Attenuation of isoprenaline-induced myocardial infarction by Rheum turkestanicum

被引:23
|
作者
Hosseini, Azar [1 ,2 ]
Rajabian, Arezoo [3 ]
Sobhanifar, Mohammad-Ali [2 ]
Alavi, Mohaddeseh Sadat [2 ]
Taghipour, Zahra [2 ]
Hasanpour, Maede [4 ]
Iranshahi, Mehrdad [4 ]
Boroumand-Noughabi, Samaneh [5 ,6 ]
Banach, Maciej [7 ,8 ]
Sahebkar, Amirhossein [4 ,9 ,10 ,11 ]
机构
[1] Mashhad Univ Med Sci, Pharmacol Res Ctr Med Plants, Mashhad, Razavi Khorasan, Iran
[2] Mashhad Univ Med Sci, Fac Med, Dept Pharmacol, Mashhad, Razavi Khorasan, Iran
[3] Mashhad Univ Med Sci, Fac Med, Dept Internal Med, Mashhad, Razavi Khorasan, Iran
[4] Mashhad Univ Med Sci, Biotechnol Res Ctr, Pharmaceut Technol Inst, Mashhad, Razavi Khorasan, Iran
[5] Mashhad Univ Med Sci, Fac Med, Dept Pathol, Mashhad, Razavi Khorasan, Iran
[6] Mashhad Univ Med Sci, Fac Med, Dept Hematol & Blood Banking, Mashhad, Razavi Khorasan, Iran
[7] Med Univ Lodz, Dept Prevent Cardiol & Lipidol, Chair Nephrol & Hypertens, Lodz, Poland
[8] Univ Zielona Gora, Cardiovasc Res Ctr, Zielona Gora, Poland
[9] Mashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Razavi Khorasan, Iran
[10] Univ Western Australia, Sch Med, Perth, WA, Australia
[11] Mashhad Univ Med Sci, Sch Pharm, Dept Biotechnol, Mashhad, Razavi Khorasan, Iran
关键词
Myocardial infarction; Isoprenaline; Oxidative stress; Rheum turkestanicum; OXIDATIVE STRESS; EXPERIMENTAL-MODEL; WISTAR RATS; ISOPROTERENOL; TOXICITY; PROTECTS; NARINGIN; EXTRACT; KIDNEY; INJURY;
D O I
10.1016/j.biopha.2022.112775
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Oxidative stress plays a major role in the pathogenesis of myocardial infarction. This study evaluated the cardioprotective effects of the hydroalcoholic extract of Rheum turkestanicum on isoprenaline-induced myocardial infarction (MI) in Wistar rats. Methods: In this study, we used liquid chromatography-mass spectrometry to determine the active compounds present in the extract. Thirty rats were divided to 5 groups (6 rats in each group). The extract was administered orally at the doses of 100 and 300 mg/kg body weight and then a subcutaneous injection of isoprenaline (85 mg/kg) was administered on the 8th and 9th days. Serum levels of lactate dehydrogenase (LDH), creatine kinase-MB (CK-MB), and creatinine kinase (CPK) were measured using standard commercial kits. Serum activities of superoxide dismutase, catalase, and cardiac levels of thiol and lipid peroxidation were also determined. Hematoxylin and eosin were used for histopathological staining. Results: Phytochemical analysis revealed the presence of 24 compounds in the hydro-ethanolic extract of R. turkestanicum. Isoprenaline increased malondialdehyde (4.002 +/- 0178, P < 0.001) while decreased thiol content (101.7 +/- 6.186, P < 0.001). Moreover, reduced activities of superoxide dismutase (139 +/- 10.88, P < 0.001) and catalase (2.812 +/- 0.215, P < 0.001), and elevated levels of LDH (1245 +/- 62.28, P < 0.001), CPK (898 +/- 23.06, P < 0.001) and CK-MB (697 +/- 50.22, P < 0.001) were observed. Pretreatment with the R. turkestanicum extract significantly reduced cardiac markers and increased thiol content as well as the activity of antioxidant enzymes. The extract attenuated the histopathological changes induced by isoprenaline. Conclusion: According to the obtained results, R. turkestanicum may be an appropriate candidate to reduce isoprenaline-induced MI through modulation of oxidative stress. Administration of the extract attenuated cardiac enzymes following isoprenaline administration. The cardioprotective action of the extract can be attributed to the bioactive antioxidant ingredients of R. turkestanicum. To identify the precise mechanisms, further investigations are required. [GRAPHICS]
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页数:7
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