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首页> 外文期刊>World Journal of Gastroenterology >Dose-related effects of dexamethasone on liver damage due to bile duct ligation in rats.
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Dose-related effects of dexamethasone on liver damage due to bile duct ligation in rats.

机译:地塞米松对大鼠胆管结扎所致肝损伤的剂量相关作用。

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摘要

AIM: To evaluate the effects of dexamethasone on liver damage in rats with bile duct ligation. METHODS: A total of 40 male Sprague-Dawley rats, weighing 165-205 g, were used in this study. Group 1 (sham-control, n = 10) rats underwent laparotomy alone and the bile duct was just dissected from the surrounding tissue. Group 2 rats (untreated, n = 10) were subjected to bile duct ligation (BDL) and no drug was applied. Group 3 rats (low-dose dexa, n = 10) received a daily dose of dexamethasone by orogastric tube for 14 d after BDL. Group 4 rats (high-dose dexa, n = 10) received a daily dose of dexamethasone by orogastric tube for 14 d after BDL. At the end of the two-week period, biochemical and histological evaluations were processed. RESULTS: The mean serum bilirubin and liver enzyme levels significantly decreased, and superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GSH-Px) values were significantly increased in low-dose dexa and high-dose dexa groups when compared to the untreatedgroup. The histopathological score was significantly less in the low-dose and high-dose dexa groups compared to the untreated rats. In the low-dose dexa group, moderate liver damage was seen, while mild liver damage was observed in the high-dose dexa group. CONCLUSION: Corticosteroids reduced liver damage produced by bile duct obstruction. However, the histopathological score was not significantly lower in the high-dose corticosteroid group as compared to the low-dose group. Thus, low-dose corticosteroid provides a significant reduction of liver damage without increased side effects, while high dose is associated not with lower fibrosis but with increased side effects.
机译:目的:评价地塞米松对胆管结扎大鼠肝损伤的影响。方法:本研究共使用40只雄性Sprague-Dawley大鼠,体重165-205 g。第1组(假对照,n = 10)大鼠仅接受剖腹手术,并从周围组织中切开胆管。第2组大鼠(未治疗,n = 10)进行了胆管结扎(BDL),并且未使用任何药物。 BDL后第3组大鼠(低剂量右旋糖酐,n = 10)通过胃胃管每日接受地塞米松14d。第4组大鼠(大剂量右旋糖酐,n = 10)在BDL后14天经口胃管接受地塞米松。在两周期间结束时,进行了生化和组织学评估。结果:与低剂量右旋糖酐和高剂量右旋糖酐相比,低剂量右旋糖酐和高剂量右旋糖酐组的平均血清胆红素和肝酶水平显着降低,超氧化物歧化酶(SOD),过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GSH-Px)值显着升高。未经治疗的组。与未治疗的大鼠相比,低剂量和高剂量右旋糖酐组的组织病理学评分明显更低。在低剂量右旋糖酐组中,观察到中度肝损伤,而在高剂量右旋糖酐组中观察到轻度肝损伤。结论:皮质类固醇可减少胆管阻塞所致的肝损害。但是,与低剂量组相比,高剂量皮质类固醇组的组织病理学评分没有明显降低。因此,低剂量的皮质类固醇可显着减少肝脏损害,而不会增加副作用,而高剂量的皮质类固醇则不会降低纤维化程度,而会增加副作用。

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