Chronic Imaging

Chronic imaging is the repeated visualization of biological structures or activity in the same subject over extended periods, allowing researchers to measure change rather than isolated snapshots. In neuroscience, it typically uses stable preparation methods, such as an implanted cranial window, together with optical or magnetic resonance imaging to relocate the same brain region and track labeled cells, neural activity, or blood flow across sessions. This longitudinal approach reveals how circuits develop, adapt, and respond to injury, learning, or treatment while reducing variation between animals. Chronic imaging therefore supports studies of neuroplasticity, disease progression, and therapeutic effects with greater temporal and cellular resolution.

Chronic Imaging - Related Videos

Research

JoVE Journal - Immunology and Infection

In vivo Imaging Method to Distinguish Acute and Chronic Inflammation

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Cited by 25 •

2013

We describe a non-invasive imaging method for distinguishing inflammatory stages. Systemic delivery of luminol reveals areas of acute inflammation dependent upon MPO activity in neutrophils. In contrast, injection of lucigenin allows for visualization of chronic inflammation dependent upon Phox activity in macrophages.

A Craniotomy Surgery Procedure for Chronic Brain Imaging

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Cited by 182 •

2008

This video and protocol demonstrate how to implant a glass-covered cranial window in rodents. These preparations can be used for chronic in vivo two-photon imaging of the neocortex over time scales of months. It may also be used for other types of imaging, including optical intrinsic signal imaging.

Chronic Imaging of Mouse Visual Cortex Using a Thinned-skull Preparation

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Cited by 20 •

2010

In this video and supplemental material, we show a protocol for chronic in vivo imaging of the intact brain using a thinned-skull preparation.

Spectral Confocal Imaging of Fluorescently tagged Nicotinic Receptors in Knock-in Mice with Chronic Nicotine Administration

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Cited by 12 •

2012

We have developed a novel technique of quantifying nicotinic acetylcholine receptor changes within subcellular regions of specific subtypes of CNS neurons to better understand the mechanisms of nicotine addiction by using a combination of approaches including fluorescent protein tagging of the receptor using the knock-in approach and spectral confocal imaging.

Research

JoVE Journal - Neuroscience
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A Thin-skull Window Technique for Chronic Two-photon In vivo Imaging of Murine Microglia in Models of Neuroinflammation

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Cited by 64 •

2010

We describe a method for repeatedly visualizing murine microglia and circulating monocytes in vivo over hours, days or weeks using transcranial two-photon microscopy. We demonstrate how to prepare a thinned-skull window that allows intermittent observation of quiescent microglia that can be activated by adjacent stereotactic injection of the HIV-1 regulatory protein Tat.

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