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Sprague-Dawley大鼠对δ阿片受体激动剂SNC80([(+)-4-[(αR)-α-[(2S,5R)-2,5-二甲基-4-(2-丙烯基)-1-哌嗪基]-(3-甲氧基苯基)甲基]-N,N-二乙基苯甲酰胺)的行为差异耐受性。

Differential behavioral tolerance to the delta-opioid agonist SNC80 ([(+)-4-[(alphaR)-alpha-[(2S,5R)-2,5-dimethyl-4-(2-propenyl)-1-piperazinyl]-(3-methoxyphenyl)methyl]-N,N-diethylbenzamide) in Sprague-Dawley rats.

作者信息

Jutkiewicz Emily M, Kaminsky Sarah T, Rice Kenner C, Traynor John R, Woods James H

机构信息

1301 MSRB III, Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109-0632, USA.

出版信息

J Pharmacol Exp Ther. 2005 Oct;315(1):414-22. doi: 10.1124/jpet.105.088831. Epub 2005 Jul 13.

Abstract

Nonpeptidic delta-opioid agonists produce a number of behaviors, such as antidepressant-like effects, locomotor stimulation, antinociception, and convulsions. To consider this class of compounds as potential therapeutics for humans, the effects of delta-opioid agonists after repeated administration must be evaluated. Therefore, the present study investigated the effects of repeated delta-opioid agonist, SNC80 ([(+)-4-[(alphaR)-alpha-[(2S,5R)-2,5-dimethyl-4-(2-propenyl)-1-piperazinyl]-(3-methoxyphenyl)-methyl]-N,N-diethylbenzamide), administration on its antidepressant-like effects in the forced swim test, locomotor activity, and convulsions in male Sprague-Dawley rats. Tolerance developed rapidly to the convulsive and locomotor-stimulating effects of SNC80 but not to the antidepressant-like effects. In addition, tolerance was evaluated at the level of the receptor-G protein interaction by measuring 5'-O-(3-[35S]thio)triphosphate binding in brains from rats that were pretreated with SNC80. With various exposure durations to SNC80, some brain regions demonstrated tolerance at different times, suggesting that adaptations in the delta-opioid system may occur during agonist exposure. Overall, the lack of observable tolerance to the antidepressant-like effects of SNC80 indicates that this class of compounds has potential as a novel antidepressant therapy.

摘要

非肽类δ-阿片受体激动剂会产生多种行为,如类抗抑郁作用、运动兴奋、抗伤害感受和惊厥。为了将这类化合物视为人类潜在的治疗药物,必须评估重复给药后δ-阿片受体激动剂的作用。因此,本研究调查了重复给予δ-阿片受体激动剂SNC80([(+)-4-[(αR)-α-[(2S,5R)-2,5-二甲基-4-(2-丙烯基)-1-哌嗪基]-(3-甲氧基苯基)-甲基]-N,N-二乙基苯甲酰胺)对雄性Sprague-Dawley大鼠在强迫游泳试验中的类抗抑郁作用、运动活性和惊厥的影响。对SNC80的惊厥和运动兴奋作用迅速产生耐受,但对类抗抑郁作用未产生耐受。此外,通过测量用SNC80预处理的大鼠脑中的5'-O-(3-[35S]硫代)三磷酸结合,在受体-G蛋白相互作用水平评估耐受性。在不同的SNC80暴露持续时间下,一些脑区在不同时间表现出耐受性,这表明在激动剂暴露期间δ-阿片受体系统可能发生适应性变化。总体而言,对SNC80的类抗抑郁作用缺乏可观察到的耐受性表明这类化合物具有作为新型抗抑郁疗法的潜力。

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