Minor T R, Winslow J L, Chang W C
Department of Psychology, University of California, Los Angeles 90024-1563.
Behav Neurosci. 1994 Apr;108(2):265-76. doi: 10.1037//0735-7044.108.2.265.
In 3 experiments, the authors examined the role of adenosine regulation in escape deficits produced by earlier exposure to inescapable shock in rats (learned helplessness). Adenosine analogs injected before escape testing mimicked the effect of earlier inescapable shock, with the magnitude of the deficit varying with dose and drug specificity for A2 adenosine receptors. Agonist-induced and stress-induced escape deficits were eliminated by pretest treatment with the centrally acting adenosine receptor antagonist theophylline but not the peripheral antagonist 8-[p-sulfophenyl]-theophylline. Finally, preexposure to an ineffective number of inescapable shocks interacted in synergy with an ineffective pretest injection of adenosine agonist to maximize deficits in escape performance. These data implicate energy regulation and a central compensatory action by adenosine in the aspects of helplessness related to conservation-withdrawal.
在3项实验中,作者研究了腺苷调节在大鼠早期暴露于不可逃避电击所导致的逃避缺陷(习得性无助)中所起的作用。在逃避测试前注射的腺苷类似物模拟了早期不可逃避电击的效果,缺陷的程度随剂量以及对A2腺苷受体的药物特异性而变化。激动剂诱导和应激诱导的逃避缺陷可通过用中枢作用的腺苷受体拮抗剂茶碱进行预测试治疗而消除,但外周拮抗剂8-[对磺基苯基]茶碱则不能。最后,预先暴露于无效次数的不可逃避电击与无效的预测试腺苷激动剂注射协同作用,以最大程度地增加逃避表现的缺陷。这些数据表明,在与保守退缩相关的无助方面,能量调节和腺苷的中枢补偿作用发挥了作用。