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伏隔核中AMPA/海人藻酸受体拮抗剂DNQX对药物诱导的条件性位置偏爱效应的影响。

Effects of the AMPA/kainate receptor antagonist DNQX in the nucleus accumbens on drug-induced conditioned place preference.

作者信息

Layer R T, Uretsky N J, Wallace L J

机构信息

Division of Pharmacology, College of Pharmacy, Ohio State University, Columbus 43210.

出版信息

Brain Res. 1993 Jul 23;617(2):267-73. doi: 10.1016/0006-8993(93)91094-9.

Abstract

Activation of AMPA/kainate glutamatergic receptors in the nucleus accumbens may be a component of the mechanism of drug induced reward. To test this hypothesis, 6,7-dinitroquinoxaline-2,3-dione (DNQX), an alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionate (AMPA)/kainate glutamatergic receptor anatagonist, was injected into the nucleus accumbens before the administration of amphetamine or morphine during the training phase (acquisition) of a conditioned place preference paradigm. Rats were then tested for place preference in the absence of drugs. In other experiments, DNQX was given before testing for place preference (expression) but not during the training phase. Bilateral injection of DNQX (1 microgram/0.5 microliters/side) inhibited acquisition of place preference to amphetamine (1 mg/kg) but not morphine (10 mg/kg). During acquisition, DNQX marginally attenuated the locomotor stimulation elicited by amphetamine during the first but not subsequent training sessions, while the combination of morphine plus DNQX produced marked akinesia during each training session. When given prior to testing, DNQX inhibited the expression of place preference induced by amphetamine and morphine but did not affect locomotor activity. The results suggest that activation of AMPA/kainate receptors is involved in the primary reward stimulation (acquisition of place preference) of amphetamine but not morphine and in behaviors elicited by memory of primary reward stimulation (expression of place preference) for both drugs. Furthermore, locomotor activity during conditioning is not necessary for acquisition of place preference.

摘要

伏隔核中α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)/海人藻酸谷氨酸能受体的激活可能是药物诱导奖赏机制的一个组成部分。为了验证这一假设,在条件性位置偏爱范式的训练阶段(习得期),在给予苯丙胺或吗啡之前,将α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)/海人藻酸谷氨酸能受体拮抗剂6,7-二硝基喹喔啉-2,3-二酮(DNQX)注入伏隔核。然后在无药物的情况下测试大鼠的位置偏爱。在其他实验中,在测试位置偏爱(表达期)之前给予DNQX,但不在训练阶段给予。双侧注射DNQX(1微克/0.5微升/侧)可抑制对苯丙胺(1毫克/千克)的位置偏爱习得,但不影响对吗啡(10毫克/千克)的位置偏爱习得。在习得期,DNQX在第一次但不是随后的训练 session 中略微减弱了苯丙胺引起的运动刺激,而吗啡加DNQX的组合在每个训练 session 中产生明显的运动不能。在测试前给予时,DNQX抑制了苯丙胺和吗啡诱导的位置偏爱表达,但不影响运动活性。结果表明,AMPA/海人藻酸受体的激活参与了苯丙胺而非吗啡的主要奖赏刺激(位置偏爱习得),以及两种药物由主要奖赏刺激记忆引发的行为(位置偏爱表达)。此外,条件反射期间的运动活性对于位置偏爱习得不是必需的。

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