时珍国医国药
時珍國醫國藥
시진국의국약
LISHIZHEN MEDICINE AND MATERIA MEDICA RESEARCH
2009年
7期
1640-1642
,共3页
王新华%金东岭%何红梅%张延霞%时志民%赵如同
王新華%金東嶺%何紅梅%張延霞%時誌民%趙如同
왕신화%금동령%하홍매%장연하%시지민%조여동
黄芩苷%抗结核药物%肝损伤%肿瘤坏死因子-α%免疫组织化学
黃芩苷%抗結覈藥物%肝損傷%腫瘤壞死因子-α%免疫組織化學
황금감%항결핵약물%간손상%종류배사인자-α%면역조직화학
Baica1in%Antituberculosis drugs%Hepatic injury%Tumor Necrosis Factor-α%Immunohistochemistry
目的 探讨黄芩苷对抗结核药物肝损伤的保护作用机制.方法 将60只小鼠完全随机分为6组,即正常对照组,肝损伤 (异烟肼+利福霉素钠) 组,联苯双酯组及黄芩苷高、中、低剂量组.给药8 d后,分别用光镜和电镜观察肝脏组织细胞病理学的改变情况,用免疫组织化学染色技术分析肿瘤坏死因子-α(TNF-α)的表达情况.结果 黄芩苷能明显减轻肝细胞变性和坏死,炎症活动程度明显减轻(P<0.05 或P<0.01);TNF-α蛋白在黄芩苷组小鼠肝脏组织内为弱阳性表达(P<0.05 或P<0.01);黄芩苷3个剂量组间小鼠肝脏病理形态学及肝脏组织内TNF-α蛋白的表达均无显著性差异(P>0.05).结论 黄芩苷对抗结核药物肝损伤的保护作用可能与抑制TNF-α蛋白表达有关.
目的 探討黃芩苷對抗結覈藥物肝損傷的保護作用機製.方法 將60隻小鼠完全隨機分為6組,即正常對照組,肝損傷 (異煙肼+利福黴素鈉) 組,聯苯雙酯組及黃芩苷高、中、低劑量組.給藥8 d後,分彆用光鏡和電鏡觀察肝髒組織細胞病理學的改變情況,用免疫組織化學染色技術分析腫瘤壞死因子-α(TNF-α)的錶達情況.結果 黃芩苷能明顯減輕肝細胞變性和壞死,炎癥活動程度明顯減輕(P<0.05 或P<0.01);TNF-α蛋白在黃芩苷組小鼠肝髒組織內為弱暘性錶達(P<0.05 或P<0.01);黃芩苷3箇劑量組間小鼠肝髒病理形態學及肝髒組織內TNF-α蛋白的錶達均無顯著性差異(P>0.05).結論 黃芩苷對抗結覈藥物肝損傷的保護作用可能與抑製TNF-α蛋白錶達有關.
목적 탐토황금감대항결핵약물간손상적보호작용궤제.방법 장60지소서완전수궤분위6조,즉정상대조조,간손상 (이연정+리복매소납) 조,련분쌍지조급황금감고、중、저제량조.급약8 d후,분별용광경화전경관찰간장조직세포병이학적개변정황,용면역조직화학염색기술분석종류배사인자-α(TNF-α)적표체정황.결과 황금감능명현감경간세포변성화배사,염증활동정도명현감경(P<0.05 혹P<0.01);TNF-α단백재황금감조소서간장조직내위약양성표체(P<0.05 혹P<0.01);황금감3개제량조간소서간장병리형태학급간장조직내TNF-α단백적표체균무현저성차이(P>0.05).결론 황금감대항결핵약물간손상적보호작용가능여억제TNF-α단백표체유관.
Objective To investigate the protective effects of baicalin on the hepatic injury induced by antituberculosis drugs in mice.Methods Sixty mice were divided randomly into 6 groups:normal control group,liver injury isoniazid and rifamycin sodium group,positive control group,baicalin groups(high,middle and low doses).The drugs were administered to mice once daily for 8 days.Light microscope and electronic microscope were used respectively to observe the histopathological changes of the hepatic cells.The expression of tumor necrosis factor-α (TNF-α) was detected by immunohistochemistry.Results Baicalin alleviated the degeneration and necrosis induced by antituberculosis drugs obviously.The level of inflammatory activity was relieved significantly (P<0.05,P<0.01).The immunoreactivity of TNF-α protein in liver cells was slightly stained in baicalin groups (P<0.05,P<0.01).There were no significant differences about the pathomorphology,the inflammatory activity and the express of TNF-α protein among baicalin groups (P>0.05).Conclusion The protective effects of baicalin on hepatic injury induced by antituberculosis drugs may be related to inhibit TNF-α protein expression.