Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Examining circadian synaptic plasticity requires housing mice under different lighting conditions (light/dark cycle, LD 12:12, and constant darkness, DD), providing access to running wheels, and sacrificing them at four defined time points within 24 h-at the beginning and middle of the day/subjective day and at the beginning and middle of the night/subjective night. Brains are then properly fixed for transmission electron microscopy (TEM). The barrel cortex, with its precise somatotopic organization, provides an ideal model for such analysis. To obtain the required brain area, the brains are tangentially cut with a vibratome, and then, sections containing the barrel cortex are selected and embedded in Polybed resin. From the prepared blocks containing the selected barrels, consecutive ultrathin sections are cut. Synaptic density, excitatory and inhibitory, is analysed from electron micrographs using the stereological dissector method. Additionally, TEM images are used for 3D reconstructions of dendritic spines. Changes in the shape of dendritic spines indicate remodeling of neurons during the day. The number of excitatory synapses peaks during sleep (day) in mice, while inhibitory synapses peak during their activity phase (in the middle of the night).

Download full-text PDF

Source
http://dx.doi.org/10.3791/68385DOI Listing

Publication Analysis

Top Keywords

barrel cortex
12
transmission electron
8
electron microscopy
8
circadian synaptic
8
synaptic plasticity
8
dendritic spines
8
microscopy visualization
4
visualization technique
4
technique analysis
4
analysis circadian
4

Similar Publications

Layer 6 corticothalamic (L6CT) neurons project to both cortex and thalamus, inducing multiple effects including the modulation of cortical and thalamic firing, and the emergence of high gamma oscillations in the cortical local field potential (LFP). We hypothesize that the high gamma oscillations driven by L6CT neuron activation reflect the dynamic engagement of intracortical and cortico-thalamo-cortical circuits. To test this, we optogenetically activated L6CT neurons in NTSR1-cre mice (both male and female) expressing channelrhodopsin-2 in L6CT neurons.

View Article and Find Full Text PDF

Examining circadian synaptic plasticity requires housing mice under different lighting conditions (light/dark cycle, LD 12:12, and constant darkness, DD), providing access to running wheels, and sacrificing them at four defined time points within 24 h-at the beginning and middle of the day/subjective day and at the beginning and middle of the night/subjective night. Brains are then properly fixed for transmission electron microscopy (TEM). The barrel cortex, with its precise somatotopic organization, provides an ideal model for such analysis.

View Article and Find Full Text PDF

Response Characteristics of Barrel Cortical Neurons in Layers IV/V of Juvenile Rats with Autism-Like Traits after Tactile Stimulation.

Physiol Behav

September 2025

Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran; Cognitive Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.

The barrel cortex is a specialized region of the primary somatosensory cortex that processes tactile information from whiskers. This study investigates how tactile stimulation (TS) affects excitatory receptive fields and surrounds suppression in barrel cortex neurons of male and female autistic-like rats, using various whisker displacement protocols. The animals were categorized into control, Valproic acid pre-treated (Val), and Val-TS treatment groups.

View Article and Find Full Text PDF

Neuronal activity in the cerebral cortex comes in surprisingly early and influences or even controls a number of important developmental process like neurogenesis, neuronal migration, myelination, formation of cortical maps and local circuits, and programmed cell death. During the late prenatal and early postnatal period, the neocortical network shows a developmental transition from sparse, synchronized, low activity patterns to continuous, desynchronized, high activity patterns. This developmental sequence has been demonstrated in various neocortical areas of different mammalian species.

View Article and Find Full Text PDF

The temporal mechanisms of activity-dependent dendritic patterning during postnatal development remain unclear because appropriate technology is lacking. Here, we demonstrate that the auxin-inducible degron 2 technology enables the rapid knockdown of target proteins at specific time points in the postnatal mouse brain. When N-methyl-D-aspartate-type glutamate receptor (NMDAR) depletion was induced from postnatal day (P)3, barrel cortex layer 4 spiny stellate neurons (barrel cells) failed to form strong asymmetry and a high tree-length variance in the dendritic patterns.

View Article and Find Full Text PDF