Isogawa K, Akiyoshi J, Hikichi T, Yamamoto Y, Tsutsumi T, Nagayama H
Department of Neuropsychiatry, Oita Medical University, Hasama-Machi, Oita 875-5593, Japan.
Neuropeptides. 2000 Jun-Aug;34(3-4):234-9. doi: 10.1054/npep.2000.0806.
Corticotropin releasing factor (CRF) is a major mediator of adaptive responsiveness to stress. We measured changes in extracellular concentrations of catecholamine and indoleamines in freely moving rats in response to administration of CRF1 antagonist CP-154,526 by using in vivo microdialysis. Dialysis probes were placed stereotaxically in either the hippocampus or the prefrontal cortex. We examined the response in the hippocampus or the prefrontal cortex to 32.0 mg/kg i.p. administration of CP-154,526. CP-154,526 reduced the extracellular concentration of norepinephrine (NE) from 30 min to 180 min and 5-hydroxytryptamine (5-HT) from 30 min to 60 min after injection in the hippocampus. CP-154,526 did not remarkably change dopamine (DA). There were no significant differences between CP-154,526 and vehicle in NE, 5-HT and DA in the prefrontal cortex. The present results indicate that CRF1 receptor antagonist produced a decrease in dialysate concentration of NE and 5-HT, but not DA, in the hippocampus. These results suggest that the CRH-1 receptor antagonist suppresses the release of NE and 5-HT in the hippocampus.
促肾上腺皮质激素释放因子(CRF)是对应激适应性反应的主要调节因子。我们通过体内微透析法,测量了自由活动大鼠在注射CRF1拮抗剂CP-154,526后,细胞外儿茶酚胺和吲哚胺浓度的变化。透析探针通过立体定位分别置于海马体或前额叶皮质。我们研究了海马体或前额叶皮质对腹腔注射32.0 mg/kg CP-154,526的反应。注射后,CP-154,526在30分钟至180分钟内降低了海马体中去甲肾上腺素(NE)的细胞外浓度,在30分钟至60分钟内降低了5-羟色胺(5-HT)的细胞外浓度。CP-154,526对多巴胺(DA)无显著影响。在前额叶皮质中,CP-154,526与赋形剂在NE、5-HT和DA方面无显著差异。目前的结果表明,CRF1受体拮抗剂使海马体中NE和5-HT的透析液浓度降低,但未使DA降低。这些结果提示,CRH-1受体拮抗剂抑制了海马体中NE和5-HT的释放。