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4-(2-(烷基硫代)苯并[d]恶唑-5-基)-2,4-二氢-3H-1,2,4-三唑-3-酮的合成与抗惊厥活性评价。

Synthesis and Evaluation of the Anticonvulsant Activities of 4-(2-(Alkylthio)benzo[d]oxazol-5-yl)-2,4-dihydro-3H-1,2,4-triazol-3-ones.

机构信息

Medical College, Jinggangshan University, No. 28, Xueyuan Road, Ji'an 343009, Jiangxi, China.

Siping Institute of Food and Drug Control, No. 357, Nanhu Road, Sipin 136000, Jilin, China.

出版信息

Molecules. 2018 Mar 25;23(4):756. doi: 10.3390/molecules23040756.

Abstract

In this study, a novel series of 4-(2-(alkylthio)benzo[]oxazol-5-yl)-2,4-dihydro-3-1,2,4-triazol-3-ones (-) was designed and synthesized. The anticonvulsant activities of these compounds were evaluated by using the maximal electroshock seizure (MES) and subcutaneous pentylenetetrazole (scPTZ) seizure models in mice. The neurotoxicity of these compounds was evaluated using the rotarod neurotoxicity test. The majority of compounds showed anti-MES activities at 100 or 300 mg/kg. Compound was considered to be the most promising, based on its potency against MES- and PTZ-induced seizures with ED values of 23.7 and 18.9 mg/kg, respectively. The TD value of was 284.0 mg/kg, which resulted in a higher protective index (PI = TD/ED) value than that of carbamazepine and valproate. In an ELISA test, compound significantly increased the γ-aminobutyric acid (GABA) content in mouse brain. In addition, pretreatment with thiosemicarbazide (an inhibitor of the GABA synthesizing enzyme) significantly decreased the activity of in the MES model, which suggests that the mechanism through which compound elicits its anticonvulsive action is at least in part through increasing the GABA level in the brain.

摘要

在这项研究中,设计并合成了一系列新型的 4-(2-(烷基硫代)苯并[1,3]恶唑-5-基)-2,4-二氢-3-[1,2,4]三唑-3-酮(-)。通过使用最大电休克惊厥 (MES) 和皮下戊四氮 (scPTZ) 惊厥模型在小鼠中评估这些化合物的抗惊厥活性。通过旋转棒神经毒性试验评估这些化合物的神经毒性。大多数化合物在 100 或 300mg/kg 时表现出抗 MES 活性。基于其对 MES 和 PTZ 诱导的惊厥的效力,化合物 被认为是最有前途的,其 ED 值分别为 23.7 和 18.9mg/kg。 的 TD 值为 284.0mg/kg,这导致其保护指数 (PI = TD/ED) 值高于卡马西平和丙戊酸。在 ELISA 测试中,化合物 显著增加了小鼠大脑中的γ-氨基丁酸 (GABA) 含量。此外,用硫代卡巴肼(GABA 合成酶抑制剂)预处理可显著降低 在 MES 模型中的活性,这表明化合物 通过至少部分增加大脑中的 GABA 水平来发挥其抗惊厥作用的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b4/6017283/2562887cc969/molecules-23-00756-g001.jpg

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