An early prenatal exposure to excess glucocorticoid leads to hypertensive offspring in sheep

被引:259
作者
Dodic, M [1 ]
May, CN
Wintour, EM
Coghlan, JP
机构
[1] Univ Melbourne, Howard Florey Inst Expt Physiol & Med, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Anat & Cell Biol, Parkville, Vic 3052, Australia
关键词
dexamethasone; hypertension; sheep;
D O I
10.1042/cs0940149
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
1. Recent studies in animals have linked fetal exposure to excess maternal glucocorticoids with the later occurrence of cardiovascular disorders, particularly hypertension. 2. To test the hypothesis that prenatal treatment could impact on adult blood pressure two groups of pregnant ewes were transported from the farm to the Institute at either 22-29 days of pregnancy (pretreatment group 1) or 59-66 days of pregnancy (pretreatment group 2), subjected to 48 h treatment with dexamethasone (0.28 mg day(-1) kg(-1) for 2 days) and then returned to the farm. The control group remained at the farm for the entire pregnancy, Lambs were then studied at approximately 4, 10 and 19 months after birth. 3, The basal mean arterial pressure in pretreatment group 1 (80 +/- 1 mmHg at 124 days; 83 +/- 1 mmHg at 309 days and 89 +/- 1 mmHg at 558 days; n = 6) was significantly different (P < 0.05 in all groups) from that in the control group of lambs (74 +/- 2 mmHg at 110 days; 76 +/- 1 mmHg at 323 days and 81 +/- 1 mmHg at 568 days; n = 7). However, prenatal glucocorticoid exposure did not alter vascular sensitivity to noradrenaline, angiotensin II and adrenocorticotropic hormone in these sheep at any of the ages studied, nor did it affect basal or adrenocorticotropic hormone-induced concentrations of cortisol or basal plasma renin concentrations in the lambs at any age. 4. These data support the hypothesis that excess glucocorticoid exposure in early pregnancy, during a critical developmental stage or 'window', programmes higher blood pressure that persists in later life.
引用
收藏
页码:149 / 155
页数:7
相关论文
共 52 条
[1]   TYPE 2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS, HYPERTENSION AND HYPERLIPEMIA (SYNDROME-X) - RELATION TO REDUCED FETAL GROWTH [J].
BARKER, DJP ;
HALES, CN ;
FALL, CHD ;
OSMOND, C ;
PHIPPS, K ;
CLARK, PMS .
DIABETOLOGIA, 1993, 36 (01) :62-67
[2]  
BARKER DJP, 1989, LANCET, V2, P577
[3]   GROWTH INUTERO, BLOOD-PRESSURE IN CHILDHOOD AND ADULT LIFE, AND MORTALITY FROM CARDIOVASCULAR-DISEASE [J].
BARKER, DJP ;
OSMOND, C ;
GOLDING, J ;
KUH, D ;
WADSWORTH, MEJ .
BRITISH MEDICAL JOURNAL, 1989, 298 (6673) :564-567
[4]   THE RELATION OF SMALL HEAD CIRCUMFERENCE AND THINNESS AT BIRTH TO DEATH FROM CARDIOVASCULAR-DISEASE IN ADULT LIFE [J].
BARKER, DJP ;
OSMOND, C ;
SIMMONDS, SJ ;
WIELD, GA .
BRITISH MEDICAL JOURNAL, 1993, 306 (6875) :422-426
[5]   FETAL NUTRITION AND CARDIOVASCULAR-DISEASE IN ADULT LIFE [J].
BARKER, DJP ;
GLUCKMAN, PD ;
GODFREY, KM ;
HARDING, JE ;
OWENS, JA ;
ROBINSON, JS .
LANCET, 1993, 341 (8850) :938-941
[6]   FETAL AND PLACENTAL SIZE AND RISK OF HYPERTENSION IN ADULT LIFE [J].
BARKER, DJP ;
BULL, AR ;
OSMOND, C ;
SIMMONDS, SJ .
BRITISH MEDICAL JOURNAL, 1990, 301 (6746) :259-262
[7]   PREDOMINANT HIGH-AFFINITY BINDING OF [DEXAMETHASONE-H-3 IN BOVINE-TISSUES IS NOT TO CLASSICAL GLUCOCORTICOID RECEPTORS [J].
BARLOW, JW ;
KRAFT, N ;
STOCKIGT, JR ;
FUNDER, JW .
ENDOCRINOLOGY, 1979, 105 (03) :827-834
[8]   TRANSPLACENTAL PASSAGE OF DEXAMETHASONE IN SHEEP [J].
BAYARD, F ;
BOULARD, C ;
RUCKEBUSCH, Y ;
LOUVET, JP .
JOURNAL OF ENDOCRINOLOGY, 1972, 54 (02) :349-+
[9]   GLUCOCORTICOID EXPOSURE INUTERO - NEW MODEL FOR ADULT HYPERTENSION [J].
BENEDIKTSSON, R ;
LINDSAY, RS ;
NOBLE, J ;
SECKL, JR ;
EDWARDS, CRW .
LANCET, 1993, 341 (8841) :339-341
[10]  
BIAN XP, 1991, J DEV PHYSIOL, V16, P331