摘要
目的观察人参皂甙(Gs)对糖皮质激素(GC)下调其受体(GR)的影响,并探讨其作用途径。方法建立大鼠肝总动脉结扎模型,分别给予GS和地塞米松(DEX)等药物干预,观察术后12h各组血清皮质酮、肝脏GR最大结合容量(GRBmax)、平衡解离常数(K)和GRmRNA水平。结果GS组和模型组皮质酮水平明显高于GS+DEX组、DEX组和正常组(均P〈0.01),GS+DEX组和DEX组皮质酮水平明显高于正常组(均P〈0.01);GS组GRBmax高于模型组(P〈0.05),GS+DEX组GRBmax明显低于模型组(P〈0.05),但高于DEX组(P〈0.01);GS组GRmRNA表达明显高于模型组(P〈0.01),DEX组则低于模型组、正常对照组和GS+DEX(P〈0.01)。结论GS虽然对肝缺血损伤大鼠血清皮质酮水平无影响,但可以部分逆转GC对GR的下调作用。
Objective Toobserve the effect of ginsenosides (GS) on the action of glucocorticoid (GC) in down-regulating glucocorticoid receptor (GR) , and to explore the mechanism. Methods The rat model with hepatic artery ligation (HAL) was established and treated with GS and dexamethasone (DEX). Serum corticosterone level, maximal GK binding capacity (GR Bmax), Kd and GR mRNA in liver cells were detected 12 h after HAL. Results The levels of corticosterone in GS group and model group were higher than those in GS + DEX group, DEX group and normal group ( all P 〈0.01 ). The levels of corticosterone in GS + DEX group and DEX group were higher than that of normal group ( both P 〈0.01 ). Compared to model group, GR Bmax in GS group was higher ( P 〈 0.05 ), GR Bmax in GS + DEX group was lower ( P 〈 0.05 ), but higher than that of DEX group (P 〈0.01 ). The expression of GR mRNA in GS group was significantly higher than model group (P 〈 0.01 ) , but GR mRNA expression in DEX group was lower than that in model group, normal group and GS + DEX group (P 〈0.01 ). Conclusion GS partially reverses the down-regulation of GC on GR Bmax and GR mRNA, but it has no effect on serum corticosterone level in the rat model with HAL.
出处
《中华内分泌代谢杂志》
CAS
CSCD
北大核心
2008年第4期425-427,共3页
Chinese Journal of Endocrinology and Metabolism
基金
“十一五”国家科技支撑计划项目(2006BA104A06)
国家自然科学基金(No.30701132)