonstrated that APS significantly reduced blood pressure in DOCA-salt- and Ang II-treated mice. Furthermore, APS reduced the inflammatory response and renal fibrosis, thereby improving renal function. Furthermore, the levels of serum creatinine, urea nitrogen, and uric acid increased in DOCA-salt-treated mice, alleviated by APS administration. At the molecular level, DOCA-salt and Ang II increased the mRNA levels of IL-1 β , IL-6, α -SMA, collagen I, and collagen III, while APS significantly inhibited these effects. APS inhibited the TGF- β 1/ILK signaling pathway, which was activated in hypertensive mice due to the administration of DOCA-salt. Conclusion: Our results suggest that APS plays a beneficial role in improving renal dysfunction in hypertensive mice.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Zheng, Huang, Tang, Li, Qin and Chen.)

Details

Language :
English
ISSN :
1663-9812
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in pharmacology
Publication Type :
Academic Journal
Accession number :
34690754
Full Text :
https://doi.org/10.3389/fphar.2021.706617