伏隔核谷氨酰胺能信号调节对急性和慢性哌甲酯的行为反应

Nicholas King, Thomas Mink, N. Kharas, N. Dafny
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引用次数: 1

摘要

哌醋甲酯(Methylphenidate, MPD)是一种作用于中枢神经系统产生行为效应的精神兴奋剂。伏隔核(NAc)参与了这一过程,但NAc的谷氨酰胺能系统在MPD行为反应中的作用尚未得到研究。采用三组动物:对照组、假NAc病变组和谷氨酰胺能特异性NAc病变组。实验第1天(ED),各组均给予生理盐水。在第2期,进行NAc手术,随后是5天的恢复期(第3-7期)。在ED 8获得术后基线记录。各组随后每天接受6次2.5 mg/kg MPD注射(ED 9-14),以产生MPD暴露的慢性效应,行为致敏,然后3天洗脱(ED 15-17),随后在ED 18再次注射2.5 mg/kg MPD。每次注射后记录机车活动60分钟。所有组在急性MPD暴露后都表现出行为活动增加,并在洗脱后维持慢性MPD暴露后出现行为敏感化。与NAc完整对照和假病变相比,谷氨酰胺能选择性伊博腾酸病变对NAc的急性和慢性MPD的水平活性反应均显著(P<0.05)减弱。谷氨酰胺能选择性伊伯tenic酸损伤后NAc的刻板印象活性在对照组基础上进一步显著增强(P<0.05)。谷氨酰胺能损伤不能调节总行进距离。这表明NAc中的谷氨酰胺能信号以不同的方式调节NAc中的行为活动回路,并提示在MPD的意志反应中起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glutaminergic Signaling in the Nucleus Accumbens Modulates the Behavioral Response to Acute and Chronic Methylphenidate
Methylphenidate (MPD) is a psychostimulant that acts on the CNS to produce behavioral effects. The nucleus accumbens (NAc) is involved in this, however the role of the NAc’s glutaminergic system in the behavioral response to MPD has not been studied. Three groups of animals were used: control, sham NAc lesions, and glutaminergic-specific (ibotenic acid toxin) NAc lesion groups. On experimental day (ED) 1, all groups received saline. On ED 2, NAc surgeries took place, followed by a 5-day recovery period (ED 3-7). On ED 8 a post-surgical baseline recording was obtained. Groups then received six daily MPD 2.5 mg/kg injections (ED 9-14) to produce a chronic effect of MPD exposure, behavioral sensitization, then three days of washout (ED 15-17), followed by a re-challenge with 2.5 mg/ kg MPD on ED 18. Locomotive activity was recorded for 60 minutes after each injection. All groups showed an increase in behavioral activity following acute MPD exposure, and developed behavioral sensitization following chronic MPD exposure that was maintained after washout. Compared to NAc intact controls and sham lesions, glutaminergic selective ibotenic acid lesions to the NAc significantly (P<0.05) attenuated the horizontal activity response to both acute and chronic MPD. Glutaminergic selective ibotenic acid lesions to the NAc also resulted in further significant (P<0.05) augmentation of stereotypic activity above the control group. The glutaminergic lesion failed to modulate total distance traveled. This indicates that glutaminergic signaling in the NAc modulates behavioral activity circuits in the NAc differently, and suggests a role in the volitional response to MPD.
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