具有神经保护作用的甘脯氨酸亲安帕平

K. N. Koliasnikova, P. Povarnina, A. V. Tallerova, Yu. N. Firsova, Sergei V. Nikolaev, T. Antipova, A. Nadorova, L. Kolik, T. Gudasheva, S. Seredenin
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引用次数: 4

摘要

先前有研究表明,神经肽环- l -脯氨酸(CPG)是AMPA受体的正向调节剂,可提高神经细胞培养中BDNF的水平。CPG的药理作用谱与BDNF一致。设计合成了二肽n -苯乙酰-甘酰基- l-脯氨酸乙酯(GZK-111)作为CPG的线性类似物。本研究的目的是揭示GZK-111的药理学特征。二肽GZK-111在体外代谢成CPG,在帕金森病细胞模型中,浓度为10-7-10-6 M时,细胞存活率提高28%。在脑缺血模型中,GZK-111在0.5 mg/kg, i.p的剂量下具有神经保护作用,使脑梗死体积减少1.6倍。与CPG相似,GZK-111在0.1 ~ 1.0 mg/kg, i.p.范围内具有立体特异性抗遗忘活性。在1.5 mg/kg剂量下观察到显著的抗焦虑作用。GZK-111在0.5 ~ 4.0 mg/kg, i.p范围内表现出镇痛活性。GZK-111给药剂量为10mg /kg/7天,每日口服,具有抗抑郁样活性。因此,GZK-111具有神经保护、促智、抗缺氧、抗焦虑、类抗抑郁和镇痛作用。因此,GZK-111可被认为是一种具有bdnf -能作用机制的具有药理活性的亲氨pakine。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glyproline Pro-Ampakine with Neuroprotective Activity
Previously it was shown that neuropeptide cyclo-L-prolylglycine (CPG) is a positive modulator of AMPA receptors, which increases BDNF level in neuronal cell cultures. The spectrum of CPG’s pharmacological effects corresponds to that of BDNF. Dipeptide N-phenylacetyl-glycyl-L-proline ethyl ester (GZK-111) was designed and synthesized as a linear analog of CPG. The aim of the present work was to reveal the pharmacological profile of GZK-111. Dipeptide GZK-111 was shown to metabolize into CPG in vitro and increased cell survival by 28% at concentrations of 10-7–10-6 M in a Parkinson’s disease cell model. In a model of cerebral ischemia, GZK-111, at a dose of 0.5 mg/kg, i.p., was found to have neuroprotective effects, reducing the cerebral infarct volume by 1.6 times. Similar to CPG, GZK-111, at the range 0.1–1.0 mg/kg, i.p., possessed a stereospecific antiamnesic activity. A significant anxiolytic effect was observed at a dose of 1.5 mg/kg. GZK-111, at the range 0.5–4.0 mg/kg, i.p., demonstrated analgesic activity. GZK-111, at a dose of 10 mg/kg/7 days, i.p., possessed antidepressant-like activity. So, the neuroprotective, nootropic, antihypoxic, anxiolytic, antidepressant-like, and analgesic effects of GZK-111 were revealed. Thus, GZK-111 can be considered as a pharmacologically active pro-ampakine with a BDNF-ergic mechanism of action.
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