口服红参对大鼠肝脏缺血再灌注损伤的影响。

Mert Çöl, Salih Tuncal, Mevlut Recep Pekcici, Koray Koşmaz, Saygın Altıner, Mehmet Şeneş, Gül Kırtıl, Neslihan Durmaz, Mehmet Alpaslan Gönültaş, Sema Hücümenoğlu
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引用次数: 0

摘要

背景:本研究通过生物化学和组织病理学评价,探讨红参(RG)对实验性肝缺血再灌注损伤(IRI)模型氧化应激和病理变化的保护作用。方法:选用体重174 ~ 232 g的Wistar-Albino雌性大鼠50只。这些动物被随机分为五组,每组10只大鼠。第一组剖腹手术后,摘除肝蒂,不做进一步手术,采集组织和血液样本。II组,剖腹手术后夹持肝动脉、门静脉60分钟诱导缺血。在不给药的情况下,于再灌注后90分钟再次手术采集组织和血液样本。III组在剖腹手术后,同样通过夹持肝动脉和门静脉60分钟诱导缺血。再灌注后48小时再次手术,再次不给药,采集组织和血液样本。IV组大鼠术前3 d经胃管给予RG 5 mg/kg/d。随后开腹,通过夹紧肝动脉和门静脉诱导缺血60分钟。在再灌注90分钟后再次手术收集组织和血液样本,术后不给药。V组术前经胃管给药RG 5 mg/kg/d,连续3天,开腹后夹持肝动脉、门静脉诱导缺血60分钟。再灌注后,大鼠术后2 d经口胃管给予相同剂量的RG,第48小时再次手术采集组织和血液样本。结果:红参无明显的组织病理学作用;然而,在生化参数上观察到差异。结论:红参对缺血再灌注损伤具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of oral administration of red ginseng on liver ischemia-reperfusion injury in rats.

Background: This study investigated the protective effect of red ginseng (RG) on oxidative stress and pathological changes in an experimental liver ischemia-reperfusion injury (IRI) model, using both biochemical and histopathological evaluations.

Methods: Fifty female Wistar-Albino rats were used, with body weights ranging from 174 g to 232 g. The animals were randomly divided into five groups, each consisting of 10 rats. After laparotomy in Group I, the hepatic pedicle was mobilized, no further procedures were performed, and tissue and blood samples were collected. In Group II, ischemia was induced by clamping the hepatic artery and portal vein for 60 minutes following laparotomy. Tissue and blood samples were collected via reoperation at 90 minutes after reperfusion, without any drug administration. In Group III, ischemia was similarly induced by clamping the hepatic artery and portal vein for 60 minutes after laparotomy. Tissue and blood samples were collected via reoperation at the 48th hour after reperfusion, again without any drug administration. In Group IV, RG was administered to the rats at a dose of 5 mg/kg/day via orogastric tube for three days preoperatively. This was followed by laparotomy and induction of ischemia through clamping of the hepatic artery and portal vein for 60 minutes. Tissue and blood samples were collected via reoperation at 90 minutes after reperfusion, with no drug administered postoperatively. In Group V, RG was administered at a dose of 5 mg/kg/day via orogastric tube for three days preoperatively, followed by laparotomy and induction of ischemia by clamping the hepatic artery and portal vein for 60 minutes. After reperfusion, the rats received RG at the same dose for two days postoperatively via orogastric tube, and tissue and blood samples were collected via re-operation at the 48th hour.

Results: Red ginseng did not show a significant histopathological effect; however, differences were observed in biochemical parameters.

Conclusion: Red ginseng may have protective effects against ischemia-reperfusion injury.

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