2002
DOI: 10.1203/01.pdr.0000036624.37481.7a
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Placental Restriction Increases the Expression of Prostaglandin Endoperoxide G/H Synthase-2 and EP2 mRNA in the Fetal Sheep Kidney during Late Gestation

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Cited by 4 publications
(6 citation statements)
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“…The upregulation of PTGS2 (39) and PFKP (40) and the downregulation of ENO2 (40) in the ileum as well as the downregulation of ELF2 (41) in the colon may be related to hypoxia, as previously reported in mammal fetuses or cell lines. In addition, the expression of most genes in lipid (OSBPL1A, MTTP, ECHS1, and APOA1 in ileum and APMAP in colon), glucose (PFKP in ileum and ALG6, B4GALT6, and UGCGL2 in colon), and protein (EIF4EBP2, CORIN, RPS43, and RPS2 in ileum) metabolism was increased in piglets with IUGR.…”
Section: Discussionsupporting
confidence: 73%
“…The upregulation of PTGS2 (39) and PFKP (40) and the downregulation of ENO2 (40) in the ileum as well as the downregulation of ELF2 (41) in the colon may be related to hypoxia, as previously reported in mammal fetuses or cell lines. In addition, the expression of most genes in lipid (OSBPL1A, MTTP, ECHS1, and APOA1 in ileum and APMAP in colon), glucose (PFKP in ileum and ALG6, B4GALT6, and UGCGL2 in colon), and protein (EIF4EBP2, CORIN, RPS43, and RPS2 in ileum) metabolism was increased in piglets with IUGR.…”
Section: Discussionsupporting
confidence: 73%
“…) and increased prostaglandin synthesis to maintain renin gene expression in the kidney (Williams et al. ). It is possible that the programming in the kidney is different than that in the heart and renal RAS is relevant in terms of the measured changes in the systemic concentrations of renin activity and ANGII.…”
Section: Discussionmentioning
confidence: 99%
“…It is possible that differences in the timing, duration, and degree of hypoxia and thus growth restriction between these models (Morrison 2008) may explain differences in the activation of the systemic RAS. In this sheep model of IUGR there are documented changes in RAS in fetal life, including a greater hypotensive response to an ACE inhibitor (Edwards et al 1999) and increased prostaglandin synthesis to maintain renin gene expression in the kidney (Williams et al 2002). It is possible that the programming in the kidney is different than that in the heart and renal RAS is relevant in terms of the measured changes in the systemic concentrations of renin activity and ANGII.…”
Section: Lbw and Plasma Renin Activity And Angii Concentrationmentioning
confidence: 96%
“…Infusion of the angiotensin‐converting enzyme inhibitor captopril after the onset of the prepartum increase in fetal cortisol concentrations from approximately 135 days gestation results in a greater hypotensive response in PR fetuses compared with normoxic fetuses 48 . Although there is no difference in the expression of renal renin mRNA between PR and control fetal sheep, there is an increase in the capacity of the kidney to synthesize prostaglandin in the PR sheep fetus and this is directly related to renin mRNA expression 74 . These changes may underlie the increased dependence on the renin–angiotensin system for maintenance of blood pressure in late gestation in the PR fetus compared with the control fetus.…”
Section: Uterine Carunclectomymentioning
confidence: 99%
“…48 Although there is no difference in the expression of renal renin mRNA between PR and control fetal sheep, there is an increase in the capacity of the kidney to synthesize prostaglandin in the PR sheep fetus and this is directly related to renin mRNA expression. 74 These changes may underlie the increased dependence on the renin-angiotensin system for maintenance of blood pressure in late gestation in the PR fetus compared with the control fetus.…”
Section: Fetal Adaptations To Placental Restriction: Cardiovascularmentioning
confidence: 99%