Pascucci Tiziana, Ventura Rossella, Latagliata Emanuele Claudio, Cabib Simona, Puglisi-Allegra Stefano
Dipartimento di Psicologia, Università La Sapienza, Rome I-00185, Italy.
Cereb Cortex. 2007 Dec;17(12):2796-804. doi: 10.1093/cercor/bhm008. Epub 2007 Feb 24.
Although the medial prefrontal cortex (mpFC) appears to constrain stress responses, indirect evidences suggest that it might determine the stress response of the mesoaccumbens dopamine (DA) system. To test this hypothesis, we first evaluated the dynamics of norepinephrine (NE) and DA release in the mpFC and of DA release in the nucleus accumbens (NAc) of acutely stressed rats. Then, we tested the effects of selective depletion of NE or DA in the mpFC (by local 6-hydroxydopamine infusion following desipramine or 1-[2[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine(GBR 12909) on stress-induced changes in mesoaccumbens DA release. Rats experiencing restraint stress for 240 min showed an initial, short-lived increase of NE outflow in the mpFC and of DA in the NAc. These responses were followed by a sustained increase of DA in the mpFC and by a decrease to below resting levels of DA in the NAc. Moreover, selective prefrontal NE depletion eliminated the increase of NE in the mpFC and of DA in the NAc, and selective depletion of mesocortical DA eliminated the enhancement of mpFC DA as well as the inhibition of mesoaccumbens DA, without affecting basal catecholamines outflow. These results demonstrate that the opposing influences of mpFC NE and DA determine mesoaccumbens DA response to stress and suggest that alterations of this mechanism may be responsible for some major psychopathological outcomes of stress.
尽管内侧前额叶皮质(mpFC)似乎能抑制应激反应,但间接证据表明它可能决定中伏隔核多巴胺(DA)系统的应激反应。为了验证这一假设,我们首先评估了急性应激大鼠mpFC中去甲肾上腺素(NE)和DA的释放动态以及伏隔核(NAc)中DA的释放动态。然后,我们测试了mpFC中NE或DA的选择性耗竭(通过在使用地昔帕明或1-[2-[双(4-氟苯基)甲氧基]乙基]-4-(3-苯基丙基)哌嗪(GBR 12909)后进行局部6-羟基多巴胺注射)对应激诱导的中伏隔核DA释放变化的影响。经历240分钟束缚应激的大鼠在mpFC中NE流出量和NAc中DA的释放量最初短暂增加。随后,mpFC中DA持续增加,而NAc中DA降至静息水平以下。此外,选择性前额叶NE耗竭消除了mpFC中NE和NAc中DA的增加,而中皮质DA的选择性耗竭消除了mpFC中DA的增强以及中伏隔核DA的抑制,且不影响基础儿茶酚胺流出。这些结果表明,mpFC中NE和DA的相反影响决定了中伏隔核DA对应激的反应,并表明该机制的改变可能是应激导致一些主要精神病理结果的原因。