Psychopharmacology Department, Institut de Recherches Servier, Centre de Recherches de Croissy, 125 Chemin de Ronde, 78290 Croissy-sur-Seine, France.
Eur Neuropsychopharmacol. 2010 Sep;20(9):599-621. doi: 10.1016/j.euroneuro.2010.04.003. Epub 2010 May 18.
Though neurokinin(1) (NK(1)) receptors are implicated in depressed states and their treatment, selective antagonists have disappointed in clinical trials. Accordingly, we designed a novel ligand, S41744 (2-piperazin-1-yl-indan-2-carboxylic-acid-(3-chloro-5-fluoro-benzyl)-methyl-amide), which both blocks NK(1) receptors and interferes with serotonin (5-HT) reuptake. S41744 mimicked the selective antagonist aprepitant in binding human (h)NK(1) receptors and in antagonising Substance-P-mediated Extracellular-Regulated-Kinase phosphorylation (pK(B), 7.7). Further, it dose-dependently (0.63-40.0 mg/kg, i.p.) displaced ex vivo [(3)H]-[Sar(9),Met(O(2))(11)]-Substance P binding to gerbil striatum, attenuated formalin-induced hind-paw licking in gerbils, and antagonised locomotion induced by i.c.v. administration of the NK(1) agonist GR73632 to guinea pigs. Like paroxetine, S41744 recognised h5-HT transporters, reduced synaptosomal uptake of 5-HT (pK(B), 7.9), and dose-dependently (0.63-10.0 mg/kg) elevated dialysis levels of 5-HT in the hippocampus and frontal cortex of freely-moving guinea pigs. Further, S41744 increased extracellular levels of 5-HT in frontal cortex and hippocampus of rats to a greater extent than paroxetine, and its inhibitory influence upon serotonergic perikarya was blunted relative to its affinity for 5-HT transporters. S41744 more potently blocked stress-induced vocalizations in guinea pigs than aprepitant and paroxetine, and it was active in forced-swim and marble-burying procedures of putative antidepressant properties in mice. While aprepitant displayed anxiolytic actions in stress-induced foot-tapping and social interaction tests in gerbils, paroxetine was anxiogenic and S41744 "neutral", reflecting balanced NK(1) antagonism and suppression of 5-HT reuptake. Moreover, S41744 shared anxiolytic actions of aprepitant in the rat Vogel Conflict Test. In conclusion, S41744 is an innovative NK(1) antagonist/5-HT reuptake inhibitor justifying further evaluation for treatment of stress-related disorders.
尽管神经激肽(1)(NK(1))受体与抑郁状态及其治疗有关,但选择性拮抗剂在临床试验中令人失望。因此,我们设计了一种新型配体 S41744(2-哌嗪-1-基-茚满-2-羧酸-(3-氯-5-氟-苄基)-甲基-酰胺),它既能阻断 NK(1)受体,又能干扰 5-羟色胺(5-HT)再摄取。S41744在结合人(h)NK(1)受体和拮抗物质 P 介导的细胞外调节激酶磷酸化(pK(B),7.7)方面模拟选择性拮抗剂阿瑞匹坦。此外,它以剂量依赖性方式(0.63-40.0mg/kg,ip)置换体外[3H]-[Sar(9),Met(O(2))(11)]物质 P 与沙鼠纹状体的结合,减轻沙鼠福尔马林诱导的后爪舔舐,拮抗 i.c.v.注射 NK(1)激动剂 GR73632 引起的豚鼠运动。与帕罗西汀一样,S41744识别 h5-HT 转运体,减少突触小体对 5-HT 的摄取(pK(B),7.9),并以剂量依赖性方式(0.63-10.0mg/kg)增加自由移动豚鼠海马和额叶皮质中 5-HT 的透析水平。此外,S41744使大鼠额叶皮质和海马中的 5-HT 水平升高的程度大于帕罗西汀,并且其对 5-HT 神经元的抑制作用相对于其对 5-HT 转运体的亲和力减弱。S41744在阻断应激诱导的豚鼠发声方面比阿瑞匹坦和帕罗西汀更有效,并且在强迫游泳和大理石埋藏程序中具有潜在的抗抑郁作用。虽然阿瑞匹坦在沙鼠应激诱导的跺脚和社交互动测试中表现出抗焦虑作用,但帕罗西汀具有焦虑作用,而 S41744“中性”,反映了平衡的 NK(1)拮抗作用和 5-HT 再摄取抑制作用。此外,S41744在大鼠沃格冲突测试中共享阿瑞匹坦的抗焦虑作用。总之,S41744 是一种创新的 NK(1)拮抗剂/5-HT 再摄取抑制剂,值得进一步评估用于治疗与应激相关的疾病。