Fernandez-Tome M P, Gonzalez Y, Del Rio J
Department of Neuropharmacology, Cajal Institute, CSIC, Madrid, Spain.
Pharmacol Biochem Behav. 1988 Feb;29(2):387-92. doi: 10.1016/0091-3057(88)90173-6.
Morphine and the enkephalin analogs DAME, DADLE and FK-33824, as well as the opioid antagonist naloxone, decrease feeding in food-deprived rats after intraventricular or subcutaneous administration, FK-33824 being by far the most potent drug tested. The administration of subeffective doses of either morphine or naloxone given by the subcutaneous route induces anorexia when given in combination with a subeffective dose of 5-HTP whereas the treatment with subeffective intraventricular doses of any of the opioids or naloxone fails to potentiate 5-HTP. Similarly, the anorexia induced by FK-33824 is blocked by either morphine or naloxone given subcutaneously but not by intraventricular administration of the same two drugs. The results appear to suggest that central or peripheral opioid receptors differentially affect feeding behavior in the rat and, on the other hand, that the interaction of opiates with the serotonergic system appears to occur preferentially in the periphery.
吗啡及脑啡肽类似物DAME、DADLE和FK - 33824,以及阿片类拮抗剂纳洛酮,在脑室内或皮下给药后,可减少食物剥夺大鼠的进食量,其中FK - 33824是目前所测试药物中最有效的。皮下给予亚有效剂量的吗啡或纳洛酮与亚有效剂量的5 - 羟色氨酸(5 - HTP)联合使用时会引起厌食,而脑室内给予亚有效剂量的任何一种阿片类药物或纳洛酮则无法增强5 - HTP的作用。同样,FK - 33824诱导的厌食可被皮下给予的吗啡或纳洛酮阻断,但不能被脑室内给予的这两种药物阻断。结果似乎表明,中枢或外周阿片受体对大鼠的进食行为有不同影响,另一方面,阿片类药物与5 - 羟色胺能系统的相互作用似乎优先发生在外周。