Kim Jeong-Hoon, Austin Jennifer D, Tanabe Lauren, Creekmore Elizabeth, Vezina Paul
Department of Physiology, Brain Korea 21 Project for Medical Science, Yonsei University Medical Center, 134 Shinchondong, Seodaemungu, Seoul 120-752, South Korea.
Eur J Neurosci. 2005 Jan;21(1):295-300. doi: 10.1111/j.1460-9568.2004.03822.x.
Repeated exposure to amphetamine (AMPH) leads to the development of behavioural sensitization that can be demonstrated in rats as enhanced locomotor responding to and self-administration of the drug. Glutamate systems are known to participate in the induction and expression of sensitization by psychostimulants. Group II metabotropic glutamate receptors (mGluRs), because they negatively regulate both vesicular and nonvesicular glutamate release, are thus well positioned to gate its expression. Here we report that the expression of locomotor sensitization by AMPH is completely prevented by a systemic injection of the selective group II mGluR agonist LY379268 at a dose that produced no effects when administered alone. The activation of group II mGluRs in AMPH-sensitized rats also reduced the enhanced overflow of both dopamine and glutamate normally observed in the nucleus accumbens, a brain region critical for the generation of locomotor and drug self-administration behaviours. To directly determine the effect of group II mGluR activation on enhanced drug self-administration, AMPH-sensitized rats were allowed to self-administer a mixture of LY379268 and AMPH. These rats continued to self-administer but did not exhibit the enhanced work output and drug intake observed in AMPH-sensitized rats self-administering AMPH alone. Thus, activating group II mGluRs prevents the expression of different manifestations of AMPH sensitization including enhanced self-administration of the drug. These receptors may represent a potentially important target for therapeutic intervention directed at drugs of abuse.
反复接触苯丙胺(AMPH)会导致行为敏化的发展,这在大鼠中表现为对该药物的运动反应增强以及自我给药增加。已知谷氨酸系统参与精神兴奋剂诱导和表达敏化。II 型代谢型谷氨酸受体(mGluRs)由于对囊泡和非囊泡谷氨酸释放均具有负调控作用,因此很适合调节其表达。在此我们报告,全身注射选择性 II 型 mGluR 激动剂 LY379268 可完全阻止 AMPH 引起的运动敏化表达,单独给予该剂量时无此效应。激活 AMPH 致敏大鼠的 II 型 mGluRs 还可减少伏隔核中通常观察到的多巴胺和谷氨酸增强的溢出,伏隔核是产生运动和药物自我给药行为的关键脑区。为直接确定 II 型 mGluR 激活对增强药物自我给药的影响,让 AMPH 致敏大鼠自我给药 LY379268 和 AMPH 的混合物。这些大鼠继续自我给药,但未表现出单独自我给药 AMPH 的 AMPH 致敏大鼠中观察到的增强的工作输出和药物摄入量。因此,激活 II 型 mGluRs 可阻止 AMPH 敏化的不同表现形式的表达,包括增强的药物自我给药。这些受体可能是针对滥用药物的治疗干预的潜在重要靶点。