尼古丁可改善吗啡引起的记忆损伤:伏隔核中N-甲基-D-天冬氨酸受体可能参与其中。

Nicotine improves morphine-induced impairment of memory: possible involvement of N-methyl-D-aspartate receptors in the nucleus accumbens.

作者信息

Ahmadi Shamseddin, Zarrindast Mohammad Reza, Haeri-Rohani Ali, Rezayof Ameneh, Nouri Maryam

机构信息

Department of Animal biology, School of Biology, University College of Science, University of Tehran, Tehran, Iran.

出版信息

Dev Neurobiol. 2007 Jul;67(8):1118-27. doi: 10.1002/dneu.20456.

Abstract

The possible involvement of N-methyl-D-aspartate (NMDA) receptors in the nucleus accumbens (NAc) in nicotine's effect on impairment of memory by morphine was investigated. A passive avoidance task was used for memory assessment in male Wistar rats. Subcutaneous (s.c.) administration of morphine (5 and 10 mg/kg) after training impaired memory performance in the animals when tested 24 h later. Pretest administration of the same doses of morphine reversed impairment of memory because of post-training administration of the opioid. Moreover, administration of nicotine (0.2 and 0.4 mg/kg, s.c.) before the test prevented impairment of memory by morphine (5 mg/kg) given after training. Impairment of memory performance in the animals because of post-training administration of morphine (5 mg/kg) was also prevented by pretest administration of a noncompetitive NMDA receptor antagonist, MK-801 (0.75 and 1 microg/rat). Interestingly, an ineffective dose of MK-801 (0.5 microg/rat) in combination with low doses (0.075 and 0.1 mg/kg) of nicotine, which had no effects alone, synergistically improved memory performance impaired by morphine given after training. On the other hand, pretest administration of NMDA (0.1 and 0.5 microg/rat), which had no effect alone, in combination with an effective dose (0.4 mg/kg, s.c.) of nicotine prevented the improving effect of nicotine on memory impaired by pretreatment morphine. The results suggest a possible role for NMDA receptors of the NAc in the improving effect of nicotine on the morphine-induced amnesia.

摘要

研究了伏隔核(NAc)中N-甲基-D-天冬氨酸(NMDA)受体在尼古丁对吗啡所致记忆损伤影响中的可能作用。采用被动回避任务对雄性Wistar大鼠的记忆进行评估。训练后皮下注射吗啡(5和10mg/kg),24小时后测试时会损害动物的记忆表现。预先注射相同剂量的吗啡可逆转因训练后注射阿片类药物所致的记忆损伤。此外,测试前皮下注射尼古丁(0.2和0.4mg/kg)可预防训练后注射吗啡(5mg/kg)所致的记忆损伤。训练后注射吗啡(5mg/kg)导致动物记忆表现受损,也可通过预先注射非竞争性NMDA受体拮抗剂MK-801(0.75和1μg/大鼠)来预防。有趣的是,无效剂量的MK-801(0.5μg/大鼠)与低剂量(0.075和0.1mg/kg)的尼古丁联合使用,单独使用时无作用,但可协同改善训练后注射吗啡所致的记忆损伤。另一方面,单独使用无作用的NMDA(0.1和0.5μg/大鼠)与有效剂量(0.4mg/kg,皮下注射)的尼古丁联合使用,可预防尼古丁对预处理吗啡所致记忆损伤的改善作用。结果表明,NAc中的NMDA受体在尼古丁对吗啡诱导的失忆的改善作用中可能发挥作用。

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