Vol 68, No 8 (2010)
Reviews
Published online: 2010-08-21
Zaburzenia genetycznych struktur mitochondrialnych i procesów energetycznych oraz ich rola w etiologii choroby niedokrwiennej serca
DOI: 10.33963/v.kp.79648
Kardiol Pol 2010;68(8):947-950.
Abstract
Apart from the theory of local inflammation in etiopathogenesis of the arteriosclerosis, hypotheses concerning the role of
mitochondria in this process arise growing interest. Some proteins of the respiratory chain (OXPHOS) are coded on mitochondrial
DNA. Their damage leads to interruption of oxidative phosphorylation, what in turns raises the free oxygen radicals
(ROS) generation. The relationship of insufficient mechanism of mitochondrial ROS elimination with the initiation of the
atherosclerosis was confirmed in experimental data. The mutagenesis of mitochondrial DNA is tied with the etiology of
coronary artery disease (CAD). Some disturbances of the structure of mt-DNA are primal. The second group is probably
determined by the effect of CAD influence on the structure of mt-DNA in cardiomyocytes. The mitochondrial energetic
transformations are described in the article, with special regard on their potential influence on the process of mt-DNA
mutagenesis and secondarily on the formation of CAD.
Kardiol Pol 2010; 68, 8: 947-950
Kardiol Pol 2010; 68, 8: 947-950
Keywords: mt-DNAcoronary artery disease