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蜂王浆对小鼠扑热息痛诱导的肝损伤的影响。

The effects of royal jelly on liver damage induced by paracetamol in mice.

作者信息

Kanbur Murat, Eraslan Gökhan, Beyaz Latife, Silici Sibel, Liman Bilal Cem, Altinordulu Sule, Atasever Ayhan

机构信息

Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Erciyes, Kayseri, Turkey.

出版信息

Exp Toxicol Pathol. 2009 Mar;61(2):123-32. doi: 10.1016/j.etp.2008.06.003. Epub 2008 Aug 6.

Abstract

The present study was undertaken to investigate the protective effect of royal jelly against paracetamol-induced liver damage. The study was conducted in 90 female Swiss Albino mice, and six groups were established. While the first group was maintained as control, Groups 2-6 were administered 200mg/kg RJ for 1 day, 200mg/kg RJ for 7 days, 400mg/kg PAR for 1 day, 200mg/kg RJ plus 400mg/kg PAR for 1 day and 200mg/kg RJ for 7 days and then second 400mg/kg PAR on the 7th day, orally, respectively. It was shown that PAR significantly increased serum ALT, AST, ALP, liver MDA levels and significantly decreased liver GSH-Px activity, when compared to the control group (Group 1). On the other hand, meaningful changes were observed in the biochemical parameters of the group which was administered long-term RJ (Group 6). The aforementioned parameters which were statistically significant were determined to have drawn closer to values of the control group, and among these, the existing statistical differences for MDA level and GSH-Px activity between the trial group (Group 6) and the control group disappeared (Group 1). Compared to the pathological changes observed in the liver parenchyma, remark cords, sinusoids and hepatocytes in the group which was administered paracetamol alone (Group 4), lesions were determined to be less severe particularly in the group (Group 6) which received royal jelly for 7 days prior to paracetamol. In conclusion, the administration of royal jelly as a hepatoprotective agent for 7 days against paracetamol-induced liver damage was determined to exhibit marked protective effect on liver tissue.

摘要

本研究旨在探讨蜂王浆对扑热息痛诱导的肝损伤的保护作用。该研究以90只雌性瑞士白化小鼠为实验对象,分为六组。第一组作为对照组,第2 - 6组分别口服给予200mg/kg蜂王浆1天、200mg/kg蜂王浆7天、400mg/kg扑热息痛1天、200mg/kg蜂王浆加400mg/kg扑热息痛1天、200mg/kg蜂王浆7天,然后在第7天给予第二次400mg/kg扑热息痛。结果显示,与对照组(第1组)相比,扑热息痛显著升高了血清谷丙转氨酶(ALT)、谷草转氨酶(AST)、碱性磷酸酶(ALP)水平以及肝脏丙二醛(MDA)水平,并显著降低了肝脏谷胱甘肽过氧化物酶(GSH - Px)活性。另一方面,长期给予蜂王浆的组(第6组)的生化参数出现了显著变化。上述具有统计学意义的参数被确定更接近对照组的值,其中,试验组(第6组)与对照组之间MDA水平和GSH - Px活性的现有统计学差异消失。与单独给予扑热息痛的组(第4组)肝脏实质、汇管区、肝血窦和肝细胞中观察到的病理变化相比,在扑热息痛给药前接受7天蜂王浆治疗的组(第6组)中,病变尤其不那么严重。总之,确定连续7天给予蜂王浆作为肝保护剂对扑热息痛诱导的肝损伤对肝脏组织具有显著的保护作用。

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