Schmidt Karl T, Schroeder Jason P, Foster Stephanie L, Squires Katherine, Smith Brilee M, Pitts Elizabeth G, Epstein Michael P, Weinshenker David
Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.
Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.
Neuropharmacology. 2017 Jun;119:134-140. doi: 10.1016/j.neuropharm.2017.04.005. Epub 2017 Apr 6.
Drug-primed reinstatement of cocaine seeking in rats is thought to reflect relapse-like behavior and is mediated by the integration of signals from mesocorticolimbic dopaminergic projections and corticostriatal glutamatergic innervation. Cocaine-primed reinstatement can also be attenuated by systemic administration of dopamine β-hydroxylase (DBH) inhibitors, which prevent norepinephrine (NE) synthesis, or by α1-adrenergic receptor (α1AR) antagonists, indicating functional modulation by the noradrenergic system. In the present study, we sought to further discern the role of NE in cocaine-seeking behavior by determining whether α1AR activation can induce reinstatement on its own or is sufficient to permit cocaine-primed reinstatement in the absence of all other AR signaling, and identifying the neuroanatomical substrate within the mesocorticolimbic reward system harboring the critical α1ARs. We found that while intracerebroventricular infusion of the α1AR agonist phenylephrine did not induce reinstatement on its own, it did overcome the blockade of cocaine-primed reinstatement by the DBH inhibitor nepicastat. Furthermore, administration of the α1AR antagonist terazosin in the medial prefrontal cortex (mPFC), but not the ventral tegmental area (VTA) or nucleus accumbens (NAc) shell, attenuated cocaine-primed reinstatement. Combined, these data indicate that α1AR activation in the mPFC is required for cocaine-primed reinstatement, and suggest that α1AR antagonists merit further investigation as pharmacotherapies for cocaine dependence.
在大鼠中,药物引发的可卡因觅求行为被认为反映了类似复发的行为,并且由中脑皮质边缘多巴胺能投射和皮质纹状体谷氨酸能神经支配的信号整合所介导。全身给予多巴胺β-羟化酶(DBH)抑制剂(可阻止去甲肾上腺素(NE)合成)或α1-肾上腺素能受体(α1AR)拮抗剂,也可减弱可卡因引发的复吸行为,这表明去甲肾上腺素能系统具有功能调节作用。在本研究中,我们试图通过确定α1AR激活是否能单独诱导复吸,或者在不存在所有其他AR信号的情况下是否足以允许可卡因引发的复吸,并确定中脑皮质边缘奖赏系统中含有关键α1AR的神经解剖学底物,来进一步了解NE在可卡因觅求行为中的作用。我们发现,虽然脑室内注入α1AR激动剂去氧肾上腺素本身不会诱导复吸,但它确实克服了DBH抑制剂奈匹西他对可卡因引发复吸的阻断作用。此外,在内侧前额叶皮质(mPFC)而非腹侧被盖区(VTA)或伏隔核(NAc)壳中给予α1AR拮抗剂特拉唑嗪,可减弱可卡因引发的复吸。综合这些数据表明,mPFC中的α1AR激活是可卡因引发复吸所必需的,这表明α1AR拮抗剂作为可卡因依赖的药物疗法值得进一步研究。