Division of Basic Medical Sciences, Mercer University School of Medicine, Macon, Georgia 31207, USA.
J Neurochem. 2012 Mar;120(5):779-94. doi: 10.1111/j.1471-4159.2011.07620.x. Epub 2012 Jan 23.
Mu opioid receptors are densely expressed in the patch compartment of striatum and contribute to methamphetamine-induced patch-enhanced gene expression and stereotypy. To further elucidate the role of mu opioid receptor activation in these phenomena, we examined whether activation of mu opioid receptors would enhance methamphetamine-induced stereotypy and prodynorphin, c-fos, arc and zif/268 expression in the patch and/or matrix compartments of striatum, as well as the impact of mu opioid receptor activation on the relationship between patch-enhanced gene expression and stereotypy. Male Sprague-Dawley rats were intrastriatally infused with d-Ala(2)-N-Me-Phe(4),Gly(5)-ol]enkephalin (DAMGO; 1 μg/μL), treated with methamphetamine (0.5 mg/kg) and killed at 45 min or 2 h later. DAMGO augmented methamphetamine-induced zif/268 mRNA expression in the patch and matrix compartments, while prodynorphin expression was increased in the dorsolateral patch compartment. DAMGO pre-treatment did not affect methamphetamine-induced arc and c-fos expression. DAMGO enhanced methamphetamine-induced stereotypy and resulted in greater patch versus matrix expression of prodynorphin in the dorsolateral striatum, leading to a negative correlation between the two. These findings indicate that mu opioid receptors contribute to methamphetamine-induced stereotypy, but can differentially influence the genomic responses to methamphetamine. These data also suggest that prodynorphin may offset the overstimulation of striatal neurons by methamphetamine.
μ 阿片受体在纹状体的斑片隔室中高度表达,并有助于甲基苯丙胺诱导的斑片增强基因表达和刻板行为。为了进一步阐明 μ 阿片受体激活在这些现象中的作用,我们研究了 μ 阿片受体的激活是否会增强甲基苯丙胺诱导的刻板行为和强啡肽原、c-fos、arc 和 zif/268 在纹状体的斑片和/或基质隔室中的表达,以及 μ 阿片受体激活对斑片增强基因表达与刻板行为之间关系的影响。雄性 Sprague-Dawley 大鼠纹状体内输注 D-Ala(2)-N-Me-Phe(4),Gly(5)-ol]enkephalin(DAMGO;1μg/μL),给予甲基苯丙胺(0.5mg/kg),然后在 45 分钟或 2 小时后处死。DAMGO 增强了甲基苯丙胺诱导的 zif/268 mRNA 在斑片和基质隔室中的表达,而强啡肽原的表达在背外侧斑片隔室中增加。DAMGO 预处理不影响甲基苯丙胺诱导的 arc 和 c-fos 表达。DAMGO 增强了甲基苯丙胺诱导的刻板行为,并导致背外侧纹状体中强啡肽原的斑片表达与基质表达之间呈负相关,导致两者之间呈负相关。这些发现表明 μ 阿片受体有助于甲基苯丙胺诱导的刻板行为,但可以对甲基苯丙胺引起的基因组反应产生不同的影响。这些数据还表明,强啡肽原可能抵消了甲基苯丙胺对纹状体神经元的过度刺激。