一种水溶性低影响安帕金原药 CX1942 及其活性分子 CX1763 的临床前特征。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Daniel P Radin, Sheng Zhong, Rok Cerne, Mohammed Shoaib, Jeffrey M Witkin, Arnold Lippa
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引用次数: 0

摘要

目的:AMPA-谷氨酸受体(AMPAR)功能障碍介导多种神经/神经精神疾病。安非他明类药物能与 AMPAR 结合,并通过异体作用增强谷氨酸诱导的电流。本报告介绍了水溶性安帕金 CX1942 原药和活性分子 CX1763 的活性:结果:CX1763 和 CX1942 能增强大鼠海马的突触传递。CX1763 可提高大鼠 5CSRTT 的注意力,减少苯丙胺诱导的小鼠多动症。CX1942 能有效逆转阿片诱导的大鼠呼吸抑制。CX1942/CX1763 的有效剂量为 2.5-10 毫克/千克。CX1763 对大鼠的致痫性可达 1500 毫克/千克:这些数据表明,CX1942 和 CX1763 在多种临床前试验中具有活性,且无明显副作用。CX1942 可作为 CX1763 的原药,在静脉注射制剂中具有高水溶性的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preclinical characterization of a water-soluble low-impact ampakine prodrug, CX1942 and its active moiety, CX1763.

Aim: AMPA-glutamate receptor (AMPAR) dysfunction mediates multiple neurological/neuropsychiatric disorders. Ampakines bind AMPARs and allosterically enhance glutamate-elicited currents. This report describes the activity of the water-soluble ampakine CX1942 prodrug and the active moiety CX1763.Results: CX1763 and CX1942 enhance synaptic transmission in hippocampi of rats. CX1763 increases attention in the 5CSRTT in rats and reduces amphetamine-induced hyperactivity in mice. CX1942 potently reverses opioid-induced respiratory depression in rats. CX1942/CX1763 was effective at 2.5-10 mg/kg. CX1763 lacked epileptogenicity up to 1500 mg/kg in rats.Conclusion: These data document that CX1942 and CX1763 are active and without prominent side effects in multiple pre-clinical assays. CX1942 could serve as a prodrug for CX1763 with the advantage of high water solubility as in an intravenous formulation.

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CiteScore
7.20
自引率
4.30%
发文量
567
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