Teich A H, McCabe P M, Gentile C G, Jarrell T W, Winters R W, Liskowsky D R, Schneiderman N
Department of Psychology, University of Miami, Coral Gables, FL 33124.
Physiol Behav. 1988;44(3):405-12. doi: 10.1016/0031-9384(88)90044-3.
Previous findings from our laboratory indicate that lesions of the auditory cortex disrupt the retention of differentially conditioned bradycardiac responses to tonal stimuli in rabbits. In the present experiment, the effect of lesions of the auditory cortex on the acquisition of differential bradycardiac conditioning was examined. The effect of lesions in the auditory cortex were compared to the effect produced by control lesions in the visual cortex. After 7 days of recovery, animals received 7 days of differential Pavlovian bradycardiac conditioning in which one tone (CS+) was paired with the unconditioned stimulus, and another tone (CS-) was never paired with the unconditioned stimulus. All animals demonstrated differential conditioning during the first 3 days of conditioning. On days 4-7, however, auditory cortex lesioned animals did not exhibit significant differential heart rate (HR) conditioning, whereas control animals with lesions in the visual cortex showed no loss of conditioning during this period. The loss of differential conditioning in animals with lesions in the auditory cortex appears to be due to an increase in the magnitude of the response to the CS-. These data support the hypothesis that the auditory cortex serves to inhibit the response to the CS- in differential conditioning of bradycardia to acoustic stimuli, and that the inhibition may be mediated by a descending corticothalamic or corticolimbic pathway.
我们实验室之前的研究结果表明,听觉皮层损伤会破坏兔子对音调刺激的差异条件性心动过缓反应的记忆。在本实验中,研究了听觉皮层损伤对差异心动过缓条件反射习得的影响。将听觉皮层损伤的影响与视觉皮层对照损伤所产生的影响进行了比较。恢复7天后,动物接受了7天的差异巴甫洛夫式心动过缓条件反射训练,其中一种音调(CS+)与无条件刺激配对,另一种音调(CS-)从未与无条件刺激配对。所有动物在条件反射训练的前3天均表现出差异条件反射。然而,在第4至7天,听觉皮层损伤的动物未表现出显著的差异心率(HR)条件反射,而视觉皮层损伤的对照动物在此期间未出现条件反射丧失。听觉皮层损伤动物差异条件反射的丧失似乎是由于对CS-反应幅度的增加。这些数据支持以下假设:在对声音刺激的心动过缓差异条件反射中,听觉皮层起到抑制对CS-反应的作用,并且这种抑制可能由皮质-丘脑或皮质-边缘系统下行通路介导。