Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2156147 | Pathology - Research and Practice | 2010 | 6 Pages |
Ischemia, hypoxia, and elevated vascular resistance disturb placental functions by increasing oxidative stress. Heat shock protein 70 (HSP70) is an oxidative stress marker. Endothelial nitric oxide synthase (eNOS) is a nitric oxide enzyme with a key role in pathologic and physiologic angiogenesis and vasculogenesis. This study was performed to investigate the role of oxidative stress in the pathogenesis of preeclampsia and intrauterine growth-restricted (IUGR) pregnancies by comparing the levels of HSP70 and eNOS in placentas from women with these diseases and those with healthy pregnancies.HSP70 and eNOS were examined using the streptavidin-biotin-peroxidase complex technique on formalin-fixed, paraffin-embedded sections from 135 placental villous tissues obtained from normal pregnancies (n = 45) and pregnancies complicated with preeclampsia (n = 45) and IUGR (n = 45). The intensity of labeling in placental tissues with antibodies to HSP70 and eNOS was scored between 0 and 3, using a semiquantitative scale.HSP70 and eNOS levels were increased in the syncytiotrophoblasts, cytotrophoblasts, and extravillous trophoblast cells of preeclamptic and IUGR placentas (P < 0.001), compared with normal pregnancies. However, their levels were increased only in the villous endothelial cells of IUGR placentas (P < 0.001).Oxidative stress is thought to play an important role in the pathogenesis of preeclampsia and IUGR pregnancies.