FETAL ENDOCRINE RESPONSES TO CHRONIC PLACENTAL EMBOLIZATION IN THE LATE-GESTATION OVINE FETUS

被引:77
作者
GAGNON, R
CHALLIS, J
JOHNSTON, L
FRAHER, L
机构
[1] ST JOSEPHS HLTH CTR,DEPT MED & BIOCHEM,LONDON,ON,CANADA
[2] ST JOSEPHS HLTH CTR,DEPT OBSTET GYNAECOL & PHYSIOL,LONDON N6A 4V2,ENGLAND
[3] UNIV WESTERN ONTARIO,LAWSON RES INST,MRC,FETAL & NEONATAL HLTH & DEV GRP,LONDON N6A 3K7,ONTARIO,CANADA
基金
英国医学研究理事会;
关键词
CHRONIC FETAL HYPOXIA; PLACENTAL INSUFFICIENCY; FETAL HORMONAL RESPONSE;
D O I
10.1016/S0002-9378(94)70309-4
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: The purpose of this study was to examine the effect of chronic fetal Placental embolization on the fetal corticotropin, cortisol, and catecholamines concentrations and on myometrial contractility pattern. STUDY DESIGN: Fourteen fetal sheep were studied (seven embolized, seven controls) for 10 days between 0.84 and 0.91 of gestation. Daily injections of nonradioactive microspheres were performed to decrease fetal arterial oxygen content by 30% to 35% of the preembolization value. Umbilical artery Doppler flow velocity waveforms were measured daily. RESULTS: Chronic fetal placental embolization produced progressive fetal hypoxemia (p < 0.001) with changes in umbilical artery Doppler flow velocity waveforms indicative of a 25% increase in placental vascular resistance (p < 0.01). In response to chronic fetal hypoxemia there was a progressive increase in baseline fetal plasma norepinephrine concentration (p < 0.001). There was a transient lburfold to fivefold increase in baseline fetal plasma cortisol levels concomitant with a significant decrease in baseline immunoreactive corticotropin between days 7 and 9 of embolization (both p < 0.05), with a return to control values by day 10. There was a 57% increase in myometrial contracture frequency in the embolized group when compared with controls (p = 0.001). CONCLUSIONS: During repetitive chronic placental damage that led to fetal hypoxemia, the fetal endocrine environment changed with time in a direction that would prevent the onset of premature activation of the hypothalamic-pituitary-adrenal axis and premature delivery.
引用
收藏
页码:929 / 938
页数:10
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