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Intermittent Fasting Ameliorated High-Fat Diet-Induced Memory Impairment in Rats via Reducing Oxidative Stress and Glial Fibrillary Acidic Protein Expression in Brain

Intermittent fasting (IF) plays an important role in the protection against metabolic syndrome-induced memory defects. This study aimed to assess the protective effects of both prophylactic and curative IF against high-fat diet (HFD)-induced memory defects in rats. The control group received a norma...

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Autores principales: Hazzaa, Suzan M., Eldaim, Mabrouk A. Abd, Fouda, Amira A., Mohamed, Asmaa Shams El Dein, Soliman, Mohamed Mohamed, Elgizawy, Eman I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822208/
https://www.ncbi.nlm.nih.gov/pubmed/33375195
http://dx.doi.org/10.3390/nu13010010
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author Hazzaa, Suzan M.
Eldaim, Mabrouk A. Abd
Fouda, Amira A.
Mohamed, Asmaa Shams El Dein
Soliman, Mohamed Mohamed
Elgizawy, Eman I.
author_facet Hazzaa, Suzan M.
Eldaim, Mabrouk A. Abd
Fouda, Amira A.
Mohamed, Asmaa Shams El Dein
Soliman, Mohamed Mohamed
Elgizawy, Eman I.
author_sort Hazzaa, Suzan M.
collection PubMed
description Intermittent fasting (IF) plays an important role in the protection against metabolic syndrome-induced memory defects. This study aimed to assess the protective effects of both prophylactic and curative IF against high-fat diet (HFD)-induced memory defects in rats. The control group received a normal diet; the second group received a HFD; the third group was fed a HFD for 12 weeks and subjected to IF during the last four weeks (curative IF); the fourth group was fed a HFD and subjected to IF simultaneously (prophylactic IF). A high-fat diet significantly increased body weight, serum lipids levels, malondialdehyde (MDA) concentration, glial fibrillary acidic protein (GFAP) and H score in brain tissue and altered memory performance. In addition, it significantly decreased reduced glutathione (GSH) concentration in brain tissue and viability and thickness of pyramidal and hippocampus granular cell layers. However, both types of IF significantly decreased body weight, serum lipids, GFAP protein expression and H score and MDA concentration in brain tissue, and improved memory performance, while it significantly increased GSH concentration in brain tissue, viability, and thickness of pyramidal and granular cell layers of the hippocampus. This study indicated that IF ameliorated HFD-induced memory disturbance and brain tissue damage and the prophylactic IF was more potent than curative IF.
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spelling pubmed-78222082021-01-23 Intermittent Fasting Ameliorated High-Fat Diet-Induced Memory Impairment in Rats via Reducing Oxidative Stress and Glial Fibrillary Acidic Protein Expression in Brain Hazzaa, Suzan M. Eldaim, Mabrouk A. Abd Fouda, Amira A. Mohamed, Asmaa Shams El Dein Soliman, Mohamed Mohamed Elgizawy, Eman I. Nutrients Article Intermittent fasting (IF) plays an important role in the protection against metabolic syndrome-induced memory defects. This study aimed to assess the protective effects of both prophylactic and curative IF against high-fat diet (HFD)-induced memory defects in rats. The control group received a normal diet; the second group received a HFD; the third group was fed a HFD for 12 weeks and subjected to IF during the last four weeks (curative IF); the fourth group was fed a HFD and subjected to IF simultaneously (prophylactic IF). A high-fat diet significantly increased body weight, serum lipids levels, malondialdehyde (MDA) concentration, glial fibrillary acidic protein (GFAP) and H score in brain tissue and altered memory performance. In addition, it significantly decreased reduced glutathione (GSH) concentration in brain tissue and viability and thickness of pyramidal and hippocampus granular cell layers. However, both types of IF significantly decreased body weight, serum lipids, GFAP protein expression and H score and MDA concentration in brain tissue, and improved memory performance, while it significantly increased GSH concentration in brain tissue, viability, and thickness of pyramidal and granular cell layers of the hippocampus. This study indicated that IF ameliorated HFD-induced memory disturbance and brain tissue damage and the prophylactic IF was more potent than curative IF. MDPI 2020-12-22 /pmc/articles/PMC7822208/ /pubmed/33375195 http://dx.doi.org/10.3390/nu13010010 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hazzaa, Suzan M.
Eldaim, Mabrouk A. Abd
Fouda, Amira A.
Mohamed, Asmaa Shams El Dein
Soliman, Mohamed Mohamed
Elgizawy, Eman I.
Intermittent Fasting Ameliorated High-Fat Diet-Induced Memory Impairment in Rats via Reducing Oxidative Stress and Glial Fibrillary Acidic Protein Expression in Brain
title Intermittent Fasting Ameliorated High-Fat Diet-Induced Memory Impairment in Rats via Reducing Oxidative Stress and Glial Fibrillary Acidic Protein Expression in Brain
title_full Intermittent Fasting Ameliorated High-Fat Diet-Induced Memory Impairment in Rats via Reducing Oxidative Stress and Glial Fibrillary Acidic Protein Expression in Brain
title_fullStr Intermittent Fasting Ameliorated High-Fat Diet-Induced Memory Impairment in Rats via Reducing Oxidative Stress and Glial Fibrillary Acidic Protein Expression in Brain
title_full_unstemmed Intermittent Fasting Ameliorated High-Fat Diet-Induced Memory Impairment in Rats via Reducing Oxidative Stress and Glial Fibrillary Acidic Protein Expression in Brain
title_short Intermittent Fasting Ameliorated High-Fat Diet-Induced Memory Impairment in Rats via Reducing Oxidative Stress and Glial Fibrillary Acidic Protein Expression in Brain
title_sort intermittent fasting ameliorated high-fat diet-induced memory impairment in rats via reducing oxidative stress and glial fibrillary acidic protein expression in brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822208/
https://www.ncbi.nlm.nih.gov/pubmed/33375195
http://dx.doi.org/10.3390/nu13010010
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