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本文引用的文献

1
Losartan chemistry and its effects via AT1 mechanisms in the kidney.氯沙坦的化学性质及其通过肾脏中AT1机制产生的作用。
Curr Med Chem. 2009;16(28):3701-15. doi: 10.2174/092986709789105000.
2
Development of fetal brain renin-angiotensin system and hypertension programmed in fetal origins.胎儿脑肾素-血管紧张素系统的发育与胎儿起源性高血压的编程
Prog Neurobiol. 2009 Apr;87(4):252-63. doi: 10.1016/j.pneurobio.2008.12.001. Epub 2009 Jan 24.
3
Regulation of angiotensin II receptors and extracellular matrix turnover in human retinal pigment epithelium: role of angiotensin II.人视网膜色素上皮中血管紧张素II受体的调节及细胞外基质周转:血管紧张素II的作用
Am J Physiol Cell Physiol. 2008 Dec;295(6):C1633-46. doi: 10.1152/ajpcell.00092.2008. Epub 2008 Oct 15.
4
Role of angiotensin II AT1 receptor activation in cardiovascular diseases.血管紧张素II 1型受体激活在心血管疾病中的作用。
Kidney Int. 2008 Dec;74(11):1379-84. doi: 10.1038/ki.2008.358. Epub 2008 Jul 23.
5
Repeated ethanol exposure during late gestation decreases nephron endowment in fetal sheep.妊娠后期反复接触乙醇会减少胎羊的肾单位数量。
Am J Physiol Regul Integr Comp Physiol. 2008 Aug;295(2):R568-74. doi: 10.1152/ajpregu.90316.2008. Epub 2008 Jun 18.
6
Growth restriction before or after birth reduces nephron number and increases blood pressure in male rats.出生前后的生长受限会减少雄性大鼠的肾单位数量并升高血压。
Kidney Int. 2008 Jul;74(2):187-95. doi: 10.1038/ki.2008.153. Epub 2008 Apr 23.
7
Angiotensin II stimulates and atrial natriuretic peptide inhibits human visceral adipocyte growth.血管紧张素II刺激而心钠素抑制人类内脏脂肪细胞生长。
Int J Obes (Lond). 2008 Feb;32(2):259-67. doi: 10.1038/sj.ijo.0803724. Epub 2007 Sep 18.
8
AT1 receptor blockade prevents interstitial and glomerular apoptosis but not fibrosis in pigs with neonatal induced partial unilateral ureteral obstruction.
Am J Physiol Renal Physiol. 2007 Jun;292(6):F1771-81. doi: 10.1152/ajprenal.00479.2006. Epub 2007 Mar 13.
9
Animal models for small for gestational age and fetal programming of adult disease.小于胎龄儿及成人疾病的胎儿编程的动物模型。
Horm Res. 2007;68(3):113-23. doi: 10.1159/000100545. Epub 2007 Mar 9.
10
Angiotensin II type 1 and bradykinin B2 receptors expressed in early stage epithelial cells derived from human embryonic stem cells.血管紧张素II 1型受体和缓激肽B2受体在源自人类胚胎干细胞的早期上皮细胞中表达。
J Cell Physiol. 2007 Jun;211(3):816-25. doi: 10.1002/jcp.20985.

长期低氧暴露对绵羊胎儿肾 AT1/AT2 受体及结构的影响。

Changes of renal AT1/AT2 receptors and structures in ovine fetuses following exposure to long-term hypoxia.

机构信息

Perinatal Biology Center, First Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Am J Nephrol. 2010;31(2):141-50. doi: 10.1159/000259901. Epub 2009 Nov 18.

DOI:10.1159/000259901
PMID:19923800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2853592/
Abstract

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, PaO(2): 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.

摘要

背景/目的:本研究旨在检验慢性低氧对绵羊胎儿肾脏发育产生不良影响的假说。

方法

从在海平面或高海拔(3801 米,PaO2:约 60 毫米汞柱)环境中维持 110 天的妊娠母羊的近足月胎儿中收集肾脏(每组 6 个胎儿)。

结果

长期高海拔低氧降低了胎儿肾脏/体重比。组织学分析显示,低氧胎儿的 Bowman 氏囊显著增大,肾小管上皮细胞肿胀。这些组织学改变仅限于皮质区,而不是髓质区。这些改变与低氧胎儿血清肌酐升高和 BUN 与肌酐比值降低有关。在肾脏的肾小球和肾小管区域检测到血管紧张素 II 受体(AT1R 和 AT2R)。慢性低氧导致 AT1R 显著增加,AT2R 蛋白和 mRNA 丰度降低,导致胎儿肾脏中 AT1R/AT2R 比值大幅增加。

结论

研究结果表明慢性低氧对胎儿肾脏 AT1R 和 AT2R 表达和功能产生不良影响,提示胎儿缺氧可能在胎儿起源的肾脏疾病发生中起作用。