Maeda Kenji, Sugino Haruhiko, Akazawa Hitomi, Amada Naoki, Shimada Jun, Futamura Takashi, Yamashita Hiroshi, Ito Nobuaki, McQuade Robert D, Mørk Arne, Pehrson Alan L, Hentzer Morten, Nielsen Vibeke, Bundgaard Christoffer, Arnt Jørn, Stensbøl Tine Bryan, Kikuchi Tetsuro
Qs' Research Institute, Otsuka Pharmaceutical Co., Ltd. Tokushima, Japan (K.M., H.S., H.A., N.A., J.S., T.F., H.Y., N.I., T.K.); Otsuka Pharmaceutical Development & Commercialization, Princeton, New Jersey (R.D.M.); Neuroscience Drug Discovery, H. Lundbeck A/S, Valby, Denmark (A.M., M.H., V.N., C.B., J.A., T.B.S.); and Lundbeck Research USA, Paramus, New Jersey (A.L.P.)
Qs' Research Institute, Otsuka Pharmaceutical Co., Ltd. Tokushima, Japan (K.M., H.S., H.A., N.A., J.S., T.F., H.Y., N.I., T.K.); Otsuka Pharmaceutical Development & Commercialization, Princeton, New Jersey (R.D.M.); Neuroscience Drug Discovery, H. Lundbeck A/S, Valby, Denmark (A.M., M.H., V.N., C.B., J.A., T.B.S.); and Lundbeck Research USA, Paramus, New Jersey (A.L.P.).
J Pharmacol Exp Ther. 2014 Sep;350(3):589-604. doi: 10.1124/jpet.114.213793. Epub 2014 Jun 19.
Brexpiprazole (OPC-34712, 7-{4-[4-(1-benzothiophen-4-yl)piperazin-1-yl]butoxy}quinolin-2(1H)-one) is a novel drug candidate in clinical development for psychiatric disorders with high affinity for serotonin, dopamine, and noradrenaline receptors. In particular, it bound with high affinity (Ki < 1 nM) to human serotonin 1A (h5-HT1A)-, h5-HT2A-, long form of human D2 (hD2L)-, hα1B-, and hα2C-adrenergic receptors. It displayed partial agonism at h5-HT1A and hD2 receptors in cloned receptor systems and potent antagonism of h5-HT2A receptors and hα1B/2C-adrenoceptors. Brexpiprazole also had affinity (Ki < 5 nM) for hD3-, h5-HT2B-, h5-HT7-, hα1A-, and hα1D-adrenergic receptors, moderate affinity for hH1 (Ki = 19 nM), and low affinity for hM1 receptors (Ki > 1000 nM). Brexpiprazole potently bound to rat 5-HT2A and D2 receptors in vivo, and ex vivo binding studies further confirmed high 5-HT1A receptor binding potency. Brexpiprazole inhibited DOI (2,5-dimethoxy-4-iodoamphetamine)-induced head twitches in rats, suggestive of 5-HT2A antagonism. Furthermore, in vivo D2 partial agonist activity of brexpiprazole was confirmed by its inhibitory effect on reserpine-induced DOPA accumulation in rats. In rat microdialysis studies, brexpiprazole slightly reduced extracellular dopamine in nucleus accumbens but not in prefrontal cortex, whereas moderate increases of the dopamine metabolites, homovanillic acid and DOPAC (3,4-dihydroxy-phenyl-acetic acid), in these areas also suggested in vivo D2 partial agonist activity. In particular, based on a lower intrinsic activity at D2 receptors and higher binding affinities for 5-HT1A/2A receptors than aripiprazole, brexpiprazole would have a favorable antipsychotic potential without D2 receptor agonist- and antagonist-related adverse effects. In conclusion, brexpiprazole is a serotonin-dopamine activity modulator with a unique pharmacology, which may offer novel treatment options across a broad spectrum of central nervous system disorders.
布雷哌唑(OPC - 34712,7 - {4 - [4 - (1 - 苯并噻吩 - 4 - 基)哌嗪 - 1 - 基]丁氧基}喹啉 - 2(1H) - 酮)是一种处于临床开发阶段的新型候选药物,用于治疗精神疾病,对5 - 羟色胺、多巴胺和去甲肾上腺素受体具有高亲和力。特别是,它以高亲和力(Ki < 1 nM)与人5 - 羟色胺1A(h5 - HT1A)、h5 - HT2A、人D2长型(hD2L)、hα1B和hα2C肾上腺素能受体结合。在克隆受体系统中,它在h5 - HT1A和hD2受体上表现出部分激动作用,对h5 - HT2A受体和hα1B/2C肾上腺素能受体具有强效拮抗作用。布雷哌唑对hD3、h5 - HT2B、h5 - HT7、hα1A和hα1D肾上腺素能受体也具有亲和力(Ki < 5 nM),对hH1具有中等亲和力(Ki = 19 nM),对hM1受体具有低亲和力(Ki > 1000 nM)。布雷哌唑在体内能强效结合大鼠5 - HT2A和D2受体,体外结合研究进一步证实其对5 - HT1A受体具有高结合效力。布雷哌唑能抑制大鼠中DOI(2,5 - 二甲氧基 - 4 - 碘苯丙胺)诱导的头部抽搐,提示其具有5 - HT2A拮抗作用。此外,布雷哌唑在体内的D2部分激动剂活性通过其对利血平诱导的大鼠多巴积累的抑制作用得到证实。在大鼠微透析研究中,布雷哌唑使伏隔核细胞外多巴胺略有减少,但前额叶皮质未出现这种情况,而这些区域中多巴胺代谢物高香草酸和DOPAC(3,4 - 二羟基苯乙酸)的适度增加也提示了其体内D2部分激动剂活性。特别是,基于其在D2受体上较低的内在活性以及对5 - HT1A/2A受体的结合亲和力高于阿立哌唑,布雷哌唑可能具有良好的抗精神病潜力,而不会产生与D2受体激动剂和拮抗剂相关的不良反应。总之,布雷哌唑是一种具有独特药理学特性的5 - 羟色胺 - 多巴胺活性调节剂,可能为广泛的中枢神经系统疾病提供新的治疗选择。