Abstract
In vivo imaging has revolutionized our understanding of biological processes in brain physiology and pathology. However, breathing-induced movement artifacts have impeded the application of this powerful tool in studies of the living spinal cord. Here we describe in detail a method to image stably and repetitively, using two-photon microscopy, the living spinal tissue in mice with dense fluorescent cells or axons, without the need for animal intubation or image post-processing. This simplified technique can greatly expand the application of in vivo imaging to study spinal cord injury, regeneration, physiology and disease.
MeSH Terms
Acepromazine/pharmacology
Anesthesia/methods
Anesthetics/pharmacology
Animals
Axons/physiology,ultrastructure
Capillaries/cytology,physiology
Cell Movement/physiology
Green Fluorescent Proteins/genetics
Image Processing, Computer-Assisted/methods
Ketamine/pharmacology
Laminectomy/methods
Mice
Mice, Transgenic
Microcirculation/cytology,physiology
Microglia/cytology,physiology
Microscopy, Confocal/methods
Neurosurgical Procedures/methods
Respiratory Physiological Phenomena/drug effects
Spinal Cord/blood supply,cytology
Staining and Labeling/methods
Stereotaxic Techniques/instrumentation
Urethane/pharmacology
Xylazine/pharmacology
Chemicals
Anesthetics
Green Fluorescent Proteins
Xylazine
Urethane
Acepromazine
Ketamine
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Davalos Dimitrios
Department of Pharmacology, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA. davalos@ucsd.edu
Lee Jae K
Smith W Bryan
Brinkman Brendan
Ellisman Mark H
Zheng Binhai
Akassoglou Katerina
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