Barton A C, Demarest K T, Moore K E
Department of Pharmacology and Toxicology, Michigan State University, East Lansing.
Neuroendocrinology. 1988 May;47(5):416-23. doi: 10.1159/000124956.
Complete or retrochiasmatic deafferentations of the mediobasal hypothalamus were made in female rats 7 days prior to experimentation in order to determine the role played by putative afferent neuronal connections (1) in maintaining the basal neuronal activity of tuberoinfundibular dopaminergic (TIDA) neurons, and (2) in the stimulatory actions of prolactin on these neurons. The neuronal activity of TIDA neurons was estimated by measuring the rates of synthesis, turnover or metabolism of dopamine (DA) in the terminals of these neurons in the median eminence. Complete deafferentation of the mediobasal hypothalamus reduced the basal rate of DA synthesis, and retrochiasmatic deafferentation decreased the rates of synthesis, turnover and metabolism of DA in the median eminence. A knife cut 1 mm rostral to the retrochiasmatic cut failed to alter basal TIDA neuronal activity. These results suggest that afferent neuronal inputs originating in or coursing through the caudal portion of the anterior hypothalamus mediate a tonic stimulatory influence on TIDA neurons in the female rat. Intracerebroventricular administration of rat prolactin or systemic administration of haloperidol (which increases circulating levels of prolactin) increased DA synthesis in the median eminence of both sham-operated rats and retrochiasmatic-deafferentated rats. Thus, the stimulatory action of prolactin was not blocked by retrochiasmatic deafferentation. In addition, elimination of the basal stimulatory action of endogenous prolactin by pretreating animals with bromocriptine reduced the rate of DA synthesis in the median eminence of both sham- and retrochiasmatic-deafferentated rats.(ABSTRACT TRUNCATED AT 250 WORDS)
(1)维持结节漏斗多巴胺能(TIDA)神经元的基础神经元活动;(2)催乳素对这些神经元的刺激作用,在实验前7天对雌性大鼠进行了下丘脑内侧基底部的完全或视交叉后去传入手术。通过测量这些神经元在正中隆起终末中多巴胺(DA)的合成、周转或代谢速率来估计TIDA神经元的活动。下丘脑内侧基底部的完全去传入降低了DA合成的基础速率,视交叉后去传入降低了正中隆起中DA的合成、周转和代谢速率。在视交叉后切口前方1毫米处的切断未能改变TIDA神经元的基础活动。这些结果表明,起源于下丘脑前部尾侧部分或通过该部分的传入神经输入对雌性大鼠的TIDA神经元介导了一种紧张性刺激影响。脑室内注射大鼠催乳素或全身注射氟哌啶醇(可提高循环中的催乳素水平)可增加假手术大鼠和视交叉后去传入大鼠正中隆起中的DA合成。因此,视交叉后去传入并未阻断催乳素的刺激作用。此外,用溴隐亭预处理动物消除内源性催乳素的基础刺激作用,可降低假手术大鼠和视交叉后去传入大鼠正中隆起中DA的合成速率。(摘要截断于250字)