Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2007
The uraemic toxin phenylacetic acid increases the formation of reactive oxygen species in vascular smooth muscle cells.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Schmidt Sven, Westhoff Timm H, Krauser Phillip, Zidek Walter, van der Giet Markus
Аннотация
BACKGROUND: Cardiovascular events are the most common cause of death in end-stage renal disease (ESRD) patients. Traditional risk factors do not sufficiently explain the marked increment in cardiovascular morbidity and mortality as compared with the general population. The role of uraemic toxins in the genesis of atherosclerosis remains elusive. Reactive oxygen species (ROS) play a major role in the development of atherosclerosis. In the present study, we describe the effect of the uraemic toxin phenylacetic acid (PAA) on the inducible nitric oxide synthase (iNOS) and the consecutive production of ROS.
METHODS: Vascular smooth muscle cells (VSMC) were stimulated by IL-1beta in the absence and presence of different concentrations of PAA (0.1-5.0 mM). Inducible NOS (iNOS) mRNA was determined by real-time PCR, iNOS protein was examined by western blotting. The NO degradation product, nitrite, was measured by Griess-assay and peroxynitrite (ONOO(-)) was assessed by hydroethidium, 2',7'-dichlorodihydro-fluorescein diacetate (H(2)DCFDA) fluorescence assays. To evaluate the iNOS cofactor tetrahydrobiopterin (BH(4)), the expression of the key enzyme GTP cyclohydrolase (GTPCH) was determined by real-time PCR.
RESULTS: PAA enhanced the IL-1beta-mediated induction of iNOS expression regarding both mRNA and protein. Nitrite was significantly increased only with high concentrations of 5 mM PAA. ONOO(-), however, was enhanced in a dose-dependent manner. GTPCH, the key enzyme in BH(4) synthesis, was not enhanced by PAA.
CONCLUSIONS: The uraemic toxin, PAA, leads to an induction of iNOS expression, resulting in an increase of ONOO(-) production. The increased production of ONOO(-) might be explained by a lack of GTPCH-catalysed BH(4) synthesis leading to an uncoupled electron transfer. Thus, PAA might contribute to the oxidative stress in ESRD patients.
METHODS: Vascular smooth muscle cells (VSMC) were stimulated by IL-1beta in the absence and presence of different concentrations of PAA (0.1-5.0 mM). Inducible NOS (iNOS) mRNA was determined by real-time PCR, iNOS protein was examined by western blotting. The NO degradation product, nitrite, was measured by Griess-assay and peroxynitrite (ONOO(-)) was assessed by hydroethidium, 2',7'-dichlorodihydro-fluorescein diacetate (H(2)DCFDA) fluorescence assays. To evaluate the iNOS cofactor tetrahydrobiopterin (BH(4)), the expression of the key enzyme GTP cyclohydrolase (GTPCH) was determined by real-time PCR.
RESULTS: PAA enhanced the IL-1beta-mediated induction of iNOS expression regarding both mRNA and protein. Nitrite was significantly increased only with high concentrations of 5 mM PAA. ONOO(-), however, was enhanced in a dose-dependent manner. GTPCH, the key enzyme in BH(4) synthesis, was not enhanced by PAA.
CONCLUSIONS: The uraemic toxin, PAA, leads to an induction of iNOS expression, resulting in an increase of ONOO(-) production. The increased production of ONOO(-) might be explained by a lack of GTPCH-catalysed BH(4) synthesis leading to an uncoupled electron transfer. Thus, PAA might contribute to the oxidative stress in ESRD patients.