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发现非手性阿莫沙平,以最大限度地提高 5-HT7 和 D2 受体拮抗作用治疗情绪障碍的获益/风险。

Discovery of Nonracemic Amisulpride to Maximize Benefit/Risk of 5-HT7 and D2 Receptor Antagonism for the Treatment of Mood Disorders.

机构信息

Sunovion Pharmaceuticals Inc, Marlborough, Massachusetts, USA.

Drug Research Division, Sumitomo Dainippon Pharma Co., Ltd., Osaka, Japan.

出版信息

Clin Pharmacol Ther. 2021 Sep;110(3):808-815. doi: 10.1002/cpt.2282. Epub 2021 Jun 12.

Abstract

In contrast to the dose-occupancy relationship in the treatment of schizophrenia, the minimal effective level of dopamine receptor 2 (D2R) blockade for antipsychotics in the treatment of bipolar depression is unknown. Lower doses aimed at reducing extrapyramidal side effects must be balanced against the need to retain the therapeutic benefit of D2R blockade on emergent cycling, mixed, manic, anxiety, and/or psychotic symptoms. Dose-reductions intended to lower D2R blockade, however, could also decrease concomitant serotonin receptor antagonism and its potential benefit on depressive symptoms. Here, we uncoupled the potential antidepressant activity in amisulpride, driven by 5-HT7 receptor (5-HT7R) antagonism, from the D2R-mediated antipsychotic activity by discovering that each enantiomer favors a different receptor. Aramisulpride was more potent at 5-HT7R relative to esamisulpride (Ki 47 vs. 1,900 nM, respectively), whereas esamisulpride was more potent at D2R (4.0 vs. 140 nM). We hypothesized that a nonracemic ratio might achieve greater 5-HT7R-mediated antidepressant effects at a lower level of D2R blockade. The dose-occupancy relationship of esamisulpride at D2R was determined by positron emission tomography (PET) imaging in human volunteers. Separately the dose-relationship of aramisulpride was established in humans using suppression of rapid eye movement (REM) sleep as a marker of 5-HT7R antagonism. These results led to the discovery of an 85:15 ratio of aramisulpride to esamisulpride (SEP-4199) that maximizes the potential for antidepressant benefit of aramisulpride via 5-HT7R and reduces esamisulpride to minimize D2R-related extrapyramidal side effects while still retaining D2R-mediated effects predicted to provide benefit in bipolar depression. The antidepressant efficacy of SEP-4199 was recently confirmed in a proof-of-concept trial for the treatment of bipolar depression (NCT03543410).

摘要

与精神分裂症治疗中的剂量-占据关系相反,抗精神病药物治疗双相情感障碍时多巴胺受体 2(D2R)阻断的最低有效水平尚不清楚。旨在减少锥体外系副作用的较低剂量必须与保留 D2R 阻断对紧急循环、混合、躁狂、焦虑和/或精神病症状的治疗益处相平衡。然而,旨在降低 D2R 阻断的剂量减少也可能降低伴随的 5-羟色胺受体拮抗作用及其对抑郁症状的潜在益处。在这里,我们通过发现每个对映体都有利于不同的受体,将氨磺必利的潜在抗抑郁活性与其 D2R 介导的抗精神病活性分离出来。氨磺必利相对于 esamisulpride 对 5-HT7R 的亲和力更强(Ki 分别为 47 和 1900 nM),而 esamisulpride 对 D2R 的亲和力更强(4.0 和 140 nM)。我们假设非对映体比例可能以较低的 D2R 阻断水平实现更大的 5-HT7R 介导的抗抑郁作用。通过正电子发射断层扫描(PET)成像在人类志愿者中确定 esamisulpride 对 D2R 的剂量-占据关系。另外,使用快速眼动(REM)睡眠抑制作为 5-HT7R 拮抗作用的标志物,在人类中建立了氨磺必利的剂量关系。这些结果导致发现了一种氨磺必利与 esamisulpride 的 85:15 比例(SEP-4199),该比例最大限度地发挥了氨磺必利通过 5-HT7R 产生的抗抑郁作用的潜力,并降低了 esamisulpride 的剂量,以最大限度地减少与 D2R 相关的锥体外系副作用,同时仍然保留预计对双相情感障碍有治疗益处的 D2R 介导作用。SEP-4199 的抗抑郁疗效最近在一项双相情感障碍治疗的概念验证试验中得到了证实(NCT03543410)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9038/8453756/74fd7fa3d43e/CPT-110-808-g003.jpg

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