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

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

Abstract

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.
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
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。
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