NO-SYNTHASE ACTIVITY IN PATIENTS WITH CORONARY HEART DISEASE ASSOCIATED WITH HYPERTENSION OF DIFFERENT AGE GROUPS

被引:24
作者
Besedina, Anna [1 ]
机构
[1] Danylo Halytsky Lviv Natl Med Univ, Dept Family Med, Lvov, Ukraine
关键词
coronary heart disease; hypertension; nitric oxide; NO-synthase; NITRIC-OXIDE SYNTHASE; OXIDATIVE STRESS; BIOLOGY; RISK; GENE; ENOS;
D O I
10.1515/jomb-2015-0008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Background: Coronary heart disease is the leading cause of death and disability worldwide. Hypertension is a major independent risk factor for the development of CHD. Abnormalities in NO generation or activity have been proposed as a major mechanism of CHD. The purpose of this article is to determine the activity of eNOS and iNOS in patients with isolated CHD and CHD associated with HT of different age groups. Methods: Fifty patients with isolated CHD and 42 patients with CHD associated with HT were enrolled in this study. NOS activity was determined by nitrite anion formed in the reaction. Results: A statistically significant increase in iNOS activity is observed in elderly donors. In patients with isolated coronary heart disease cNOS activity is statistically significantly reduced with respect to the control group. The reduction of enzymatic activity of cNOS is more expressed in elderly patients than in middle-aged patients with coronary heart disease. Alterations in eNOS activity are more expressed in patients with coronary heart disease associated with hypertension than in patients with isolated coronary heart disease. Against the background of cNOS inhibition in the patients, a sharp increase in iNOS activity is observed. Conclusions: It has been shown that disturbance of endothelial function in patients with coronary heart disease associated with hypertension is characterized by reduced endothelial NO synthesis by cNOS and increased systemic NO synthesis due to increased iNOS activity. It has been found that the lack of endothelial NO and hyperproduction of "harmful" NO by iNOS are more expressed in elderly patients.
引用
收藏
页码:43 / 49
页数:7
相关论文
共 32 条
[1]
Abolhalaj M., 2013, J BIOMARKERS, P1
[2]
Endothelial nitric oxide gene polymorphisms, nitric oxide production and coronary artery disease risk in a South Indian population [J].
Angeline, T. ;
Isabel, W. ;
Tsongalis, Gregory J. .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2010, 89 (03) :205-208
[3]
Apykhtina EL, 2007, UKRAINIAN BIOCH J, V5, P204
[4]
Discovery of the nitric oxide signaling pathway and targets for drug development [J].
Bryan, Nathan S. ;
Bian, Ka ;
Murad, Ferid .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2009, 14 :1-+
[5]
Aging-induced phenotypic changes and oxidative stress impair coronary arteriolar function [J].
Csiszar, A ;
Ungvari, Z ;
Edwards, JG ;
Kaminski, P ;
Wolin, MS ;
Koller, A ;
Kaley, G .
CIRCULATION RESEARCH, 2002, 90 (11) :1159-1166
[6]
OXIDATIVE AND NITROSATIVE STRESS IN STABLE RENAL TRANSPLANT RECIPIENTS WITH RESPECT TO THE IMMUNOSUPPRESSION PROTOCOL - DIFFERENCES OR SIMILARITIES? [J].
Cvetkovic, Tatjana ;
Velickovic-Radovanovic, Radmila ;
Stojanovic, Dijana ;
Stefanovic, Nikola ;
Ignjatovic, Aleksandra ;
Stojanovic, Ivana ;
Sladojevic, Nikola ;
Ignjatovic, Aleksandra ;
Stojanovic, Ivana ;
Sladojevic, Nikola ;
Pavlovic, Dusica .
JOURNAL OF MEDICAL BIOCHEMISTRY, 2015, 34 (03) :295-303
[7]
De Backer G G., 2009, Medicographia, V31, P343
[8]
Ethanol Metabolism and Effects: Nitric Oxide and its Interaction [J].
Deng, Xin-Sheng ;
Deitrich, Richard A. .
CURRENT CLINICAL PHARMACOLOGY, 2007, 2 (02) :145-153
[9]
Nitric oxide-dependent endothelial function and cardiovascular disease [J].
Desjardins, F. ;
Balligand, J. -L. .
ACTA CLINICA BELGICA, 2006, 61 (06) :326-334
[10]
Vascular Endothelial Function and Hypertension: Insights and Directions [J].
Dharmashankar, Kodlipet ;
Widlansky, Michael E. .
CURRENT HYPERTENSION REPORTS, 2010, 12 (06) :448-455