Departments of Psychology, Pharmacology, and Health and Human Physiology, and the Cardiovascular Center, The University of Iowa, Iowa City, IA 52242, USA.
Pharmacol Biochem Behav. 2011 May;98(3):440-8. doi: 10.1016/j.pbb.2011.02.016. Epub 2011 Feb 22.
Behavioral sensitization involves increases in the magnitude of a response to a stimulus after repeated exposures to the same response initiator. Administration of psychomotor stimulants and the induction of appetitive motivational states associated with natural reinforcers like sugar and salt are among experimental manipulations producing behavioral sensitization. In rats, repeated administration of the mineralocorticoid agonist deoxycorticosterone acetate (DOCA) initially induces incremental increases in daily hypertonic saline consumption (i.e., sensitization of sodium appetite) in spite of the retention of sodium. The present studies investigated whether sodium appetite sensitization induced by DOCA shares mechanisms similar to those of psychomotor stimulant-induced sensitization, and whether there is evidence for reciprocal cross-sensitization. In Experiments 1 and 3, rats received control or cocaine treatments to induce locomotor sensitization. A week later DOCA (or vehicle) was administered to generate a sodium appetite. Animals pretreated with cocaine showed a greater sodium appetite. In Experiment 2, the order of the putative sensitizing treatments was reversed. Rats first received either a series of DOCA or vehicle treatments either with or without access to saline and were later tested for sensitization of the locomotor response to cocaine. Animals pretreated with DOCA without access to saline showed greater locomotor responses to cocaine than animals receiving vehicle treatments. Together these experiments indicate that treatments generating a sustained salt appetite and producing cocaine-induced psychomotor responses show reciprocal behavioral cross-sensitization. The underlying mechanisms accounting for this relationship may be the fact that psychostimulants and an unresolved craving for sodium can act as potent stressors.
行为敏化是指在重复暴露于相同的反应启动器后,对刺激的反应幅度增加。施用精神兴奋剂和诱导与天然强化物(如糖和盐)相关的食欲动机状态是产生行为敏化的实验操作之一。在大鼠中,反复给予盐皮质激素激动剂脱氧皮质酮乙酸盐(DOCA)最初会导致每日高渗盐水消耗的增量增加(即钠食欲的敏化),尽管保留了钠。目前的研究调查了 DOCA 诱导的钠食欲敏化是否与精神兴奋剂诱导的敏化具有相似的机制,以及是否有相互交叉敏化的证据。在实验 1 和 3 中,大鼠接受对照或可卡因处理以诱导运动敏化。一周后,给予 DOCA(或载体)以产生钠食欲。用可卡因预处理的动物表现出更强的钠食欲。在实验 2 中,假定的敏化处理的顺序被颠倒。大鼠首先接受一系列 DOCA 或载体处理,要么有盐水摄入,要么没有盐水摄入,然后测试对可卡因引起的运动反应的敏化作用。没有盐水摄入的 DOCA 预处理动物对可卡因的运动反应比接受载体处理的动物更强。这些实验共同表明,产生持续盐食欲和产生可卡因引起的运动反应的治疗方法表现出相互的行为交叉敏化。导致这种关系的潜在机制可能是这样一个事实,即精神兴奋剂和对钠的未解决的渴望可以作为强烈的应激源。