Angiotensin II type 2 receptor blocker PD123319 has more beneficial effects than losartan on ischemia–reperfusion injury and oxidative damage in isolated rat heart

Author:

Kilic Aysu1,Ustunova Savas1,Usta Cansu2,Bulut Huri3,Meral Ismail1,Demirci Tansel Cihan4,Gurel Gurevin Ebru4

Affiliation:

1. Department of Physiology, Faculty of Medicine, Bezmialem Vakif University, 34093 Fatih, Istanbul, Turkey.

2. Institute of Graduate Studies in Science and Engineering, Istanbul University, 34134 Fatih, Istanbul, Turkey.

3. Department of Medical Biochemistry, Faculty of Medicine, Bezmialem Vakif University, 34093 Fatih, Istanbul, Turkey.

4. Department of Biology, Faculty of Science, Istanbul University, 34134 Fatih, Istanbul, Turkey.

Abstract

Our study aimed to determine the effects of losartan and PD123319 in ischemia–reperfusion (IR) injury in isolated perfused rat heart. The study used 40 male Wistar albino rats that were grouped as Control, IR, and IR treatment groups that received losartan (20 mg/kg), PD123319 (20 mg/kg), and losartan+PD123319. The hearts were attached to Langendorff isolated heart system by employing in situ cannulation method, and cardiodynamic parameters were recorded during the experiment. At the end of experiment, hearts were retained for biochemical analysis and all data were statistically evaluated. A partial recovery of cardiodynamic parameters was observed in all treatment groups. A significant increase in oxidative stress parameters were seen in the IR group, whereas all treatment groups exhibited lower increase. Furthermore, levels of all antioxidant parameters were significantly lower in the IR group, but higher in the treatment groups. Effects on all parameters were much more remarkable in the PD123319 group. Levels of angiotensin II and renin were increased (P < 0.001) with IR application and decreased (P < 0.001) with the treatment of both antagonists. In conclusion, treatment of losartan and PD123319 played a cardioprotective role against IR injury, PD123319 being more effective in this protection.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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