Martin-Iverson M T, Dourish C T
Merck Sharp and Dohme Research Laboratories, Neuroscience Research Centre, Harlow, Essex, UK.
Psychopharmacology (Berl). 1988;96(3):370-4. doi: 10.1007/BF00216064.
The effects of selective D-2 and D-1 dopamine (DA) receptor agonists on food consumption were investigated in free-feeding rats. A selective D-2 receptor agonist, (+)-4-propyl-9-hydroxynaphthoxazine (PHNO), increased the consumption of standard food pellets in the dose range of 7.5-120 micrograms/kg, while SKF 38393 (5.0 mg/kg), a selective D-1 receptor agonist, decreased food pellet intake. The increase in food pellet intake produced by PHNO was blocked by haloperidol (an antagonist relatively selective for the D-2 receptor at the dose used, 0.05 mg/kg) and SCH 23390 (20 micrograms/kg, a D-1 receptor selective antagonist). Increasing "arousal" by disturbance associated with repeated food weighing also increased food pellet consumption, but did not diminish PHNO-elicited feeding. However, the same range of doses of PHNO (7.5-120 micrograms/kg) which increased food pellet intake decreased consumption of a liquid diet, and had no overall effect on a highly palatable liquid diet. The increase in consumption of solid food induced by PHNO appears to be secondary to enhancement of chewing behaviors. In contrast, the decrease in food intake induced by SKF 39393 may be due to a direct action of the drug on neural feeding mechanisms.
在自由进食的大鼠中研究了选择性D-2和D-1多巴胺(DA)受体激动剂对食物消耗的影响。选择性D-2受体激动剂(+)-4-丙基-9-羟基萘恶嗪(PHNO)在7.5-120微克/千克的剂量范围内增加了标准食物颗粒的消耗量,而选择性D-1受体激动剂SKF 38393(5.0毫克/千克)则减少了食物颗粒的摄入量。PHNO引起的食物颗粒摄入量增加被氟哌啶醇(在所使用的剂量0.05毫克/千克时对D-2受体相对选择性的拮抗剂)和SCH 23390(20微克/千克,一种D-1受体选择性拮抗剂)阻断。与重复称重食物相关的干扰增加“唤醒”也增加了食物颗粒的消耗量,但并没有减少PHNO引起的进食。然而,增加食物颗粒摄入量的相同剂量范围的PHNO(7.5-120微克/千克)减少了流食的消耗量,并且对高度可口的流食没有总体影响。PHNO引起的固体食物消耗量增加似乎是咀嚼行为增强的继发结果。相比之下,SKF 39393引起的食物摄入量减少可能是由于药物对神经进食机制的直接作用。