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Bruchpilot (BRP) protein is a scaffolding presynaptic protein that has been detected in the nervous system of Drosophila melanogaster. BRP assembles a presynaptic active zone and is responsible for calcium channel clustering and release of a neurotransmitter from synaptic vesicles. We have used the antibody nc82 against BRP to visualize presynaptic elements of tetrad synapses formed between the photoreceptor terminals and postsynaptic cells in the first optic neuropil (lamina) of the Drosophila optic lobe. In the lamina several circadian rhythms have been detected including rhythms in plasticity of synapses and neurons. The aim of this study was to examine whether BRP protein is involved in the circadian plasticity of tetrad synapses in the lamina. We have examined the BRP level, measured as the fluorescence intensity of immunolabeling, at different times of a light/dark (LD 12:12) regime and constant darkness (DD). We have found that BRP oscillates during the day. In LD 12:12 its level increases two times, in the morning and in the evening. However, these two peaks in BRP abundance are regulated differently. The morning peak is predominantly regulated by light since it is not present in norpA7 phototransduction mutant but it also depends on the circadian clock gene per. In turn the evening peak is regulated by the brain pacemaker. This peak is present in DD as well as in the norpA7 in LD but is absent in clock gene mutants.
The reception of sensory information is an active process in which sensory input and motor behaviour influence each other. Mice explore the environment by rhythmically moving their whiskers. As a result, their representations in the somatosensory cortex are modulated. In the present study, we analyzed daily structural changes in the barrel cortex associated with locomotor activity level of the C57/BL mouse strain. The locomotor activity was monitored using running wheels. In a day/night regime (LD 12:12), maximum of the activity of animals was at the beginning of the night and minimum in the first half of the day. Using serial EM sections of the barrel cortex of mice, sacrificed in the period of their high or low locomotor activity, we found an increase in numerical density of synapses during the low activity period. In particular, we observed up-regulation of the density of excitatory synapses located on dendritic spines (mostly single-synapse spines). We also detected a slight increase in the density of inhibitory synapses, located on both dendritic shafts and spines, during the high activity period. It seems that in LD 12:12 conditions high locomotor activity of animals leads to the elimination of singlesynapse spines. In conclusion, in LD 12:12 conditions there are cyclical, daily changes in the density of synapses and dendritic spines in mouse barrel cortex, which are associated with the daily locomotor activity pattern of the animal.
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