Przegaliński E, Jaworska L, Konarska R, Gołembiowska K
Institute of Pharmacology, Polish Academy of Sciences, Kraków.
Neuropeptides. 1991 Jul;19(3):189-95. doi: 10.1016/0143-4179(91)90118-3.
The effect of alpha-methyl-p-tyrosine (alpha-MT), FLA-63, amphetamine, apomorphine and quinpirole on the concentration of thyrotropin-releasing hormone (TRH) in the striatum and nucleus accumbens was studied in rats. It has been found that the TRH content was increased in both those structures after alpha-MT, an inhibitor of tyrosine hydroxylase which reduced the concentration of both dopamine (DA) and noradrenaline (NA), but not after FLA-63, an inhibitor of DA-beta-hydroxylase which decreased the NA level without affecting DA. On the other hand, the indirectly acting dopaminomimetic amphetamine, the non-selective DA receptor agonist apomorphine, and the selective D2 receptor agonist quinpirole reduced the TRH level in the striatum, but not in the nucleus accumbens. Moreover, the decrease in the striatal peptide content induced by DA-mimetics was antagonized by the selective D2-receptor antagonist sulpiride, but not by the selective D1 receptor antagonist SCH 23390. The effect of amphetamine was not modified by the selective alpha 1-adrenoceptor antagonist prazosin. These results indicate that DA and D2 receptors play a significant role in the regulation of the striatal TRH.
研究了α-甲基-对-酪氨酸(α-MT)、氟阿尼酮(FLA-63)、苯丙胺、阿扑吗啡和喹吡罗对大鼠纹状体和伏隔核中促甲状腺激素释放激素(TRH)浓度的影响。已发现,酪氨酸羟化酶抑制剂α-MT使多巴胺(DA)和去甲肾上腺素(NA)浓度均降低后,这两个结构中的TRH含量均增加,但多巴胺β-羟化酶抑制剂FLA-63使NA水平降低而不影响DA后,TRH含量未增加。另一方面,间接作用的拟多巴胺药苯丙胺、非选择性DA受体激动剂阿扑吗啡和选择性D2受体激动剂喹吡罗降低了纹状体中的TRH水平,但未降低伏隔核中的TRH水平。此外,DA模拟物诱导的纹状体肽含量降低被选择性D2受体拮抗剂舒必利拮抗,但未被选择性D1受体拮抗剂SCH 23390拮抗。苯丙胺的作用未被选择性α1-肾上腺素能受体拮抗剂哌唑嗪改变。这些结果表明,DA和D2受体在纹状体TRH的调节中起重要作用。