PubMed · 3831710
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D Dellarosa, L E Bourne. 1985. Surface form and the spacing effect.. https://doi.org/10.3758/bf03198324
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The firing rates of primary auditory cortex (A1) neurons are known to be modulated only at the onset, offset, and change of a tonal stimulus in anesthetized animals. The tonal response pattern has been rarely investigated in alert animals. We investigated the time-course of A1 neuron responses to a steady tonal stimulus in alert cats. We found four types of firing responses based on statistical evaluation of the time course of the firing rate. The tonic cells (38 cells) showed a significant (P<0.05) firing increase throughout the stimulus period after a relatively long latency (mean, 25.3 ms) with little tendency of adaptation. The phasic-tonic cells (22 cells) showed a significant firing increase throughout the stimulus period after a medium latency (19.8 ms) with tendency of adaptation to less than a half of the maximum excitation level. Phasic cells (15 cells) responded, after a short latency (10.2 ms), at onset and offset of the stimuli. The unresponsive cells (26 cells) did not show a significant firing increase during stimuli. The findings suggest that there is a functional difference between each type of cells: the tonic cells encode information of static auditory signals in their firing rates; the phasic-tonic cells, of the changing auditory signal during the stimulus period; and the phasic cells, of rapid change of the auditory signal at onset and offset.
Altered behavioural and physiological responsivity following a short session of foot shocks in the rat has proven to be a stable and clinically relevant model of stress-induced sensitisation. However, a number of key factors influencing effect size or direction have not previously been reported. Rats underwent a single, 15-min session of foot shocks and were exposed to a variety of novel stressful challenges 1 or 2 weeks later. Sensitised behavioural responses (increased immobility) in preshocked rats remained present over 3 days of repeated exposure to noise stress. In mild novel challenges (open field, empty cage), behavioural sensitisation and defecation was most clearly expressed at the beginning of the dark phase (evening). Higher-arousal challenges (prod, noise) caused increased behavioural inhibition in preshocked rats at all three time points (morning, afternoon, evening). Female preshocked rats showed a different pattern of behavioural and defecation sensitisation than preshocked males. The robustness of the model makes it suitable for further investigations into the mechanisms and vulnerability factors involved in the long-term consequences of stress.
To study the effects of linguistic background on auditory processing, magnetoencephalographic responses for pure tones (120 Hz, 1 and 4 kHz), [u] and a complex tone (with three pure tone components corresponding to the three lowest formant frequencies of [u]) were recorded in ten Finnish and ten Swedish speaking Finnish males. Auditory cortical activation, maximal at about 100 ms after stimulus onset, was stronger in the right hemisphere (RH) for all stimuli. At 175-225 ms, Swedish speaking subjects had larger inter-hemispheric differences and different signal morphology in the RH than Finnish speaking subjects, suggesting that linguistic background influences basic auditory processes. Possibly, Swedish speaking subjects had retained a juvenile response component due to their bilingual surrounding after early childhood.