蜂毒对维拉帕米胚胎毒性对小家鼠产前肝脏和肾脏发育的保护作用

IF 1.1 Q3 BIOLOGY
Amin A. Seleem
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引用次数: 2

摘要

维拉帕米是一种钙通道阻滞剂,广泛用于治疗心血管异常、高血压和心绞痛。蜂毒具有抗肿瘤、抗炎、抗风湿、镇痛和神经保护作用。本研究将70只怀孕雌性小鼠分为两组,第一组主要分为3个亚组,对照组,维拉帕米(40 mg/kg)每日1次和2次,从妊娠0天至E10雌性划伤。第二主组从妊娠第7天起分为4个亚组,对照组、维拉帕米每日单剂量(40 mg/kg)、蜂毒注射(150 μg/kg/BW)和维拉帕米联合蜂毒治疗,于妊娠第14、17天处死雌鼠。本研究结果表明,维拉帕米处理组在第一次主实验中出现流产和子宫胚胎再吸收现象。在第二个主要实验中,维拉帕米处理组在E14和E17时发育的肝脏和肾脏的组织学图结构异常,热休克蛋白和BAK的免疫组织化学表达改变,与E17时的超微结构异常有关。蜂毒处理组与对照组结构相似,维拉帕米联合蜂毒处理组对维拉帕米胚胎毒性有改善作用。综上所述,蜂毒可作为一种治疗药物,对维拉帕米对肝脏和肾脏发育的毒性有一定的治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculus

Verapamil is a calcium channel blocker that has been widely used in the treatment of cardiovascular abnormalities, hypertension and angina pectoris. The present study investigates the effect of bee venom against verapamil embryotoxicity, bee venom (BV) is characterized with anticancer, anti-inflammatory, anti-rheumatoid, pain-relieving and neuroprotective agents. The current study was carried out on 70 pregnant female mice which were divided into two main groups, the first main group divided into three subgroups, control, treated with single and twice dose daily of verapamil (40 mg/kg) that was treated from zero day of gestation to scarification of females at E10. The second main group that was treated from the seventh day of gestation was divided into four subgroups, control, treated with single dose daily of verapamil (40 mg/kg), injected with bee venom (150 μg/kg/BW) and treated with verapamil combined with bee venom, the females were sacrificed at E14 and E17. The results of this study showed that verapamil treated groups once or twice daily in the first main experiment showed abortion and resorption of uteri embryos. In the second main experiment, developing liver and kidney at E14 and E17 in verapamil treated group showed abnormal architecture of histological picture and alterations of immunohistochemical expression of heat shock protein and BAK that were associated with ultrastructure abnormalities at E17. Bee venom treated group showed the similar structure as control, verapamil combined with bee venom treated group exhibited amelioration against verapamil embryotoxicity. In conclusion, bee venom could be considered as a therapeutic agent and it has a curative effect against the toxicity of verapamil during development of liver and kidney.

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