Devroye Céline, Haddjeri Nasser, Cathala Adeline, Rovera Renaud, Drago Filippo, Piazza Pier Vincenzo, Artigas Francesc, Spampinato Umberto
Inserm U1215, Neurocentre Magendie, Physiopathology of Addiction and Traumatic Memories Group, Bordeaux F-33000, France; Université de Bordeaux, Bordeaux F-33000, France.
Inserm U1208, Stem Cell and Brain Research Institute, 69500 Bron, France; Université Lyon 1, 69373 Lyon, France.
Neuropharmacology. 2017 Jun;119:91-99. doi: 10.1016/j.neuropharm.2017.04.001. Epub 2017 Apr 5.
Recent studies have shown that serotonin receptor (5-HTR) antagonists exert opposite facilitatory and inhibitory effects on dopamine (DA) release in the medial prefrontal cortex (mPFC) and the nucleus accumbens (NAc), respectively, thereby leading to the proposal that these compounds could provide an interesting pharmacological tool for treating schizophrenia. Although the mechanisms underlying these effects remain unknown, several data in the literature suggest that 5-HTRs located into the mPFC could participate in this interaction. The present study, using in vivo microdialysis and electrophysiological recordings in rats, assessed this hypothesis by means of two selective 5-HTR (WAY 100635) and 5-HTR (RS 127445) antagonists. WAY 100635, administered either subcutaneously (0.16 mg/kg, s.c) or locally into the mPFC (0.1 μM), blocked the changes of mPFC and NAc DA release induced by the intraperitoneal administration of RS 127445 (0.16 mg/kg, i.p.). The administration of RS 127445 (0.16 mg/kg, i.p.) increased both dorsal raphe nucleus (DRN) 5-HT neuron firing rate and 5-HT outflow in the mPFC. Likewise, mPFC 5-HT outflow was increased following the intra-DRN injection of RS 127445 (0.032 μg/0.2 μl). Finally, intra-DRN injection of RS 127445 increased and decreased DA outflow in the mPFC and the NAc, respectively, these effects being reversed by the intra-mPFC perfusion of WAY 100635. These results demonstrate the existence of a functional interplay between mPFC 5-HTRs and DRN 5-HTRs in the control of the DA mesocorticolimbic system, and highlight the clinical interest of this interaction, as both receptors represent an important pharmacological target for the treatment of schizophrenia.
最近的研究表明,血清素受体(5 - HTR)拮抗剂分别对内侧前额叶皮质(mPFC)和伏隔核(NAc)中的多巴胺(DA)释放产生相反的促进和抑制作用,因此有人提出这些化合物可能为治疗精神分裂症提供一种有趣的药理学工具。尽管这些作用背后的机制尚不清楚,但文献中的一些数据表明,位于mPFC中的5 - HTRs可能参与了这种相互作用。本研究在大鼠体内使用微透析和电生理记录,通过两种选择性5 - HTR(WAY 100635)和5 - HTR(RS 127445)拮抗剂评估了这一假设。皮下注射(0.16 mg/kg,皮下)或局部注射到mPFC(0.1 μM)的WAY 100635,可阻断腹腔注射RS 127445(0.16 mg/kg,腹腔注射)诱导的mPFC和NAc中DA释放的变化。腹腔注射RS 127445(0.16 mg/kg,腹腔注射)可增加背侧中缝核(DRN)5 - HT神经元的放电率以及mPFC中的5 - HT流出量。同样,在DRN内注射RS 127445(0.032 μg/0.2 μl)后,mPFC中的5 - HT流出量增加。最后,DRN内注射RS 127445分别增加和减少了mPFC和NAc中的DA流出量,mPFC内灌注WAY 100635可逆转这些作用。这些结果证明了在DA中脑皮质边缘系统的控制中,mPFC 5 - HTRs和DRN 5 - HTRs之间存在功能相互作用,并突出了这种相互作用的临床意义,因为这两种受体都是治疗精神分裂症的重要药理学靶点。