中华内分泌代谢杂志
中華內分泌代謝雜誌
중화내분비대사잡지
CHINESE JOURNAL OF ENDOCRINOLOGY AND METABOLISM
2012年
5期
419-422
,共4页
尉希清%谭洪勇%张金国%张洪生%陈昱%胡玲爱%刘志华
尉希清%譚洪勇%張金國%張洪生%陳昱%鬍玲愛%劉誌華
위희청%담홍용%장금국%장홍생%진욱%호령애%류지화
辛伐他汀%高糖%心肌细胞%NADPH氧化酶%活性氧簇
辛伐他汀%高糖%心肌細胞%NADPH氧化酶%活性氧簇
신벌타정%고당%심기세포%NADPH양화매%활성양족
Simvastatin%High glucose%Cardiomyocytes%NADPH oxidase subunits%Reactive oxygen species
取原代培养的SD雄性乳鼠心肌细胞在高糖刺激下加入10-7、10-6和10-5mol/L辛伐他汀作用72 h.结果显示,与对照组比较,高糖组心肌细胞活力明显降低(P<0.01),乳酸脱氢酶(LDH)活性显著增加(P<0.01),NADPH氧化酶亚基p22phox、p47phox mRNA表达和活性氧簇(ROS)水平明显增高(均P<0.05);与高糖组比较,辛伐他汀各组心肌细胞活力明显增加(P<0.05),LDH活性显著降低(P<0.05),p22phox、p47phox mRNA表达和ROS水平明显降低,且辛伐他汀浓度对心肌细胞活力的影响呈剂量依赖效应.这些结果提示辛伐他汀能够抑制NADPH氧化酶亚基的基因表达,减轻高糖引起的心肌损伤.
取原代培養的SD雄性乳鼠心肌細胞在高糖刺激下加入10-7、10-6和10-5mol/L辛伐他汀作用72 h.結果顯示,與對照組比較,高糖組心肌細胞活力明顯降低(P<0.01),乳痠脫氫酶(LDH)活性顯著增加(P<0.01),NADPH氧化酶亞基p22phox、p47phox mRNA錶達和活性氧簇(ROS)水平明顯增高(均P<0.05);與高糖組比較,辛伐他汀各組心肌細胞活力明顯增加(P<0.05),LDH活性顯著降低(P<0.05),p22phox、p47phox mRNA錶達和ROS水平明顯降低,且辛伐他汀濃度對心肌細胞活力的影響呈劑量依賴效應.這些結果提示辛伐他汀能夠抑製NADPH氧化酶亞基的基因錶達,減輕高糖引起的心肌損傷.
취원대배양적SD웅성유서심기세포재고당자격하가입10-7、10-6화10-5mol/L신벌타정작용72 h.결과현시,여대조조비교,고당조심기세포활력명현강저(P<0.01),유산탈경매(LDH)활성현저증가(P<0.01),NADPH양화매아기p22phox、p47phox mRNA표체화활성양족(ROS)수평명현증고(균P<0.05);여고당조비교,신벌타정각조심기세포활력명현증가(P<0.05),LDH활성현저강저(P<0.05),p22phox、p47phox mRNA표체화ROS수평명현강저,차신벌타정농도대심기세포활력적영향정제량의뢰효응.저사결과제시신벌타정능구억제NADPH양화매아기적기인표체,감경고당인기적심기손상.
Ventricular myocytes from hearts of the neonatal SD rats were treated with 10-7,10-6,and 10-5 mol/L simvastatin for 72 hours under high glucose condition. Compared with control group,the viability of cadiomyocyte was significantly lower in high glucose group (P<0.01 ).The activity of lactate dehydrogenase,the relative expressions of NADPH oxidase subunits p22phox,p47phox mRNA,and reactive oxygen species level in the high glucose group were higher than those of control group ( all P<0.05).lndexes mentioned above were significantly improved by simvastatin treatment in a dose-dependent manner.These results suggest that simvastatin ameliorates high glucose-induced injury of cardiomyocytes via increasing the expression of NADPH oxidase mRNA.