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Biomedical subjects

D A Popplewell

Publications and source records attributed to D A Popplewell.

7 recordsLinked to original sources

Visual form discrimination from luminance or disparity cues: functional anatomy by PET.

With the purpose of elucidating the functional fields involved in the discrimination of visual form based either on luminance or binocular disparity cues, we used PET to measure changes in regional cerebral blood flow (rCBF) in ten volunteers while they performed visual discrimination tasks. The averaged standardized subtraction images (delta rCBF) were analysed for statistically significant changes between the form tasks and their reference tasks. Twenty cortical fields in the visual association areas and the prefrontal cortex were engaged by the discrimination of visual form based upon disparity cues, whereas only four fields showed increased activity during the discrimination of visual form created by luminance cues. The only functional field activated in both conditions was in the left fusiform gyrus. The present findings extend our earlier observations, namely that disparate functional networks of activated fields in the human brain can perform the discrimination of visual form perceptually defined by different visual cues.

Adult↗

Visual form discrimination from color or motion cues: functional anatomy by positron emission tomography.

To explore the extent to which various cortical functional pathways are involved in processing and analyzing different types of information that yield the same perceptual entity, we mapped anatomical structures in the human brain participating in the discrimination of visual forms mediated either by motion or color cues. Changes in regional cerebral blood flow were measured in 10 young male volunteers with positron emission tomography and with [15O]butanol. During the measurements, the subjects performed four visual discrimination tasks (form-from-motion, motion alone, form-from-color, and color alone discrimination). The individual regional cerebral blood flow images were standardized in shape and size with the help of a computerized brain atlas. Subtraction images were determined and averaged across data from all subjects. The resulting images were analyzed for statistically significant changes between specific and reference tasks. The discrimination of form by means of motion cues activated functional fields bilaterally in the inferior and lateral occipital gyri, in the lingual, anterior cingulate, middle frontal and orbitofrontal gyri, and in the left fusiform and right inferior temporal gyri. Form discrimination by color cues resulted in activation bilaterally in the inferior temporal, lateral occipital, and orbitofrontal gyri, the left precuneus and intraparietal sulcus, and the right precentral gyrus. The regions engaged in the two kinds of form discrimination did not overlap, demonstrating that differences in visual forms mediated by color or motion cues are processed and analyzed by disparate networks of functional fields in human cerebral cortex.

Adult↗

A behavioural and pharmacological examination of phenylethylamine-induced anorexia and hyperactivity--comparisons with amphetamine.

The discovery that trace amine beta-phenylethylamine (PEA) has a number of properties in common with amphetamine (AMPH) has led to the suggestion that PEA may be a neuromodulator of catecholamine release or an "endogenous amphetamine." The present study compared PEA-induced behavioural changes (anorexia and hyperactivity) with AMPH-induced changes in feeding and motor activity. The first experiment examined the effects of PEA (0-35 mg/kg) on the temporal profile of feeding. The results from this experiment revealed important differences between the effects of PEA as compared with AMPH, in particular PEA failed to increase the rate of eating that is characteristic of AMPH-induced anorexia. The second experiment concurrently measured food intake and motor activity following equi-anorectic doses of PEA and AMPH and pretreatment with the neuroleptic pimozide. Pimozide attenuated PEA-induced hyperactivity, AMPH-induced hyperactivity and AMPH-induced anorexia, but failed to attenuate PEA-induced anorexia. These findings are discussed in relation to the possible mechanisms of action of PEA and AMPH.

Animals↗

A microcomputer system designed for psychological and behavioural experiments.

This paper describes a relatively cheap MC6809-based microcomputer designed to run experiments in real-time, and to use the hardware and software facilities of a larger (HOST) computer. Each microcomputer is capable of controlling a wide range of psychological and behavioural experiments, and includes 32K RAM, 4K EPROM, 32 digital input lines, 32 digital output lines, analogue/digital converters, and programmable timers. Any programming language may be used, providing a cross-compiler generating MC6809 executable code exists for the HOST. Following over a year of use we can confirm that this system provides an effective method of running psychological and behavioural experiments.

Computers↗

Feeding rate and meal patterns in the laboratory rat.

Many manipulations used in the study of feeding (e.g., changes of food taste or texture, anorectic drugs) affect the rate of food consumption. Consequent changes in meal patterning might reflect either direct effects of the manipulation or alternatively might result from indirect effects of the changed rate of intake. In the experiment reported here a direct reduction in the permitted rate of food intake resulted in a clear reduction of meal size and an increase in meal frequency in rats. We explore the extent to which this finding is predicted by quantitative models of the regulation of food intake.

Animals↗

The effect of fenfluramine on the microstructure of feeding and drinking in the rat.

1. The effects of three doses of fenfluramine on feeding and drinking in the rat were examined. 2. Feeding and drinking were subdivided into meals and bouts, and the changes in feeding/drinking were expressed in terms of meal/bout frequency, meal/bout size, meal/bout length, and eating/drinking rate. 3. The changes in these parameters were examined over different time periods after the injection. 4. Significant changes in the distribution of inter-response intervals within meals were found in time period 1 with 5 mg/kg and 10 mg/kg doses of fenfluramine. Videotape and computer analysis showed that the changes in inter-response interval histograms differed significantly from those seen in normal animals approaching satiety. Drinking parameters also changed. 5. Compensatory increases in feeding were observed in time period 4 with the 10 mg/kg dose. 6. The difficulties in designing and interpreting experiments in feeding are discussed, and the action of fenfluramine as an anorectic drug is considered.

Animals↗