Dogru Segun, Yasar Ekrem, Yesilkaya Akin
Department of Medical Biochemistry, Akdeniz University Medical School, 07058 Antalya, Turkey.
Department of Biophysics, Akdeniz University Medical School, 07058 Antalya, Turkey.
Biomed Rep. 2024 Sep 18;21(6):171. doi: 10.3892/br.2024.1859. eCollection 2024 Dec.
Hyperuricemia during hypertension is associated with aberrant vascular functions and increased oxidative stress, which affects endothelial dysfunction. Nevertheless, the molecular mechanisms underlying the effects of uric acid on vascular smooth muscle cells (VSMCs) through oxidative stress remain unclear. The aim of the present study was to investigate the dose- and time-dependent effects of uric acid on oxidative stress and p53 protein expression in VSMCs. VSMCs were incubated with various concentrations of uric acid (0-50 mg/dl) for different time periods (1-24 h). Thiobarbituric acid reactive substances (TBARs), protein carbonylation and nitric oxide (NO) levels were determined using appropriate assay kits. Superoxide anion release was detected using the Görlach method. Western blotting was performed to determine the protein expression levels of p53. The findings demonstrated that the application of uric acid led to an increase in protein carbonylation and superoxide anion levels while causing a decrease in NO levels. Conversely, no significant effect was observed on TBARS levels. Additionally, it was observed that high concentrations of uric acid suppressed p53 expression at 6, 12 and 24 h. The present study provided evidence that the influence of uric acid on oxidative stress was more closely associated with time than dose; however, not all effects observed were strictly time-dependent.
高血压期间的高尿酸血症与血管功能异常和氧化应激增加有关,而氧化应激会影响内皮功能障碍。然而,尿酸通过氧化应激对血管平滑肌细胞(VSMCs)产生影响的分子机制仍不清楚。本研究的目的是探讨尿酸对VSMCs氧化应激和p53蛋白表达的剂量和时间依赖性影响。将VSMCs与不同浓度的尿酸(0-50mg/dl)孵育不同时间段(1-24小时)。使用适当的检测试剂盒测定硫代巴比妥酸反应性物质(TBARs)、蛋白质羰基化和一氧化氮(NO)水平。使用Görlach方法检测超氧阴离子释放。进行蛋白质印迹法以确定p53的蛋白质表达水平。研究结果表明,尿酸的应用导致蛋白质羰基化和超氧阴离子水平增加,同时导致NO水平降低。相反,未观察到对TBARS水平有显著影响。此外,观察到高浓度尿酸在6、12和24小时抑制p53表达。本研究提供的证据表明,尿酸对氧化应激的影响与时间的关系比与剂量的关系更密切;然而,并非所有观察到的影响都严格依赖于时间。