期刊文献+

微小RNA 30c增加有氧运动训练小鼠心室顺应性的研究 被引量:8

MicroRNA 30c Involved in the Improvement of Ventricular Compliance Promoted by Aerobic Exercise Training in Mice
在线阅读 下载PDF
导出
摘要 目的:探讨有氧运动训练对小鼠心脏形态结构、功能及心室肌微小RNAs(micro RNAs,miRNAs)的影响,研究关健miRNA在心脏对运动适应过程中的调节作用。方法:KM雄性小鼠随机分为安静对照组和8周有氧运动训练组,每组各10只。有氧运动训练组小鼠进行为期8周的无负重有氧训练,每周训练5天,前5周,每天早上固定时间运动1次,后3周每天在早上和晚上固定时间分别运动1次;第1周每次运动时间为30min,随后每周增加10min直至90min。有氧运动训练完成后,首先使用超声心动图检测全部小鼠心脏各项形态学和功能学指标,随后将小鼠颈椎脱位猝死取心肌组织,使用基因芯片扫描两组差异表达的miRNAs,使用实时定量PCR技术验证miRNA-1,-133a,-29和-30c4个关键差异表达的miRNA,同时使用荧光定量PCR和酶联免疫吸附技术检测小鼠心肌组织结缔组织生长因子(connective tissue growth factor,CTGF)基因和蛋白的表达。结果:有氧运动训练明显提高了小鼠心室内径、心壁厚度和功能学指标Ratio E/A,提示运动诱导小鼠心脏生理性肥大,增加了心室顺应性;与安静对照组相比,8周有氧运动训练后小鼠心肌组织中miRNA-1和-133a显著下降(P<0.05),而miRNA-29和-30c则显著升高(P<0.05);同时有氧运动训练组小鼠心肌组织中CTGF基因和蛋白的表达低于对照组,差异具有统计学意义(P<0.05);进一步研究发现,有氧运动训练组小鼠心肌组织中miRNA-30c表达量与CTGF蛋白表达量呈负相关(相关系数r=-0.818,P=0.004)。结论:有氧运动训练通过增加心室肌组织中miRNA-30c的表达量,抑制心肌组织中CTGF的表达和浓度,从而提高运动引起心脏生理性肥大过程中心室顺应性,有利于心脏功能的正常有效发挥。 Objective:To explore the effects of aerobic exercise training on the cardiac structure and miRNAs, and analyze their role in cardiac adaption induced by aerobic exercise training. Methods: Male KM mice (n= 10/group) were randomized into two groups: 8 weeks aerobic exercise training group and sedentary control group. Mice in training group undertook a swim- ming protocol for 8 weeks, 5days/wk, from the 1st to 5th week, mice were trained one time a day in the morning, from the 6th to 8th week, mice were trained twice a day with a 12 h inter- val. In the 1st week, the training time was 30 min, and the time was increased 10 min per week until to 90 min. After the aerobic exercise training, all mice were measured by echocar- diography. MiRNAs analysis was performed by miRNA microarray and confirmed by real-time PCR. The level of connective tissue growth factor (CTGF) gene expression was determined by real-time PCR, CTGF protein concentration was assessed by ELISA. Results:Aerobic exercise training improved aerobic capacity, left ventricular and induced cardiac hypertrophy. MiRNAs- 1 and 133 a were siginificant downregulated in training group ( P 〈 0.05 ), however, miRNAs- 29c and 30c expression increased in training group (P〈0.05), correlated with a decrease in CTGF gene expression in training group (P〈0.05). Furthermore, miRNA-30 c was inversely correlated to CTGF protein contration in training group (r =-0.818, P= 0.05). Conclusion: Aerobic exercise training could increase miRNA-30c expression and decrease CTGF gene ex- pression and concentration in the heart, which is relevant to the improved left ventricular com- pliance and beneficial cardiac effects.
出处 《体育科学》 CSSCI 北大核心 2013年第9期70-76,共7页 China Sport Science
关键词 有氧运动 心脏 心室顺应性 微小RNA 动物实验 aerobic exercise heart ventricular compliance miRNA mice animal experiment
  • 相关文献

参考文献21

  • 1冯伟,张幼怡.MicroRNA基因及其靶位点的单核苷酸多态性与疾病易感性[J].生理科学进展,2010,41(6):443-445. 被引量:4
  • 2王映霞,吴宜林.微小RNA在肿瘤转移中的调节作用[J].国际病理科学与临床杂志,2010,30(6):501-506. 被引量:2
  • 3赵永才.运动对C57BL/6小鼠心肌miRNA的影响及其在心脏肥大中的调节作用[J].体育科学,2012,32(6):62-68. 被引量:9
  • 4AN P,PERUSSE L,RANKINEN T,et al.Familial aggregation of exercise heart rate and blood pressure in response to 20 weeks of endurance training:the HERITAGE family study[J].Int J Sports Med,2003,24(1):57-62.
  • 5BAGGA S,BRACHT J,HUNTER S,et al.Regulation by let-7 and lin-4 miRNAs results in target mRNA degradation[J].Cell,2005,122(4):553-563.
  • 6CASTOLDI G,DI GIOIA C R,BOMBARDI C,et al.MiR-133a regulates collagen 1A1:potential role of miR-133a in myocardial fibrosis in angiotensin Ⅱ-dependent hypertension[J].J Cell Phys,2012,227(2):850-856.
  • 7CATALUCCI D,GALLO P,CONDORELLI G.MicroRNAs in cardiovascular biology and heart disease[J].Circ Cardiovasc Genet,2009,2 (4):402-408.
  • 8DUISTERS R F,TIJSEN A J,SCHROEN B,et al.miR-133 and miR-30 regulate connective tissue growth factor:implications for a role of microRNAs in myocardial matrix remodeling[J].Circ Res,2009,104(2):170-178.
  • 9EHLERT T,SIMON P,MOSER D A.Epigenetics in sports[J].Sports Med,2013,43(2):93-110.
  • 10IGARASHI A,OKOCHI H,BRADHAM D M,et al.Regulation of connective tissue growth factor gene expression in human skin fibroblasts and during wound repair[J].Mol Biol Cell,1993,4(6):637.

二级参考文献37

  • 1Duan R,Pak C,Jin P.Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA.Hum Mol Genet,2007,16:1124-1131.
  • 2Saunders MA,Liang H,Li WH.Human polymorphism at microRNAs and microRNA target sites.Proc Natl Acad Sci USA,2007,104:3300-3305.
  • 3Jazdzewski K,Liyanarachchi S,Swierniak M,et al.Polymorphic mature microRNAs from passenger strand of pre-miR-146a contribute to thyroid cancer.Proc Natl Acad Sci USA,2009,106:1502-1505.
  • 4Xu B,Feng NH,Li PC,et al.A functional polymorphism in Pre-miR-146a gene is associated with prostate cancer risk and mature miR-146a expression in vivo.Prostate,2010,70:467-472.
  • 5Christensen BC,Avissar-Whiting M,Ouellet LG,et al.Mature miRNA sequence polymorphism in MIR196A2 is associated with risk and prognosis of head and neck cancer.Clin Cancer Res,2010,16:3713-3720.
  • 6Zhou B,Rao L,Peng Y,et al.Common genetic polymorphisms in pre-microRNAs were associated with increased risk of dilated cardiomyopathy.Clin Chim Acta,2010,411:1287-1290.
  • 7Abelson JF,Kwan KY,O' Roak BJ,et al.Sequence variants in SLITRK1 are associated with Tourette's syndrome.Science,2005,310:317-320.
  • 8Martin MM,Buckenberger JA,Jiang J,et al.The human angiotensin II type 1 receptor +1166 A/C polymorphism attenuates microrna-155 binding.J Biol Chem,2007,282:24262-24269.
  • 9Sethupathy P,Borel C,Gagnebin M,et al.Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region:a mechanism for functional single-nucleotide polymorphisms related to phenotypes.Am J Hum Genet,2007,81:405-413.
  • 10Sethupathy P,Collins FS.MicroRNA target site polymorphisms and human disease.Trends Genet,2008,24:489-497.

共引文献12

同被引文献116

  • 1Vander Josédas Neves,Tiago Fernandes,Fernanda Roberta Roque,Ursula Paula RenóSoci,Stéphano Freitas Soares Melo,Edilamar Menezes de Oliveira.Exercise training in hypertension:Role of microRNAs[J].World Journal of Cardiology,2014,6(8):713-727. 被引量:9
  • 2张钧,陈晓莺,许豪文.运动对心肌细胞中凋亡调控基因表达的影响[J].体育科学,2005,25(8):79-82. 被引量:29
  • 3马延超,常芸,张缨.运动心脏重塑过程中降钙素基因相关肽基因的表达[J].中国运动医学杂志,2006,25(2):168-170. 被引量:7
  • 4ALESSANDRA CARE, DANIELE CATALUCCI, FEDERICA FELICETTI, et al. MicroRNA 133 controls cardiac hypertrophy [J]. Nature Med,2007,13:613-618.
  • 5AMBROS V. MicroRNA pathways in flies and worms:growth, death, fat, stress, and timing[J]. Cell, 2003,113 : 673-676.
  • 6BARRY S P, DAVIDSON S M, TOWNSEND P A. Molecular regulation of cardiac hypertrophy[J]. Int J Biochem Cell Biol, 2008,40:2023-2039.
  • 7BARTEL D P. MicroRNAs: Genomics, biogenesis, mechanism, and function[J]. Cell, 2004,23 ; 116(2) : 281-297.
  • 8BIANCA C BERNARDO, KATE L WEEKS, LYNETTE PRE- TORIUS, et al. Molecular distinction between physiological and pathological cardiac hypertrophy: Experimental findings and therapeutic strategies [J].Pharrnacol Therapeutics, 2010, 128: 191-227.
  • 9BOLUYT M O, LOYD A M, ROTH M H, et al. Activation of JNK in rat heart by exercise: effect of training[J]. Am J Physi-ol-Heart Circ Physiol, 2003,285:2639-2647.
  • 10DANISH SAYED, CHULL HONG, IENG YI CHEN, et al. MicroRNAs play an essential role in the development of cardiac hypertrophy[J]. Circ Res, 2007,100 : 416-424.

引证文献8

二级引证文献43

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部