期刊文献+

FECH基因rs1787997多态性与有氧耐力训练后左心室结构功能关联性研究

Association between the rs1787997 Polymorphism in FECH Gene and Left Ventricular Structure and Function in Men of Han Nationality in Northern China
下载PDF
导出
摘要 目的:选取中国北方汉族男性亚铁螯合酶(FECH)基因rs1787997多态位点,与耐力训练前后左心室结构、功能指标进行关联性研究,探讨该多态位点作为预测有氧耐力训练后左心室结构、功能指标适应性改变的分子标记。方法:选取102名中国北方汉族男性健康受试者,以95%-105%个体无氧阈强度进行5 000米跑训练,每周3次,共18周,训练前后测定安静及递增负荷下左心室结构与功能等指标。使用PCR-RFLP和测序方法解析该基因多态性的分布特征,并进行该多态与上述生理指标进行关联性分析。结果:有氧耐力训练前,CG基因型受试者在安静状态下的室间隔收缩末厚度(IVSS)、左室后壁收缩末厚度(PWS)、在100W负荷下的心动周期(100W/T)均显著性高于CC型或GG型(P<0.05)。有氧耐力训练后,CG基因型受试者在150W负荷、恢复期时心动周期增加的幅度(△150W/T、△reT)均显著性高于GG型(P<0.05)。结论:在FECH基因rs1787997多态性中,CG基因型在左心室结构与功能的初始水平上面不仅具有较高的遗传优势,还具有较高的耐力训练敏感性,可以作为预测有氧耐力训练敏感性的分子标记。 Objective: To investigate the association between the rs1787997 polymorphism of FECH gene and left ventricular structure and function, and explore the feasibility that SNP rs1787997 has as genetic mark for predicting the effect of aerobic endurance training in men of Han nationality in Northern China. Methods : 102 healthy young male soldiers of Han Nationality in Northern China were recruited to undergo 18 -week 5000m running with the intensity of 95% -105% anaerobic threshold with 3 times a week. Left ventricular structure and function parameters under different loads were measured before and after protocol. The PCR -RFLP and gene sequencing was used to analyze the distribution of this polymorphism. The association of the polymorphism with initial endurance capacity and endurance training response was analyzed. Results : ( 1 ) Before 18 - week 5000m running, the initial mean value of the inter ventricular septal wall thickness systolic (IVSS), left ventricular posterior wall systolic (PWS), cardiac cycle (T) under 100W load in CG genotype were significantly higher than in CC or GG genotype( P 〈 0.05 ). (2)After 18 -week 5000m running, the increased degree of cardiac cycle(T) under 150W load and recovery in CG genotype was significantly higher than in GG genotype ( P 〈 0.05 ). Conclusion : In the rs1787997 polymorphism of FECH Gene, CC genotype has not only initial genetic advantage, but also higher training response in cardiac structure and function to aerobic training, and it could be the genetic marker in predicting endurance training response.
出处 《成都体育学院学报》 CSSCI 北大核心 2014年第6期57-61,共5页 Journal of Chengdu Sport University
基金 国家科技部课题<优秀长跑运动员选材分子遗传学指标的研究>(2003BA904B04)基金资助
关键词 亚铁螯合酶 基因多态性 左心室结构 功能 ferrochelatase gene polymorphism aerobic performance left ventricular structure function
  • 相关文献

参考文献9

  • 1Navarro S, Del Hoyo P, and Campos Y, et al. Increased mito- chondrial respiratory chain enzyme activities correlate with minor extent of liver damage in mice suffering from erythropoietic proto- porphyria[ J ]. Exp Dermatol,2005,14 ( 1 ) : 26 - 33.
  • 2Bloomer J, Wang Y, Singhal A, et al. Molecular studies of liver disease in erythropoietic protoporphyria[ J ]. J Clin Gastroenterol, 2005,39(4 Suppl 2) : S167 -75.
  • 3Lyoumi S, Abitbol M, Andrieu V, et al. Increased plasma transferrin, altered body iron distribution, and microeytie hypoehro- mic anemia in ferroehelatase - deficient mice [ J ]. Blood,2007,109 (2) : 811 -8.
  • 4Tsiftsoglou AS, Tsamadou AI, Papadopoulou LC. Heine as key regulator of major mammalian eellular functions : Molecular, cel- lular and pharmacological aspects [ J ]. Pharmacol Ther, 2006, 111 : 327 - 345.
  • 5Gatta, LB,Vitali M,Verardi R, et al. Inhibition of heine syn- thesis alters Amyloid Preeursor Protein proeessing [ J ]. J Neural Transm, 2009,116( 1 ) : 79 - 88.
  • 6刘海平,胡扬.HIF-1α基因C1772T多态性与有氧耐力训练后左心室结构功能关联性研究[J].体育科学,2009,29(6):62-66. 被引量:3
  • 7Timmons JA, Jansson E, Fischer H, et al. Modulation of ex- tracellular matrix genes reflects the magnitude of physiological ad- aptation to aerobic exercise training in human [ J ]. BMC Biol, 2005,3 : 19.
  • 8Tlmmons JA, Larsson O, Jansson E, et al. Human muscle gene expression responses to endurance training provide a novel perspective on Duchenne muscular dystrophy [ J ]. FASEB J, 2005, 19:750 - 760.
  • 9Shastry BS. SNP alleles in human disease and evolution [ J ]. J Hum Genet, 2002,47 ( 11 ) :561 - 6.

二级参考文献11

  • 1ABBATE A, SCARPA S, SANTINI D, et al. Myocardial expression of survivin, an apoptosis inhibitor, in aging and heart failure. An experimental study in the spontaneously hypertensive rat[J].Int J Cardiol, 2006, (111) : 371-376.
  • 2BALLIGAND J L, CANNON P J. Nitric oxide synthases and cardiac muscle. Autocrine and paraerine influences[J].Arterioscler Thromb Vasc Bio1,1997, (17) : 1846- 1858
  • 3BOUCHARD C,BOULAY M,THIBAULT M C,et al. Training of submaximal working capacity: frequency, intensity, duration, and their interactions[J]. J Sport Med Phys Fitness, 1980, (20) : 29- 40.
  • 4BOUCHARD C, MALINA R M. Genetics of physiological fitness and motor performance[J]. Exe Sport Sci Rev,1983, (11): 306-339.
  • 5ERSLEV A J, SCHUSTER S J ,CAIRO J. Erythropoietin and its clinical promise[J]. Eur J Haematol, 1989, (43) : 367-373.
  • 6JUNG F,PALMER LA, ZHOU N, et al. Hypoxic regulation of inducible nitric oxide synthase via hypoxia inducible factor-1 in cardiac myocytes[J]. Circ Res, 2000, (86):319-325.
  • 7LEGAZ ARRESE A, SERRANO OSTARIZ E, GONZALEZ CARRETERO M, et al. Echocardiography to measure fitness of elite runners[J]. J Am Soc Echocardiogr, 2005, (18) : 419-426.
  • 8PLUIM B M,ZWINDERMAN A H,VAN DER LAARSE A,et al. The athlete's heart. A meta-analysis of cardiac structure and function[J]. Circulation, 2000, (101) : 336-344.
  • 9SEMENZA G L. HIF-1:mediator of physiological and patho-physiological responses to hypoxia[J]. J Appl Physiol, 2000, (88) :1474- 1480.
  • 10TANIMOTO K, YOSHIGA K, EGUCHI H, et al. Hypoxia-inducible factor-1alpha polymorphisms associated with enhanced transactivation capacity, implying clinical significance[J]. Cardnogenesis,2003, (24) : 1779 -1783.

共引文献2

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