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N-丙基-2,2-二苯基-2-羟基乙酰胺,一种新型的α-羟基酰胺,具有抗惊厥、抗焦虑和抗抑郁样作用,能抑制电压门控钠离子通道。

N-propyl-2,2-diphenyl-2-hydroxyacetamide, a novel α-hydroxyamide with anticonvulsant, anxiolytic and antidepressant-like effects that inhibits voltage-gated sodium channels.

机构信息

Universidad de Buenos Aires, Consejo Nacional de lnvestigaciones Científicas y Técnicas, Instituto de Química y Fisicoquímica Biológicas, Facultad de Farmacia y Bioquímica, Junín 956 (C1113AAD), Ciudad de Buenos Aires, Argentina.

Universidad Nacional de La Plata, Consejo Nacional de lnvestigaciones Científicas y Técnicas, Instituto de Estudios Inmunopatológicos y Fisiológicos, 47 street and 115 (B1900BJW), La Plata, Argentina.

出版信息

Eur J Pharmacol. 2018 Jan 15;819:270-280. doi: 10.1016/j.ejphar.2017.11.048. Epub 2017 Dec 5.

DOI:10.1016/j.ejphar.2017.11.048
PMID:29217174
Abstract

In patients with epilepsy, anxiety and depression are the most frequent psychiatric comorbidities but they often remain unrecognized and untreated. We report herein the antidepressant-like activity in two animal models, tail suspension and forced swimming tests, of six anticonvulsants α-hydroxyamides. From these, N-propyl-2,2-diphenyl-2-hydroxyacetamide (compound 5) emerged not only as the most active as anticonvulsant (ED = 2.5mg/kg, MES test), but it showed the most remarkable antidepressant-like effect in the tail suspension and forced swimming tests (0.3-30mg/kg, i.p.); and, also, anxiolytic-like action in the plus maze test (3-10mg/kg, i.p.) in mice. Studies of its mechanism of action, by means of its capacity to act via the GABA receptor ([H]-flunitrazepam binding assay); the 5-HT receptor ([H]-8-OH-DPAT binding assay) and the voltage-gated sodium channels (either using the patch clamp technique in hNa 1.2 expressed in HEK293 cell line or using veratrine, in vivo) were attempted. The results demonstrated that its effects are not likely related to 5-HT or GABAergic receptors and that its anticonvulsant and antidepressant-like effect could be due to its voltage-gated sodium channel blocking properties.

摘要

在癫痫患者中,焦虑和抑郁是最常见的精神共病,但它们常常未被识别和治疗。我们在此报告六种抗惊厥α-羟基酰胺在两种动物模型(悬尾和强迫游泳试验)中的抗抑郁样活性。在这些化合物中,N-丙基-2,2-二苯基-2-羟基乙酰胺(化合物 5)不仅作为最有效的抗惊厥剂(ED=2.5mg/kg,MES 试验),而且在悬尾和强迫游泳试验中表现出最显著的抗抑郁样作用(0.3-30mg/kg,ip);并且在小鼠的加迷宫试验中也表现出类苯并二氮䓬样作用(3-10mg/kg,ip)。通过其通过 GABA 受体的作用能力([H]-氟硝西泮结合测定)、5-HT 受体([H]-8-OH-DPAT 结合测定)和电压门控钠离子通道(使用在 HEK293 细胞系中表达的 hNa 1.2 的膜片钳技术或使用藜芦碱,体内)来研究其作用机制的尝试。结果表明,其作用可能与 5-HT 或 GABA 能受体无关,其抗惊厥和抗抑郁样作用可能归因于其电压门控钠离子通道阻断特性。

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