Protective Effect of Pycnogenol® on Cisplatin Induced-Cardiotoxicity in Rats
Journal Title: Meandros Medical and Dental Journal - Year 2018, Vol 19, Issue 3
Abstract
Objective: This study investigated the cardiotoxicity of cisplatin (CIS) on rat heart by using the oxidative damage of the rat myocardium, troponin I and serum S100A1 levels. Previous studies have reported that cell-protective effect of Pycnogenol® (PYC) depended on its antioxidant and anti-inflammatory properties. Hence, the myocardial protective effect of PYC was investigated in this study. Materials and Methods: Rats were randomly grouped to four with 5 rats in each group. The groups were consisted of control group, PYC group: 10 mg/kg PYC for 7 days, CIS group: 15 mg/kg single injection of CIS on the 5th day, CIS + PYC group: 10 mg/kg PYC for 7 days, plus 15 mg/kg single injection of CIS on the 5th day. Heart and serum samples were acquired subsequently. Results: CIS and PYC co-treatment group had increased catalase level (from 43.61±15.16 to 60.80±21.36, p<0.019) and prevented troponin I elevation (from 7.34±6.20 to 3.03±1.36). The S100A1 level was significantly reduced by CIS (from 10.25±8.8 to 3.99±2.87, p<0.035) and was restored by PYC treatment (32.07±29.23). Conclusion: Injured cardiomyocytes released troponin I after exposure to CIS and PYC, which can protect the cells from CIS cardiotoxicity, increased the tissue catalase level. Additionally, PYC treatment increased serum level of S100A1.
Authors and Affiliations
Ufuk Eryılmaz, Saliha Aksun, Buket Demirci
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