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作 者:李萍[1] 陶立坚[2] 胡国龄[3] 谭德明[3]
机构地区:[1]天津市传染病医院,天津市肝病研究所天津300192 [2]中南大学湘雅医院肾病研究所 [3]中南大学湘雅医院传染病研究所
出 处:《中国临床药理学与治疗学》2007年第7期782-785,共4页Chinese Journal of Clinical Pharmacology and Therapeutics
摘 要:目的:探讨吡啶酮类化合物1-(3-氟苯基)-5-甲基-2-(1H)吡啶酮(FMP)抗肝纤维化的机制。方法:MTT法观察FMP对肝星状细胞(HSC)增殖的影响,免疫细胞化学观察FMP对HSCⅠ、Ⅲ型胶原表达的影响。结果:FMP200、300、400、500、600μg/mL在24、48h可抑制HSC增殖,显著强于阳性对照组(P<0.05)。免疫细胞化学显示FMP在200μg/mL可抑制HSCⅠ、Ⅲ型胶原蛋白表达。结论:FMP治疗肝纤维化的原理可能与抑制HSC增殖和HSCⅠ、Ⅲ型胶原蛋白表达有关。AIM: To explore the mechanism of 1-(3- fluorophenyl )-5-methyl-2- ( 1H ) pyridone ( FMP ) against hepatic fibrosis. METHODS: The inhibitory effect of FMP on hepatic stellate cells(HSC) proliferation was observed by MTF, and the expression levels of collagen type Ⅰ, Ⅲ protein of HSC were detected by immunocytochemistry. RESULTS: HSC proliferation was decreased after incubation with FMP for 48 h at the dosage range from 200μg/mL to 600 μg/mL compared with that in control group, and FMP could also significantly decrease the protein expression of collagen type Ⅰ, Ⅲ at the dosage of 200μg/mL. CONCLUSION: FMP can inhibit the proliferation of HSC and decrease the expression of type Ⅰ, Ⅲ collagen, which are related to the mechanism of FMP treating hepatic fibrosis.
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