Rat Cortical Dissection

Rat cortical dissection is a laboratory method for isolating cerebral cortical tissue from rat brains, enabling researchers to examine neural development in a defined region. The procedure uses anatomical landmarks to separate the cortex from surrounding brain structures, often preserving the tissue for downstream processing such as sectioning, molecular analysis, or cell culture. In developmental biology, dissected cortex supports studies of progenitor proliferation, neuronal differentiation, migration, and tissue maturation across developmental stages. By providing region-specific material, the method links cellular and molecular changes to brain development and can improve experimental models of neurodevelopmental disorders.

Rat Cortical Dissection - Related Videos

Research

JoVE Journal - Neuroscience

Isolation of Cerebrospinal Fluid from Rodent Embryos for use with Dissected Cerebral Cortical Explants

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Cited by 20 •

2013

The ventricular cerebrospinal fluid (CSF) bathes the neuroepithelial and cerebral cortical progenitor cells during early brain development in the embryo. Here we describe the method developed to isolate ventricular CSF from rodent embryos of different ages in order to investigate its biological function. In addition, we demonstrate our cerebral cortical explant dissection and culture technique that allows for explant growth with minimal volumes of culture medium or CSF.

Bilaminar Co-culture of Primary Rat Cortical Neurons and Glia

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Cited by 26 •

2011

Here we provide a protocol for culturing rat cortical neurons in the presence of a glial feeder layer. The cultured neurons establish polarity and create synapses, and can be separated from the glia for use in various applications, such as electrophysiology, calcium imaging, cell survival assays, immunocytochemistry, and RNA/DNA/protein isolation.

Quantification of Filamentous Actin (F-actin) Puncta in Rat Cortical Neurons

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Cited by 8 •

2016

Filamentous actin (F-actin) plays an important role in spinogenesis, synaptic plasticity, and synaptic stability. Quantification of F-actin puncta is therefore a useful tool to study the integrity of synaptic structures. This protocol describes the procedures of quantifying F-actin puncta labeled with Phalloidin in low-density primary cortical neuronal cultures.

Modulating Cortical Excitability in a Rat Using Repetitive Transcranial Magnetic Stimulation

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2025

Source: Beom, J., et al. Repetitive Transcranial Magnetic Stimulation to the Unilateral Hemisphere of Rat Brain. J. Vis. Exp. (2016)This video demonstrates the application of repetitive transcranial magnetic stimulation (rTMS) in anesthetized rats to modulate cortical excitability. The procedure involves determining the motor threshold (MT) to establish baseline stimulation, followed by applying rTMS at an intensity above the MT to induce neuronal depolarization. This stimulation triggers...

Research

JoVE Journal - Biology
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Preparing E18 Cortical Rat Neurons for Compartmentalization in a Microfluidic Device

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Cited by 26 •

2007

In this video we demonstrate the preparation of E18 Cortical Rat Neurons.

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