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Biomedical subjects

J L Altman

Publications and source records attributed to J L Altman.

9 recordsLinked to original sources
PubMed1979

Drugs and the discrimination of duration.

The effects of lysergic acid diethylamide (LSD), d-amphetamine (AMP), chlorpromazine (CPZ), and the most active isomer of marihuana (delta9 - THC) on timing behavior were analyzed with a two-choice, discrete trial procedure in which pigeons were trained to discriminate visual stimuli that differed with respect to duration ('long' vs. 'short'). LSD (0.01, 0.04, 0.16 mg/kg) decreased response speed (increased latency), but otherwise had no significant effects on performance of the discrimination. d-Amphetamine (1.0, 2.0, 4.0 mg/kg) increased perseveration of 'spatial bias' and, at a dose of 4.0 mg/kg, lowered response speed. This compound did not significantly alter accuracy (percentage correct). CPZ (7.5, 15.0, 30.0 mg/kg) significantly decreased accuracy and, at a dose of 30.0 mg/kg, significantly lowered speed; THC also decreased accuracy and lowered speed. Neither CPZ nor THC significantly altered perseveration.

Animals↗
PubMed1979

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↗
PubMed1976

A behavioral paradigm for the evaluation of narcotic antagonists.

We have developed an experimental paradigm for the behavioral evaluation of narcotic antagonists. The study specifically examined the heroin-seeking behavior of hard-core narcotic addicts on a research ward under blocked and unblocked conditions. Each patient served as his own control. A long-term follow-up program in the community, with aftercare services, was utilized to determine the relationship between behavior observed on the research ward and behavior that occurred in the community. While preliminary one-month follow-up data offered some cause for an optimistic view of narcotic antagonist treatment, behavioral data observed on the research ward raised serious doubts about the possibility of extinguishing heroin self-administration with antagonists. The behavioral data were not consistent with laboratory descriptions of extinction. Rather, the data suggested that narcotic antagonist programs should emphasize the development of contingencies for the reinforcement of narcotic antagonist self-administration to ensure an opiate-free state, instead of focusing on an extinction approach.

Adult↗
PubMed1976

Analysis and modification of opiate reinforcement.

The authors describe a research protocol for the evaluation of narcotic antagonists which examines the heroin-seeking behavior of hard-core heroin addicts on a research ward under blocked and unblocked conditions. Each patient served as his own control. This paper serves as an introduction to a series of papers which follow dealing with behavioral, psychiatric, and aftercare results. It describes detailed methods and preliminary results for the first 21 subjects admitted to the study. More specific results are reported in the papers that follow.

Adult↗
PubMed1976

Opiate antagonists and the modification of heroin self-administration behavior in man: an experimental study.

The heroin self-administration behavior of 8 inpatient heroin addicts was examined for 10 days under blocked (i.e., following ingestion of narcotic antagonists--naloxone or naltrexone) and unblocked (no antagonist) conditions. In the unblocked state, subjects injected all the available heroin, but they ceased heroin use almost completely following antagonist administration. Possible explanations for these results are discussed along with their implications for treatment.

Adult↗
PubMedDate not supplied

Para-chlorophenylalanine, serotonin and killing behavior.

Both p-chlorophenylalanine (PCPA) and PCPA methyl ester were found to reliably induce mouse-killing in non-killer rats only when unusually large doses were used (three successive daily injections of 300 mg/kg) and brain serotonin (5-HT) concentration was drastically reduced (about 90 percent). Neither three doses of 100 mg/kg of PCPA nor p-chloroamphetamine (3 times 3.5 mg/kg) caused similar effects in spite of the fact that these compounds depleted brain 5-HT by 85 percent and 60 percent, respectively. PCPA-induced mouse killing was reversed by 5-HTP (100 mg/kg) only when this serotonin precursor completely restored levels of 5-HT. The topography of PCPA-induced killing did not resemble normal interspecies aggression and was also directed toward fat pups. These findings suggest that 5-HT depletion might facilitate nonspecific killing reactions, but is not a sufficient condition to induce the species-specific predatory behavior in rats.

5-Hydroxytryptophan↗
PubMedDate not supplied

LSD and fixed-internal responding in the rat.

A series of 6 doses of lysergic acid diethylamide-25 (LSD) altered the bar-pressing behavior of 6 rats maintained on a fixed-interval, 5 min (FI 5) schedule of reinforcement. High doses of LSD (0.16, 0.32 mg/kg) depressed overall rates of responding. Low response rates, which occurred during the first half of the interval between successive reinforcements, were increased by low (0.01, 0.02 mg/kg), moderate (0.04, 0.08 mg/kg), and high doses of LSD; high rates of responding which occurred during the final half of the interval were decreased only by high doses of LSD. All doses (except the lowest) decreased the Index of Curvature, a statistic describing the temporal distribution of responses. The results were discussed in terms of baseline rate of responding and the presence or absence of timing behavior.

Animals↗