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首页> 外文期刊>International Journal of Pharmacology >Asiatic Acid Enhances Antioxidant and Anti-inflammatory Activity to Suppress Isoproterenol Induced Cardiotoxicity
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Asiatic Acid Enhances Antioxidant and Anti-inflammatory Activity to Suppress Isoproterenol Induced Cardiotoxicity

机译:亚洲酸增强抗氧化和抗炎活性,以抑制异丙肾上腺素诱导的心脏毒性

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Background and Objective: Myocardial infarction (heart attack) owing to ischemia is the primary contributor to most of the death caused by cardiovascular disease s (CVDs). This pre-clinical study was framed to investigate the beneficial efficacy of Asiatic acid (AA) against isoproterenol (ISO)-induced myocardial infraction (MI) in experimental rats. Materials and Methods: Healthy male rats (n = 32), were separated into four groups with 8 rats in each group. Group I rats were given only saline (control), group II rats were orally administrated with AA (20 mg kg?1) for 7 days (AA alone), group III rats were induced with ISO (100 mg kg?1, s.c) for 2 consecutive days (MI model), group IV rats were pre-treated (5 days) and co-treated (6th and 7th day) with AA (20 mg kg?1 via orally) and followed by induction of ISO (AA+ISO). Results: Rats pre and co-treated with AA for 7 days and followed by ISO induction (group IV rats)results in considerable increase in the activities of ATPases (Na2+/K+ and Mg2+) and endogenous antioxidants (CAT, SOD, GPx) as well as substantial decrease in the levels of heart weight, heart to body weight ratio, lipid peroxidation product (MDA), Ca2+ ATPases, cardiac markers (cTnT, CK-MB, LDH) and inflammatory markers (IL-6, IL-1β, TNF-α).Moreover, administration with AA greatly reduced the pathological changes (edema, necrosis, neutrophil infiltration) in cardiac tissue and lookalike as a control group. Conclusion: Taken together, that treatment with AA considerably attenuated the ISO-induced cardiotoxicity or MI by exhibiting potent antioxidant and anti-inflammatory activity. However, further studies (clinical trials) are required to support its importance against Myocardial infarction.
机译:背景与目的:缺血导致的心肌梗塞(心脏病发作)是导致心血管疾病(CVD)死亡的主要原因。这项临床前研究旨在研究亚洲酸(AA)对异丙肾上腺素(ISO)诱导的大鼠心肌梗死(MI)的有益疗效。材料与方法:健康雄性大鼠(n = 32)分为四组,每组8只。 I组大鼠仅给予生理盐水(对照组),II组大鼠口服AA(20 mg kg ?1 )7天(仅AA),III组大鼠用ISO诱导(100)连续2天(MI模型)给予mg kg ?1 ,sc),对IV组大鼠进行预处理(5天),并与AA(20 mg kg ?1 经口),然后诱导ISO(AA + ISO)。结果:AA预处理和联合治疗7天,然后进行ISO诱导的大鼠(IV组)导致ATPase活性显着增加(Na 2 + / K + < / SUP>和Mg 2 + )和内源性抗氧化剂(CAT,SOD,GPx)以及心脏重量,心脏与体重之比,脂质过氧化产物(MDA)的水平大幅下降, Ca 2 + ATPases,心脏标志物(cTnT,CK-MB,LDH)和炎症标志物(IL-6,IL-1β,TNF-α)。心脏组织中的水肿(水肿,坏死,中性粒细胞浸润)与对照组相似。结论:综上所述,AA治疗具有有效的抗氧化和抗炎活性,可大大减轻ISO引起的心脏毒性或MI。但是,需要进一步的研究(临床试验)以支持其对心肌梗塞的重要性。

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