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Biomedical subjects

P Lewis

Publications and source records attributed to P Lewis.

At least 217 records · Page 12Linked to original sources

Pathophysiologic studies in human rabies.

Six patients with proved rabies were studied with a combination of clinical, physiologic and pathologic technics. Three were given a type of intensive care but died with evidence of respiratory failure. Although circulatory failure did not develop in any of the six patients, three had supraventricular arrhythmias: interstitial myocarditis was found in one of these and rabies virus was isolated from the myocardium of another. Inspiratory muscle spasm was the dominant clinical feature in all cases. This occurred as part of the hydrophobic response and followed stimulation of the upper respiratory tract and skin. Hydrophobia may represent an exaggerated respiratory tract irritant reflex with associated arousal. Later in the course of the disease, various patterns of periodic and ataxic breathing were observed. Widespread brain stem encephalitis was discovered at autopsy, with particular involvement of the neighborhood of the nucleus ambiguous in two of three patients examined. In one patient cerebral metabolism was grossly abnormal, with greatly reduced cerebral oxygen consumption suggesting irreversible brain damage. Respiratory and circulatory disturbances may well be immediate causes of death in patients with rabies, but the present studies reemphasize the severity of the encephalitis which remains the ultimate barrier to survival. In the developing countries in which rabies is still a major problem and in which the cost precludes intensive care, the clinical management of rabies can aim only to reduce suffering by heavy sedation.

Adolescent↗

Synthesis and adrenoreceptor blocking action of aziridinium ions derived from phenoxybenzamine and dibenamine.

Crystalline perchlorate salts of aziridinium ions derived from phenoxybenzamine and dibenamine were prepared. Both aziridinium ions were tested on the rat vas deferens and found to possess alpha-adrenergic potencies which were nearly identical with those of the parent compounds. The hydrolysis rates of phenoxybenzamine and dibenamine aziridinium ions (2a,b) in physiological medium were found to be 6.0 4 x 10(-4) and 8.35 x 10(-4) sec-1, respectively. The rates of cyclization of the parent amines to 2a and 2b in aqueous medium were 1.9 x 10(-2) and 7.2 x 10(-3) sec-1, respectively. The potencies and kinetic profiles indicate that the aziridinium ion is the only active species in alpha-adrenergic blockade. Moreover, differences in potency between phenoxybenzamine and dibenamine appear to be exclusively to a difference in receptor affinity rather than to a difference in intrinsic alkylating ability.

Adrenergic alpha-Antagonists↗

Negative reinforcement with shock-frequency increase.

Two avoidance-conditioning experiments in which responding delayed shocks are reported. Rats receiving an average of two shocks per minute (imposed condition) could produce, by pressing a bar, a 3-min alternate condition. Six (Experiment I) or more (Experiment II) shocks occurred in the alternate condition. All shocks in the alternate condition were delayed and delivered at 1-sec intervals. With long delays, all subjects produced the alternate condition and spent a large percentage of each session in the alternate condition. The first experiment demonstrated that the longer the delay from onset of the alternate condition to onset of the shocks, the more session time spent in the alternate condition. The second experiment indicated that despite increased shock frequency, behavior is acquired and maintained when responding leads to sufficient delay. Individual subjects produced the alternate condition by bar pressing in essentially one of two patterns. One pattern, termed postshock, involved bar pressing immediately after shock; the other, termed posttransition, involved responding immediately after the transition from the alternate to the imposed condition. These results indicate that shock-frequency reduction is not necessary for avoidance conditioning; delay to shock onset is sufficient.

Journal Article↗

Integrated delays to shock as negative reinforcement.

Rats were shocked at the rate of two per minute until they pressed a lever. In Experiment I, shocks were delivered at variable-time intervals averaging 30 sec; in Experiment II, shocks were delivered at fixed-time intervals of 30 sec. A response produced an alternate condition for a fixed-time period. The shock frequency following a response, calculated over the whole alternate condition, was two per minute. The pattern of shocks in the alternate condition was controlled so that the first shock occurred at the same time as it would have occurred had the response not been emitted; the remaining shocks were delayed until near the end of the alternate condition. Bar pressing was acquired in both experiments. This finding is not explained by two-factor theories of avoidance and is inconsistent with the notion that overall shock-frequency reduction is necessary for negative reinforcement. The data imply that responding is determined by the integrated delays to each shock following a response versus the integrated delays to shock in the absence of a response.

Journal Article↗

Preference for signalled reinforcement.

Key pecking was reinforced on a two-component multiple schedule. A variable-interval schedule controlled reinforcement in both components. During one component, access to reinforcement was preceded by a tone; in the other component, a standard unsignalled schedule was in effect. After performance stabilized, subjects were given a choice between the signalled and unsignalled schedules. They were placed in the chamber with the unsignalled schedule in effect on the right key. A single response on the left, or changeover, key produced the signalled schedule for 1 min. Both pigeons in Experiment I pecked the changeover key at a rate sufficient to remain under the signalled schedule for over 90% of the session. Removing and reintroducing the tone demonstrated that the changeover-key responses were due to the occurrence of the tone. In Experiment II, when pecking the changeover key produced the unsignalled schedule, pecking the changeover key declined. The results may be explained either in terms of Hendry's information hypothesis or as escape from an intermittent positive reinforcement schedule.

Journal Article↗

Negatively reinforced key pecking.

A reinforcement-switching procedure was used to produce negatively reinforced key pecking in pigeons. First, key pecking on a chain schedule (fixed-interval 10-sec variable-interval 60-sec) was conditioned using grain reinforcement. Second, intermittent shock in the initial link was introduced at a low intensity and gradually increased. Third, food reinforcement in the terminal link was eliminated. With shock at 90 V occurring on the average every 3 sec, initial-link pecking was maintained with no terminal-link food. Three of four pigeons responded consistently at shock intensities of 90, 70, and 50 V but not at 30 V. A fourth pigeon responded at but not below 90 V. Rate of response was directly related to shock frequency. Eliminating food deprivation did not affect the negatively reinforced performance.

Journal Article↗

The relative aversiveness of signalled vs unsignalled avoidance.

Subjects avoided shock by pressing on one lever under an unsignalled condition, but by pressing a separate lever they changed the condition to signalled avoidance for 1-min periods. Signalled avoidance periods were identified by a correlated stimulus. All eight subjects responded to change the unsignalled schedule to a signalled one. Once contact with signalled avoidance was made, subjects continued responding to remain in that condition. Other tests showed that changeover responding was greater when the correlated stimulus was presented without the signal than when the signal was presented without the correlated stimulus. An analysis based upon shock and shock-free periods is presented.

Journal Article↗