Bellissimo Nick, Anderson G Harvey
Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, ON, Canada M5S 3E2.
J Nutr. 2003 Jul;133(7):2319-25. doi: 10.1093/jn/133.7.2319.
The hypothesis of these studies was that all fats and carbohydrates suppress food intake, at least in part, via cholecystokinin-A receptors (CCKAR). Fat (coconut oil, beef tallow, olive and safflower oil) and carbohydrate (cornstarch, sucrose, glucose and fructose) preloads were given intragastrically (1 g/4 mL) 30 min before feeding. Devazepide (0.25 mg/kg), a CCKAR antagonist, was given intraperitoneally at 60 or 30 min before or with each of the macronutrient preloads. Devazepide reversed food intake suppression caused by all fat and carbohydrate sources, but the effect was not consistently related to the time of devazepide administration or to any specific feeding interval. Among the fats, coconut and olive oil were most responsive to devazepide. The effect of all carbohydrates on food intake was decreased by devazepide. We conclude that CCKAR play a role in food intake suppression caused by all fats and carbohydrates, but their role is dependent upon the composition of the fat or carbohydrate.
这些研究的假设是,所有脂肪和碳水化合物至少部分通过胆囊收缩素A受体(CCKAR)抑制食物摄入。在喂食前30分钟经胃内给予脂肪(椰子油、牛油、橄榄油和红花油)和碳水化合物(玉米淀粉、蔗糖、葡萄糖和果糖)预负荷(1克/4毫升)。CCKAR拮抗剂地伐西匹(0.25毫克/千克)在每次宏量营养素预负荷前60分钟或30分钟或与预负荷同时腹腔注射。地伐西匹逆转了所有脂肪和碳水化合物来源引起的食物摄入抑制,但这种作用与地伐西匹给药时间或任何特定喂食间隔没有始终如一的关联。在脂肪中,椰子油和橄榄油对地伐西匹反应最明显。地伐西匹降低了所有碳水化合物对食物摄入的影响。我们得出结论,CCKAR在所有脂肪和碳水化合物引起的食物摄入抑制中起作用,但其作用取决于脂肪或碳水化合物的组成。