Fan Qiong-Yin, Xue Rui, Li Ying, Zhang Ting-Ting, He Xin-Hua, Fan Shi-Yong, Li Yun-Feng, Zhong Bo-Hua, Zhang You-Zhi, Li Jin
Department of New Drug Evaluation, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
CNS Neurosci Ther. 2016 Aug;22(8):700-6. doi: 10.1111/cns.12567. Epub 2016 May 20.
The present study was conducted to evaluate the antidepressant-like effects of ZBH2012001, a novel potential serotonin and norepinephrine reuptake inhibitor (SNRI).
Competitive binding assays, calcium flow, and cAMP detection methods were used to determine the affinity of ZBH2012001 for serotonin transporters (SERTs) and norepinephrine transporters (NETs), as well as its selectivity over dopamine transporters (DATs) and 16 other G-protein-coupled receptors (GPCRs) or iron channels. The antidepressant-like effects of ZBH2012001 were determined using the tail suspension test, forced swim test, and learned helplessness paradigm. The pharmacokinetics and acute toxicity of ZBH2012001 were also assessed.
ZBH2012001 exhibited a moderate affinity to SERTs and NETs (Ki values were 35.3 ± 2.86 and 225 ± 26.0 nM, respectively); it had no effects on the DATs or the 16 other GPCRs or iron channels. Data from behavioral tests indicated that ZBH2012001 exhibited superior antidepressant-like effects compared with duloxetine (one of the most used SNRIs) in the three depression models. The pharmacokinetic evaluation of ZBH2012001 indicated that the absolute bioavailability value was 60.5%, and the acute toxicity test indicated that LD50 of ZBH2012001 was 346 mg/kg.
These findings suggest that ZBH2012001 is a novel SNRI with superior antidepressant-like effects, lower acute toxicity and a better pharmacokinetic profile compared with duloxetine. Thus, ZBH2012001 may have potential therapeutic effects in depression disorders.
本研究旨在评估新型潜在的5-羟色胺和去甲肾上腺素再摄取抑制剂(SNRI)ZBH2012001的抗抑郁样作用。
采用竞争性结合试验、钙流和环磷酸腺苷(cAMP)检测方法,以确定ZBH2012001对5-羟色胺转运体(SERTs)和去甲肾上腺素转运体(NETs)的亲和力,以及其对多巴胺转运体(DATs)和其他16种G蛋白偶联受体(GPCRs)或离子通道的选择性。使用悬尾试验、强迫游泳试验和习得性无助范式来确定ZBH2012001的抗抑郁样作用。还评估了ZBH2012001的药代动力学和急性毒性。
ZBH2012001对SERTs和NETs表现出中等亲和力(Ki值分别为35.3±2.86和225±26.0 nM);对DATs或其他16种GPCRs或离子通道无作用。行为测试数据表明,在三种抑郁模型中,ZBH2012001与度洛西汀(最常用的SNRIs之一)相比,表现出更强的抗抑郁样作用。ZBH2012001的药代动力学评估表明,绝对生物利用度值为60.5%,急性毒性试验表明,ZBH2012001的半数致死量(LD50)为346 mg/kg。
这些发现表明,与度洛西汀相比,ZBH2012001是一种新型SNRI,具有更强的抗抑郁样作用、更低的急性毒性和更好的药代动力学特征。因此,ZBH2012001可能对抑郁症具有潜在的治疗作用。