中国糖尿病杂志
中國糖尿病雜誌
중국당뇨병잡지
CHINESE JOURNAL OF DIABETES
2011年
3期
197-200
,共4页
梁湘樱%张红杰%朱凌云%罗云%李菁%项阳%张辰宇
樑湘櫻%張紅傑%硃凌雲%囉雲%李菁%項暘%張辰宇
량상앵%장홍걸%주릉운%라운%리정%항양%장신우
过氧化物酶体增殖物激活受体γ共激活因子-1α%胰岛素抵抗%金银花%ob/ob小鼠
過氧化物酶體增殖物激活受體γ共激活因子-1α%胰島素牴抗%金銀花%ob/ob小鼠
과양화물매체증식물격활수체γ공격활인자-1α%이도소저항%금은화%ob/ob소서
Peroxisome proliferators-activated receptor-γ coactivator-1%Insulin resistance% Lonicera japonica thunb% ob/ob mice
目的:检测金银花提取物对小鼠肝脏和L02细胞中过氧化物酶体增殖物激活受体γ(PPART)共激活因子-1αPGC-1α表达及对胰岛素抵抗(IR)的影响.方法:分别将ob/ob小鼠、C57/B6J小鼠和L02细胞随机分为对照组和实验组,实验组给予金银花提取物,对照组给予生理盐水.给药后检测小鼠肝脏和L02细胞PGC-1α表达.结果:与对照组相比,实验组ob/ob小鼠给予金银花提取物后肝脏PGC-1α mRNA和蛋白表达下调(P<0.05或P<0.01);而实验组C57/B6J小鼠给药后肝脏PGC-1α mRNA表达与对照组比较无统计学差异.给药5d后实验组ob/ob小鼠FPG降低,但实验组与对照组组间胰岛素水平无统计学差异,实验组FPG/FIns比值显著降低.胰岛素耐量实验显示金银花提取物改善了ob/ob小鼠的IR.脂肪酸培养L02细胞,给予金银花提取物后PGC-1α mRNA表达下调(P<0.05),而正常培养L02细胞PGC-1αmRNA表达无变化.结论:金银花提取物可以下调PGC-1α在肝脏中的病理性高表达,降低血糖,改善IR.
目的:檢測金銀花提取物對小鼠肝髒和L02細胞中過氧化物酶體增殖物激活受體γ(PPART)共激活因子-1αPGC-1α錶達及對胰島素牴抗(IR)的影響.方法:分彆將ob/ob小鼠、C57/B6J小鼠和L02細胞隨機分為對照組和實驗組,實驗組給予金銀花提取物,對照組給予生理鹽水.給藥後檢測小鼠肝髒和L02細胞PGC-1α錶達.結果:與對照組相比,實驗組ob/ob小鼠給予金銀花提取物後肝髒PGC-1α mRNA和蛋白錶達下調(P<0.05或P<0.01);而實驗組C57/B6J小鼠給藥後肝髒PGC-1α mRNA錶達與對照組比較無統計學差異.給藥5d後實驗組ob/ob小鼠FPG降低,但實驗組與對照組組間胰島素水平無統計學差異,實驗組FPG/FIns比值顯著降低.胰島素耐量實驗顯示金銀花提取物改善瞭ob/ob小鼠的IR.脂肪痠培養L02細胞,給予金銀花提取物後PGC-1α mRNA錶達下調(P<0.05),而正常培養L02細胞PGC-1αmRNA錶達無變化.結論:金銀花提取物可以下調PGC-1α在肝髒中的病理性高錶達,降低血糖,改善IR.
목적:검측금은화제취물대소서간장화L02세포중과양화물매체증식물격활수체γ(PPART)공격활인자-1αPGC-1α표체급대이도소저항(IR)적영향.방법:분별장ob/ob소서、C57/B6J소서화L02세포수궤분위대조조화실험조,실험조급여금은화제취물,대조조급여생리염수.급약후검측소서간장화L02세포PGC-1α표체.결과:여대조조상비,실험조ob/ob소서급여금은화제취물후간장PGC-1α mRNA화단백표체하조(P<0.05혹P<0.01);이실험조C57/B6J소서급약후간장PGC-1α mRNA표체여대조조비교무통계학차이.급약5d후실험조ob/ob소서FPG강저,단실험조여대조조조간이도소수평무통계학차이,실험조FPG/FIns비치현저강저.이도소내량실험현시금은화제취물개선료ob/ob소서적IR.지방산배양L02세포,급여금은화제취물후PGC-1α mRNA표체하조(P<0.05),이정상배양L02세포PGC-1αmRNA표체무변화.결론:금은화제취물가이하조PGC-1α재간장중적병이성고표체,강저혈당,개선IR.
Objective To explore the effects of extracts of Lonicera japonica Thunb. on hepatic PGC-1α expression and insulin resistance in mice and L02 cell. Methods C57/B6J mice were divided into control group (group A)and Lonicera japonica Thunb.-treated group (group B). The ob/ob mice were divided into control group (group C)and Lonicera japonica Thunb.-treated group (group D). L02 cells cultured in normal medium were divided into control group (group a) and Lonicera japonica Thunb.-treated group(group b). L02 cells cultured in medium with FFA (free fatty acid) were divided into control group(group c)and Lonicera japonica Thunb.-treated group (group d). The basal blood glucose and insulin were measured and insulin tolerance test(ITT) was done in ob/ob mice.PGC-1α mRNA and protein expressions were detected by q-RT-PCR and Western blot respectively. Results Hepatic mRNA expression of PGC-1α were significantly decreased in group d versus group c(P<0.05) and in group D versus group C(P<0.05) , while were similar in group b versus group a and in group B versus group A (all P>0.05).Hepatic protein expression of PGC-1α was significantly lower in group D than in group C(P<0.01). Basal blood glucose were significantly lower in group D than in group C (P<0.05), while insulin secretion were similar (P>0.05). Hepatic insulin resistance in group D was improved according to the results of ITT. Conclusions Lonicera japonica Thunb. decreases the pathologically high expression of PGC-1α mRNA in liver and basal blood glucose, and improves insulin resistance .