Kojima Shinya, Ueno Naohiko, Asakawa Akihiro, Sagiyama Kenichirou, Naruo Tetsuro, Mizuno Shigeto, Inui Akio
Department of Behavioral Medicine, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1, Sakuragaoka, Kagoshima-City 890-8520, Japan.
Peptides. 2007 Feb;28(2):459-63. doi: 10.1016/j.peptides.2006.09.024. Epub 2007 Jan 4.
PP administration induces negative energy balance by suppressing food intake and gastric emptying while increasing energy expenditure in rodents. The mechanism of PP actions involves the changes in the expression of hypothalamic feeding-regulatory peptides and the activity of the vago-vagal and vago-sympathetic reflex arc. PP-overexpressing mice we developed exhibited the thin phenotype with decreased food intake and gastric emptying rate. Plasma cholecystokinin (CCK) concentrations were increased in the transgenic mice and CCK-1 receptor antagonist improved the anorexia of the animals. These results, together with the previous notion of PP as an anti-CCK hormone in pancreatic exocrine secretion and gallbladder contraction, indicate that PP-CCK interactions may be either antagonistic or synergistic and the transgenic mice may exhibit the mixed phenotype by overproduction of PP and CCK.
胰多肽(PP)给药通过抑制啮齿动物的食物摄入和胃排空,同时增加能量消耗来诱导负能量平衡。PP作用的机制涉及下丘脑进食调节肽表达的变化以及迷走-迷走和迷走-交感反射弧的活动。我们培育的PP过表达小鼠表现出消瘦的表型,食物摄入量和胃排空率降低。转基因小鼠血浆胆囊收缩素(CCK)浓度升高,CCK-1受体拮抗剂改善了动物的厌食症。这些结果,连同之前关于PP在胰腺外分泌和胆囊收缩中作为抗CCK激素的观点,表明PP-CCK相互作用可能是拮抗或协同的,转基因小鼠可能因PP和CCK的过量产生而表现出混合表型。