Kageyama H, Kita T, Toshinai K, Guan J-L, Date Y, Takenoya F, Kato S, Matsumoto H, Ohtaki T, Nakazato M, Shioda S
Department of Anatomy, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.
J Neuroendocrinol. 2006 Jan;18(1):33-41. doi: 10.1111/j.1365-2826.2005.01382.x.
Galanin-like peptide (GALP) is produced in neurones in the hypothalamic arcuate nucleus and is implicated in the neural control of feeding behaviour. Previously, we have reported that GALP immunoreactive fibres were in direct contact with orexin/hypocretin immunoreactive neurones in the rat lateral hypothalamus using double-immunofluorescence. Centrally administered GALP is known to stimulate feeding behaviour. However, the target neurones of this action have not been clarified. The present study aimed to determine features of the GALP-mediated neuronal feeding pathway in rat. Accordingly, at the ultrastructural level, GALP-immunoreactive axon terminals were found to make synapses on orexin/hypocretin immunoreactive cell bodies and dendritic processes in the lateral hypothalamus. c-Fos immunoreactivity was expressed in orexin/hypocretin-immunoreactive neurones but not in melanin concentrating hormone-immunoreactive neurones in the lateral hypothalamus at 90 min after the application of GALP by i.c.v. infusion. Furthermore, to determine whether GALP regulates feeding behaviour via orexin/hypocretin neurones, the feeding behaviour of rats was studied following GALP i.c.v. injection with or without anti-orexin A and B immunoglobulin (IgG) pretreatment. The anti-orexin IgGs markedly inhibited GALP-induced hyperphagia. These results suggest that orexin/hypocretin-containing neurones in the lateral hypothalamus are targeted by GALP, and that GALP-induced hyperphagia is mediated via orexin/hypocretin neurones in the rat hypothalamus.
甘丙肽样肽(GALP)在下丘脑弓状核的神经元中产生,并参与进食行为的神经控制。此前,我们曾报道,利用双重免疫荧光技术发现,大鼠下丘脑外侧区中,GALP免疫反应性纤维与食欲素/下丘脑泌素免疫反应性神经元直接接触。已知中枢给予GALP可刺激进食行为。然而,这一作用的靶神经元尚未明确。本研究旨在确定大鼠中GALP介导的神经元进食途径的特征。因此,在超微结构水平上,发现GALP免疫反应性轴突终末在下丘脑外侧区与食欲素/下丘脑泌素免疫反应性细胞体和树突形成突触。通过脑室内注射给予GALP后90分钟,下丘脑外侧区中,食欲素/下丘脑泌素免疫反应性神经元表达c-Fos免疫反应性,而黑色素浓集激素免疫反应性神经元则未表达。此外,为了确定GALP是否通过食欲素/下丘脑泌素神经元调节进食行为,在给予或不给予抗食欲素A和B免疫球蛋白(IgG)预处理的情况下,对大鼠进行GALP脑室内注射后,研究其进食行为。抗食欲素IgG显著抑制GALP诱导的摄食过多。这些结果表明,下丘脑外侧区中含食欲素/下丘脑泌素的神经元是GALP的作用靶点,且GALP诱导的摄食过多是通过大鼠下丘脑的食欲素/下丘脑泌素神经元介导