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NO Level and Endothelial NO Synthase Gene Polymorphism (Glu298Asp) in the Patients with Coronary Artery Disease from the Turkish Population
引用本文:Afrasyap L,Ozturk G. NO Level and Endothelial NO Synthase Gene Polymorphism (Glu298Asp) in the Patients with Coronary Artery Disease from the Turkish Population[J]. Acta biochimica et biophysica Sinica, 2004, 36(10): 661-666
作者姓名:Afrasyap L  Ozturk G
作者单位:Department of Physiology,Faculty of Medicine,Maltepe University,Maltepe-Istanbul Turkey
摘    要:A healthy endothelium plays a core role in cardiovascu-lar control [1]. In the endothelial cell, nitric oxide (NO) issynthesized by the endothelial nitric oxide synthase (eNOS)encoded by a 26-exon gene (NOS 3) located on chromo-some 7 [2]. Besides its regulatory functions on vasomotortone and blood flow, endothelial NO is known to inhibitthe platelet activation and modulate migration and growthof the vascular smooth muscle [3]. Indirect evidence sug-gests that alterations of the NO pathwa…

关 键 词:一氧化氮 内皮一氧化氮合酶 基因多态性 土耳其人 冠心病

NO level and endothelial NO synthase gene polymorphism (Glu298Asp) in the patients with coronary artery disease from the Turkish population
Afrasyap Lale,Ozturk Guler. NO level and endothelial NO synthase gene polymorphism (Glu298Asp) in the patients with coronary artery disease from the Turkish population[J]. Acta biochimica et biophysica Sinica, 2004, 36(10): 661-666
Authors:Afrasyap Lale  Ozturk Guler
Affiliation:Department of Biochemistry, Faculty of Health, Mugla University, Mugla, Turkey. laledr@yahoo.com.
Abstract:Nitric oxide is synthesized from L-arginine by endothelial nitric oxide synthase encoded by eNOS gene. This study was performed to investigate the relationship between the serum nitric oxide level and eNOS gene polymorphism in the Turkish population with angiographically diagnosed coronary artery disease (63.47 +/- 9.10 years old, n=250) and control subjects without any history and/or risk factors of coronary artery disease (60.71 +/- 9.14 years old, n=150). Griess assay and PCR-RFLP analysis were used to measure the serum nitric oxide metabolites and genotypes, respectively. It was found that Glu/Glu, Glu/Asp and Asp/Asp genotype frequencies of the eNOS were 49.3%, 41.3% and 9.3% respectively in the control group, and 45.6%, 41.2% and 13.2% in the patient group. Serum nitric oxide levels were (32.56 +/- 17.26) microM in controls and (29.84 +/- 11.88) microM in patients. Neither the frequencies of the Glu298Asp genotypes nor the serum nitricoxide levels showed a significant difference between the groups. There was also no correlation between serum nitric oxide levels and the frequencies of the eNOS genotypes. Result showed that the coronary artery disease of the Turkish population seemed to develop without any alterations in eNOS Glu298Asp genotype frequency and the serum nitric oxide level.
Keywords:coronary artery disease  genetics  nitric oxide  polymorphism  population  
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