Funk D, Li Z, Shaham Y, Lê A D
Department of Neuroscience, Center for Addiction and Mental Health, Toronto, Ontario, Canada M5S 2S1.
Neuroscience. 2003;122(1):1-4. doi: 10.1016/j.neuroscience.2003.08.003.
Using a rat relapse model, we have shown that infusion of a corticotropin-releasing factor (CRF) receptor antagonist into the median raphe nucleus (MRN) blocks footshock stress-induced reinstatement of alcohol seeking in rats. The goal of the present study was to begin identifying brain sites potentially involved in this effect. For this purpose, we measured levels of c-fos mRNA in discrete nuclei of the rat brain following exposure to intermittent footshock, which was preceded by intra-MRN infusions of a CRF receptor antagonist, d-Phe CRF (0 or 50 ng). Exposure to intermittent footshock increased the expression of c-fos mRNA in a number of brain regions previously shown to be responsive to stressful stimuli. Pretreatment with d-Phe CRF in the MRN selectively attenuated the increases in c-fos mRNA induced by footshock in the central nucleus of the amygdala (CeA). These findings are consistent with previous data on the important role for the CeA in stress-induced reinstatement of drug seeking. These results also suggest that inhibition of CeA activity may contribute to the blockade of alcohol-seeking induced by footshock that we have observed following injections of d-Phe into the MRN.
利用大鼠复发模型,我们已经表明,向中缝核(MRN)注射促肾上腺皮质激素释放因子(CRF)受体拮抗剂可阻断电击应激诱导的大鼠酒精觅求行为的恢复。本研究的目的是开始确定可能参与此效应的脑区。为此,我们在间歇性电击前向MRN内注射CRF受体拮抗剂d-Phe CRF(0或50 ng),然后测量大鼠脑内离散核团中c-fos mRNA的水平。暴露于间歇性电击会增加先前已证明对压力刺激有反应的多个脑区中c-fos mRNA的表达。在MRN中用d-Phe CRF预处理可选择性减弱电击诱导的杏仁核中央核(CeA)中c-fos mRNA的增加。这些发现与先前关于CeA在应激诱导的药物觅求行为恢复中的重要作用的数据一致。这些结果还表明,抑制CeA活性可能有助于阻断我们在向MRN注射d-Phe后观察到的电击诱导的酒精觅求行为。