亚慢性敌敌畏致Wistar大鼠心脏毒性:黑草油的缓解作用

A. Imam, M. Busari, M. Adana, M. Ajibola, A. Ibrahim, F. Sulaimon, M. Ajao
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引用次数: 5

摘要

背景:近几十年来,由于滥用有机磷而造成的意外中毒已成为一种地方病,尤其是在发展中国家,再加上令人满意的解毒剂的可用性有限。因此,我们研究了黑草油(NSO)在敌敌畏(DDVP)诱导的Wistar大鼠心脏毒性后的心脏保护作用。材料与方法:取Wistar大鼠24只,随机分为4组(n = 6);实验ⅰ组给予对照组葵花籽油(1 ml/kg)和敌敌畏(8.8 mg/kg),实验ⅱ组和实验ⅲ组分别口服敌敌畏+ NSO (8.8 mg/kg +1 ml/kg)和NSO (1 ml/kg)。这些动物被安乐死;经心导管从右心房采血,离心,提取血浆,分析总胆固醇(TC)、甘油三酯、高密度脂蛋白胆固醇和低密度脂蛋白胆固醇(LDL-C)水平。同时,从左心脏收集心肌组织,处理并染色一般结构(苏木精和伊红)和弹性形态(orcein)。结果:DDVP显著(P≤0.05)提高血浆TC、LDL水平、动脉粥样硬化和动脉粥样硬化指标(TC/HDL-C和LDL- c /HDL-C比值),但与NSO合用可防止这种情况发生。组织学检查显示,DDVP导致心脏组织的病理表现,如缺乏条纹,心肌出血和坏死样特征。结论:NSO对ddvp的心脏毒性有一定的减弱作用。
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Subchronic dichlorvos-induced Cardiotoxicity in Wistar rats: Mitigative efficacy of Nigella sativa oil
BACKGROUND: Accidental poisoning from indiscriminate use of organophosphates have become endemic in recent decades, most especially in developing nations, coupled with the limitations of the availability of satisfactory antidotes. AIM OF THE STUDY: Thus, we investigated the cardioprotective efficacy of Nigella sativa oil (NSO) following dichlorvos dichlorvos (DDVP)-induced cardiotoxicity in Wistar rats. MATERIALS AND METHODS: A total of 24 Wistar rats were randomly divided into four groups (n = 6); the control was administered sunflower oil (1 ml/kg), DDVP (8.8 mg/kg) to the experimental Group I, whereas DDVP + NSO (8.8 mg/kg +1 ml/kg) and NSO (1 ml/kg) was administered orally to the experimental Groups II and III, respectively. The animals were euthanized; blood was transcardially collected from the right atrium, centrifuged, and plasma extracted to analyze levels of total cholesterol (TC), triglycerides, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol (LDL-C). While cardiac muscle tissue was collected from the left heart, processed and stained for general architecture (hematoxylin and eosin) and elastic morphology (orcein). RESULTS: DDVP significantly (P ≤ 0.05) increased the plasma levels of TC, LDL, atherogenic and atherosclerotic indices (TC/HDL-C and LDL-C/HDL-C ratios), but this was prevented by co-administration with NSO. Histological investigations showed that DDVP resulted in the pathological appearance of cardiac tissues, such as the lack of striations, myocardial hemorrhage, and necrosis-like features. CONCLUSION: It can be concluded that NSO was able to attenuate DDVP-induced cardiotoxicity.
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