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首页> 外文期刊>BMC Neuroscience >Synergistic effect of CART (cocaine- and amphetamine-regulated transcript) peptide and cholecystokinin on food intake regulation in lean mice
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Synergistic effect of CART (cocaine- and amphetamine-regulated transcript) peptide and cholecystokinin on food intake regulation in lean mice

机译:CART(可卡因和苯丙胺调节的转录物)肽和胆囊收缩素对瘦小鼠食物摄入调节的协同作用

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Background CART (cocaine- and amphetamine-regulated transcript) peptide and cholecystokinin (CCK) are neuromodulators involved in feeding behavior. This study is based on previously found synergistic effect of leptin and CCK on food intake and our hypothesis on a co-operation of the CART peptide and CCK in food intake regulation and Fos activation in their common targets, the nucleus tractus solitarii of the brainstem (NTS), the paraventricular nucleus (PVN), and the dorsomedial nucleus (DMH) of the hypothalamus. Results In fasted C57BL/6 mice, the anorexigenic effect of CART(61-102) in the doses of 0.1 or 0.5 μg/mouse was significantly enhanced by low doses of CCK-8 of 0.4 or 4 μg/kg, while 1 mg/kg dose of CCK-A receptor antagonist devazepide blocked the effect of CART(61-102) on food intake. After simultaneous administration of 0.1 μg/mouse CART(61-102) and of 4 μg/kg of CCK-8, the number of Fos-positive neurons in NTS, PVN, and DMH was significantly higher than after administration of each particular peptide. Besides, CART(61-102) and CCK-8 showed an additive effect on inhibition of the locomotor activity of mice in an open field test. Conclusion The synergistic and long-lasting effect of the CART peptide and CCK on food intake and their additive effect on Fos immunoreactivity in their common targets suggest a co-operative action of CART peptide and CCK which could be related to synergistic effect of leptin on CCK satiety.
机译:背景CART(可卡因和苯丙胺调节的转录物)肽和胆囊收缩素(CCK)是参与进食行为的神经调节剂。这项研究基于先前发现的瘦素和CCK对食物摄入的协同作用,以及我们关于CART肽和CCK在食物摄入调节和共同目标中的Fos激活(脑干孤束核( NTS),下丘脑室旁核(PVN)和背侧核(DMH)。结果在禁食的C57BL / 6小鼠中,低剂量的0.4或4μg/ kg的CCK-8剂量为0.1或0.5μg/ kg时,CART(61-102)的厌食作用明显增强,而1 mg / kg的CCK-8剂量较低。公斤剂量的CCK-A受体拮抗剂devazepide阻断了CART(61-102)对食物摄入的影响。在同时施用0.1μg/小鼠CART(61-102)和4μg/ kg CCK-8之后,NTS,PVN和DMH中Fos阳性神经元的数量显着高于施用每种特定肽后的数量。此外,在野外试验中,CART(61-102)和CCK-8对抑制小鼠的自发活动具有累加作用。结论CART肽和CCK对食物摄取的协同和持久作用以及它们对共同目标的Fos免疫反应性的累加作用提示CART肽和CCK的协同作用可能与瘦素对CCK的协同作用有关饱腹感。

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