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5-(4-氯苯基)-2-(吗啉-4-基甲基)-2,4-二氢-3H-1,2,4-三唑-3-硫酮的4-取代衍生物对小鼠的抗伤害感受作用。

The antinociceptive effect of 4-substituted derivatives of 5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione in mice.

作者信息

Joanna Listos, Talarek Sylwia, Orzelska Jolanta, Fidecka Sylwia, Wujec Monika, Plech Tomasz

机构信息

Medical University, Lublin, Poland,

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2014 Apr;387(4):367-75. doi: 10.1007/s00210-013-0938-0. Epub 2013 Dec 11.

DOI:10.1007/s00210-013-0938-0
PMID:24326964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3964309/
Abstract

The aim of the present experiments was to examine the antinociceptive activity of 4-substituted derivatives of 5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione in mice. The compounds were synthesized using the so-called Mannich reaction and their structures were confirmed using IR and 1H-NMR spectra. The antinociceptive activity was investigated in two behavioral tests: the hot plate test and the writhing test. For preliminary estimation of other behavioral effects, the locomotor activity of mice, the motor coordination in the rota-rod test, and the myorelaxation in the chimney test were also studied. The changes in body temperature of animals were also recorded. We demonstrated that all examined compounds produced antinociceptive effect, both in the hot plate test and in the writhing test, without impact on the motor coordination and myorelaxation of animals. The pharmacological effect of all drugs has been developed within 60 min after administration of drugs; and in two cases (T-103 and T-104), it has been a short-lasting effect (up to 90 min). Two compounds (T-100 and T-102) also inhibited the locomotor activity of animals. T-104 induced the changes in body temperature of mice. Generally, we demonstrated that combination of two different heterocyclic systems (morpholine and 1,2,4-triazole) might be beneficial for reduction of nociception.

摘要

本实验的目的是研究5-(4-氯苯基)-2-(吗啉-4-基甲基)-2,4-二氢-3H-1,2,4-三唑-3-硫酮的4-取代衍生物在小鼠体内的抗伤害感受活性。这些化合物采用所谓的曼尼希反应合成,其结构通过红外光谱和1H-核磁共振光谱得到证实。在两项行为测试中研究了抗伤害感受活性:热板试验和扭体试验。为了初步评估其他行为效应,还研究了小鼠的运动活性、转棒试验中的运动协调性以及烟囱试验中的肌松作用。还记录了动物体温的变化。我们证明,所有受试化合物在热板试验和扭体试验中均产生抗伤害感受作用,且对动物的运动协调性和肌松作用无影响。所有药物的药理作用在给药后60分钟内显现;在两种情况下(T-103和T-104),作用持续时间较短(长达90分钟)。两种化合物(T-100和T-102)还抑制了动物的运动活性。T-104引起了小鼠体温的变化。总体而言,我们证明两种不同杂环系统(吗啉和1,2,4-三唑)的组合可能有利于减轻伤害感受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/eb54f18e774b/210_2013_938_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/35e18b3670c9/210_2013_938_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/5348dde70092/210_2013_938_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/ec518f39122f/210_2013_938_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/eb54f18e774b/210_2013_938_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/35e18b3670c9/210_2013_938_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/5348dde70092/210_2013_938_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/ec518f39122f/210_2013_938_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/3964309/eb54f18e774b/210_2013_938_Fig3_HTML.jpg

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