Instrumental conditioning of photic evoked potentials: Mechanisms and properties of late component modification

1972 ◽  
Vol 9 (5) ◽  
pp. 851-858 ◽  
Author(s):  
J.P. Rosenfeld ◽  
Robert L. Owen
2002 ◽  
Vol 9 (4) ◽  
pp. 261-272 ◽  
Author(s):  
J. M. J. Knippenberg ◽  
E. L. J. M. van Luijtelaar ◽  
J. H. R. Maes

Male Wistar rats were subjected to a differential Pavlovian fear conditioning procedure in which one of two tones (6 or 10 kHz) was followed by an electric shock (CS+) and the other was not (CS-). Before and after fear conditioning, we recorded the evoked potentials elicited byCS+andCS-from electrodes aimed at the lateral nucleus of the amygdala. Before conditioning, a slow, negative component with peak amplitude around 150 ms was present in the evoked potentials. This component was sensitive to habituation. After fear conditioning, bothCS+andCS-elicited the same late component, albeit with a larger amplitude. This enhancement was temporary: decreasing amplitude was observed in the course of CS test presentations under extinction. Prior research revealed a comparable slow component in the amygdala of the cat under similar experimental conditions. The collective results indicate that the large late component in the amygdala is enhanced by fear conditioning, suggesting that such enhancement reflects the anticipation of a biologically significant event.


1986 ◽  
Vol 65 (3) ◽  
pp. 392-397 ◽  
Author(s):  
Kyu Ho Lee ◽  
Jun Kim ◽  
Jin Mo Chung

✓ A late component of the cortical evoked potential elicited by somatosensory afferent input was studied in cats anesthetized with α-chloralose. Cortical evoked potentials were recorded from the somatosensory-motor cortex during stimulation of the sural nerve with graded intensities. The stimulus intensity was adjusted to activate Aαβ fibers only, then both Aαβ and Aδ fibers, and both A and C fibers, as judged by afferent volleys monitored from the sural nerve proximal to the stimulating site. In addition to early components reported previously, a very late component was identified at a latency of 400 to 600 msec following stimulation of the sural nerve with intensities above threshold for Aδ fibers. A further increase in stimulation intensity to include activation of C fibers did not reveal any more components. This late component was depressed by a systemic intravenous injection of morphine (2 mg/kg), and intravenous naloxone (0.1 mg/kg) reversed the effect of morphine. The late component of the evoked potential could also be recorded from subcortical tissue after decortication of the sensorimotor cortex. From these results, it appears that a very late component of the cortical evoked potential can be recorded from cats anesthetized with α-chloralose. The late component is evoked by activation of peripheral Aδ fibers. Furthermore, its morphine sensitivity suggests that this component may be elicited by nociceptive afferent fibers. If further investigations prove this, the late component, which is analogous to human long-latency potentials, could be used in an experimental model for pain research.


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