Manaker S, Engber T M, Knight P B, Winokur A
J Neurochem. 1985 Oct;45(4):1315-8. doi: 10.1111/j.1471-4159.1985.tb05561.x.
Rats received intraventricular (i.v.t.) injections of 5,7-dihydroxytryptamine (5,7-DHT) (100-600 micrograms). Some animals also received intraperitoneal injections of the 5-hydroxytryptamine uptake blocker fluoxetine (FX) (20 mg/kg) or the norepinephrine uptake blocker desmethylimipramine (DMI) (48 mg/kg) 30-90 min prior to i.v.t. 5,7-DHT. Rats were killed between 2 and 35 days following i.v.t. 5,7-DHT, brains were dissected, and regions were assayed for thyrotropin-releasing hormone (TRH) by radioimmunoassay. Dose-dependent increases in TRH content following i.v.t. 5,7-DHT were noted in the brainstem and hippocampus. DMI pretreatment blocked the increase in hippocampal TRH, but not in brainstem TRH. FX pretreatment was ineffective in blocking any increases in TRH content. These results suggest differential regulation of regional TRH content by interactions with specific neurotransmitter systems.
给大鼠进行脑室内(i.v.t.)注射5,7 - 二羟基色胺(5,7 - DHT)(100 - 600微克)。一些动物在脑室内注射5,7 - DHT前30 - 90分钟还接受了腹腔注射5 - 羟色胺摄取阻断剂氟西汀(FX)(20毫克/千克)或去甲肾上腺素摄取阻断剂去甲丙咪嗪(DMI)(48毫克/千克)。在脑室内注射5,7 - DHT后的2至35天内处死大鼠,解剖大脑,并通过放射免疫测定法检测各区域的促甲状腺激素释放激素(TRH)。脑室内注射5,7 - DHT后,在脑干和海马体中观察到TRH含量呈剂量依赖性增加。DMI预处理可阻断海马体中TRH的增加,但不能阻断脑干中TRH的增加。FX预处理在阻断TRH含量的任何增加方面均无效。这些结果表明,通过与特定神经递质系统的相互作用,区域TRH含量存在差异调节。