医学研究与教育
醫學研究與教育
의학연구여교육
MEDICAL RESEARCH AND EDUCATION
2013年
1期
29-32
,共4页
潘文超%周玉娟%段斐%王英超%孟连柱%任明%杨琳
潘文超%週玉娟%段斐%王英超%孟連柱%任明%楊琳
반문초%주옥연%단비%왕영초%맹련주%임명%양림
复方甘草酸苷(CG)%免疫性肝损伤%刀豆蛋白A
複方甘草痠苷(CG)%免疫性肝損傷%刀豆蛋白A
복방감초산감(CG)%면역성간손상%도두단백A
compound glycyrrhizin(CG)%hepatic damage%concanavalin A
目的观察复方甘草酸苷对免疫性肝损伤小鼠的保护作用.方法将50只小鼠随机分为正常对照组、模型组、复方甘草酸苷高、中、低剂量组[400、200、100 mg/(kg?d)],用药7 d,腹腔注射,正常对照组、模型组注射等量生理盐水,除正常对照组外,其余各组尾静脉注射20 mg/kg刀豆蛋白A(Con A).12 h后测定血清谷草转氨酶(AST)、谷丙转氨酶(ALT),计算肝脏、脾脏指数,测定血清TNF–α含量.结果与模型组比较,高、中、低剂量的复方甘草酸苷均能明显降低Con A介导的肝损伤小鼠肝、脾指数,降低血清中AST、ALT的水平,明显降低血清中TNF-α的含量.结论复方甘草酸苷对Con A所致免疫性肝损伤小鼠具有保护作用.
目的觀察複方甘草痠苷對免疫性肝損傷小鼠的保護作用.方法將50隻小鼠隨機分為正常對照組、模型組、複方甘草痠苷高、中、低劑量組[400、200、100 mg/(kg?d)],用藥7 d,腹腔註射,正常對照組、模型組註射等量生理鹽水,除正常對照組外,其餘各組尾靜脈註射20 mg/kg刀豆蛋白A(Con A).12 h後測定血清穀草轉氨酶(AST)、穀丙轉氨酶(ALT),計算肝髒、脾髒指數,測定血清TNF–α含量.結果與模型組比較,高、中、低劑量的複方甘草痠苷均能明顯降低Con A介導的肝損傷小鼠肝、脾指數,降低血清中AST、ALT的水平,明顯降低血清中TNF-α的含量.結論複方甘草痠苷對Con A所緻免疫性肝損傷小鼠具有保護作用.
목적관찰복방감초산감대면역성간손상소서적보호작용.방법장50지소서수궤분위정상대조조、모형조、복방감초산감고、중、저제량조[400、200、100 mg/(kg?d)],용약7 d,복강주사,정상대조조、모형조주사등량생리염수,제정상대조조외,기여각조미정맥주사20 mg/kg도두단백A(Con A).12 h후측정혈청곡초전안매(AST)、곡병전안매(ALT),계산간장、비장지수,측정혈청TNF–α함량.결과여모형조비교,고、중、저제량적복방감초산감균능명현강저Con A개도적간손상소서간、비지수,강저혈청중AST、ALT적수평,명현강저혈청중TNF-α적함량.결론복방감초산감대Con A소치면역성간손상소서구유보호작용.
Objective To study the protective effect of compound glycyrrhizin (CG) on hepatic injury Induced by Con A. Methods 50 mice of BALB/C species were randomly divided into normal group, model group, high, medium, low-dose CG-treated group (400, 200, 100 mg?kg-1?d-1), CG-treated group were injected into peritoneal cavity, the normal and model groups were given normal saline. After 7 days, beside mice in normal group, other groups were injected with concanavalin A (Con A) 20 mg/kg via the tail vein to damage mice’s liver. After 12 hour, the index of liver and spleen were calculated .Using automatic biochemical analyzer, the alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in serum were examined, using ELISA for determination of the serum cytokines:tumor necrosis factor alpha (TNF-α). Results Compared with model group, high, medium, low-dose CG-treated group could significantly decrease the activity of AST and ALT and the index of liver and spleen in mice, and CG also could significantly reduce the inflammatory cytokines TNF-αlevel. Conclusion CG is effective in protecting immunological liver injury in mice induced by Con A.