Przegaliński E, Jaworska L, Budziszewska B
Institute of Pharmacology, Polish Academy of Sciences, Kraków.
Neuropeptides. 1993 Nov;25(5):277-82. doi: 10.1016/0143-4179(93)90044-b.
In the present study we examined the influence of dopamine (DA) stimulants: amphetamine (an agent releasing DA), apomorphine (a non-selective agonist of DA receptors), quinpirole (a selective agonist of D2 receptors) and SKF-38393 (a selective agonist of D1 receptors) on the in vitro release of thyrotropin-releasing hormone (TRH) from the rat striatal slices and nucleus accumbens fragments. It was shown that amphetamine, apomorphine and quinpirole (all those drugs added in concentrations of 10(-8)-10(-5) M), concentration-dependently increased the release of TRH, a more potent effect being observed in striatal slices. On the other hand, SKF-38393 (10(-6)-10(-5) M) was ineffective. Furthermore, the increases in the TRH release from the striatal slices, induced by 10(-5) M of amphetamine, apomorphine or quinpirole, were completely blocked by the selective D2 receptor antagonist sulpiride (10(-5) M), but not by the selective D1 receptors antagonist SCH-23390 (10(-5) M). These results indicate that stimulation of D2 receptors is responsible for the TRH release from the striatum and nucleus accumbens in vitro, and that this effect may be involved in the decrease in the peptide content in the striatum following DA stimulants, observed earlier in in vivo studies.
在本研究中,我们检测了多巴胺(DA)兴奋剂:苯丙胺(一种释放DA的药物)、阿扑吗啡(DA受体的非选择性激动剂)、喹吡罗(D2受体的选择性激动剂)和SKF-38393(D1受体的选择性激动剂)对大鼠纹状体切片和伏隔核碎片中促甲状腺激素释放激素(TRH)体外释放的影响。结果表明,苯丙胺、阿扑吗啡和喹吡罗(所有这些药物添加浓度为10^(-8)-10^(-5) M)均浓度依赖性地增加TRH的释放,在纹状体切片中观察到更强的效应。另一方面,SKF-38393(10^(-6)-10^(-5) M)无效。此外,10^(-5) M苯丙胺、阿扑吗啡或喹吡罗诱导的纹状体切片中TRH释放的增加,被选择性D2受体拮抗剂舒必利(10^(-5) M)完全阻断,但未被选择性D1受体拮抗剂SCH-23390(10^(-5) M)阻断。这些结果表明,D2受体的刺激负责体外纹状体和伏隔核中TRH的释放,并且这种效应可能与体内研究中先前观察到的DA兴奋剂后纹状体中肽含量的降低有关。