Synthesis and Investigation of the Antidepressant Properties of Novel Analogs of Arginine-Vasopressin

被引:0
|
作者
Borodina, K., V [1 ]
Savanets, O. N. [1 ]
Pustyulga, E. S. [1 ]
Martinovich, V. P. [1 ]
Kravchenko, E., V [1 ]
Olgomets, L. M. [1 ]
Golubovich, V. P. [1 ]
机构
[1] Byelarussian Acad Sci, Inst Bioorgan Chem, Minsk 220141, BELARUS
关键词
peptides; arginine-vasopressin; computer modeling; intranasal administration; depression; rats; FORCED SWIM TEST; V1A RECEPTOR; BINDING-SITE; FRAGMENT; 4-9; POSITIONS; RAT-BRAIN; LOCALIZATION; CONFORMATIONS;
D O I
10.1134/S1068162022030050
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A search for novel antidepressant analogs of arginine-vasopressin (AVP) by a computer modeling revealed the following peptide analogs of the C-terminal part of AVP: N-Ac-D-Ser-Pro-D-Arg-Gly-NH2, N-Ac-Phe-Pro-Arg-Gly-NH2, and N-Ac-Trp-Pro-Arg-Gly-NH2. Syntheses of the modeled compounds were described in this article. The compounds that could potentially exhibit the antidepressant activity were examined in the forced swimming test. N-Ac-Trp-Pro-Arg-Gly-NH2 (0.1, 1.0, and 10.0 mu g/kg) and N-Ac-D-Ser-Pro-D-Arg-Gly-NH2 (1.0 mu g/kg) were shown to have the highest similarity to the fluoxetine reference antidepressant according to a number of parameters after the intranasal administration to the Wistar male rats.
引用
收藏
页码:576 / 588
页数:13
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