Changes of Renal AT1/AT2 Receptors and Structures in Ovine Fetuses following Exposure to Long-Term Hypoxia

被引:23
作者
Mao, Caiping [1 ]
Hou, Jianquan [1 ]
Ge, Jianyi [1 ]
Hu, Yali [2 ]
Ding, Yang [1 ]
Zhou, Yun [1 ]
Zhang, Huiying [1 ]
Xu, Zhice [1 ,2 ,3 ]
Zhang, Lubo [1 ,3 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Perinatal Biol Ctr, Suzhou 2135007, Peoples R China
[2] Nanjing Univ, Drum Tower Hosp, Nanjing 210008, Peoples R China
[3] Loma Linda Univ, Sch Med, Ctr Perinatal Biol, Dept Physiol & Pharmacol, Loma Linda, CA USA
关键词
Hypoxia; Angiotensin II receptors; Ovine fetus; GLOMERULAR-FILTRATION-RATE; ANGIOTENSIN-II RECEPTORS; REDUCES NEPHRON NUMBER; SERUM CREATININE; VASOPRESSIN RELEASE; HUMAN PREADIPOCYTES; FOS EXPRESSION; FETAL SHEEP; CELLS; TYPE-2;
D O I
10.1159/000259901
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: The present study tested the hypothesis that chronic hypoxia adversely affects renal development in the ovine fetus. Methods: Kidneys were collected from near-term fetuses of pregnant ewes maintained at sea level or high altitude (3,801 m, PaO2 : approx. 60 mm Hg) for 110 days (n = 6 for each group). Results: Long-term high altitude hypoxia reduced the fetal kidney/body weight ratio. Histological analysis showed a significant enlargement in the Bowman's space and swelling of tubule epithelial cells in the kidney of the hypoxic fetus. The histological alterations were limited to the cortical, but not medullary, zone. These alterations were associated with an increase in serum creatinine and a decrease in the BUN-to-creatinine ratio in hypoxic fetuses. Angiotensin II receptors (AT(1)R and AT(2)R) were detected in the glomerular and tubular regions of the kidney. Chronic hypoxia caused a significant increase in AT(1)R and a decrease in AT(2)R protein and mRNA abundance, resulting in a large increase in the AT(1)R/AT(2)R ratio in the fetal kidney. Conclusion: The results demonstrate an adverse effect of chronic hypoxia on renal AT(1)R and AT(2)R expression and functions in the fetus, suggesting a possible role of fetal hypoxia in the programming of renal diseases in fetal origins. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:141 / 150
页数:10
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