Maternal hypertension and progeny blood pressure -: Role of aldosterone and 11β-HSD

被引:26
作者
Gomez-Sanchez, EP
Gomez-Sanchez, CE
机构
[1] Harry S Truman Mem Vet Hosp, Res Serv, Columbia, MO 65201 USA
[2] Univ Missouri, Dept Internal Med, Div Endocrinol Diabet & Metab, Columbia, MO USA
关键词
hypertension; essential; aldosterone; mineralocorticoids; glucocorticoids; 11 beta-hydroxysteroid dehydrogenase; gestation; carbenoxolone; 11; alpha-hydroxyprogesterone;
D O I
10.1161/01.HYP.33.6.1369
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Epidemiological and experimental evidence suggests that gestational events modulate the level of blood pressure that will be "normal" for the individual as an adult. Glucocorticoid excess during gestation is associated with low birth weight, a large placenta, and adult hypertension in humans and animals. It has been proposed that the deficiency in placental 11 beta-hydroxysteroid dehydrogenase activity in humans produces a gestational hormonal milieu, notwithstanding normal circulating levels of glucocorticoids, that predisposes the adult progeny to hypertension. Animal studies indicate that maternal hypertension, excess glucocorticoids, and hydroxysteroid dehydrogenase inhibition program adult blood pressure. Blood pressures of Sprague-Dawley rat dams were manipulated during gestation with continuous intracerebroventricular infusions of vehicle, aldosterone, 11 alpha-hydroxyprogesterone, or carbenoxolone at doses known to produce hypertension with no renal effects or with subcutaneous infusions of larger, equally hypertensinogenic doses that produce systemic effects. Blood pressures of all treated dams were significantly greater (P<0.01) during gestation than those of the vehicle ICV control rats but not significantly different from each other. The blood pressures of both male and female progeny (n greater than or equal to 6 per group, comprising representatives from at least 4 litters) were measured after 6 weeks of age. No significant difference was found in the blood pressure of the pups regardless of the maternal gestational blood pressure or treatment with an enzyme inhibitor, even after high-salt diet challenge.
引用
收藏
页码:1369 / 1373
页数:5
相关论文
共 38 条
[31]  
TONOLO G, 1988, J HYPERTENS, V6, P25
[32]   Carbenoxolone damages endothelium and enhances vasoconstrictor action in aortic rings [J].
Ullian, ME ;
HazenMartin, DJ ;
Walsh, LG ;
Davda, RK ;
Egan, BM .
HYPERTENSION, 1996, 27 (06) :1346-1352
[33]   Tissue-specific messenger ribonucleic acid expression of 11β-hydroxysteroid dehydrogenase types 1 and 2 and the glucocorticoid receptor within rat placenta suggests exquisite local control of glucocorticoid action [J].
Waddell, BJ ;
Benediktsson, R ;
Brown, RW ;
Seckl, JR .
ENDOCRINOLOGY, 1998, 139 (04) :1517-1523
[34]  
WALKER BR, 1994, J HYPERTENS, V12, P33
[35]   Molecular analysis of 11 beta-hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excess [J].
White, PC ;
Mune, T ;
Rogerson, FM ;
Kayes, KM ;
Agarwal, AK .
STEROIDS, 1997, 62 (01) :83-88
[36]   11 beta-hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess [J].
White, PC ;
Mune, T ;
Agarwal, AK .
ENDOCRINE REVIEWS, 1997, 18 (01) :135-156
[37]  
WU JN, 1994, HYPERTENS RES, V17, P243
[38]   DETERMINANTS OF CARDIAC FIBROSIS IN EXPERIMENTAL HYPERMINERALOCORTICOID STATES [J].
YOUNG, M ;
HEAD, G ;
FUNDER, J .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 269 (04) :E657-E662