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GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome

Wolfram syndrome (WS) is a rare neurodegenerative disorder that is mainly characterized by diabetes mellitus, optic nerve atrophy, deafness, and progressive brainstem degeneration. Treatment with GLP-1 receptor agonists has shown a promising anti-diabetic effect in WS treatment in both animal models...

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Autores principales: Seppa, Kadri, Toots, Maarja, Reimets, Riin, Jagomäe, Toomas, Koppel, Tuuliki, Pallase, Maia, Hasselholt, Stine, Krogsbæk Mikkelsen, Maiken, Randel Nyengaard, Jens, Vasar, Eero, Terasmaa, Anton, Plaas, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823542/
https://www.ncbi.nlm.nih.gov/pubmed/31673100
http://dx.doi.org/10.1038/s41598-019-52295-2
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author Seppa, Kadri
Toots, Maarja
Reimets, Riin
Jagomäe, Toomas
Koppel, Tuuliki
Pallase, Maia
Hasselholt, Stine
Krogsbæk Mikkelsen, Maiken
Randel Nyengaard, Jens
Vasar, Eero
Terasmaa, Anton
Plaas, Mario
author_facet Seppa, Kadri
Toots, Maarja
Reimets, Riin
Jagomäe, Toomas
Koppel, Tuuliki
Pallase, Maia
Hasselholt, Stine
Krogsbæk Mikkelsen, Maiken
Randel Nyengaard, Jens
Vasar, Eero
Terasmaa, Anton
Plaas, Mario
author_sort Seppa, Kadri
collection PubMed
description Wolfram syndrome (WS) is a rare neurodegenerative disorder that is mainly characterized by diabetes mellitus, optic nerve atrophy, deafness, and progressive brainstem degeneration. Treatment with GLP-1 receptor agonists has shown a promising anti-diabetic effect in WS treatment in both animal models and in human patients. Since previous research has tended to focus on investigation of the WS first symptom, diabetes mellitus, the aim of the present study was to examine liraglutide effect on WS-associated neurodegeneration. We took 9-month-old Wfs1 knock-out (KO) animals that already had developed glucose intolerance and treated them with liraglutide for 6 months. Our research results indicate that 6-month liraglutide treatment reduced neuroinflammation and ameliorated endoplasmic reticulum (ER) stress in the inferior olive of the aged WS rat model. Liraglutide treatment also protected retinal ganglion cells from cell death and optic nerve axons from degeneration. According to this, the results of the present study provide novel insight that GLP-1 receptor agonist liraglutide has a neuroprotective effect in the WS rat model.
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spelling pubmed-68235422019-11-12 GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome Seppa, Kadri Toots, Maarja Reimets, Riin Jagomäe, Toomas Koppel, Tuuliki Pallase, Maia Hasselholt, Stine Krogsbæk Mikkelsen, Maiken Randel Nyengaard, Jens Vasar, Eero Terasmaa, Anton Plaas, Mario Sci Rep Article Wolfram syndrome (WS) is a rare neurodegenerative disorder that is mainly characterized by diabetes mellitus, optic nerve atrophy, deafness, and progressive brainstem degeneration. Treatment with GLP-1 receptor agonists has shown a promising anti-diabetic effect in WS treatment in both animal models and in human patients. Since previous research has tended to focus on investigation of the WS first symptom, diabetes mellitus, the aim of the present study was to examine liraglutide effect on WS-associated neurodegeneration. We took 9-month-old Wfs1 knock-out (KO) animals that already had developed glucose intolerance and treated them with liraglutide for 6 months. Our research results indicate that 6-month liraglutide treatment reduced neuroinflammation and ameliorated endoplasmic reticulum (ER) stress in the inferior olive of the aged WS rat model. Liraglutide treatment also protected retinal ganglion cells from cell death and optic nerve axons from degeneration. According to this, the results of the present study provide novel insight that GLP-1 receptor agonist liraglutide has a neuroprotective effect in the WS rat model. Nature Publishing Group UK 2019-10-31 /pmc/articles/PMC6823542/ /pubmed/31673100 http://dx.doi.org/10.1038/s41598-019-52295-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Seppa, Kadri
Toots, Maarja
Reimets, Riin
Jagomäe, Toomas
Koppel, Tuuliki
Pallase, Maia
Hasselholt, Stine
Krogsbæk Mikkelsen, Maiken
Randel Nyengaard, Jens
Vasar, Eero
Terasmaa, Anton
Plaas, Mario
GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome
title GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome
title_full GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome
title_fullStr GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome
title_full_unstemmed GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome
title_short GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome
title_sort glp-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of wolfram syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823542/
https://www.ncbi.nlm.nih.gov/pubmed/31673100
http://dx.doi.org/10.1038/s41598-019-52295-2
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