Wahlestedt C, Karoum F, Jaskiw G, Wyatt R J, Larhammar D, Ekman R, Reis D J
Department of Neurology and Neuroscience, Cornell University Medical College, New York, NY 10021.
Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2078-82. doi: 10.1073/pnas.88.6.2078.
Repeated administration of cocaine elicits substantial, long-lasting, but reversible reductions in neuropeptide Y (NPY) and NPY mRNA in the rat cerebral cortex and nucleus accumbens. The NPY reduction appears to be mediated through a decrease in NPY biosynthesis, occurring transneuronally, perhaps in response to changes in synaptic dopamine associated with mesolimbic and mesocortical dopamine neurons. The medial prefrontal cortex appears necessary for maintenance of cocaine's action on this neuronal network since excitotoxic lesions of this area prevented (lesion before cocaine) and reversed (lesion after cocaine) the reductions in NPY elicited by the cocaine. NPY may be a sensitive marker for chronic cocaine use. Its decrease may relate to the anxiety and depression associated with cocaine withdrawal in humans.
反复给予可卡因会导致大鼠大脑皮层和伏隔核中神经肽Y(NPY)及其mRNA显著、持久但可逆地减少。NPY的减少似乎是通过NPY生物合成的减少介导的,这种减少跨神经元发生,可能是对与中脑边缘和中脑皮质多巴胺神经元相关的突触多巴胺变化的反应。内侧前额叶皮层似乎是维持可卡因对该神经元网络作用所必需的,因为该区域的兴奋性毒性损伤可预防(在给予可卡因前损伤)和逆转(在给予可卡因后损伤)由可卡因引起的NPY减少。NPY可能是长期使用可卡因的一个敏感标志物。其减少可能与人类可卡因戒断相关的焦虑和抑郁有关。