Woody C D, Wang X F, Gruen W E
Mental Retardation Research Center, Brain Research Institute, UCLA Medical Center 90024, USA.
Brain Res. 1998 Apr 6;789(1):74-83. doi: 10.1016/s0006-8993(98)00017-1.
Recordings were made from 95 units of the dentate nucleus of naive cats to determine if patterns of response to 70 dB clicks could be distinguished from those to another acoustic stimulus (a hiss) of approximately equal sound pressure level. Further studies of an additional 309 units were conducted to determine if unit excitability and the response to clicks changed after Pavlovian conditioning in which blink responses were elicited by the clicks as conditioned stimuli. Over 50% of units tested before conditioning responded to click or hiss with increased activity, and 8% responded in the first 4-8 ms after the onset of the rapidly rising click. Cross-correlation of the respective 160 ms poststimulus histogram averages of mean activity showed dissimilar patterns of response to clicks and hisses (Pearson product-moment correlation coefficient + 0.02). Thus the averaged population responses distinguished these stimuli. In addition, individual cells were found in each behavioral state that responded selectively to either click or hiss. After conditioning with click as the conditioned stimulus, the number of units responding in the first 4-8 ms to click increased to 23%. The mean magnitude of activity 4-8 ms after presenting the click increased after conditioning but not after sensitization produced by backward pairing of the stimuli used for conditioning. After backward pairing only 6% of the units responded in the first 4-8 ms to click. The changes in activity after conditioning were accompanied by increases in neural excitability to intracellularly applied depolarizing current. In contrast with the changes in activity, the increases in neural excitability were also found after backward pairing. We conclude that short as well as long latency acoustic transmissions to click change in the dentate nucleus after conditioning, that changes in response to click are expressed in 4-8 ms responsive cells, and that many of these cells have different patterns of spike activity in response to click and hiss. The findings support the hypothesis that the dentate nucleus can play a significant role in short as well as long latency, adaptive acoustic transmission that can enhance the response to an acoustic signal used as a Pavlovian conditioned stimulus.
对95只未接受过训练的猫的齿状核中的神经元进行记录,以确定对70分贝咔哒声的反应模式是否能与对声压水平大致相同的另一种听觉刺激(嘶嘶声)的反应模式区分开来。对另外309个神经元进行了进一步研究,以确定在经典条件反射后,神经元兴奋性和对咔哒声的反应是否发生变化,在该条件反射中,咔哒声作为条件刺激引发眨眼反应。超过50%的在条件反射前测试的神经元对咔哒声或嘶嘶声的反应是活动增加,8%的神经元在快速上升的咔哒声开始后的前4 - 8毫秒内有反应。对平均活动的各自160毫秒刺激后直方图平均值进行互相关分析,结果显示对咔哒声和嘶嘶声的反应模式不同(皮尔逊积矩相关系数 + 0.02)。因此,平均群体反应能够区分这些刺激。此外,在每种行为状态下都发现了对咔哒声或嘶嘶声有选择性反应的单个细胞。以咔哒声作为条件刺激进行条件反射后,在最初4 - 8毫秒内对咔哒声有反应的神经元数量增加到了23%。呈现咔哒声后4 - 8毫秒内活动的平均幅度在条件反射后增加,但在用于条件反射的刺激进行反向配对产生的敏感化后没有增加。仅在反向配对后,只有6%的神经元在最初4 - 8毫秒内对咔哒声有反应。条件反射后活动的变化伴随着对细胞内施加的去极化电流的神经兴奋性增加。与活动变化相反,在反向配对后也发现了神经兴奋性的增加。我们得出结论,在条件反射后,齿状核中对咔哒声的短潜伏期和长潜伏期听觉传递都会发生变化,对咔哒声反应的变化在4 - 8毫秒有反应的细胞中表现出来,并且这些细胞中的许多对咔哒声和嘶嘶声有不同的放电活动模式。这些发现支持了这样一种假设,即齿状核在短潜伏期和长潜伏期的适应性听觉传递中都可以发挥重要作用,这种传递可以增强对用作经典条件刺激的听觉信号的反应。