Mamoun A H, Bergström J, Södersten P
Department of Renal Medicine, Karolinska Institute, Huddinge, Sweden.
Am J Physiol. 1997 Sep;273(3 Pt 2):R972-80. doi: 10.1152/ajpregu.1997.273.3.R972.
Male rats ingested about half as much of an intraorally infused (1 ml/min) carbohydrate solution compared with a protein solution. Blood levels of cholecystokinin octapeptide (CCK-8) had increased to 13.6 +/- 1.4 and 16.7 +/- 1.7 pmol/l when the rats stopped ingesting carbohydrate or protein and continued to increase to 35.6 +/- 3.2 pmol/l 30 min after the carbohydrate meal and 34.4 +/- 3.5 pmol/l 60 min after the protein meal. Intraperitoneal injection of CCK-8 (0.6-5.0 micrograms) inhibited and injection of the CCKA-receptor antagonist L-364, 718 (20-80 micrograms) facilitated carbohydrate intake, but neither CCK-8 nor L-364,718 affected protein intake. The results suggest that CCK-8 is not involved in regulating the duration of a protein meal but may be involved in regulating carbohydrate intake. The postprandial period of suppression of protein intake correlated with the disappearance of some amino acids, e.g., Arg, Tyr, and Trp, in the blood, and this may be of importance for protein ingestion, since these amino acids are neurotransmitter precursors.
与蛋白质溶液相比,雄性大鼠经口输注(1毫升/分钟)碳水化合物溶液的摄入量约为其一半。当大鼠停止摄入碳水化合物或蛋白质时,胆囊收缩素八肽(CCK - 8)的血药浓度分别升至13.6±1.4和16.7±1.7皮摩尔/升,在摄入碳水化合物餐后30分钟继续升至35.6±3.2皮摩尔/升,摄入蛋白质餐后60分钟升至34.4±3.5皮摩尔/升。腹腔注射CCK - 8(0.6 - 5.0微克)会抑制碳水化合物摄入,而注射CCKA受体拮抗剂L - 364,718(20 - 80微克)则会促进碳水化合物摄入,但CCK - 8和L - 364,718均不影响蛋白质摄入。结果表明,CCK - 8不参与调节蛋白质餐的持续时间,但可能参与调节碳水化合物摄入。餐后蛋白质摄入的抑制期与血液中某些氨基酸(如精氨酸、酪氨酸和色氨酸)的消失有关,这可能对蛋白质摄入很重要,因为这些氨基酸是神经递质前体。