Gołembiowska K, Wedzony K
Institute of Pharmacology, Polish Academy of Sciences, Kraków.
Pol J Pharmacol. 1993 May-Jun;45(3):299-308.
Intrastriatal administration of ipsapirone (IPSA, 0.5 and 1 mM), an agonist of 5-HT1A serotonergic receptors, enhanced in a dose-dependent manner DA release in the rat striatum, without affecting levels of the DA metabolites DOPAC and HVA. The IPSA evoked-enhancement of DA release was followed by a decrease in 5-HIAA concentration. The effects of intrastriatal administration of IPSA were mimicked by 8-OH-DPAT (0.5 mM), another agonist of 5-HT1A receptors, and were antagonized by the peripheral administration of metergoline (5 mg/kg ip) and intrastriatal administration of NAN-190 (0.5 mM). IPSA given peripherally (10 mg/kg ip) also enhanced DA release; that effect was accompanied by an increase in DOPAC and HVA levels. It is postulated that IPSA increases the release of DA from nigrostriatal terminals via activation of striatal 5-HT1A receptors in a manner independent of the activation of 5-HT1A receptors in the dorsal raphe nuclei.
向大鼠纹状体内注射5-HT1A 5-羟色胺能受体激动剂ipsapirone(IPSA,0.5和1 mM),可使纹状体内多巴胺(DA)释放呈剂量依赖性增强,且不影响DA代谢产物3,4-二羟基苯乙酸(DOPAC)和高香草酸(HVA)的水平。IPSA引起的DA释放增强之后,5-羟吲哚乙酸(5-HIAA)浓度降低。向纹状体内注射8-OH-DPAT(0.5 mM),另一种5-HT1A受体激动剂,可模拟IPSA的作用,而外周注射麦角林(5 mg/kg腹腔注射)和向纹状体内注射NAN-190(0.5 mM)可拮抗IPSA的作用。外周给予IPSA(10 mg/kg腹腔注射)也可增强DA释放;该作用伴随着DOPAC和HVA水平升高。据推测,IPSA通过激活纹状体5-HT1A受体增加黑质纹状体终末DA的释放,其方式独立于中缝背核5-HT1A受体的激活。