Membrane potential dye imaging of ventromedial hypothalamus neurons from adult mice to study glucose sensing

Studies of neuronal activity are often performed using neurons from rodents less than 2 months of age due to the technical difficulties associated with increasing connective tissue and decreased neuronal viability that occur with age. Here, we describe a methodology for the dissociation of healthy h...

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Bibliographic Details
Published inJournal of visualized experiments Vol. 81; no. 81; pp. 1 - 9
Main Authors Vazirani, Reema P, Fioramonti, Xavier, Routh, Vanessa H
Format Journal Article
LanguageEnglish
Published United States JoVE 2013
MyJove Corporation
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Summary:Studies of neuronal activity are often performed using neurons from rodents less than 2 months of age due to the technical difficulties associated with increasing connective tissue and decreased neuronal viability that occur with age. Here, we describe a methodology for the dissociation of healthy hypothalamic neurons from adult-aged mice. The ability to study neurons from adult-aged mice allows the use of disease models that manifest at a later age and might be more developmentally accurate for certain studies. Fluorescence imaging of dissociated neurons can be used to study the activity of a population of neurons, as opposed to using electrophysiology to study a single neuron. This is particularly useful when studying a heterogeneous neuronal population in which the desired neuronal type is rare such as for hypothalamic glucose sensing neurons. We utilized membrane potential dye imaging of adult ventromedial hypothalamic neurons to study their responses to changes in extracellular glucose. Glucose sensing neurons are believed to play a role in central regulation of energy balance. The ability to study glucose sensing in adult rodents is particularly useful since the predominance of diseases related to dysfunctional energy balance (e.g. obesity) increase with age.
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PMCID: PMC3992114
Correspondence to: Vanessa H. Routh at routhvh@umdnj.edu
ISSN:1940-087X
1940-087X
DOI:10.3791/50861