Department of Medicine, Division Hepatology, Gastroenterology, and Endocrinology, Charité, Campus Virchow, Universitätsmedizin Berlin, Berlin, Germany.
Department of Medicine, Division of Digestive Diseases, CURE Digestive Diseases Research Center and Center for Neurobiology of Stress, UCLA and Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA, USA.
Peptides. 2010 Jun;31(6):1118-1123. doi: 10.1016/j.peptides.2010.03.013. Epub 2010 Mar 20.
Cholecystokinin (CCK) plays a role in the short-term inhibition of food intake. Cocaine- and amphetamine-regulated transcript (CART) peptide has been observed in neurons of the paraventricular nucleus (PVN). It has been reported that intracerebroventricular injection of CART peptide inhibits food intake in rodents. The aim of the study was to determine whether intraperitoneally (ip) injected CCK-8S affects neuronal activity of PVN-CART neurons. Ad libitum fed male Sprague-Dawley rats received 6 or 10 microg/kg CCK-8S or 0.15M NaCl ip (n=4/group). The number of c-Fos-immunoreactive neurons was determined in the PVN, arcuate nucleus (ARC), and the nucleus of the solitary tract (NTS). CCK-8S dose-dependently increased the number of c-Fos-immunoreactive neurons in the PVN (mean+/-SEM: 102+/-6 vs. 150+/-5 neurons/section, p<0.05) and compared to vehicle treated rats (18+/-7, p<0.05 vs. 6 and 10 microg/kg CCK-8S). CCK-8S at both doses induced an increase in the number of c-Fos-immunoreactive neurons in the NTS (65+/-13, p<0.05, and 182+/-16, p<0.05). No effect on the number of c-Fos neurons was observed in the ARC. Immunostaining for CART and c-Fos revealed a dose-dependent increase of activated CART neurons (19+/-3 vs. 29+/-7; p<0.05), only few activated CART neuron were observed in the vehicle group (1+/-0). The present observation shows that CCK-8S injected ip induces an increase in neuronal activity in PVN-CART neurons and suggests that CART neurons in the PVN may play a role in the mediation of peripheral CCK-8S's anorexigenic effects.
胆囊收缩素(CCK)在短期抑制食物摄入中发挥作用。可卡因和安非他命调节转录本(CART)肽已在室旁核(PVN)的神经元中观察到。据报道,脑室注射 CART 肽可抑制啮齿动物的食物摄入。本研究的目的是确定腹腔内(ip)注射 CCK-8S 是否会影响 PVN-CART 神经元的神经元活性。自由进食的雄性 Sprague-Dawley 大鼠接受 6 或 10μg/kg CCK-8S 或 0.15M NaCl ip(n=4/组)。在 PVN、弓状核(ARC)和孤束核(NTS)中测定 c-Fos 免疫反应性神经元的数量。CCK-8S 剂量依赖性地增加了 PVN 中 c-Fos 免疫反应性神经元的数量(平均值+/-SEM:102+/-6 与 150+/-5 个/节,p<0.05),与载体处理的大鼠相比(18+/-7,p<0.05 与 6 和 10μg/kg CCK-8S)。CCK-8S 两种剂量均增加了 NTS 中 c-Fos 免疫反应性神经元的数量(65+/-13,p<0.05,和 182+/-16,p<0.05)。在 ARC 中,c-Fos 神经元的数量没有变化。CART 和 c-Fos 的免疫染色显示激活的 CART 神经元数量呈剂量依赖性增加(19+/-3 与 29+/-7;p<0.05),仅在载体组中观察到少量激活的 CART 神经元(1+/-0)。本观察表明,CCK-8S 腹腔内注射可增加 PVN-CART 神经元的神经元活性,并表明 PVN 中的 CART 神经元可能在介导外周 CCK-8S 的厌食作用中发挥作用。