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J Eggermont

Publications and source records attributed to J Eggermont.

57 records · Page 4Linked to original sources

The neurochrome. An identity preserving representation of activity patterns from neural populations.

Recording of simultaneous but separated activity of neural populations overwhelms the experimenter with a large amount of information. A clearly structured display technique the "Neurochrome" is introduced, usable on-line and real-time. It shows neural activity patterns while preserving neural identity by employing a color code. The Neurochrome assists the experimenter in generating and verifying hypotheses about neural correlations and stimulus-event relations already during the experiment. In auditory research single neurons are characterized by their spectro-temporal sensitivity to auditory stimuli. A straightforward generalization of this concept, applicable to neural populations, is proposed leading to a global indication of a populations' activity to stimuli: the Multi-Unit Spectro-Temporal Sensitivity. This approach is inversely related to the Neurochrome, the latter however containing more information. The combination of both approaches seems quite powerful in the investigation of neural assemblies. The procedures are illustrated with examples of extracellular multiunit recordings from the auditory midbrain of the grassfrog (Rana temporaria L.).

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Isolation of a plasma-membrane fraction from gastric smooth muscle. Comparison of the calcium uptake with that in endoplasmic reticulum.

1. A plasma-membrane fraction was isolated from the smooth muscle of the pig stomach by using differential and sucrose-density-gradient centrifugations. When the centrifugation was carried out after preloading the crude microsomal fraction with Ca2+ in the presence of oxalate, the contamination of the plasma-membrane fraction by endoplasmic reticulum was decreased and a fraction enriched in endoplasmic reticulum vesicles filled with calcium oxalate crystals was obtained. 2. The plasmalemmal and endoplasmic-reticulum membranes could be distinguished by differences in the activity of marker enzymes and in the cholesterol content and by their different permeability to oxalate and phosphate. Oxalate and phosphate stimulated the Ca2+ uptake in the endoplasmic reticulum much more than in the plasmalemmal vesicles. In the plasma-membrane vesicles 40 mM-phosphate was more effective for stimulating the Ca2+ uptake than was 5 mM-oxalate, but the reverse was seen in the endoplasmic reticulum. 3. The high cholesterol/phospholipid ratio of the crude microsomal fraction are of the majority of the vesicles present in the crude microsomal fraction are of plasmalemmal origin. 4. The Ca2+ pump of the plasmalemmal and endoplasmic-reticulum vesicles could be differentiated by their different sensitivities to calmodulin. However, the two Ca2+-transport ATPases did not differ by their sensitivity to vanadate nor by the energization of the Ca2+ transport by different nucleoside triphosphates.

Animals↗