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Biomedical subjects

S Schottenfeld

Publications and source records attributed to S Schottenfeld.

6 recordsLinked to original sources

Specific oculomotor deficit after acute methadone. I. Saccadic eye movements.

Changes in saccadic eye movements before and after up to 10 mg oral methadone were measured electrooculographically in nontolerant nondependent humans. Undershoot of initial saccades increased with increasing size of horizontal target displacement (to 36 degrees) from a central viewing position. Dosage as low as 5 mg caused significant increase in saccade undershoot especially to target displacements greater than 10-15 degrees. Latency from target displacement to onset of initial saccade also increased after methadone. These results, in combination with the lack of significant drug effect on latency between initial saccade and corrective saccade, and on initial saccade duration, maximum velocity, and time to maximum velocity indicate methadone action on specific sensory, rather than motor, components of saccadic response. The similarity of alteration of saccadic response after methadone and after lesion of the upper layers of the superior colliculus in primates, as reported in the literature, suggests that opiate binding sites in the upper layers of the superior colliculus may be physiologically active.

Adult

Specific oculomotor deficit after acute methadone. II. Smooth pursuit eye movements.

Changes in smooth pursuit eye tracking of targets moving sinusoidally in horizontal and vertical planes before and after up to 10 mg oral methadone were measured electrooculographically in nontolerant nondependent humans. Methadone depressed the gain of horizontal tracking movements at most frequencies tested (0.2 - 1.6 Hz) without changing target-eye phase relationships. Lack of change in target-eye cross-correlation functions after methadone and examination of individual records indicate that gain reduction was due to the eye failing to follow the target to the full extent of target excusion (+5 degrees from eyes straight ahead view). Possible mechanisms and the practical consequences of methadone action on smooth pursuit were discussed.

Adult

Methadone depression of visual signal detection performance.

In order to determine the origin of a previously reported slowing of simple visual reaction time in subjects receiving single doses of oral methadone, three well-trained subjects performed. a modified double flash detection task several times after single doses of 5 mg and 10 mg of oral methadone and a placebo. A Theory of Signal Detectability analysis allowed for a clear distinction between drug-induced changes in visual sensitivity and changes in response bias. It was found that methadone reduced visual sensitivity. The peak depression in detection as well as the duration of the depressed performance were dose-related. Depression in performance paralleled the subjective effect of the drug in each subject. Averaged visual evoked potentials showed significant changes at peak drug effect to the onset of each of the pair of stimuli. It was concluded that methadone depresses visual function by acting on the visual parts of the central nervous system. The retina, midbrain and thalamic visual nuclei were discussed as possible sites of action of methadone.

Adult

Performance differences between addicts and non-addicts.

Methadone addicts and non-addict controls were tested before and after receiving up to 10 mg of methadone on simple visual reaction time tests and on a vigilance type visual attention test. Addicts were faster than controls on pre-drug testing, although there were no pre-drug differences between groups on the attention task. Addicts maintained faster reaction times than controls even when money was offered as an incentive for speed. Additional methadone did not affect addict performance on any of the tasks. Methadone slowed control reaction times in a dose-related fashion. No significant attention decrements were seen after methadone in controls. Visual reaction time differences between addicts and controls cannot be attributed to group differences in motivation or ability to attend. Slowing of reaction time with acute dose of methadone in controls cannot be attributed to the effect of the drug on attention. An hypothesized drug-induced decrease in visual sensitivity with acute dose in controls and a drug-induced increase in visual sensitivity with chronic dose in addicts can account for the presented data.

Adult

An automated laboratory control system: collection and analysis of behavioral and electro-physiological data.

A system of man-machine interactive PDP-11 assembly language programs is described which presents stimuli to a subject and records and analyzes behavioral and evoked potential data. The system was designed for researchers with no knowledge of computer programming and enables the user to create complicated sequences of stimulus presentations ("trials") and sequences of successive trials ("runs"), with no new programming required. The system is written for DEC.s DECLAB 11/40 system.

Behavior