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Antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats

In the brain, propionic acid (PA) can cross cell membranes and accumulate within cells, leading to intracellular acidification, which may alter neurotransmitter release (NT), communication between neurons, and behavior. Such elevation in levels of PA constitutes a neurodevelopmental metabolic disord...

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Autores principales: Al‐Salem, Huda S., Al‐Yousef, Hanan M., Ashour, Abdelkader E., Ahmed, Atallah F., Amina, Musarat, Issa, Iman S., Bhat, Ramesa Shafi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500755/
https://www.ncbi.nlm.nih.gov/pubmed/32994972
http://dx.doi.org/10.1002/fsn3.1813
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author Al‐Salem, Huda S.
Al‐Yousef, Hanan M.
Ashour, Abdelkader E.
Ahmed, Atallah F.
Amina, Musarat
Issa, Iman S.
Bhat, Ramesa Shafi
author_facet Al‐Salem, Huda S.
Al‐Yousef, Hanan M.
Ashour, Abdelkader E.
Ahmed, Atallah F.
Amina, Musarat
Issa, Iman S.
Bhat, Ramesa Shafi
author_sort Al‐Salem, Huda S.
collection PubMed
description In the brain, propionic acid (PA) can cross cell membranes and accumulate within cells, leading to intracellular acidification, which may alter neurotransmitter release (NT), communication between neurons, and behavior. Such elevation in levels of PA constitutes a neurodevelopmental metabolic disorder called propionic acidemia, which could clinically manifest as autism. The purpose of this study was to investigate the protective effects of different fractions of bee pollen (BP) on PA‐induced autism in rats, and to evaluate their effects on the expression of liver and renal biomarkers. Groups of rats received treatments of different fractions of BP at a dose of 250 mg/kg of body weight/day for a period of 1 month. Normal control group I and group II were orally administered with phosphate‐buffered saline and propionic acid, respectively, for 3 days. BP contains various health‐promoting phenolic components. Different fractions of BP administered pre‐ and post‐treatment with PA showed significant reduction in the levels of liver and renal biomarkers (p < .05). Also, a significant enhancement in the levels of glutathione S‐transferase (GST), catalase CAT), and ascorbic acid (VIT C) was observed. Supplementation with BP significantly reduced biochemical changes in the liver, kidneys, and brain of rats with PA‐induced toxicity. It exhibited protective effects against oxidative damage and reactive oxygen species produced by PA‐induced adverse reactions in rats. Taken together, our study shows that BP possesses protective effects in PA‐induced liver and kidney damage.
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spelling pubmed-75007552020-09-28 Antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats Al‐Salem, Huda S. Al‐Yousef, Hanan M. Ashour, Abdelkader E. Ahmed, Atallah F. Amina, Musarat Issa, Iman S. Bhat, Ramesa Shafi Food Sci Nutr Original Research In the brain, propionic acid (PA) can cross cell membranes and accumulate within cells, leading to intracellular acidification, which may alter neurotransmitter release (NT), communication between neurons, and behavior. Such elevation in levels of PA constitutes a neurodevelopmental metabolic disorder called propionic acidemia, which could clinically manifest as autism. The purpose of this study was to investigate the protective effects of different fractions of bee pollen (BP) on PA‐induced autism in rats, and to evaluate their effects on the expression of liver and renal biomarkers. Groups of rats received treatments of different fractions of BP at a dose of 250 mg/kg of body weight/day for a period of 1 month. Normal control group I and group II were orally administered with phosphate‐buffered saline and propionic acid, respectively, for 3 days. BP contains various health‐promoting phenolic components. Different fractions of BP administered pre‐ and post‐treatment with PA showed significant reduction in the levels of liver and renal biomarkers (p < .05). Also, a significant enhancement in the levels of glutathione S‐transferase (GST), catalase CAT), and ascorbic acid (VIT C) was observed. Supplementation with BP significantly reduced biochemical changes in the liver, kidneys, and brain of rats with PA‐induced toxicity. It exhibited protective effects against oxidative damage and reactive oxygen species produced by PA‐induced adverse reactions in rats. Taken together, our study shows that BP possesses protective effects in PA‐induced liver and kidney damage. John Wiley and Sons Inc. 2020-08-14 /pmc/articles/PMC7500755/ /pubmed/32994972 http://dx.doi.org/10.1002/fsn3.1813 Text en © 2020 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Al‐Salem, Huda S.
Al‐Yousef, Hanan M.
Ashour, Abdelkader E.
Ahmed, Atallah F.
Amina, Musarat
Issa, Iman S.
Bhat, Ramesa Shafi
Antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats
title Antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats
title_full Antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats
title_fullStr Antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats
title_full_unstemmed Antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats
title_short Antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats
title_sort antioxidant and hepatorenal protective effects of bee pollen fractions against propionic acid‐induced autistic feature in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500755/
https://www.ncbi.nlm.nih.gov/pubmed/32994972
http://dx.doi.org/10.1002/fsn3.1813
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