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作 者:魏琳琳[1] 郑素军[1] 陈煜[1] 赵军[1] 丁美[1] 段钟平[1]
机构地区:[1]首都医科大学附属北京佑安医院人工肝中心,北京市100069
出 处:《世界华人消化杂志》2008年第23期2610-2614,共5页World Chinese Journal of Digestology
基 金:国家科技攻关计划引导项目;No.2003BA753C;2007年高等学校博士学科点专项科研基金;No.20070025009~~
摘 要:目的:研究N-乙酰半胱氨酸(N-acetylcysteine,NAC)对慢性重型肝炎肝衰竭时肝细胞解毒代谢功能的影响,并比较NAC与还原型谷胱甘肽(GSH)的疗效.方法:体外慢性重型肝炎患者血浆(chronic severe hepatitis plasma,CSHP)培养C3A细胞,并同时分别加入大、中、小三个剂量NAC及对应剂量的GSH,以正常血浆(normal human plasma,NHP)及培养基(100 mL/L FBS-MEM)为对照,分别于24、48、72h3个时间点检测细胞内GSH及脂质过氧化物(MDA)的含量,并检测安定代谢量的变化.结果:24、48、72h3个时间点,培养基组、正常血浆组、各剂量NAC治疗组和GSH治疗组C3A细胞中GSH含量与安定代谢量均分别高于慢性重型肝炎血浆组(GSH:F=246.116,235.489,201.536,均P<0.01;安定代谢量:F=306.812,476.722,502.061,均P<0.01),而慢性重型肝炎血浆组C3A细胞中MDA含量均分别高于上述各组(F=332.48,662.349,492.983,均P<0.01).慢性重型肝炎血浆+NAC组与慢性重型肝炎血浆+GSH组比较,前者细胞内的GSH含量和对安定的代谢量,大、中、小剂量组均分别高于后者对应剂量组(P<0.01),而前者细胞内的MDA含量,大、中、小剂量组均分别低于后者对应剂量组(P<0.01).结论:NAC可以显著改善慢性重型肝炎肝衰竭时肝细胞解毒代谢功能,GSH也有相似功效,且相同摩尔剂量的NAC效果要优于GSH.AIM: To investigate the effects of N-acetylcysteine (NAC) on hepatocyte (using C3A immortalized cell line) detoxification and biological metabolism, and to compare the therapeutic effect between NAC and GSH (reduced glutathione). METHODS: C3A cells were cultured with chronic severe hepatitis plasma (CSHP), while NAC and GSH were added to the medium with a dosage of 25 mmol/L, 5 mmol/L or 1 mmol/L, respectively. Meanwhile, C3A cells cultured with normal human plasma (NHP) or 100 mL/L FBS-MEM were as controls. The contents of GSH and MDA in C3A cells and the metabolic rate of diazepam were detected 24, 48 and 72 h after administration, respectively. RESULTS: Comparison between groups showed that the content of intra-cellular GSH and the metabolic rate of diazepam in C3A cells were significantly higher at 24, 48 and 72 h in the FBS-MEM group, the NHP group and the groups added NAC or GSH in CSHP than those in the CSHP group (GSH: F = 246.116, 235.489, 201.536, all P 〈 0.01; diazepam: F = 306.812, 476.722, 502.061, all P 〈 0.01), but the content of intra-celluar MDA in the CSHP group was markedly higer than those in the other groups (F = 332.48, 662.349, 492.983, all P 〈 0.01). The content of intra-celluar GSH and the metabolic rate of diazepam in C3A cells in the CSHP + NAC groups were higher than those in the CSHP + GSH groups (comparison between the same dosage: P 〈 0.01), but the content of intra-celluar MDA was in the opposite situation (P 〈 0.01). CONCLUSION: NAC can obviously improve the detoxification and biological metabolism of C3A cells cultured in CSHP. NAC is superior to GSH at the same dosage.
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