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C B Dahl

Publications and source records attributed to C B Dahl.

4 recordsLinked to original sources

Aversive and compensatory classical conditioning with diazepam as conditional stimulus.

The purpose of the first experiment was to investigate whether diazepam could acquire anxiogenic properties by signalling an aversive event. Rats were trained in an operant chamber in the pentylenetetrazol (PTZ) model of anxiety. Thereafter the animals were divided into groups that received classical diazepam conditioning (Group 1), and conditioning of diazepam + tone (Group 2). In the test phase diazepam was injected prior to placement in the operant chamber. Group 2 selected the PTZ-appropriate lever more often than the other groups, indicating that the tone induced anxiety, and diazepam did not. Tones and shock may therefore be more easily associated than diazepam and shock. The second experiment investigated this. Rats were trained the same way as in the first experiment. Thereafter the experimental group received injections of a small dose of diazepam prior to a second injection of a large dose of diazepam. The hypothesis was that a compensatory anxiogenic conditional response to diazepam's anxiolytic effect should be elicited by the small dose. There were no differences between the groups in lever selection, indicating that a compensatory anxiogenic response was not elicited.

Animals↗

Lack of self-administration of different fenfluramine isomers in rats.

Twelve rats were tested in an animal model for self-administration of dl-, d-, and l-fenfluramine. Amphetamine and saline were used as reference substances. In addition to being tested on the reference substances amphetamine and saline, each rat was only tested on one drug and dose. Analyses of variance were performed to assert that high rates of self-administration were maintained on amphetamine whereas saline gave low rates of responding. The results showed that all three forms of fenfluramine (dl-fenfluramine 0.1, 0.5, 2.0 mg/kg; d-fenfluramine 0.05, 0.1, 0.25, 1.0 mg/kg; l-fenfluramine 0.1, 0.5, 1.0, 2.0 mg/kg) differed significantly from amphetamine, but not from saline. As d-fenfluramine is both more effective in reducing food intake, and has less sedative action than dl-fenfluramine, it may be an improvement in the pharmacotherapy of obesity.

Animals↗

An open field study of antidepressant drugs.

Eight psychotropic drugs, mainly acting on the catecholaminergic systems, were investigated in an open field setting. All drugs but one showed a significant reduction in overall activity over time. Only piribedil at 32 mg/kg showed an increase, while 2 mg/kg showed a decrease over time. Amineptine and nomifensine significantly increased and salbutamol significantly decreased both ambulation and rearing with dose. For viloxazine, metapramine, piribedil and piracetam no significant dose effects were revealed at the doses tested. It is concluded that no clear correlation between clinically reported antidepressant efficacy and the selected open field variables can be demonstrated. However, some of the dopaminergic drugs have substantial activating properties, which might render them dependence-producing properties.

Albuterol↗

Tissue level related stereotyped behaviour after intravenous amphetamine in rats.

In the first experiment, open field activity was studied in rats after different intravenous doses of d-amphetamine (0.5, 2, 4, 6, 8 mg/kg) at three time points (1-5, 28-32, 58-62 min.). Ambulation and rearing initially increased with increasing amphetamine doses, but at 8 mg/kg the registered activity was replaced by stereotyped disintegrated behaviour. In the second experiment plasma and brain levels of d-amphetamine were determined (at 3, 30 and 60 min.) after 5 different intravenous doses of d-amphetamine (0.25, 0.5, 2, 4, 8 mg/kg). Ambulation and rearing where then plotted against the tissue levels. There was initially a positive correlation between activity and tissue level. At a certain level a maximum was reached, followed by a decline with increasing tissue levels. At 3 min., the decline started after 15 micrograms/g of amphetamine in the brain tissue, at 30 min. this level was 3, and at 60 min. 2 micrograms/g. It is concluded that at least 5 times higher brain concentrations are needed to elicit stereotyped behaviour, than to maintain it later on.

Animals↗