新的原始NT-3模拟二肽GTS-302的药理学活性谱研究

D. M. Nikiforov, P. Povarnina, T. Gudasheva, A. Nadorova, L. Kolik, E. Valdman, J. V. Vakhitova, S. Seredenin
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引用次数: 0

摘要

背景:神经退行性疾病、抑郁、焦虑和认知障碍的发病机制与神经营养因子-3缺失的关联决定了开发具有类似作用机制的药物的前景。由于全尺寸神经营养因子-3的使用受到不理想的药代动力学特性的限制,因此有必要制造低分子量的神经营养因子-3模拟物,使其在系统给药时具有活性。V.V. Zakusov药理学研究所开发了一种二聚体二肽,模拟神经营养因子-3的第4环,六亚甲基二胺双(N-氧化丁基- l-谷氨酰胺- l-天冬酰胺)GTS-302,可激活TrkC和TrkB受体。目的:研究GTS-302的药理活性谱。材料及МETHODS:研究GTS-302腹腔给药后的药理作用。在小鼠急性和给药7 d后的强迫游泳实验中研究了GTS-302的抗抑郁样活性。急性给药后,分别在小鼠升高+迷宫实验和大鼠新物体识别实验中研究了该二肽的抗焦虑和认知活性。采用热板法研究了GTS-302急性给药后对小鼠疼痛敏感性的影响。结果:GTS-302在0.5、1.0、5.0和10mg /kg急性给药后表现出抗抑郁样活性。给药7 d后,GTS-302的抗抑郁样活性在效应量和统计学意义上更为显著。二肽GTS-302在1.0、5.0和10.0 mg/kg剂量下表现出抗焦虑和认知活性,不影响疼痛敏感性。结论:低分子神经营养因子-3的模拟物二肽GTS-302在全身给药后的药理学谱显示,它具有许多全尺寸神经营养因子所特有的神经精神作用。这使我们可以考虑将GTS-302作为一种潜在的神经精神药物。
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The study of the spectrum of pharmacological activity of the new original NT-3 mimetic dipeptide GTS-302
BACKGROUND: The association of the pathogenesis of neurodegenerative diseases, depression, anxiety, and cognitive disorders with the deficit of neurotrophin-3 determines the prospect of creating drugs with a similar mechanism of action. Since the use of full-size neurotrophin-3 is limited by unsatisfactory pharmacokinetic properties, it is relevant to create low-molecular-weight mimetics of neurotrophin-3 that are active when administered systemically. A dimeric dipeptide mimetic of the 4th loop of neurotrophin-3, hexamethylenediamide bis(N--oxibutyryl-L-glutamyl-L-asparagine) GTS-302, which activates TrkC and TrkB receptors, has been developed at the V.V. Zakusov Research Institute of Pharmacology. AIM: The aim of this study was to investigate the spectrum of pharmacological activity of GTS-302. MATERIALS AND МETHODS: The pharmacological effects of GTS-302 were investigated following its intraperitoneal administration. The antidepressant-like activity of GTS-302 was studied in the forced swim test in mice after acute and 7-day administration. The anxiolytic and cognitive activity of the dipeptide were studied in the elevated plus maze test in mice and the novel object recognition test in rats after acute administration, respectively. The effect of GTS-302 on pain sensitivity was studied in the hot plate test in mice after acute administration. RESULTS: It was found that GTS-302 exhibits antidepressant-like activity after acute administration at doses of 0.5, 1.0, 5.0 and 10 mg/kg. After 7-day administration, the antidepressant-like activity of GTS-302 was more pronounced in terms of effect size and statistical significance. The dipeptide GTS-302 at doses of 1.0, 5.0 and 10.0 mg/kg showed anxiolytic and cognitive activity and did not affect pain sensitivity. CONCLUSIONS: The pharmacological spectrum of the low-molecular-weight mimetic of neurotrophin-3, dipeptide GTS-302, revealed upon systemic administration includes a number of neuropsychotropic effects characteristic of the full-sized neurotrophin. This allows us to consider GTS-302 as a potential neuropsychotropic drug.
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