Farningham D A, Mercer J G, Lawrence C B
Rowett Research Institute, Bucksburn, Aberdeen, UK.
Physiol Behav. 1993 Sep;54(3):437-42. doi: 10.1016/0031-9384(93)90232-5.
The satiety effects of the hormone, cholecystokinin (CCK), and propionate, an important gluconeogenic substrate, were studied in ad lib-fed sheep. Hepatic portal infusion of either sodium propionate (1.2 mmol/min) or sulphated CCK-8 (sCCK-8; 18.3 pmol/kg/min) had no effect on food intake. However, together, they decreased intake by 44%; similar to the effect of 2.4 mmol/min propionate alone. CCK infusions reduced the frequency of reticular contractions in the presence or absence of propionate. The effects of infusions on motility and food intake were, therefore, dissociated. Further studies demonstrated axonal transport of CCK binding sites in the ovine vagus. Binding sites accumulated to a similar extent on both sides of a ligature indicating the existence of both anterograde and retrograde transport which was limited to a small proportion of fibres. Binding incubations carried out in the presence of the CCK receptor antagonists, MK-329 and L-365,260, indicated that the majority of binding sites, if not the total population, possessed pharmacology typical of type B CCK receptors.
在自由采食的绵羊中研究了激素胆囊收缩素(CCK)和丙酸(一种重要的糖异生底物)的饱腹感效应。肝门静脉输注丙酸钠(1.2 mmol/分钟)或硫酸化CCK-8(sCCK-8;18.3 pmol/千克/分钟)对采食量均无影响。然而,二者共同作用时,采食量降低了44%;这与单独输注2.4 mmol/分钟丙酸的效果相似。无论有无丙酸存在,CCK输注均降低了网状收缩频率。因此,输注对运动性和采食量的影响是分离的。进一步研究表明,CCK结合位点在绵羊迷走神经中有轴突运输。结合位点在结扎线两侧积累的程度相似,表明存在顺行和逆行运输,且仅限于一小部分纤维。在CCK受体拮抗剂MK-329和L-365,260存在的情况下进行的结合孵育表明,大多数结合位点(即使不是全部)具有典型的B型CCK受体药理学特性。