Narváez Manuel, Millón Carmelo, Borroto-Escuela Dasiel, Flores-Burgess Antonio, Santín Luis, Parrado Concepción, Gago Belén, Puigcerver Araceli, Fuxe Kjell, Narváez José Angel, Díaz-Cabiale Zaida
Universidad de Málaga, Instituto de Investigación Biomédica, Facultad de Medicina, Málaga, Spain.
Brain Struct Funct. 2015 Jul;220(4):2289-301. doi: 10.1007/s00429-014-0788-7. Epub 2014 May 20.
Galanin (GAL) and neuropeptide Y (NPY) are neuropeptides involved in behaviors associated with anxiety. Both neuropeptides interact in several central functions. However, the potential behavioral and cellular interactions between them in anxiety are unknown. GAL was found to act through GAL receptor 2 (GALR2) to enhance NPYY1 receptor (NPYY1R)-mediated anxiolytic behaviors in rats. Using receptor autoradiography, c-Fos expression and in situ proximity ligation assay, the medial paracapsular intercalated nuclei of the amygdala were determined to be a key area in the interaction probably involving the formation of GALR2/NPYY1R heteroreceptor complexes. In cell cultures costimulation of GALR2 and NPYY1R induced changes in the functions of these receptors. The changes involved a potentiation of the decrease in the phosphorylation of CREB induced by NPYY1R and a delay in the internalization of NPYY1R. These results indicate that GALR2/NPYY1R interactions can provide a novel integrative amygdaloid mechanism in anxiety.
甘丙肽(GAL)和神经肽Y(NPY)是参与焦虑相关行为的神经肽。这两种神经肽在多种中枢功能中相互作用。然而,它们在焦虑方面潜在的行为和细胞相互作用尚不清楚。研究发现,甘丙肽通过甘丙肽受体2(GALR2)发挥作用,增强大鼠中神经肽Y Y1受体(NPYY1R)介导的抗焦虑行为。通过受体放射自显影、c-Fos表达和原位邻近连接分析,确定杏仁核内侧囊周插入核是这种相互作用的关键区域,可能涉及GALR2/NPYY1R异源受体复合物的形成。在细胞培养中,GALR2和NPYY1R的共刺激诱导了这些受体功能的变化。这些变化包括NPYY1R诱导的CREB磷酸化减少的增强以及NPYY1R内化的延迟。这些结果表明,GALR2/NPYY1R相互作用可为焦虑提供一种新的杏仁核整合机制。