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10.2353/ajpath.2010.090800

http://scihub22266oqcxt.onion/10.2353/ajpath.2010.090800
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20952590!2993274!20952590
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suck abstract from ncbi

pmid20952590      Am+J+Pathol 2010 ; 177 (6): 2950-62
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  • Effects of hypoxia-inducible factor-1alpha overexpression in pregnant mice: possible implications for preeclampsia and intrauterine growth restriction #MMPMID20952590
  • Tal R; Shaish A; Barshack I; Polak-Charcon S; Afek A; Volkov A; Feldman B; Avivi C; Harats D
  • Am J Pathol 2010[Dec]; 177 (6): 2950-62 PMID20952590show ga
  • Preeclampsia and intrauterine growth restriction (IUGR) are pregnancy-specific disorders that share a common pathophysiology. Hypoxia-inducible factor-1alpha (HIF-1alpha) is a transcription factor that plays an important role in placental development. HIF-1alpha is elevated in preeclamptic placentas and induces soluble vascular endothelial growth factor receptor-1 (sFLT-1), a central factor in preeclampsia and IUGR pathogenesis. Our objective was to investigate the effects of HIF-1alpha overexpression on pregnancy in mice. C57BL/6J pregnant mice were systemically administered either adenovirus expressing stabilized HIF-1alpha (cytomegalovirus [CMV]-HIF), luciferase control (CMV-Luc), or saline on gestational day 8. Pregnant mice overexpressing HIF-1alpha had significantly elevated blood pressure and proteinuria compared with pregnant controls. HIF-1alpha mice showed fetal IUGR, decreased placental weights, and histopathological placental abnormalities compared with control mice. Glomerular endotheliosis, the hallmark lesion of preeclampsia, was demonstrated in the kidneys of these mice relative to the normal histology in control mice. Moreover, liver enzyme levels were significantly elevated, whereas complete blood counts revealed significant anemia and thrombocytopenia in CMV-HIF mice compared with controls. Blood smears confirmed microangiopathic hemolytic anemia in CMV-HIF mice, consistent with HELLP (hemolysis, elevated liver enzymes, and low platelets)-like syndrome. CMV-HIF mice showed elevation in serum sFLT-1 and soluble endoglin, providing a mechanistic explanation for the observations. Collectively, our results suggest a possible role for HIF-1alpha in the pathogenesis of both preeclampsia and IUGR.
  • |*Disease Models, Animal[MESH]
  • |*Mice[MESH]
  • |Animals[MESH]
  • |Female[MESH]
  • |Fetal Growth Retardation/genetics/metabolism/pathology[MESH]
  • |Hypoxia-Inducible Factor 1, alpha Subunit/*genetics/metabolism/physiology[MESH]
  • |Liver/metabolism/pathology[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Mice, Transgenic[MESH]
  • |Placenta Diseases/genetics/metabolism/pathology[MESH]
  • |Placenta/metabolism/physiology[MESH]
  • |Pre-Eclampsia/*genetics/metabolism/pathology[MESH]
  • |Pregnancy/*genetics/metabolism[MESH]
  • |Tissue Distribution[MESH]
  • |Transgenes/genetics[MESH]


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