Short-term high-fat feeding exacerbates degeneration in retinitis pigmentosa by promoting retinal oxidative stress and inflammation

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Title: Short-term high-fat feeding exacerbates degeneration in retinitis pigmentosa by promoting retinal oxidative stress and inflammation
Authors: Kutsyr, Oksana | Noailles, Agustina | Martínez Gil, Natalia | Maestre-Carballa, Lucia | Martinez-Garcia, Manuel | Maneu, Victoria | Cuenca, Nicolás | Lax, Pedro
Research Group/s: Neurobiología del Sistema Visual y Terapia de Enfermedades Neurodegenerativas (NEUROVIS) | Ecología Microbiana Molecular
Center, Department or Service: Universidad de Alicante. Departamento de Fisiología, Genética y Microbiología | Universidad de Alicante. Departamento de Óptica, Farmacología y Anatomía
Keywords: Retinal degeneration | Neurodegeneration | Cell death | Gut microbiome
Knowledge Area: Biología Celular | Fisiología | Microbiología | Farmacología
Issue Date: 19-Oct-2021
Publisher: National Academy of Sciences
Citation: PNAS. 2021, 118(43): e2100566118. https://doi.org/10.1073/pnas.2100566118
Abstract: A high-fat diet (HFD) can induce hyperglycemia and metabolic syndromes that, in turn, can trigger visual impairment. To evaluate the acute effects of HFD feeding on retinal degeneration, we assessed retinal function and morphology, inflammatory state, oxidative stress, and gut microbiome in dystrophic retinal degeneration 10 (rd10) mice, a model of retinitis pigmentosa, fed an HFD for 2 to 3 wk. Short-term HFD feeding impaired retinal responsiveness and visual acuity and enhanced photoreceptor degeneration, microglial cell activation, and Müller cell gliosis. HFD consumption also triggered the expression of inflammatory and oxidative markers in rd10 retinas. Finally, an HFD caused gut microbiome dysbiosis, increasing the abundance of potentially proinflammatory bacteria. Thus, HFD feeding drives the pathological processes of retinal degeneration by promoting oxidative stress and activating inflammatory-related pathways. Our findings suggest that consumption of an HFD could accelerate the progression of the disease in patients with retinal degenerative disorders.
Sponsor: This work was supported by grants from the Spanish Ministry of the Economy and Competitiveness (RTI2018-094248-B-I00), Spanish Ministry of Science and Innovation cofinanced by European Regional Development Fund (MICINN-FEDER PID2019-106230RB-I00), Instituto de Salud Carlos III co-financed by European Regional Development Fund (RETICS-FEDER-RD16/0008/0016), Asociación Retina Asturias (ASOCIACIONRETINA1-20I), Federación de Asociaciones de Retinosis Pigmentaria de España and Fundación Lucha Contra la Ceguera (FUNDALUCE18-01), and Generalitat Valenciana (PROMETEO/2021/024, IDIFEDER/2017/064).
URI: http://hdl.handle.net/10045/118819
ISSN: 0027-8424 (Print) | 1091-6490 (Online)
DOI: 10.1073/pnas.2100566118
Language: eng
Type: info:eu-repo/semantics/article
Rights: © 2021 National Academy of Sciences
Peer Review: si
Publisher version: https://doi.org/10.1073/pnas.2100566118
Appears in Collections:INV - EMM - Artículos de Revistas
INV - NEUROVIS - Artículos de Revistas

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