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Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy

BACKGROUND: Diabetic neuropathy is a complication of diabetes mellitus that develops in about 50% of people with diabetes. Despite its widespread occurrence and devastating effects, this complication is still not fully understood, and there is no treatment available to prevent its development. METHO...

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Autores principales: Peeraer, Eve, Van Lutsenborg, An, Verheyen, An, De Jongh, Raf, Nuydens, Rony, Meert, Theo F
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085264/
https://www.ncbi.nlm.nih.gov/pubmed/21559351
http://dx.doi.org/10.2147/JPR.S15452
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author Peeraer, Eve
Van Lutsenborg, An
Verheyen, An
De Jongh, Raf
Nuydens, Rony
Meert, Theo F
author_facet Peeraer, Eve
Van Lutsenborg, An
Verheyen, An
De Jongh, Raf
Nuydens, Rony
Meert, Theo F
author_sort Peeraer, Eve
collection PubMed
description BACKGROUND: Diabetic neuropathy is a complication of diabetes mellitus that develops in about 50% of people with diabetes. Despite its widespread occurrence and devastating effects, this complication is still not fully understood, and there is no treatment available to prevent its development. METHODS: In this study, immunocytochemistry for activating transcription factor 3, a marker for cell injury, was used to investigate the stress response in dorsal root ganglion neurons in both in vitro and ex vivo models of diabetic neuropathy. RESULTS: Our findings showed increased activating transcription factor 3 expression in hyperglycemic culture conditions and in dorsal root ganglion neurons isolated from diabetic rats. Glial cell line-derived neurotrophic factor, a substance with known neuroprotective properties, was able to reduce diabetes mellitus-induced neuronal stress in vitro, while gabapentin and carbamazepine, currently used to treat neuropathic pain, showed only limited effects. CONCLUSION: Growth factors may have a therapeutic benefit as neurotrophic agents in the treatment of diabetic peripheral neuropathy, but gabapentin and carbamazepine have no direct protective effect on sensory neurons. This research also indicates that immunocytochemistry for activating transcription factor 3 is a valuable tool for evaluation of pharmacological substances in dorsal root ganglion cultures.
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spelling pubmed-30852642011-05-10 Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy Peeraer, Eve Van Lutsenborg, An Verheyen, An De Jongh, Raf Nuydens, Rony Meert, Theo F J Pain Res Original Research BACKGROUND: Diabetic neuropathy is a complication of diabetes mellitus that develops in about 50% of people with diabetes. Despite its widespread occurrence and devastating effects, this complication is still not fully understood, and there is no treatment available to prevent its development. METHODS: In this study, immunocytochemistry for activating transcription factor 3, a marker for cell injury, was used to investigate the stress response in dorsal root ganglion neurons in both in vitro and ex vivo models of diabetic neuropathy. RESULTS: Our findings showed increased activating transcription factor 3 expression in hyperglycemic culture conditions and in dorsal root ganglion neurons isolated from diabetic rats. Glial cell line-derived neurotrophic factor, a substance with known neuroprotective properties, was able to reduce diabetes mellitus-induced neuronal stress in vitro, while gabapentin and carbamazepine, currently used to treat neuropathic pain, showed only limited effects. CONCLUSION: Growth factors may have a therapeutic benefit as neurotrophic agents in the treatment of diabetic peripheral neuropathy, but gabapentin and carbamazepine have no direct protective effect on sensory neurons. This research also indicates that immunocytochemistry for activating transcription factor 3 is a valuable tool for evaluation of pharmacological substances in dorsal root ganglion cultures. Dove Medical Press 2011-02-14 /pmc/articles/PMC3085264/ /pubmed/21559351 http://dx.doi.org/10.2147/JPR.S15452 Text en © 2011 Peeraer et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Peeraer, Eve
Van Lutsenborg, An
Verheyen, An
De Jongh, Raf
Nuydens, Rony
Meert, Theo F
Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy
title Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy
title_full Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy
title_fullStr Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy
title_full_unstemmed Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy
title_short Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy
title_sort pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085264/
https://www.ncbi.nlm.nih.gov/pubmed/21559351
http://dx.doi.org/10.2147/JPR.S15452
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