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Aali, Ehsan, Ghaznavi, Habib, Soltanpour, Mohammad Soleiman, Mahmoudian, Massoud, Shafiei, Massoumeh. (1399). Cardioprotective Effects of Mebudipine in a Rat Model of Doxorubicin-Induced Heart Failure. سامانه مدیریت نشریات علمی, 46(2), 136-143. doi: 10.30476/ijms.2019.82057.0
Ehsan Aali; Habib Ghaznavi; Mohammad Soleiman Soltanpour; Massoud Mahmoudian; Massoumeh Shafiei. "Cardioprotective Effects of Mebudipine in a Rat Model of Doxorubicin-Induced Heart Failure". سامانه مدیریت نشریات علمی, 46, 2, 1399, 136-143. doi: 10.30476/ijms.2019.82057.0
Aali, Ehsan, Ghaznavi, Habib, Soltanpour, Mohammad Soleiman, Mahmoudian, Massoud, Shafiei, Massoumeh. (1399). 'Cardioprotective Effects of Mebudipine in a Rat Model of Doxorubicin-Induced Heart Failure', سامانه مدیریت نشریات علمی, 46(2), pp. 136-143. doi: 10.30476/ijms.2019.82057.0
Aali, Ehsan, Ghaznavi, Habib, Soltanpour, Mohammad Soleiman, Mahmoudian, Massoud, Shafiei, Massoumeh. Cardioprotective Effects of Mebudipine in a Rat Model of Doxorubicin-Induced Heart Failure. سامانه مدیریت نشریات علمی, 1399; 46(2): 136-143. doi: 10.30476/ijms.2019.82057.0

Cardioprotective Effects of Mebudipine in a Rat Model of Doxorubicin-Induced Heart Failure

Iranian Journal of Medical Sciences
مقاله 8، دوره 46، شماره 2، خرداد 2021، صفحه 136-143    اصل مقاله (265.68 K)
نوع مقاله: Original Article(s)
شناسه دیجیتال (DOI): 10.30476/ijms.2019.82057.0
نویسندگان
Ehsan Aali1، 2؛ Habib Ghaznavi3؛ Mohammad Soleiman Soltanpour4؛ Massoud Mahmoudian5؛ Massoumeh Shafiei* 5
1Department of Pharmacology, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran
2Gifted and Talented Students Center, Iran University of Medical Sciences, Tehran, Iran
3Department of Pharmacology, Zahedan University of Medical Sciences, Zahedan, Iran
4Department of Medical Laboratory Sciences, School of Paramedical Sciences, Zanjan University of Medical Sciences, Zanjan, Iran
5Department of Pharmacology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
چکیده
Background: Mebudipine, a dihydropyridine calcium-channel blocker (CCB), shows greater time- and voltage-dependent inhibitory effects than nifedipine. Its significant negative chronotropic effects without having considerable negative inotropic properties may make it a suitable candidate for the pharmacotherapy of heart failure (HF). This study aimed to investigate the possible beneficial action of mebudipine in a rat model of HF.
Methods: The present study carried out in the Department of Pharmacology at the Iran University of Medical Sciences during the years of 2009-2011. An experimental model of HF was induced in male Wistar rats using doxorubicin (DOX). The rats were divided into five groups with seven animals in each group: normal control group, DOX-induced HF control groups, and treatment groups. The animals were administered DOX for 15 days. A consistent deterioration occurred after a four-week rest period. The animals were then treated with intraperitoneal mebudipine (0.5 mg/kg) and intraperitoneal amlodipine (0.35 mg/kg), as well as an equal volume of distilled water for 15 days. The plasma levels of big endothelin-1 (BET-1), creatine kinase-myocardial band (CK-MB), lactate dehydrogenase (LDH), aspartate aminotransferase (AST), and alanine aminotransferase (ALT), as well as the clinical status (heart rate and blood pressure), were assessed before and after treatment. Statistical analysis was performed with SPSS software using parametric and nonparametric ANOVA.
Results: Mebudipine and amlodipine reversed the increased plasma BET-1 values in the treated animals when compared with the HF control group (0.103 and 0.112 vs 0.231 pg/mL, respectively). The increased plasma levels of AST, ALT, CK-MB, and LDH were also reversed in the HF animals that received mebudipine or amlodipine.
Conclusion: The administration of mebudipine to HF animals, akin to amlodipine, palliated the clinical and biochemical signs of the disease in the present study.
The abstract was presented in the Iranian Congress of Physiology and Pharmacology as a poster and published in the Scientific Information Database as a supplement (2015; Vol 22).
کلیدواژه‌ها
Mebudipine؛ Amlodipine؛ Endothelin-1؛ Heart failure؛ Doxorubicin
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