Boland F J, Stern M H
Pharmacol Biochem Behav. 1980 Feb;12(2):239-48. doi: 10.1016/0091-3057(80)90363-9.
Subjects were 70 Wistar rats showing either low preference for aversive alcohol solutions or a high preference induced by hypothalamic stimulation. Experiments 1 and 2 showed that a large lithium chloride injection.(3 meq/kg) suppressed alcohol intake only if alcohol was tasted. Pairing lithium contiguously with water or intubed alcohol failed to reduce subsequent alcohol intake despite the concurrent presence of high serum lithium levels. In Experiments 3 and 4 a series of seven lithium injections increased rather than decreased alcohol intake if lithium was allowed to accumulate in the blood and brain during alcohol exposure while the transitory sickness associated with each injection was prevented from association with the taste of alcohol. When sickness was allowed to occur during alcohol exposure a suppression of intake resulted after two injections. Contrary to current interpretations these results suggest that the suppression of voluntary alcohol intake by acute and chronic lithium administration is due to a learned taste aversion rather than to a pharmacological mechanism specific to alcohol;
实验对象为70只Wistar大鼠,它们对厌恶性酒精溶液表现出低偏好或因下丘脑刺激而表现出高偏好。实验1和实验2表明,大剂量注射氯化锂(3毫当量/千克)仅在品尝酒精时才会抑制酒精摄入。将锂与水或插管注入的酒精连续配对,尽管同时存在高血清锂水平,但未能减少随后的酒精摄入量。在实验3和实验4中,如果在酒精暴露期间让锂在血液和大脑中积累,同时防止每次注射相关的短暂疾病与酒精味道相关联,那么一系列七次锂注射会增加而不是减少酒精摄入量。当在酒精暴露期间允许疾病发生时,两次注射后会导致摄入量受到抑制。与当前的解释相反,这些结果表明,急性和慢性锂给药对自愿酒精摄入的抑制是由于习得的味觉厌恶,而不是由于特定于酒精的药理机制;