Deeva O A, Pantileev A S, Rybina I V, Yarkova M A, Gudasheva T A, Seredenin S B
Zakusov Research Institute of Pharmacology, 125315, Moscow, Russia.
Dokl Biochem Biophys. 2019 May;484(1):17-20. doi: 10.1134/S1607672919010046. Epub 2019 Apr 22.
On the basis of the first dipeptide ligand of TSPO, N-carbobenzoxy-L-tryptophanyl-L-isoleucine amide (GD-23), which was obtained by us earlier, we synthesized a new dipeptide, N-phenylpropionyl-L-tryptophanyl-L-leucine amide (GD-102). GD-102 exhibited anxiolytic activity in the open field test in BALB/c mice and in the elevated plus maze test in ICR mice. The minimum effective dose of GD-102 was one order of magnitude lower than that of GD-23. Compound PK11195, a selective antagonist of TSPO, completely blocked the anxiolytic activity of GD-102, which testified to the involvement of TSPO in the realization of the anxiolytic effect of GD-102. The results were confirmed by molecular docking data.
基于我们之前获得的TSPO的首个二肽配体N-苄氧羰基-L-色氨酰-L-异亮氨酸酰胺(GD-23),我们合成了一种新的二肽,即N-苯丙酰-L-色氨酰-L-亮氨酸酰胺(GD-102)。GD-102在BALB/c小鼠的旷场试验和ICR小鼠的高架十字迷宫试验中表现出抗焦虑活性。GD-102的最小有效剂量比GD-23低一个数量级。TSPO的选择性拮抗剂化合物PK11195完全阻断了GD-102的抗焦虑活性,这证明TSPO参与了GD-102抗焦虑作用的实现。分子对接数据证实了这些结果。