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“三联”单胺神经递质摄取抑制剂DOV 102,677的药理学特征

Pharmacological profile of the "triple" monoamine neurotransmitter uptake inhibitor, DOV 102,677.

作者信息

Popik Piotr, Krawczyk Martyna, Golembiowska Krystyna, Nowak Gabriel, Janowsky Aaron, Skolnick Phil, Lippa Arnold, Basile Anthony S

机构信息

Behavioral Neuroscience Laboratory, Institute of Pharmacology, Polish Academy of Sciences, Smetna 12, 31-343, Krakow, Poland.

出版信息

Cell Mol Neurobiol. 2006 Jul-Aug;26(4-6):857-73. doi: 10.1007/s10571-006-9012-5. Epub 2006 Apr 25.

Abstract
  1. The molecular and behavioral pharmacology of DOV 102,677 is characterized. 2. This characterization was performed using radioligand binding and neurotransmitter uptake assays targeting the monoamine neurotransmitter receptors. In addition, the effects of DOV 102,677 on extracellular neurotransmitter levels were investigated using in vivo microdialysis. Finally, the effects of DOV 102,677 in the forced swim test, locomotor function, and response to prepulse inhibition was investigated.3. DOV 102,677 is a novel, "triple" uptake inhibitor that suppresses [(3)H]dopamine (DA), [(3)H]norepinephrine (NE) and [(3)H]serotonin (5-HT) uptake by recombinant human transporters with IC(50) values of 129, 103 and 133 nM, respectively. Radioligand binding to the dopamine (DAT), norepinephrine (NET), and serotonin (SERT) transporters is inhibited with k (i) values of 222, 1030, and 740 nM, respectively. DOV 102,677 (20 mg/kg IP) increased extracellular levels of DA and 5-HT in the prefrontal cortex to 320 and 280% above baseline 100 min after administration. DA levels were stably increased for the duration (240 min) of the study, but serotonin levels declined to baseline by 200 min after administration. NE levels increased linearly to a maximum of 348% at 240 min post-dosing. Consistent with these increases in NE levels, the density of beta-adrenoceptors was selectively decreased in the cortex of rats treated with DOV 102,677 (20 mg/kg per day, PO, 35 days). 4. DOV 102,677 dose-dependently reduced the amount of time spent immobile by rats in the forced swim test, a model predictive of antidepressant activity, with a minimum effective dose (MED) of 20 mg/kg and a maximal efficacy comparable to imipramine. This decrease in immobility time did not appear to result from increased motor activity. Further, DOV 102,677 was as effective as methylphenidate in reducing the amplitude of the startle response in juvenile mice, without notably altering motor activity. 5. In summary, DOV 102,677 is an orally active, "balanced" inhibitor of DAT, NET and SERT with therapeutic versatility in treating neuropsychiatric disorders beyond depression.
摘要
  1. 对DOV 102,677的分子和行为药理学特性进行了表征。2. 这种表征是通过针对单胺神经递质受体的放射性配体结合和神经递质摄取试验来进行的。此外,使用体内微透析研究了DOV 102,677对细胞外神经递质水平的影响。最后,研究了DOV 102,677在强迫游泳试验、运动功能以及对预脉冲抑制反应中的作用。3. DOV 102,677是一种新型的“三重”摄取抑制剂,它通过重组人转运体抑制[(3)H]多巴胺(DA)、[(3)H]去甲肾上腺素(NE)和[(3)H]5-羟色胺(5-HT)的摄取,IC(50)值分别为129、103和133 nM。与多巴胺(DAT)、去甲肾上腺素(NET)和5-羟色胺(SERT)转运体的放射性配体结合受到抑制,k (i)值分别为222、1030和740 nM。腹腔注射20 mg/kg的DOV 102,677使前额叶皮质中DA和5-HT的细胞外水平在给药后100分钟分别比基线水平升高320%和280%。在研究持续时间(240分钟)内,DA水平持续稳定升高,但5-羟色胺水平在给药后200分钟降至基线。NE水平在给药后240分钟线性升高至最大值348%。与NE水平的这些升高一致,在用DOV 102,677(每天20 mg/kg,口服,35天)治疗的大鼠皮质中,β-肾上腺素能受体的密度选择性降低。4. 在强迫游泳试验中,DOV 102,677剂量依赖性地减少了大鼠不动的时间,该试验是一种预测抗抑郁活性的模型,最小有效剂量(MED)为20 mg/kg,最大疗效与丙咪嗪相当。不动时间的减少似乎不是由运动活动增加引起的。此外,DOV 102,677在降低幼年小鼠惊吓反应幅度方面与哌甲酯一样有效,且对运动活动没有明显影响。5. 总之,DOV 102,677是一种口服活性的DAT、NET和SERT的“平衡”抑制剂,在治疗除抑郁症之外的神经精神疾病方面具有治疗多功能性。

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