Thalamus Isolation

Thalamus isolation is a neuroscience dissection technique used to separate the thalamus from surrounding brain tissue for focused structural, physiological, or molecular analysis. The procedure relies on anatomical landmarks and precise tissue handling to identify thalamic boundaries while preserving neuronal circuits, nuclei, and cellular integrity. Isolated thalamic tissue can support ex vivo electrophysiology, imaging, gene-expression studies, and pharmacological experiments that examine sensory relay, motor coordination, arousal, and sleep-related pathways. By reducing experimental complexity and enabling direct access to thalamic neurons, the technique helps researchers investigate circuit function and model changes associated with neurological disorders.

Thalamus Isolation - Related Videos

Research

JoVE EoE - Neuronal Culture Techniques

Generation of Medial Thalamus-Anterior Cingulate Cortex Slices from Mouse Brains

0 Views •

2025

The video demonstrates the preparation of medial thalamus-anterior cingulate cortex (MT-ACC) slices from mouse brains. A mouse's brain is dissected, cuts are made to expose the MT-ACC pathway, and slices are generated using a vibratome. The MT-ACC slices are then maintained in oxygenated artificial cerebrospinal fluid.

Education

JoVE Core - Anatomy and Physiology

Diencephalon: Thalamus and Information Relay

0 Views •

2025

The thalamus, often called “the gateway to the cerebral cortex,” is vital in processing and directing sensory and motor signals throughout the brain. Almost all inputs destined for the cerebral cortex, except for olfactory signals, are relayed through the thalamus. The thalamus is a sophisticated relay station, channeling information from various brain regions to the cerebral cortex, as well as a filter, prioritizing certain signals over others based on current physiological states or needs.

Cortex-, Hippocampus-, Thalamus-, Hypothalamus-, Lateral Septal Nucleus- and Striatum-specific In Utero Electroporation in the C57BL/6 Mouse

0 Views •

Cited by 14 •

2016

This protocol describes in detail how to specifically transfect different regions in the C57BL/6 central nervous system via in utero electroporation. Included in this protocol are detailed instructions for transfections of regions that develop into the cortex, hippocampus, thalamus, hypothalamus, lateral septal nucleus and striatum.

Research

JoVE Journal - Neuroscience
Free Sample

Mouse in Utero Electroporation: Controlled Spatiotemporal Gene Transfection

0 Views •

Cited by 49 •

2011

A gene transfer method into the developing mouse brain is described by using a unique surgical method and special shape of electrodes. This unique technique allows transfection of plasmid DNA temporally and spatially, which will aid many neuroscientists in studying brain development.

Vasodilation of Isolated Vessels and the Isolation of the Extracellular Matrix of Tight-skin Mice

0 Views •

Cited by 1 •

2017

We describe the isolation of cardiac extracellular matrix from C57Bl/6J control mice, tight-skin mice, and tight-skin mice treated with the IRF5 inhibitory peptide. We also describe the vasodilation studies on the isolated vessels from C57Bl/6J, tight-skin mice and tight-skin mice treated with the IRF5 inhibitory peptide.

View All Results

FAQs

Related Topics