Peculiarities of behavioral reactions of albino rats exposed to stress and introduction of non-opiate analogues of leu-enkephalins in the early ontogenic periods

Timur Amirov, E. Sazonova
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Abstract

The authors studied behavioral reactions of 7-day and 30-day-old albino Wistar rats, exposed to intrauterine hypoxia as well as emotional-pain stress and were introduced peptides - non-opiate analogues of leu-enkephalins in the neonatal periods of ontogenesis. The authors found that exposure to intrauterine hypoxia as well as emotional-pain stumuli led to slowdown of sensor-motor reflexes maturation in 7-day-old animals (duration of turning in the test "Negative geotropism" increased by 66 %); 30-day-old animals in this experimental group demonstrated increased anxiety and "motor disinhibition" in the tests "Elevated plus-maze" and "Open field". Daily introduction from the second to sixth day of life of 100 mkg/kg peptide NALE (H - Phe - D-Ala Gly - Phe - Leu - Arg - OH) practically neutralizes negative early and remote behavioral consequences of intrauterine hypoxia as well as neonatal emotional-pain stress. Neuroprotective effect is less significantly expressed during introduction of 100 mkg/kg of the peptide G (H - Phe - D-Ala - Gly - Phe - Leu - Gly - OH) from the second to sixth day of life, differing from NALE by replacement of C-ending aminoacid from Arg to Gly. Nitrogen oxide blockade by the accompanying introduction of L-NAME (50mg/kg) hinders the realization of both early (in 7-day-old animals), and remote (in 30-day-old animals) neuroprotective effects of peptide NALE.
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白化大鼠暴露于应激和引入亮氨酸脑啡肽的非阿片类类似物在早期发病期的行为反应的特点
作者研究了7天和30天大的白化Wistar大鼠,暴露于宫内缺氧和情绪疼痛应激,并在新生儿期引入亮氨酸脑啡肽的非阿片类类似物的行为反应。作者发现,暴露于宫内缺氧以及情绪-疼痛刺激导致7日龄动物的感觉-运动反射成熟速度减慢(在“负向地性”测试中翻转的时间增加了66%);30日龄大鼠在“高架+迷宫”和“开阔场地”实验中表现出焦虑和“运动去抑制”的增加。从出生的第2天到第6天,每天引入100毫克/公斤的肽NALE (H - Phe - D-Ala - Gly - Phe - Leu - Arg - OH),实际上可以中和宫内缺氧和新生儿情绪疼痛应激的早期和远程负面行为后果。在出生后第2天至第6天,引入100 mg /kg肽G (H - Phe - D-Ala - Gly - Phe - Leu - Gly - OH)时,神经保护作用的表达不那么显著,与NALE不同的是,c端氨基酸从Arg替换为Gly。同时引入L-NAME (50mg/kg)的氮氧化物阻断会阻碍肽NALE早期(7日龄动物)和远期(30日龄动物)神经保护作用的实现。
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