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Localisation of cannabinoid receptor 1 in rat dorsal root ganglion using in situ hybridisation and immunohistochemistry

In this study we used in situ hybridisation and double-labelling immunohistochemistry to characterise cannabinoid receptor 1 (CB 1) expression in rat lumbar dorsal root ganglion (DRG) neurons. Approximately 25% of DRG neurons expressed CB 1 mRNA and displayed immunoreactivity for CB 1. Sixty-nine pe...

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Bibliographic Details
Published in:Neuroscience 2003-01, Vol.119 (3), p.803-812
Main Authors: Bridges, D, Rice, A.S.C, Egertová, M, Elphick, M.R, Winter, J, Michael, G.J
Format: Article
Language:English
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Summary:In this study we used in situ hybridisation and double-labelling immunohistochemistry to characterise cannabinoid receptor 1 (CB 1) expression in rat lumbar dorsal root ganglion (DRG) neurons. Approximately 25% of DRG neurons expressed CB 1 mRNA and displayed immunoreactivity for CB 1. Sixty-nine percent to 82% of CB 1-expressing cells were also immunoreactive for neurofilament 200, indicative of myelinated A-fibre neurons, which tend to be large- and medium-sized DRG neurons (>600 μm 2). Approximately 10% of CB1-expressing cells also expressed transient receptor potential vanilloid family ion channel 2 (TRPV2), the noxious heat-transducing channel found in medium to large lightly myelinated Aδ-fibre DRG neurons. Seventeen percent to 26% of CB 1-expressing cells co-stained using Isolectin B4, 9–10% for calcitonin gene-related peptide and 11–20% for transient receptor potential vanilloid family ion channel 1 (TRPV1), predominantly markers of small non-myelinated C-fibre DRG neurons (
ISSN:0306-4522
1873-7544
DOI:10.1016/S0306-4522(03)00200-8