Oltipraz attenuates the progression of heart failure in rats through inhibiting oxidative stress and inflammatory response
Y. Tang, M. Guo, X.-Y. Ma, W.-P. Sun, M.-H. Hao, H.-Y. Zhu Department of Cardiology, Beijing Luhe Hospital, Capital Medical University, Beijing, China. tangyu7810@126.com
OBJECTIVE: To evaluate the effect of oltipraz (OPZ) on isoproterenol-induced heart failure (HF) and heart function. We also explore the underlying molecular mechanism of OPZ.
MATERIALS AND METHODS: The rats were randomly divided into four groups, including normal control group, isoproterenol (ISO) group, ISO +100 mg/kg OPZ group, and OPZ group. Hemodynamic parameters, such as left-ventricular systolic pressure, were statistically analyzed. Besides, plasma levels of brain natriuretic peptide (BNP), pro-inflammatory cytokines and antioxidant markers were assessed by using enzyme-linked immunosorbent assay (ELISA). Moreover, histopathological examination was applied to assess the degree of cardiac interstitial fibrosis.
RESULTS: OPZ could statistically improve the hemodynamic parameters of the heart function, and could also obviously attenuate cardiac interstitial fibrosis in ISO-induced HF rats when compared with the ISO group. Besides, plasma level of BNP in ISO +100 mg/kg OPZ group dramatically decreased in comparison with that of ISO group. Moreover, compared with ISO group, OPZ treatment significantly reduced the levels of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). Moreover, OPZ treatment remarkably increased the levels of antioxidant markers such as superoxide dismutase (SOD) and glutathione peroxidase (GPx) in ISO-induced HF rats.
CONCLUSIONS: OPZ administration may provide experimental evidence for the possible effect of OPZ on isoproterenol-induced heart failure in rats. Moreover, OPZ administration may have potential utility for the treatment of heart failure.
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To cite this article
Y. Tang, M. Guo, X.-Y. Ma, W.-P. Sun, M.-H. Hao, H.-Y. Zhu
Oltipraz attenuates the progression of heart failure in rats through inhibiting oxidative stress and inflammatory response
Eur Rev Med Pharmacol Sci
Year: 2018
Vol. 22 - N. 24
Pages: 8918-8923
DOI: 10.26355/eurrev_201812_16661