[STUDY OF INHIBITOR CONDITIONING IN THE RAT. ACTION OF AMPHETAMINE, CHLORPROMAZINE AND CHOLINERGIC AGENTS].
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The electrical responses of the thalamic pulvinar (of its analogue, the nucleus lateralis posterior (nLP)) to light stimuli of various intensity were recorded in awake rabbits, and their interrelationships with the responses of the retina, superior colliculi, and visual cortex were analyzed. It is postulated that a major role in the afferent supply of the rabbit nLP belongs to the optic track and the superior colliculi. The presence was demonstrated of a highly organized analyzer of the reticular control of nLP function that is of a facilitatory character. The most important role in reticular influence belongs to its adrenoresponsive mechanism. An inhibitory influence was demonstrated for the visual and sensorimotor regions of the cerebral cortex on the nLP neuronal apparatus producing responses to light stimuli. The influence of the visual cortex are the most pronounced and stable.
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The activity of individual neurons of the visual cortex was recorded simultaneously in behavioral experiments on monkeys before and after the systemic administration of a blocker of M-cholinoreceptors, amizil (0.8-1.0 mg/kg). The animals were trained to delayed visual differentiation of stimuli of various colors. After the administration of amizil, the characteristics of recognition deteriorated substantially: the duration of the storage of information in short-term memory sharply declined, while the time of the motoric reaction increased. The deterioration of these characteristics was accompanied by inhibition of the activity of the neurons of the visual cortex, inhibition which depended on the stage of recognition, and which intensified when there was an increase in the delay interval. The results obtained suggest that cholinergic mechanisms of the visual cortex are included in visual recognition, and apparently play various functional roles at various stages of behavior.
Monkeys performed a task of delayed visual differentiation of differently colored stimuli in behavioral experiments. The impulse activity of individual neurons of the prefrontal and inferotemporal cortex before and after the systemic administration of a blocker of M-cholinoreceptors, amyzil (0.8-1.0 mg/kg), was recorded simultaneously. Deterioration of the characteristics of recognition induced by amyzil was accompanied mainly by a significant increase in the activity of neurons of the prefrontal cortex which was dependant on the stage of recognition, and intensified with an increase in the delay interval. The impulse activity of the neurons of the inferotemporal cortex varied in the process without a regular pattern: at some stages of recognition it increased, at others it was inhibited. Amyzil induced a substantial decrease in the coefficients of cross correlation between the simultaneous respondent reactions of groups of neurons of the prefrontal and inferotemporal cortex. The results obtained point to the fact that the cholinergic structures of the inferotemporal and prefrontal cortex participate, at various stages of visual recognition in monkeys, in the formation of the dynamic functional systems which make their specific contribution to informational processes.
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Experiments on rhesus macaques were used to study the relationship between the characteristics of delayed visual differentiation and stimulus properties in conditions of pharmacological treatment with the m-cholinoreceptor blocker amizil, with the aim of identifying how modification of cholinergic structures affects different types of information. Disturbances to short-term memory for all stimuli consisted of reductions in the duration of retention and increases in motor reaction times, but occurred at different doses of the blocker: amizil at a dose of 0.3 mg/kg significantly decreased the retention duration for information relating to spatial relationships. Delayed discrimination of shape, contrast, and size worsened after treatment with amizil at a dose of 0.45-0.50 mg/kg, while decreases in the duration of short-term storage of information relating to color started after amizil doses of 0.6-0.8 mg/kg. It is suggested that the short-term memory system includes a set of neurophysiological mechanisms in which the cholinergic structures are organized differently and whose specific properties result in differences in the characteristics of short-term storage of different types of visual information.
Experiments reported in this study have been performed in order to investigate cholinergic and GABA-ergic neurotransmitter systems and substance P in the realization of internal inhibition and pain reinforcement. This was accomplished during the elaboration of inhibitory and defensive conditioned reflexes to light flashes in alert, nonimmobilized rabbits. Present results together with a review of past research indicate that the cholinergic system is directly involved in transmitting the effects of pain reinforcement to neocortical neurons. Substance P, a neuropeptide, reduces the background activity of neocortical and hippocampal neurons and the response of cortical neurons to pain and positive conditioned stimuli. The cholinergic system and substance P exert a modulating effect on the elaboration of internal inhibition. Phenybut, a GABA derivative capable of penetrating the blood-brain barrier, enhances inhibitory hyperpolarization in the cerebral cortex and improves discrimination between the inhibitory and reinforcing light flashes. It appears, therefore, that the GABA-ergic system plays a leading part in the elaboration of internal inhibition. Neuronal activity and slow potential changes in response to positive conditioned and pain stimuli occur in the same direction after administering the preparations, and the dynamics of these changes is different from that in responses to inhibitory stimuli. It may be supposed on these grounds that the neurotransmitter and neuromodulator systems studied possess a considerable degree of plasticity.
Experiments employing ultrasound technique showed that nonselective blockade of central muscarinic cholinoceptors with amizyl significantly increases the number and lifespan of rats highly resistant to acute massive blood loss. This pretreatment increased individual resistance of the circulatory system to posthemorrhagic hypoxia (blood pressure and portal blood flow rate). Preliminary blockade of central nicotinic cholinoceptors and peripheral muscarinic cholinoceptors with cyclodol and methacin, respectively, had no effect on the percentage of rats highly and low resistant to acute blood loss. Preliminary blockade of peripheral muscarinic cholinoceptors with methacin prevented the decrease in the cardiac output in low resistant animals during the posthemorrhagic period.