急性口服BDNF环4二肽模拟双(n -单琥珀酰-l -seryl- l-赖氨酸)六亚二胺对小鼠抑郁模型有活性

P. Povarnina, Yulia N. Firsova, Anna V. Tallerova, Аrmen G. Mezhlumyan, Sergey V. Kruglov, Tatiana A. Antipova, Tatiana A. Gudasheva, Sergey B. Seredenin
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引用次数: 1

摘要

低分子模拟物BDNF GSB-106是一种取代二聚二肽,双(n -单琥珀酰-l -seryl- l-赖氨酸)六亚二胺,由Zakusov药理学研究所设计合成。该二肽激活TrkB、PI3K/AKT和MAPK/ ERK。GSB-106是一种潜在的抗抑郁药。在多项啮齿动物试验中检测到其抗抑郁活性(0.1-1.0 mg/kg, ip;0.5-5.0 mg/kg, po)。在本研究中,GSB-106在C57Bl/6小鼠的10天社会失败应激后急性口服(0.1 mg/kg)可完全消除糖偏好试验中的快感缺乏表现,并增加紊乱的海马突触发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The BDNF Loop 4 Dipeptide Mimetic Bis(N-monosuccinyl-L-seryl-L-lysine)hexamethylenediamide Is Active in a Depression Model in Mice after Acute Oral Administration
Low-molecular mimetic BDNF GSB-106, which is a substituted dimeric dipeptide, bis(N-monosuccinyl-L-seryl-L-lysine) hexamethylenediamide, was designed and synthesized in the V. V. Zakusov Research Institute of Pharmacology. The dipeptide activates TrkB, PI3K/AKT, and MAPK/ ERK. GSB-106 is being developed as a potential antidepressant. Its antidepressant activity was detected in a number of rodent tests (0.1–1.0 mg/kg, ip; 0.5–5.0 mg/kg, po). In the present study, GSB-106 was shown to completely eliminate the manifestation of anhedonia in the sucrose preference test and to increase disturbed hippocampal synaptogenesis at acute oral administration (0.1 mg/kg) after 10-day social defeat stress in C57Bl/6 mice.
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