Drug Research Division, Sumitomo Pharma Co., Ltd., Osaka, 554-0022, Japan.
Laboratory of Molecular Pharmacology, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, 920-1192, Japan.
Psychopharmacology (Berl). 2024 Nov;241(11):2223-2239. doi: 10.1007/s00213-024-06629-2. Epub 2024 Jun 10.
Current treatment of major depressive disorder is facing challenges, including a low remission rate, late onset of efficacy, and worsening severity due to comorbid symptoms such as psychosis and cognitive dysfunction. Serotonin (5-HT) neurotransmission is involved in a wide variety of psychiatric diseases and its potential as a drug target continues to attract attention.
The present study elucidates the effects of a novel 5-HT modulator, DSP-6745, on depression and its comorbid symptoms.
In vitro radioligand binding and functional assays showed that DSP-6745 is a potent inhibitor of 5-HT transporter and 5-HT, 5-HT, and 5-HT receptors. In vivo, DSP-6745 (6.4 and 19.1 mg/kg as free base, p.o.) increased the release of not only 5-HT, norepinephrine, and dopamine, but also glutamate in the medial prefrontal cortex. The results of in vivo mouse phenotypic screening by SmartCube® suggested that DSP-6745 has a behavioral signature combined with antidepressant-, anxiolytic-, and antipsychotic-like signals. A single oral dose of DSP-6745 (6.4 and 19.1 mg/kg) showed rapid antidepressant-like efficacy in the rat forced swim test, even at 24 h post-dosing, and anxiolytic activity in the rat social interaction test. Moreover, DSP-6745 (12.7 mg/kg, p.o.) led to an improvement in the apomorphine-induced prepulse inhibition deficit in rats. In the marmoset object retrieval with detour task, which is used to assess cognitive functions such as attention and behavioral inhibition, DSP-6745 (7.8 mg/kg, p.o.) enhanced cognition.
These data suggest that DSP-6745 is a multimodal 5-HT receptor antagonist and a 5-HT transporter inhibitor and has the potential to be a rapid acting antidepressant with efficacies in mitigating the comorbid symptoms of depression.
目前,重度抑郁症的治疗面临着诸多挑战,包括缓解率低、疗效出现较晚以及因精神病和认知功能障碍等合并症而导致病情恶化。血清素(5-HT)神经传递涉及到广泛的精神疾病,其作为药物靶点的潜力仍然备受关注。
本研究旨在阐明新型 5-HT 调节剂 DSP-6745 对抑郁症及其合并症症状的作用。
体外放射性配体结合和功能测定显示,DSP-6745 是一种强效的 5-HT 转运体和 5-HT、5-HT 和 5-HT 受体抑制剂。在体内,DSP-6745(以游离碱计,口服 6.4 和 19.1mg/kg)不仅增加了内侧前额叶皮质中 5-HT、去甲肾上腺素和多巴胺的释放,还增加了谷氨酸的释放。通过 SmartCube®进行的体内小鼠表型筛选结果表明,DSP-6745 具有结合抗抑郁药、抗焦虑药和抗精神病药特征的行为特征。单次口服 DSP-6745(6.4 和 19.1mg/kg)在大鼠强迫游泳试验中表现出快速的抗抑郁样作用,甚至在给药后 24 小时,以及在大鼠社交互动试验中表现出抗焦虑作用。此外,DSP-6745(12.7mg/kg,口服)可改善大鼠阿扑吗啡诱导的前脉冲抑制缺陷。在用于评估注意力和行为抑制等认知功能的狨猴物体检索回避任务中,DSP-6745(7.8mg/kg,口服)增强了认知能力。
这些数据表明,DSP-6745 是一种多模态 5-HT 受体拮抗剂和 5-HT 转运体抑制剂,有可能成为一种快速起效的抗抑郁药,具有缓解抑郁症合并症的疗效。