胎儿生长迟缓对绵羊中枢和外周儿茶酚胺能通路发育的影响。

Journal of developmental physiology Pub Date : 1992-11-01
K Oyama, J Padbury, A Martinez, B Chappell, H Stein, J Humme
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摘要

研究了假手术对照和单脐动脉结扎(SUAL)诱导的生长迟缓新生羊脑区去甲肾上腺素和多巴胺含量及α 1和β肾上腺素能受体机制。与其他器官系统相比,脑重量的相对保存证明了脑节约。大脑的去甲肾上腺素和多巴胺含量不受SUAL的影响。这与褐色脂肪中去甲肾上腺素水平下降形成对比,棕色脂肪通常是神经密集支配的外周组织。α - 1和β -肾上腺素能受体数量和亲和状态在两组之间相似。受体与鸟嘌呤核苷酸刺激蛋白之间的偶联以及激动剂刺激的腺苷酸环化酶活性不受SUAL的影响。脑区域DNA含量和蛋白质/DNA比值在两组间无显著差异。这些数据表明,单脐动脉结扎引起的胎儿生长迟缓改变了绵羊的外周而不是中枢儿茶酚胺能通路。特异性儿茶酚胺信号转导系统的生长和表达在大脑中受到保护。
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Effects of fetal growth retardation on the development of central and peripheral catecholaminergic pathways in the sheep.

Regional norepinephrine and dopamine content and cerebral alpha 1- and beta-adrenergic receptor mechanisms were studied in the brain of sham operated control and single umbilical artery ligation (SUAL) induced growth retarded newborn sheep. Brain sparing was evidenced by relative preservation of brain weight compared to other organ systems. Norepinephrine and dopamine content of the brain were not affected by SUAL. This is in contrast to decreased norepinephrine levels in the brown fat, a normally densely innervated peripheral tissue. Alpha 1- and beta-adrenergic receptor numbers and affinity states were similar between the two groups. Coupling between beta-receptor and guanine nucleotide stimulatory protein and agonist stimulated adenylyl cyclase activity were unaffected by SUAL. Brain regional DNA content and protein/DNA ratios were not different between the two groups. These data suggest that single umbilical artery ligation induced fetal growth retardation modifies peripheral but not central catecholaminergic pathways in the sheep. Both growth and expression of specific catecholaminergic signal transduction system are protected in the brain.

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Thyroid hormone status correlates inversely with expression of the growth hormone receptor gene in rats immediately after birth. Decreased norepinephrine turnover rate in the brown adipose tissue of pre-obese fa/fa Zucker rats. Modification of thermogenic capacity in neonatal pigs by changes in thyroid status during late gestation. Analysis of beat-to-beat heart rate changes during sleep-waking states in normal infants. Abdominal vibration alters sleep state in fetal sheep.
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