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机构地区:[1]安徽医科大学第二附属医院消化内科,合肥230601
出 处:《中国新药杂志》2017年第14期1643-1648,共6页Chinese Journal of New Drugs
基 金:安徽省公益性研究联动计划资助项目(1501ld04046);安徽医科大学校科研基金资助项目(2015xkj127);安徽省自然科学基金资助项目(1708085QH192)
摘 要:目的:探讨乌骨藤提取物对四氯化碳(CCl_4)致慢性肝损伤模型大鼠的保护作用。方法:50只SD大鼠随机分为空白对照组,模型组,乌骨藤低、中、高剂量(10,20,40 mg·kg^(-1))组。以CCl_4皮下注射每周2次制备慢性肝损伤模型。同时各给药组每天灌胃(ig)给药1次,连续6周。计算大鼠的肝脏和脾脏指数;检测血清ALT,AST和肝组织中SOD,MDA,GSH-Px和Hyp水平;HE染色法检测肝组织病理变化;ELISA法检测大鼠血清IL-2水平;流式细胞术检测大鼠外周血T淋巴细胞亚群(CD3^+,CD4^+,CD8^+)的变化情况。结果:给予不同剂量乌骨藤治疗慢性肝损伤模型大鼠后,大鼠肝脾指数、血清ALT,AST,MDA和Hyp水平均不同程度降低,SOD,GSH-Px,IL-2水平升高,升高或降低的差异均以乌骨藤高剂量组尤为显著(P<0.01,P<0.05);乌骨藤显著改善大鼠肝组织病理损伤;大鼠外周血CD3^+和CD4^+亚群细胞比例下降,CD8^+细胞比例上升,CD4^+/CD8^+比值降低。结论:乌骨藤提取物对CCl4诱导的大鼠慢性肝损伤有保护作用,作用可能与其平衡T淋巴细胞亚群,调节免疫功能有关。Objective: To investigate the protective effects of Marsdeniatenacissima extract on CC14-induced chronic liver injury in rats. Methods: Fifty SD rats were randomly divided into the following groups: normal control group, model group, low-, middle- and high-dose M. tenacissima groups ( 10, 20, 40 mg· kg- 1 ) CC14 was given to rats by subcutaneous injection to make liver injury model. At the same time, the treatment groups were intragastricly administered with M. tenacissima twice a week for six weeks. The liver and spleen indexes of rats were calculated. The activities of ALT, AST in serum and SOD, MDA, GSH-Px and Hyp in liver tissues were tested. Histopathology of liver was observed by HE staining. The level of IL-2 in serum was tested by ELISA. The T lymphocytes ( CD3 + , CD4+, CD8 +) in blood were detected by using flow cytometer. Results : Compared with the model group, M. tenaclssima-treated groups showed decreases in the activities of ALT, AST, SOD, MDA, GSHPx and Hyp, and an increase in IL-2 level. Moreover, the pathological damage of liver tissue was obviously improved by M. tenacissima. Furthermore, the proportions of CD3 +, CD4+, CD4+/CD8+ were reduced, while that of CD8 + cells was up-regulated. Conclusion: Marsdeniatenacissima extract has protective effect on CC14-induced chronic liver injury in rats, which might be associated with its regulation of immunological function by counterbalance the T lymphocyte subsets.
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