Severe nutritional restriction in pregnant rats aggravates hypertension, altered vascular reactivity, and renal development in spontaneously hypertensive rats offspring

被引:33
作者
Franco, MDP
Arruda, RMMP
Fortes, ZB
de Oliveira, SF
Carvalho, MHC
Tostes, RCA
Nigro, D
机构
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Pharmacol, Lab Hypertens, BR-05508900 Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Pharmacol, Lab Hypertens, BR-05508900 Sao Paulo, Brazil
[3] Univ Sao Paulo, Inst Biomed Sci, Dept Histol, Reprod Biol Lab, BR-05508900 Sao Paulo, Brazil
关键词
blood pressure; fetal undernutrition; gender; spontaneously hypertensive rats; vascular reactivity;
D O I
10.1097/00005344-200203000-00008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epidemiologic studies suggest that intrauterine undernutrition plays an important role in the development of arterial hypertension in adulthood. The aim of the current study was to evaluate whether severe nutritional restriction during pregnancy can aggravate hypertension, vascular reactivity changes, and renal development in spontaneously hypertensive rat (SHR) offspring. To investigate the potential existence of gender differences, both male and female offspring of pregnant SHRs on a restricted diet were studied in adulthood. Female pregnant SHRs were fed either normal or 50% of the normal intake diets, during the whole gestational period. Arterial blood pressure and nephron number were determined. Norepinephrine, acetylcholine, and sodium nitroprusside responses in isolated aortic rings from the offspring (male and female, when they reached adulthood) were also evaluated. In the SHR offspring (male and female) the intrauterine undernutrition further increased the blood pressure levels, increased the response to norepinephrine, and decreased the response to acetylcholine, without altering the response to sodium nitroprusside. In addition, it induced a decrease in the number of nephrons in the kidney from adult offspring. In conclusion, fetal undernutrition aggravates hypertension and the endothelial dysfunction along with an impairment of renal development in both male and female SHRs.
引用
收藏
页码:369 / 377
页数:9
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