中国实验动物学报
中國實驗動物學報
중국실험동물학보
ACTA LABORATORIUM ANIMALIS SCIENTIA SINICA
2014年
4期
1-5
,共5页
孟哲颖%王玉%南淑良%林艳端%徐卫平%胡兵%申锷
孟哲穎%王玉%南淑良%林豔耑%徐衛平%鬍兵%申鍔
맹철영%왕옥%남숙량%림염단%서위평%호병%신악
miR-182%糖尿病%心脏功能%心肌肥大%自噬%小鼠
miR-182%糖尿病%心髒功能%心肌肥大%自噬%小鼠
miR-182%당뇨병%심장공능%심기비대%자서%소서
Mir-182%Diabetes%Cardiac function%Cardiac hypertrophy%Autophagy%Mice
目的:探讨miR-182模拟物对1型糖尿病小鼠心脏功能的影响及可能作用机制。方法40只8周龄雄性C57小鼠随机分为正常对照组(n=5),miR-182模拟物对照组(n=5),1型糖尿病组(n=15),1型糖尿病+miR-182模拟物治疗组(n=15)。腹腔注射链脲佐菌素(STZ)建立1型糖尿病动物模型。实验于8周末结束,采用小动物用高分辨超声仪测量小鼠心脏功能;运用透射电镜观察心肌组织超微结构改变;利用real-time PCR技术检测心肌组织β-肌球蛋白重链(β-MHC),α-肌球蛋白重链(α-MHC),心房钠尿肽(ANP),I型(Col I)和III型胶原(Col III) mRNA及miR-182 mRNA的表达含量。结果①miR-182模拟物可改善1型糖尿病小鼠的心脏功能,增加心脏射血分数及左室短轴缩短率(P<0.01);②miR-182模拟物可降低糖尿病小鼠心肌组织ANP、Col I、Col III的表达及β/a-MHC比值(P<0.01);③miR182模拟物可改善1型糖尿病小鼠心肌超微结构变化,减轻自噬。结论MiR-182模拟物能改善1型糖尿病小鼠的心脏功能,其机制可能与减轻心肌肥大和心肌纤维化,减轻线粒体结构损伤及减轻自噬有关。
目的:探討miR-182模擬物對1型糖尿病小鼠心髒功能的影響及可能作用機製。方法40隻8週齡雄性C57小鼠隨機分為正常對照組(n=5),miR-182模擬物對照組(n=5),1型糖尿病組(n=15),1型糖尿病+miR-182模擬物治療組(n=15)。腹腔註射鏈脲佐菌素(STZ)建立1型糖尿病動物模型。實驗于8週末結束,採用小動物用高分辨超聲儀測量小鼠心髒功能;運用透射電鏡觀察心肌組織超微結構改變;利用real-time PCR技術檢測心肌組織β-肌毬蛋白重鏈(β-MHC),α-肌毬蛋白重鏈(α-MHC),心房鈉尿肽(ANP),I型(Col I)和III型膠原(Col III) mRNA及miR-182 mRNA的錶達含量。結果①miR-182模擬物可改善1型糖尿病小鼠的心髒功能,增加心髒射血分數及左室短軸縮短率(P<0.01);②miR-182模擬物可降低糖尿病小鼠心肌組織ANP、Col I、Col III的錶達及β/a-MHC比值(P<0.01);③miR182模擬物可改善1型糖尿病小鼠心肌超微結構變化,減輕自噬。結論MiR-182模擬物能改善1型糖尿病小鼠的心髒功能,其機製可能與減輕心肌肥大和心肌纖維化,減輕線粒體結構損傷及減輕自噬有關。
목적:탐토miR-182모의물대1형당뇨병소서심장공능적영향급가능작용궤제。방법40지8주령웅성C57소서수궤분위정상대조조(n=5),miR-182모의물대조조(n=5),1형당뇨병조(n=15),1형당뇨병+miR-182모의물치료조(n=15)。복강주사련뇨좌균소(STZ)건립1형당뇨병동물모형。실험우8주말결속,채용소동물용고분변초성의측량소서심장공능;운용투사전경관찰심기조직초미결구개변;이용real-time PCR기술검측심기조직β-기구단백중련(β-MHC),α-기구단백중련(α-MHC),심방납뇨태(ANP),I형(Col I)화III형효원(Col III) mRNA급miR-182 mRNA적표체함량。결과①miR-182모의물가개선1형당뇨병소서적심장공능,증가심장사혈분수급좌실단축축단솔(P<0.01);②miR-182모의물가강저당뇨병소서심기조직ANP、Col I、Col III적표체급β/a-MHC비치(P<0.01);③miR182모의물가개선1형당뇨병소서심기초미결구변화,감경자서。결론MiR-182모의물능개선1형당뇨병소서적심장공능,기궤제가능여감경심기비대화심기섬유화,감경선립체결구손상급감경자서유관。
Objective To investigate the effects of miR-182 mimics on cardiac function in type 1 diabetic mice and explore the mechanisms of action .Methods Forty 8-week-old C57 mice were randomly divided into 4 groups:control group (n=5), miR-182 mimics control groups group (n=5), type 1 diabetes group (n=15) and type 1 diabetes treated by miR-182 mimics (n=15).Eight weeks after modeling , the cardiac function was evaluated by a high-resolution ultra-sonic imaging system for small animals (Vevo 2100).The samples of cardiac tissue was used to observe the ultrastructural changes by electron microscopy and to detect the expression levels of β-MHC,α-MHC, ANP, Col I, Col III and miR-182 mRNA .Results ①MiR-182 mimics improved the cadiac function of type 1 diabetic mice with an increase of left ventricu-lar function and left ventricular short axis fractional shortening ( P<0.01);②MiR-182 mimics significantly decreased the expression level of ANP , Col I, Col III protein and the ratio of β/α-MHC in cardiac tissue;③MiR-182 mimics induced ul-trastructural changes of cardiac tissue in type 1 diabetic mice and the phenomenon of autophagy .Conclusions MiR-182 mimics may improve the cardiac function of type 1 diabetic mice , which is associated with decreased expression of hypertro-phy-related gene ANP,β/α-MHC ratio and expression of Col I, Col III, reduction of mitochondrial damage and autophagy .