玄参醇提物对大鼠心肌梗死的有益作用

IF 1 Q4 PHARMACOLOGY & PHARMACY Jundishapur Journal of Natural Pharmaceutical Products Pub Date : 2023-07-09 DOI:10.5812/jjnpp-134493
Sevda Shayesteh, A. Garjani, S. Azadi, P. Asgharian
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引用次数: 0

摘要

背景:心肌梗死(MI)是心血管疾病死亡的主要原因。再灌注是最有害的阶段,伴随着心肌细胞的炎症、氧化和凋亡级联反应,损害心脏组织的血液动力学和组织学状态。玄参属以其物种的心脏保护作用而闻名,在之前的研究中显示出对血压和心律失常的有益影响。目的:就心肌梗死的发病机制及玄参属植物的心脏保护作用,评价了玄参对心肌梗死的保护作用。在干预组中,在第一次ISO注射后两小时,通过管饲法(24小时间隔)给予5、10和20mg/kg的阿托帕坦提取物三天。通过将导管插入右颈动脉和左心室来测量心脏血液动力学参数。评估总抗氧化状态(TAS)、丙二醛(MDA)和乳酸水平以及组织病理学变化。结果:MI的诱导伴随着中动脉压(MAP)、左心室收缩压(LVSP)和总抗氧化状态(TAS)水平的下降。相反,MI组的心率、左心室舒张末期压(LVEDP)、丙二醛(MDA)和乳酸水平升高。玄参治疗增加了MAP、LVSP和TAS水平,并显著降低了心率、LVEDP、MDA和乳酸水平。此外,阿托帕坦治疗可防止心肌梗死后的组织病理学变化。结论:阿托帕坦对心肌梗死的改善作用表明其作为补充心脏保护药物的潜力。
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The Beneficial Effects of Scrophularia atropatana Methanolic Extract on Myocardial Infarction in Rats
Background: Myocardial infarction (MI) is the leading cause of death among cardiovascular diseases. Reperfusion, the most harmful phase, is accompanied by inflammatory, oxidative, and apoptotic cascades in cardiomyocytes, impairing the hemodynamic and histologic status of the cardiac tissue. The Scrophularia genus is well known for the cardioprotective effects of its species, showing beneficial impacts on blood pressure and arrhythmias in previous studies. Objectives: Regarding the mechanisms involved in MI and the cardioprotective effects of the Scrophularia genus, in this study, we evaluated the cardioprotective effects of Scrophularia atropatana on MI. Methods: Isoproterenol (ISO) injections (100 mg/kg, sc, 24-hour intervals) were used to induce MI in rats. In intervention groups, two hours after the first ISO injection, 5, 10, and 20 mg/kg S. atropatana extract was administered by gavage (24-hour intervals) for three days. Cardiac hemodynamic parameters were measured by placing a catheter into the right carotid artery and the left ventricle. Total antioxidant status (TAS), malondialdehyde (MDA) and lactate levels, and histopathologic changes were evaluated. Results: Induction of MI was accompanied by declined median arterial pressure (MAP), left ventricular systolic pressure (LVSP), and total antioxidant status (TAS) levels. In contrast, the heart rate, left ventricle end-diastolic pressure (LVEDP), malondialdehyde (MDA), and lactate levels were elevated in the MI group. Scrophularia atropatana treatment increased the MAP, LVSP, and TAS levels and significantly reduced the heart rate, LVEDP, MDA, and lactate levels. Also, S. atropatana treatment prevented histopathologic changes post-MI. Conclusions: The improving effects of S. atropatana on MI injuries suggest its potential as a complementary cardioprotective medication.
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