Issue 26, 2018, Issue in Progress

Thymoquinone protects against cardiac damage from doxorubicin-induced heart failure in Sprague-Dawley rats

Abstract

Heart failure is a complex end stage result of various cardiovascular diseases, and has a poor prognosis. The mechanisms for the development and progression of heart failure have always been an important topic in cardiovascular research, and previous studies have shown that thymoquinone (TQ) protects against cardiotoxicity and cardiac damage. The aim of this study was to investigate the possible protective effects of thymoquinone against cardiac damage in doxorubicin (DOX)-induced heart failure in Sprague-Dawley Rats (SDR). Forty-five male SDR were randomly divided into three groups and administered different treatment regimens for 8 weeks. Left ventricular fractional shortening (LVFS) and ejection fraction (LVEF) were higher in the DOX + TQ group than those in the DOX group. Significant pathophysiology changes (HE and Masson staining) were observed in rats of the DOX group compared to those of the DOX + TQ group. The addition of Thymoquinone inhibited DOX-induced cardiac fibrosis (TGF-β, Smad3, collagen I, collagen III, and α-SMA) and apoptosis (P53, bcl-2, caspase-3, caspase-9, and BAX) in SDR, indicating that thymoquinone may be a potential therapeutic target for cardiac damage caused by DOX-induced heart failure.

Graphical abstract: Thymoquinone protects against cardiac damage from doxorubicin-induced heart failure in Sprague-Dawley rats

Article information

Article type
Paper
Submitted
31 Jan 2018
Accepted
26 Mar 2018
First published
18 Apr 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 14633-14639

Thymoquinone protects against cardiac damage from doxorubicin-induced heart failure in Sprague-Dawley rats

Z. Pei, J. Hu, Q. Bai, B. Liu, D. Cheng, H. Liu, R. Na and Q. Yu, RSC Adv., 2018, 8, 14633 DOI: 10.1039/C8RA00975A

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