氟美松对急性肝损伤大鼠肝细胞FasFas配体表达和细胞凋亡的影响
氟美松,,氟美松;内毒素;肝损伤;Fas,Fas配体;凋亡,1材料和方法,2结果,3讨论,【参考文献】
Effects of dexamethasone on Fas/Fas ligand expression and apoptosis of hepatocytes in rats with LPSinduced acute liver injuryZHOU GaoSu1, ZHANG ZhenShu2, WANG Fan1, LIN HanJun1, ZHU Jie1
1Ward for Senior Cadres, General Hospital, Beijing Military Region, Beijing 100026, China, 2Department of Gastroenterology, Nanfang Hospital, First Military Medical University, Guangzhou 510515, China
【Abstract】 AIM: To investigate the changes of expression of hepatocytes apoptosis and Fas/Fas ligand (FasL) in lipopolysaccharide (LPS)induced acute liver injury in rats and the effects of treatment by dexamethasone and to evaluate the potential role and mechanism in the pathogenesis of acute liver injury. METHODS: Expression of Fas/FasL protein and mRNA was detected using immunohistochemistry and in situ hybridization, respectively. Apoptosis was determined by terminal UTP nick end labelling (TUNEL) in rats during every phase of acute liver injury. RESULTS: Expression of Fas/FasL protein and mRNA was upregulated and correlated with the increased apoptosis in hepatocytes of rats with lipopolysaccharide (LPS)induced acute liver injury (P<0.05). The administration of dexamethasone suppressed apoptosis as well as expression of Fas/FasL protein and mRNA (P<0.05). CONCLUSION: Dysregulation of apoptosis and activation of Fas/FasL system may play a key role in the pathogenesis of LPSinduced acute liver injury in rats, which worsens the early stage acute liver injury. The protective effects of dexamethasone may obstruct the activation of Fas/FasL system and apoptosis of hepatocytes in rats with LPSinduced acute liver injury and thus alleviate liver damage. ......
您现在查看是摘要页,全文长 9625 字符。