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Omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice

OBJECTIVE: Diabetic retinopathy (DR) is associated with hyperglycemia-driven microvascular pathology and neuronal compromise in the retina. However, DR is also linked to dyslipidemia. As omega-3 (ω-3) polyunsaturated fatty acids (PUFAs) are protective in proliferative retinopathy, we investigated th...

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Autores principales: Sapieha, P, Chen, J, Stahl, A, Seaward, M R, Favazza, T L, Juan, A M, Hatton, C J, Joyal, J-S, Krah, N M, Dennison, R J, Tang, J, Kern, T S, Akula, J D, Smith, L E H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408641/
https://www.ncbi.nlm.nih.gov/pubmed/23448719
http://dx.doi.org/10.1038/nutd.2012.10
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author Sapieha, P
Chen, J
Stahl, A
Seaward, M R
Favazza, T L
Juan, A M
Hatton, C J
Joyal, J-S
Krah, N M
Dennison, R J
Tang, J
Kern, T S
Akula, J D
Smith, L E H
author_facet Sapieha, P
Chen, J
Stahl, A
Seaward, M R
Favazza, T L
Juan, A M
Hatton, C J
Joyal, J-S
Krah, N M
Dennison, R J
Tang, J
Kern, T S
Akula, J D
Smith, L E H
author_sort Sapieha, P
collection PubMed
description OBJECTIVE: Diabetic retinopathy (DR) is associated with hyperglycemia-driven microvascular pathology and neuronal compromise in the retina. However, DR is also linked to dyslipidemia. As omega-3 (ω-3) polyunsaturated fatty acids (PUFAs) are protective in proliferative retinopathy, we investigated the capacity of ω-3PUFAs to preserve retinal function in a mouse model of type 2 diabetes mellitus (T2DM). DESIGN: Male leptin-receptor-deficient (db/db) mice were maintained for 22 weeks (4 weeks–26 weeks of life) on calorically and compositionally matched diets, except for 2% enrichment in either ω-3 or ω-6PUFAs. Visual function was assessed at 9, 14 and 26 weeks by electroretinography. Retinal capillary and neuronal integrity, as well as glucose challenge responses, were assessed on each diet. RESULTS: The ω-3PUFA diet significantly preserved retinal function in the mouse model of T2DM to levels similar to those observed in nondiabetic control mice on normal chow. Conversely, retinal function gradually deteriorated in db/db mice on a ω-6PUFA-rich diet. There was also an enhanced ability of ω-3PUFA-fed mice to respond to glucose challenge. The protection of visual function appeared to be independent of cytoprotective or anti-inflammatory effects of ω-3PUFAs. CONCLUSION: This study identifies beneficial effects of dietary ω-3PUFAs on visual function in T2DM. The data are consistent with dyslipidemia negatively impacting retinal function. As ω-3PUFA lipid dietary interventions are readily available, safe and inexpensive, increasing ω-3PUFA intake in diabetic patients may slow the progression of vision loss in T2DM.
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spelling pubmed-34086412012-07-31 Omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice Sapieha, P Chen, J Stahl, A Seaward, M R Favazza, T L Juan, A M Hatton, C J Joyal, J-S Krah, N M Dennison, R J Tang, J Kern, T S Akula, J D Smith, L E H Nutr Diabetes Original Article OBJECTIVE: Diabetic retinopathy (DR) is associated with hyperglycemia-driven microvascular pathology and neuronal compromise in the retina. However, DR is also linked to dyslipidemia. As omega-3 (ω-3) polyunsaturated fatty acids (PUFAs) are protective in proliferative retinopathy, we investigated the capacity of ω-3PUFAs to preserve retinal function in a mouse model of type 2 diabetes mellitus (T2DM). DESIGN: Male leptin-receptor-deficient (db/db) mice were maintained for 22 weeks (4 weeks–26 weeks of life) on calorically and compositionally matched diets, except for 2% enrichment in either ω-3 or ω-6PUFAs. Visual function was assessed at 9, 14 and 26 weeks by electroretinography. Retinal capillary and neuronal integrity, as well as glucose challenge responses, were assessed on each diet. RESULTS: The ω-3PUFA diet significantly preserved retinal function in the mouse model of T2DM to levels similar to those observed in nondiabetic control mice on normal chow. Conversely, retinal function gradually deteriorated in db/db mice on a ω-6PUFA-rich diet. There was also an enhanced ability of ω-3PUFA-fed mice to respond to glucose challenge. The protection of visual function appeared to be independent of cytoprotective or anti-inflammatory effects of ω-3PUFAs. CONCLUSION: This study identifies beneficial effects of dietary ω-3PUFAs on visual function in T2DM. The data are consistent with dyslipidemia negatively impacting retinal function. As ω-3PUFA lipid dietary interventions are readily available, safe and inexpensive, increasing ω-3PUFA intake in diabetic patients may slow the progression of vision loss in T2DM. Nature Publishing Group 2012-07 2012-07-23 /pmc/articles/PMC3408641/ /pubmed/23448719 http://dx.doi.org/10.1038/nutd.2012.10 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Sapieha, P
Chen, J
Stahl, A
Seaward, M R
Favazza, T L
Juan, A M
Hatton, C J
Joyal, J-S
Krah, N M
Dennison, R J
Tang, J
Kern, T S
Akula, J D
Smith, L E H
Omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice
title Omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice
title_full Omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice
title_fullStr Omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice
title_full_unstemmed Omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice
title_short Omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice
title_sort omega-3 polyunsaturated fatty acids preserve retinal function in type 2 diabetic mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408641/
https://www.ncbi.nlm.nih.gov/pubmed/23448719
http://dx.doi.org/10.1038/nutd.2012.10
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