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重复给予胍丁胺治疗可减轻小鼠尼古丁致敏作用:α2肾上腺素能受体的调节作用

Repeated agmatine treatment attenuates nicotine sensitization in mice: modulation by alpha2-adrenoceptors.

作者信息

Kotagale Nandkishor Ramdas, Taksande Brijesh Gulabrao, Gahane Avinash Yashwant, Ugale Rajesh Ramesh, Chopde Chandrabhan Tukaram

机构信息

Division of Neuroscience, Department of Pharmacology, Shrimati Kishoritai Bhoyar College of Pharmacy, New Kamptee, Nagpur, Maharashtra, India.

出版信息

Behav Brain Res. 2010 Dec 1;213(2):161-74. doi: 10.1016/j.bbr.2010.04.049. Epub 2010 May 5.

Abstract

Agmatine [2-(4-aminobutyl)guanidine] is an endogenous amine proposed as a neurotransmitter/neuromodulator that binds to multiple target receptors in brain. Besides, many central and peripheral functions, agmatine have been implicated in the process of drug addiction. The purpose of the present study was to examine the effects of centrally injected agmatine on nicotine induced locomotor sensitization in Swiss male mice. Our data shows that repeated injections of nicotine (0.4 mg/kg, sc, twice daily for 7 days) gradually increased locomotion during 7 days development period or after 3 days (nicotine) withdrawal phase challenged with nicotine (0.4 mg/kg, sc) on day 11. Mice were pretreated with agmatine (40-80 microg, icv) or agents known to increase endogenous brain agmatine levels [e.g. an agmatine biosynthetic precursor, L-arginine (80 microg, icv), ornithine decarboxylase inhibitor, difluoromethyl-ornithine (50 microg, icv), diamine oxidase inhibitor, aminoguanidine (25 microg, icv) and agmatinase inhibitor, arcaine (50 microg, icv)] 30 min before daily first nicotine injection or during nicotine withdrawal phase. All these treatments attenuated the development as well as incubation of locomotor sensitization to nicotine. Coadministration of agmatine (20 microg, icv) and alpha(2)-adrenoreceptors agonist, clonidine (0.1 microg, icv) evoked synergistic inhibition of nicotine sensitization. Conversely, prior administration of alpha(2)-adrenoceptor antagonist, yohimbine (5mg/kg, ip) or idazoxan (0.4 mg/kg, ip) reversed the inhibitory effect of agmatine on nicotine sensitization. There was no significant difference in activity between mice injected with any of these agents/saline alone and saline/saline groups. These data indicate that agmatine attenuates nicotine induced locomotor sensitization via a mechanism which may involve alpha(2)-adrenergic receptors. Thus, agmatine might have therapeutic implications in the treatment of nicotine addiction and deserve further investigations.

摘要

胍丁胺[2-(4-氨基丁基)胍]是一种内源性胺,被认为是一种神经递质/神经调质,可与大脑中的多种靶受体结合。此外,除了许多中枢和外周功能外,胍丁胺还与药物成瘾过程有关。本研究的目的是研究脑室内注射胍丁胺对瑞士雄性小鼠尼古丁诱导的运动敏化的影响。我们的数据表明,重复注射尼古丁(0.4mg/kg,皮下注射,每天两次,共7天)在7天的发育期或在第11天用尼古丁(0.4mg/kg,皮下注射)激发的3天(尼古丁)戒断期后逐渐增加运动。在每天首次注射尼古丁前30分钟或在尼古丁戒断期,小鼠用胍丁胺(40-80μg,脑室内注射)或已知可增加脑内源性胍丁胺水平的药物预处理[例如胍丁胺生物合成前体L-精氨酸(80μg,脑室内注射)、鸟氨酸脱羧酶抑制剂二氟甲基鸟氨酸(50μg,脑室内注射)、二胺氧化酶抑制剂氨基胍(25μg,脑室内注射)和胍丁胺酶抑制剂阿卡林(50μg,脑室内注射)]。所有这些处理均减弱了对尼古丁运动敏化的发展以及潜伏期。胍丁胺(20μg,脑室内注射)与α2-肾上腺素能受体激动剂可乐定(0.1μg,脑室内注射)共同给药可协同抑制尼古丁敏化。相反,预先给予α2-肾上腺素能受体拮抗剂育亨宾(5mg/kg,腹腔注射)或咪唑克生(0.4mg/kg,腹腔注射)可逆转胍丁胺对尼古丁敏化的抑制作用。单独注射这些药物/生理盐水的小鼠与生理盐水/生理盐水组之间的活动没有显著差异。这些数据表明,胍丁胺通过可能涉及α2-肾上腺素能受体的机制减弱尼古丁诱导的运动敏化。因此,胍丁胺在尼古丁成瘾治疗中可能具有治疗意义,值得进一步研究。

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