Puzserova Angelika, Ilovska Veronika, Balis Peter, Slezak Peter, Bernatova Iveta
Institute of Normal and Pathological Physiology, Centre of Excellence for Examination of Regulatory Role of Nitric Oxide in Civilization Diseases, Slovak Academy of Sciences, Sienkiewiczova 1, 813 71 Bratislava, Slovakia.
Institute of Normal and Pathological Physiology, Centre of Excellence for Examination of Regulatory Role of Nitric Oxide in Civilization Diseases, Slovak Academy of Sciences, Sienkiewiczova 1, 813 71 Bratislava, Slovakia ; Institute of Medical Biochemistry, Jessenius Faculty of Medicine, Comenius University, Mala Hora 4, 036 01 Martin, Slovakia.
Biomed Res Int. 2014;2014:658479. doi: 10.1155/2014/658479. Epub 2014 Mar 20.
The present study was designed to evaluate the effects of vascular aging in juvenescence on endothelial function in femoral arteries and to assess differences between normotensive and hypertensive rats. The aim of the study was to determine if age affected nitric oxide- (NO-) mediated relaxations in normotensive and hypertensive rats. Juvenile (7-week-old) and young adult (22-week-old) male Wistar-Kyoto (WKY) and spontaneously hypertensive rats (SHR) were used in this study. Femoral artery (FA) reactivity was determined by wire myograph and NO synthase activity by conversion of [(3)H]-L-arginine. During juvenescence systolic blood pressure (tail-cuff) increased significantly only in SHR, while NO synthesis decreased significantly in both strains. Endothelium-dependent relaxations to acetylcholine were reduced in the FA of SHR compared to age-matched WKY at both ages, yet these parameters were unchanged in adult rats compared with juvenile animals. The NO-dependent component of vasorelaxation was markedly reduced, whereas the NO-independent component was increased in adult compared to juvenile rats in both strains. The endothelial dysfunction in SHR at both ages was associated with reduction of NO-independent mechanisms. In conclusion, aging in early periods of life was associated with reduction of vascular NO production and bioavailability in both strains investigated. This reduction was however fully compensated by accentuation of NO-independent mechanisms.
本研究旨在评估青春期血管衰老对股动脉内皮功能的影响,并评估正常血压大鼠和高血压大鼠之间的差异。该研究的目的是确定年龄是否会影响正常血压大鼠和高血压大鼠中一氧化氮(NO)介导的舒张功能。本研究使用了幼年(7周龄)和年轻成年(22周龄)的雄性Wistar-Kyoto(WKY)大鼠和自发性高血压大鼠(SHR)。通过线肌张力测定仪测定股动脉(FA)反应性,并通过[(3)H]-L-精氨酸的转化测定NO合酶活性。在青春期,收缩压(尾袖法)仅在SHR中显著升高,而在两个品系中NO合成均显著降低。与年龄匹配的WKY相比,两个年龄段的SHR的FA中对乙酰胆碱的内皮依赖性舒张均降低,但与幼年动物相比,成年大鼠的这些参数没有变化。与幼年大鼠相比,两个品系的成年大鼠中血管舒张的NO依赖性成分明显降低,而NO非依赖性成分增加。两个年龄段的SHR中的内皮功能障碍与NO非依赖性机制的减少有关。总之,在研究的两个品系中,生命早期的衰老与血管NO生成和生物利用度的降低有关。然而,这种降低通过NO非依赖性机制的增强得到了完全补偿。