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Investigating Migraine-Like Behavior Using Light Aversion in Mice.
Wang, Mengya; Mason, Bianca N; Sowers, Levi P; Kuburas, Adisa; Rea, Brandon J; Russo, Andrew F.
Afiliación
  • Wang M; Department of Neuroscience and Pharmacology, University of Iowa.
  • Mason BN; School of Behavioral and Brain Sciences, University of Texas at Dallas.
  • Sowers LP; Center for the Prevention and Treatment of Visual Loss, Veterans Administration Health Center, Iowa City, IA; Department of Molecular Physiology and Biophysics, University of Iowa.
  • Kuburas A; Department of Molecular Physiology and Biophysics, University of Iowa.
  • Rea BJ; Center for the Prevention and Treatment of Visual Loss, Veterans Administration Health Center, Iowa City, IA; Department of Molecular Physiology and Biophysics, University of Iowa.
  • Russo AF; Center for the Prevention and Treatment of Visual Loss, Veterans Administration Health Center, Iowa City, IA; Department of Molecular Physiology and Biophysics, University of Iowa; Department of Neurology, University of Iowa; andrew-russo@uiowa.edu.
J Vis Exp ; (174)2021 08 11.
Article en En | MEDLINE | ID: mdl-34459825
Migraine is a complex neurological disorder characterized by headache and sensory abnormalities, such as hypersensitivity to light, observed as photophobia. Whilst it is impossible to confirm that a mouse is experiencing migraine, light aversion can be used as a behavioral surrogate for the migraine symptom of photophobia. To test for light aversion, we utilize the light/dark assay to measure the time mice freely choose to spend in either a light or dark environment. The assay has been refined by introducing two critical modifications: pre-exposures to the chamber prior to running the test procedure and adjustable chamber lighting, permitting the use of a range of light intensities from 55 lux to 27,000 lux. Because the choice to spend more time in the dark is also indicative of anxiety, we also utilize a light-independent anxiety test, the open field assay, to distinguish anxiety from light-aversive behavior. Here, we describe a modified test paradigm for the light/dark and open field assays. The application of these assays is described for intraperitoneal injection of calcitonin gene-related peptide (CGRP) in two mouse strains and for optogenetic brain stimulation studies.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trastornos Migrañosos Tipo de estudio: Etiology_studies Idioma: En Revista: J Vis Exp Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trastornos Migrañosos Tipo de estudio: Etiology_studies Idioma: En Revista: J Vis Exp Año: 2021 Tipo del documento: Article