Slotkin T A, Slepetis R J
J Pharmacol Exp Ther. 1984 Jul;230(1):53-61.
Thyroid status is thought to play a major role in establishing the time course of development of sympathetic nerve pathways. Hypothyroidism induced by perinatal administration of propylthiouracil to developing rats resulted in substantial deficits in cardiac norepinephrine levels that persisted into adulthood. This shortfall was not accompanied by compensatory receptor supersensitivity or by increased utilization of remaining transmitter. Indeed neonatal hypothyroidism is known to result in end-organ subsensitivity and the norepinephrine turnover rate, an index of spontaneous activity of the neuron, was found to be markedly subnormal. The ability of cardiac sympathetic neurons to release transmitter upon pharmacological challenge was also compromised by hypothyroidism: in control neonates, administration of tyramine resulted in displacement of norepinephrine from nerve terminals, a response which was present very early in development. Hypothyroid rats did not develop the ability to release transmitter in response to tyramine until 10 days postnatally and a fully mature response was not apparent until weeks later. Ontogeny of the capability to release norepinephrine in response to hypotension (baroreflex) also was assessed through administration of hydralazine, a direct arteriolar vasodilator; control rats showed a characteristic development of this response at the end of the 2nd postnatal week, whereas hypothyroid rats did not show any potential for norepinephrine release until young adulthood (41 days). In comparison to cardiac sympathetic neurons, an overall evaluation of central catecholaminergic pathways in whole brain indicated a much smaller effect of hypothyroidism, with no (norepinephrine) or only minor (dopamine) deficits in transmitter content and smaller, transient reductions in turnover.(ABSTRACT TRUNCATED AT 250 WORDS)
甲状腺状态被认为在交感神经通路发育的时间进程确立中起主要作用。在发育中的大鼠围产期给予丙硫氧嘧啶诱导甲状腺功能减退,导致心脏去甲肾上腺素水平大幅降低,这种降低持续到成年期。这种不足并未伴有代偿性受体超敏反应或剩余递质利用率增加。事实上,已知新生儿甲状腺功能减退会导致终末器官反应性降低,并且发现去甲肾上腺素周转率(神经元自发活动的一个指标)明显低于正常水平。甲状腺功能减退还损害了心脏交感神经元在药理学刺激下释放递质的能力:在对照新生儿中,给予酪胺会导致去甲肾上腺素从神经末梢移位,这种反应在发育早期就存在。甲状腺功能减退的大鼠直到出生后10天才发展出对酪胺释放递质的能力,并且直到数周后才出现完全成熟的反应。还通过给予肼屈嗪(一种直接的小动脉血管扩张剂)来评估对低血压(压力反射)释放去甲肾上腺素能力的个体发生;对照大鼠在出生后第二周结束时显示出这种反应的特征性发展,而甲状腺功能减退的大鼠直到成年早期(41天)才显示出任何去甲肾上腺素释放的潜力。与心脏交感神经元相比,对全脑中枢儿茶酚胺能通路的总体评估表明,甲状腺功能减退的影响要小得多,递质含量没有(去甲肾上腺素)或只有轻微(多巴胺)不足,周转率有较小的、短暂的降低。(摘要截断于250字)