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Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke
BACKGROUND: Post-stroke functional recovery is severely impaired by type 2 diabetes (T2D). This is an important clinical problem since T2D is one of the most common diseases. Because weight loss-based strategies have been shown to decrease stroke risk in people with T2D, we aimed to investigate whet...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697500/ https://www.ncbi.nlm.nih.gov/pubmed/34937562 http://dx.doi.org/10.1186/s12933-021-01426-z |
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author | Karampatsi, Dimitra Zabala, Alexander Wilhelmsson, Ulrika Dekens, Doortje Vercalsteren, Ellen Larsson, Martin Nyström, Thomas Pekny, Milos Patrone, Cesare Darsalia, Vladimer |
author_facet | Karampatsi, Dimitra Zabala, Alexander Wilhelmsson, Ulrika Dekens, Doortje Vercalsteren, Ellen Larsson, Martin Nyström, Thomas Pekny, Milos Patrone, Cesare Darsalia, Vladimer |
author_sort | Karampatsi, Dimitra |
collection | PubMed |
description | BACKGROUND: Post-stroke functional recovery is severely impaired by type 2 diabetes (T2D). This is an important clinical problem since T2D is one of the most common diseases. Because weight loss-based strategies have been shown to decrease stroke risk in people with T2D, we aimed to investigate whether diet-induced weight loss can also improve post-stroke functional recovery and identify some of the underlying mechanisms. METHODS: T2D/obesity was induced by 6 months of high-fat diet (HFD). Weight loss was achieved by a short- or long-term dietary change, replacing HFD with standard diet for 2 or 4 months, respectively. Stroke was induced by middle cerebral artery occlusion and post-stroke recovery was assessed by sensorimotor tests. Mechanisms involved in neurovascular damage in the post-stroke recovery phase, i.e. neuroinflammation, impaired angiogenesis and cellular atrophy of GABAergic parvalbumin (PV)+ interneurons were assessed by immunohistochemistry/quantitative microscopy. RESULTS: Both short- and long-term dietary change led to similar weight loss. However, only the latter enhanced functional recovery after stroke. This effect was associated with pre-stroke normalization of fasting glucose and insulin resistance, and with the reduction of T2D-induced cellular atrophy of PV+ interneurons. Moreover, stroke recovery was associated with decreased T2D-induced neuroinflammation and reduced astrocyte reactivity in the contralateral striatum. CONCLUSION: The global diabetes epidemic will dramatically increase the number of people in need of post-stroke treatment and care. Our results suggest that diet-induced weight loss leading to pre-stroke normalization of glucose metabolism has great potential to reduce the sequelae of stroke in the diabetic population. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12933-021-01426-z. |
format | Online Article Text |
id | pubmed-8697500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86975002022-01-05 Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke Karampatsi, Dimitra Zabala, Alexander Wilhelmsson, Ulrika Dekens, Doortje Vercalsteren, Ellen Larsson, Martin Nyström, Thomas Pekny, Milos Patrone, Cesare Darsalia, Vladimer Cardiovasc Diabetol Original Investigation BACKGROUND: Post-stroke functional recovery is severely impaired by type 2 diabetes (T2D). This is an important clinical problem since T2D is one of the most common diseases. Because weight loss-based strategies have been shown to decrease stroke risk in people with T2D, we aimed to investigate whether diet-induced weight loss can also improve post-stroke functional recovery and identify some of the underlying mechanisms. METHODS: T2D/obesity was induced by 6 months of high-fat diet (HFD). Weight loss was achieved by a short- or long-term dietary change, replacing HFD with standard diet for 2 or 4 months, respectively. Stroke was induced by middle cerebral artery occlusion and post-stroke recovery was assessed by sensorimotor tests. Mechanisms involved in neurovascular damage in the post-stroke recovery phase, i.e. neuroinflammation, impaired angiogenesis and cellular atrophy of GABAergic parvalbumin (PV)+ interneurons were assessed by immunohistochemistry/quantitative microscopy. RESULTS: Both short- and long-term dietary change led to similar weight loss. However, only the latter enhanced functional recovery after stroke. This effect was associated with pre-stroke normalization of fasting glucose and insulin resistance, and with the reduction of T2D-induced cellular atrophy of PV+ interneurons. Moreover, stroke recovery was associated with decreased T2D-induced neuroinflammation and reduced astrocyte reactivity in the contralateral striatum. CONCLUSION: The global diabetes epidemic will dramatically increase the number of people in need of post-stroke treatment and care. Our results suggest that diet-induced weight loss leading to pre-stroke normalization of glucose metabolism has great potential to reduce the sequelae of stroke in the diabetic population. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12933-021-01426-z. BioMed Central 2021-12-22 /pmc/articles/PMC8697500/ /pubmed/34937562 http://dx.doi.org/10.1186/s12933-021-01426-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Original Investigation Karampatsi, Dimitra Zabala, Alexander Wilhelmsson, Ulrika Dekens, Doortje Vercalsteren, Ellen Larsson, Martin Nyström, Thomas Pekny, Milos Patrone, Cesare Darsalia, Vladimer Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke |
title | Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke |
title_full | Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke |
title_fullStr | Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke |
title_full_unstemmed | Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke |
title_short | Diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke |
title_sort | diet-induced weight loss in obese/diabetic mice normalizes glucose metabolism and promotes functional recovery after stroke |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697500/ https://www.ncbi.nlm.nih.gov/pubmed/34937562 http://dx.doi.org/10.1186/s12933-021-01426-z |
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