Isolated Hippocampal Preparation

An isolated hippocampal preparation is an ex vivo neuroscience method in which hippocampal tissue is separated from the brain and maintained for controlled study of neural function. Researchers preserve viable circuits by placing the tissue, often as acute slices or an intact isolated hippocampus, in oxygenated artificial cerebrospinal fluid under carefully regulated conditions. This setup enables direct recording and manipulation of neuronal activity, synaptic transmission, and plasticity while reducing the complexity of the intact brain. Isolated hippocampal preparations are widely used to investigate learning and memory mechanisms, long-term potentiation, epilepsy, neuropharmacology, and the cellular effects of disease or experimental treatments.

Isolated Hippocampal Preparation - Related Videos

Research

JoVE Journal - Neuroscience

Isolation and Culture of Hippocampal Neurons from Prenatal Mice

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Cited by 183 •

2012

We provide a protocol for the culture of highly purified hippocampal neurons from prenatal mouse brains without the use of a feeder glial cell layer.

Isolation and Expansion of Adult Canine Hippocampal Neural Precursors

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Cited by 3 •

2016

The canine brain is a valuable model in which to study adult neurogenesis. Presented here are protocols for isolating and expanding adult canine hippocampal neural precursor cells from primary brain tissue.

Tuning in the Hippocampal Theta Band In Vitro: Methodologies for Recording from the Isolated Rodent Septohippocampal Circuit

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Cited by 4 •

2017

Here, we present a protocol for recording rhythmic neuronal network theta and gamma oscillations from an isolated whole hippocampal preparation. We describe the experimental steps from extraction of the hippocampus to details of field, unitary and whole-cell patch clamp recordings as well as optogenetic pacing of the theta rhythm.

Organotypic Hippocampal Slice Cultures

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Cited by 52 •

2011

We describe a method to prepare organotypic hippocampal slices that can be easily adapted to other brain regions. Brain slices are laid on porous membranes and culture media is allowed to form an interface. This method preserves the gross architecture of the hippocampus for up to 2 weeks in culture.

Research

JoVE Journal - Neuroscience
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Preparation of Acute Hippocampal Slices from Rats and Transgenic Mice for the Study of Synaptic Alterations during Aging and Amyloid Pathology

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Cited by 62 •

2011

This article outlines procedures for preparing hippocampal slices from rats and transgenic mice for the study of synaptic alterations associated with brain aging and age-related neurodegenerative diseases, such as Alzheimer’s disease.

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