Cardioprotective effect of hydroalcoholic leaf extract of Jatropha mollissima on isoproterenol-induced myocardial infarction in rats

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Abstract
Pharmacognosy Magazine,2021,17,06,s251-s256.
Published:September 2021
Type:Original Article
Authors:
Author(s) affiliations:

Muhammad Omer Iqbal1, Imran Ahmad Khan2, Ashira Manzoor3, Shafia Arshad4, Asad Saleem Sial5, Eshwa Dar6, Abdul Rashid Shaikh6
1 Key Laboratory of Marine Drugs (Ministry of Education), Shandong Provincial Key Laboratory of Glycoscience and Glycoengineering, School of Medicine and Pharmacy, Ocean University of China, Qingdao, Shandong 266003, China; Fatima Tu Zahra, Department of Life Sciences, Muhammad Institute of Medical and Allied Sciences, Multan, Pakistan
2 Fatima Tu Zahra, Department of Life Sciences, Muhammad Institute of Medical and Allied Sciences, Multan; Department of Pharmacology, The Islamia University of Bahawalpur, Pakistan
3 Fatima Tu Zahra, Department of Life Sciences, Muhammad Institute of Medical and Allied Sciences, Multan, Pakistan
4 Faculty of Medicine and Allied Health Sciences, The Islamia University of Bahawalpur, Bahawalpur, Pakistan
5 Department of Pharmacognosy, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan
6 Department of Pharmacology, Faculty of Pharmacy, University of Lahore, Pakistan

Abstract:

We aim to explore various effects of doses of Jatropha mollissima against isoproterenol-induced myocardial infarction in the rat. Rats were divided into 6 groups (10 rats in each). Group-1 was normal to control, and Group-2 was considered intoxicated isoproterenol (ISP) (100 mg/kg, s. c.) Group-3 was treated with standard drug carvedilol, while Group-4, 5, and 6 were treatment groups and treated with J. mollissima extract at the doses of 400, 600, and 800 mg/kg, respectively. Preliminary phytochemistry, histopathological variation in the myocardium, antioxidant potential, and cardiac biomarkers (serum glutamic oxaloacetic transaminase, triglyceride, 2,4,6-trinitrotoluene, serum glutamic pyruvic transaminase, lactate dehydrogenase, and creatine kinase muscle–brain fraction), cardiac rate, electrocardiographing, and pressurization rate index were estimated. This study indicates that the extract proved to have cardioprotective potential and significantly reduced the cardiac biomarkers in a dose-dependent fashion because of flavonoid contents and antioxidant property. The histopathological analysis shows marked improvement in J. mollissima groups handled in comparison with ISP. The present evaluation suggests that J. mollissima has exceptional cardioprotective potential contrary to toxicity caused by isoproterenol. We recommend further studies at the molecular level to frame the exact mechanism of action.

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Images
Histopathological sections of the rat kidney; (a) Control (b) ISP (c) SD (d) ISP + JM (400 mg/kg) (e) ISP + JM (600 mg/kg) (f) ISP + JM (800 mg/kg). ISP: Isoproterenol; SD: Standard drug; JM: Jatropha mollissima
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