Corticotrophin-releasing hormone and fetal responses in human pregnancy

被引:44
|
作者
Sandman, CA
Wadhwa, P
Glynn, L
Chicz-Demet, A
Porto, M
Garite, TJ
机构
[1] Univ Calif Irvine, Dept Psychiat & Human Behav, Irvine, CA 92697 USA
[2] Univ Kentucky, Dept Behav Sci, Lexington, KY 40535 USA
[3] Univ Calif Irvine, Dept Obstet & Gynecol, Irvine, CA 92697 USA
关键词
D O I
10.1111/j.1749-6632.1999.tb07879.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During human pregnancy, maternal and fetal compartments of the human placenta produce and release corticotrophic-releasing hormone (CRH), Elevations of placental CRH are associated with decreased gestational length (including preterm delivery). The effects of elevated placental CRH on human fetal neurological development are not known. Pregnant women in the 31st and 32nd week of gestation consented to procedures for collection of blood and measurement of fetal heart rate (FHR) in response to a series of 40 vibroacoustic stimuli (VAS), Measures of habituation and dishabituation were calculated from the FBR. All subjects were followed to delivery. Fetuses (N = 33) of women with highly elevated CRH were least responsive (p < ,03) to stimulation after presentation of a novel (dishabituating) stimulus with control far parity, fetal gender, medical (antepartum) risk, and gestational length at term, In a larger sample (N = 156) a polynomial model predicted the pattern of FHR reactivity for the first 15 trials. Placental CRH concentration significantly predicted FHR reactivity after controlling for the effects of trial number, baseline FHR, inter-trial interval, and presence of uterine contractions. Increased maternal CRH levels were significantly related to the length of gestation after controlling for the effects of fetal gender, parity, and medical risk (p = ,05), The relationship between length of gestation and FHR was not significant suggesting separate actions of CRH on these events. Elevated placental CRH appears to accelerate certain developmental events (gestational length) and may influence the fetal nervous system. The impaired fetal responses to novelty and increased arousal observed in this study suggest that neurological systems map be targets for placental CRH during sensitive developmental periods.
引用
收藏
页码:66 / 75
页数:10
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