Rolka K, Kolasa K, Kleinrok Z, Kupryszewski G
Pol J Pharmacol Pharm. 1986 Jul-Aug;38(4):391-402.
Syntheses of [D-Ala2, D-Leu5]-enkephalin, methyl ester of [D-Ala2, D-Leu3]-enkephalin, methylamides and dimethylamides of [D-Leu5]-enkephalin and [D-Ala2, D-Leu5]-enkephalin are described together with their analgesic activity determined on the basis of four analgesic tests: the hot-plate method, the reaction to electric stimulus, the tail immersion test and the frequency of writhing syndrome test. The neurotoxicity was estimated by the rota-rod test. The most pronounced analgesic effect was induced by compound: [D-Ala2, D-Leu5]-enkephalin, [D-Ala2, D-Leu5-OMe]-enkephalin and [D-Ala2, D-Leu5-NMe2]-enkephalin. In the tail immersion test all analogs did not exhibit analgesic activity.
描述了[D-丙氨酸2,D-亮氨酸5]-脑啡肽、[D-丙氨酸2,D-亮氨酸3]-脑啡肽甲酯、[D-亮氨酸5]-脑啡肽和[D-丙氨酸2,D-亮氨酸5]-脑啡肽的甲基酰胺和二甲基酰胺的合成,以及基于四种镇痛试验确定的它们的镇痛活性:热板法、对电刺激的反应、尾部浸入试验和扭体综合征试验频率。通过旋转棒试验评估神经毒性。化合物[D-丙氨酸2,D-亮氨酸5]-脑啡肽、[D-丙氨酸2,D-亮氨酸5-OMe]-脑啡肽和[D-丙氨酸2,D-亮氨酸5-NMe2]-脑啡肽诱导出最明显的镇痛效果。在尾部浸入试验中,所有类似物均未表现出镇痛活性。