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急性尼古丁对安非他命刺激行为和多巴胺释放的敏化作用需要激活含有β2 亚基的烟碱型乙酰胆碱受体和谷氨酸 N-甲基-D-天冬氨酸受体。

The sensitizing effect of acute nicotine on amphetamine-stimulated behavior and dopamine efflux requires activation of β2 subunit-containing nicotinic acetylcholine receptors and glutamate N-methyl-D-aspartate receptors.

机构信息

Department of Pharmacology, University of Michigan Medical School, 1301 Medical Science Research Building III, 1150 W. Medical Center Drive, Ann Arbor, MI 48109-5632, USA.

出版信息

Neuropharmacology. 2011 Jun;60(7-8):1126-34. doi: 10.1016/j.neuropharm.2010.10.003. Epub 2010 Oct 28.

Abstract

Nicotine has been demonstrated to enhance the subsequent use of illicit drugs in animals and humans. We previously demonstrated in female, Holtzman rats that one low dose of nicotine will potentiate locomotor activity and dopamine (DA) efflux in response to a subsequent low dose of d-amphetamine (AMPH) given 1-4 h later. In the present study, we show this also occurs in male rats and characterize the receptors required for the rapid sensitizing effect of nicotine on AMPH-stimulated locomotor behavior and AMPH-induced DA efflux. Pretreatment of male, Holtzman rats with a low dose (0.1 mg/kg, i.p.) of nicotine 2-4 h before a challenge with AMPH (0.32 mg/kg, i.p.) enhanced locomotor behavior as compared to saline pretreatment. Dihydro-β-erythroidine (DHβE), a relatively selective antagonist at β2 subunit-containing (β2∗) nicotinic acetylcholine receptors (nAChR), but not methyllycaconitine (MLA), a relatively selective antagonist at α7 nAChRs, blocked the sensitizing effect of nicotine on AMPH-stimulated locomotor activity. Pretreatment with varenicline, a partial agonist selective for β2∗ nAChRs, blocked the sensitizing effect of nicotine on AMPH-stimulated locomotor behavior. Nicotine pretreatment sensitized AMPH-induced DA overflow in slices from ventral (nucleus accumbens, NAc), but not dorsal striatum as compared to saline-pretreated rats. Nicotine sensitization of the DA overflow was blocked by DHβE. Pretreatment with the glutamate N-methyl-D-aspartate (NMDA) receptor antagonist (+)-MK-801 (0.1 mg/kg, s.c.) 30 min before nicotine blocked sensitization of both locomotion and DA overflow in response to AMPH challenge. These results demonstrate that activation of the β2∗ nAChRs and NMDA receptors are required for the rapid sensitizing effect of nicotine on AMPH actions. This article is part of a Special Issue entitled 'Trends in neuropharmacology: in memory of Erminio Costa'.

摘要

尼古丁已被证明可增强动物和人类随后使用非法药物的能力。我们之前在雌性霍尔茨曼大鼠中证明,单次低剂量尼古丁会增强随后给予的低剂量 d-苯丙胺(AMPH)的运动活性和多巴胺(DA)外排,1-4 小时后给予。在本研究中,我们表明这也发生在雄性大鼠中,并描述了尼古丁对 AMPH 刺激的运动行为和 AMPH 诱导的 DA 外排的快速敏化作用所需的受体。在 AMPH(0.32 mg/kg,ip)挑战前 2-4 小时,雄性霍尔茨曼大鼠用低剂量(0.1 mg/kg,ip)尼古丁预处理可增强运动行为,与盐水预处理相比。二氢-β-erythroidine(DHβE),一种相对选择性的β2亚单位(β2∗)烟碱型乙酰胆碱受体(nAChR)拮抗剂,但不是甲基lycaconitine(MLA),一种相对选择性的α7 nAChR 拮抗剂,阻断了尼古丁对 AMPH 刺激的运动活性的敏化作用。用 varenicline 预处理,一种选择性的β2∗nAChR 部分激动剂,阻断了尼古丁对 AMPH 刺激的运动行为的敏化作用。尼古丁预处理敏化了 AMPH 诱导的腹侧(伏隔核,NAc)而不是背侧纹状体切片中的 DA 溢出,与用盐水预处理的大鼠相比。DHβE 阻断了尼古丁敏化的 DA 溢出。在尼古丁预处理前 30 分钟用谷氨酸 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂(+)-MK-801(0.1 mg/kg,sc)预处理,阻断了对 AMPH 挑战的运动和 DA 溢出的敏化。这些结果表明,β2∗nAChR 和 NMDA 受体的激活是尼古丁对 AMPH 作用的快速敏化作用所必需的。本文是题为“神经药理学趋势:纪念 Erminio Costa”的特刊的一部分。

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