Ebenezer I S
Neuropharmacology. 1986 Jun;25(6):639-43. doi: 10.1016/0028-3908(86)90217-0.
This paper reports the generation of cortical slow potentials (SP), similar to the human contingent negative variation, in rats anaesthetised with urethane. Rats previously implanted with silver/silver chloride electrodes for recording slow potentials from the frontal cortex were anaesthetised with urethane, and given extensive associative conditioning in which a 100 msec, 70 dB tone (S1) preceded electric tail shock (S2). The S1-S2 interval was initially set at 0.5 sec, and increased over a number of training sessions to 3 sec. Negative slow potential responses developed during the interval between S1 and S2. Once the slow potential response was fully developed, it persisted without habituation during subsequent sessions. Withholding tail shock (S2) resulted in a rapid extinction of the slow potential response to S1 alone. In further experiments, rats (n = 8) that generated steady slow potentials under urethane, were injected with saline (n = 4) or nicotine (0.4 mg/kg, s.c.; n = 4), and their responses measured 0-10, 15-25 and 30-40 min after administration. While saline did not affect the magnitude of the slow potential responses compared with pre-saline control values, nicotine (0.4 mg/kg) caused significant decreases in the magnitude of slow potentials during all the measurement intervals. These results demonstrate that cortical slow potentials can be generated in rats anaesthetised with urethane, and that these slow potentials are sensitive to drugs such as nicotine. The slow potential responses measured in the rat anaesthetised with urethane thus have similar characteristics to those generated in the conscious rat. Such a preparation may therefore prove useful in carrying out experiments on slow potentials that were previously difficult or impossible in conscious animals.
本文报道了在用氨基甲酸乙酯麻醉的大鼠中产生的皮层慢电位(SP),类似于人类的关联性负变化。先前植入银/氯化银电极以记录额叶皮层慢电位的大鼠用氨基甲酸乙酯麻醉,并给予广泛的联合条件反射训练,其中100毫秒、70分贝的音调(S1)先于电尾击(S2)出现。S1 - S2间隔最初设定为0.5秒,并在多次训练过程中增加到3秒。在S1和S2之间的间隔期间出现了负性慢电位反应。一旦慢电位反应完全形成,在随后的训练过程中它会持续存在而不产生习惯化。停止给予尾击(S2)会导致对单独S1的慢电位反应迅速消退。在进一步的实验中,在用氨基甲酸乙酯麻醉下产生稳定慢电位的大鼠(n = 8),分别注射生理盐水(n = 4)或尼古丁(0.4毫克/千克,皮下注射;n = 4),并在给药后0 - 10分钟、15 - 25分钟和30 - 40分钟测量它们的反应。与注射生理盐水前的对照值相比,生理盐水不影响慢电位反应的幅度,而尼古丁(0.4毫克/千克)在所有测量间隔期间均导致慢电位幅度显著降低。这些结果表明,在用氨基甲酸乙酯麻醉的大鼠中可以产生皮层慢电位,并且这些慢电位对尼古丁等药物敏感。因此,在用氨基甲酸乙酯麻醉的大鼠中测量的慢电位反应具有与清醒大鼠中产生的慢电位反应相似的特征。因此,这样的制备方法可能被证明在进行先前在清醒动物中难以或不可能进行的慢电位实验中是有用的。