Czirr S A, Reid L D
Brain Res Bull. 1986 Nov;17(5):639-42. doi: 10.1016/0361-9230(86)90195-4.
Mildly deprived rats (18-hr of deprivation of water) were given the opportunity to take a solution of sucrose daily for periods of either 10, 18, 31, 56, or 100 min. After daily intakes stabilized and prior to a session, rats were given an injection of either morphine sulfate, 1.0 mg/kg, or naloxone hydrochloride, 2.5 mg/kg, an agonist and an antagonist, respectively, at the opioid receptors. Naloxone, as expected, decreased intakes regardless of the test-session's length. Morphine decreased intakes of the shorter sessions, but increased intake of the longest session. Subsequently, injections of morphine were given 56 min into a 100-min session. These injections also increased intake. Morphine's effects in potentiating intake seem to have special relevance with respect to the continuance of ingestion. Variations across experiments, in duration of test-sessions, could account for the variations in conclusions drawn about whether or not morphine and other agonists potentiate intake of ingesta.
轻度剥夺大鼠(剥夺水分18小时)每天有机会饮用蔗糖溶液,时间分别为10、18、31、56或100分钟。在每日摄入量稳定后且在一次实验前,给大鼠分别注射硫酸吗啡(1.0毫克/千克)或盐酸纳洛酮(2.5毫克/千克),它们分别是阿片受体的激动剂和拮抗剂。不出所料,无论实验时长如何,纳洛酮都会减少摄入量。吗啡减少了较短实验时长的摄入量,但增加了最长实验时长的摄入量。随后,在100分钟的实验进行到56分钟时注射吗啡。这些注射也增加了摄入量。吗啡在增强摄入量方面的作用似乎与摄食的持续有关。不同实验中实验时长的差异,可能解释了关于吗啡和其他激动剂是否增强摄入物摄入量所得出结论的差异。