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Riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat

Tartrazine is a synthetic yellowish dye considered one of the most common food colorants. Extensive usage of tartrazine in humans led to harmful health impacts. To investigate the impact of tartrazine administration on the cerebellum and to assess the potential role of riboflavin co-administration i...

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Autores principales: Ismail, Omnia I., Rashed, Noha A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652251/
https://www.ncbi.nlm.nih.gov/pubmed/36369258
http://dx.doi.org/10.1038/s41598-022-23894-3
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author Ismail, Omnia I.
Rashed, Noha A.
author_facet Ismail, Omnia I.
Rashed, Noha A.
author_sort Ismail, Omnia I.
collection PubMed
description Tartrazine is a synthetic yellowish dye considered one of the most common food colorants. Extensive usage of tartrazine in humans led to harmful health impacts. To investigate the impact of tartrazine administration on the cerebellum and to assess the potential role of riboflavin co-administration in the adult male albino rat. Four groups of adult albino rats were included in this study. Group I was supplied with distilled water. Group II was supplied tartrazine orally at a dose of 7.5 mg/kg BW dissolved in distilled water. Group III was supplied with tartrazine at the same previously mentioned dose and riboflavin orally at a dose of 25 mg/kg BW dissolved in distilled water. Group IV was supplied with riboflavin at the same previously mentioned dose. The study was conducted for 30 days then rats were sacrificed, weighted and the cerebella extracted and handled for light, ultrastructural and immunohistochemical evaluation. It was found with tartrazine treatment focal areas of Purkinje cell loss leaving empty spaces, a broad spread of neuronal affection to the degree of the disappearance of some of the granular cells, reduced the thickness of the molecular and granular layers, and strong positive GFAP immunoreactions. With riboflavin coadministration restored continuous Purkinje layer with normal appeared Purkinje cells, but some cells were still shrunken and vacuolated as well as the molecular and granular cell layers appeared normal. Tartrazine had deleterious effects on the cerebellar cytoarchitecture, and riboflavin co-administration alleviated these neurotoxic effects.
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spelling pubmed-96522512022-11-15 Riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat Ismail, Omnia I. Rashed, Noha A. Sci Rep Article Tartrazine is a synthetic yellowish dye considered one of the most common food colorants. Extensive usage of tartrazine in humans led to harmful health impacts. To investigate the impact of tartrazine administration on the cerebellum and to assess the potential role of riboflavin co-administration in the adult male albino rat. Four groups of adult albino rats were included in this study. Group I was supplied with distilled water. Group II was supplied tartrazine orally at a dose of 7.5 mg/kg BW dissolved in distilled water. Group III was supplied with tartrazine at the same previously mentioned dose and riboflavin orally at a dose of 25 mg/kg BW dissolved in distilled water. Group IV was supplied with riboflavin at the same previously mentioned dose. The study was conducted for 30 days then rats were sacrificed, weighted and the cerebella extracted and handled for light, ultrastructural and immunohistochemical evaluation. It was found with tartrazine treatment focal areas of Purkinje cell loss leaving empty spaces, a broad spread of neuronal affection to the degree of the disappearance of some of the granular cells, reduced the thickness of the molecular and granular layers, and strong positive GFAP immunoreactions. With riboflavin coadministration restored continuous Purkinje layer with normal appeared Purkinje cells, but some cells were still shrunken and vacuolated as well as the molecular and granular cell layers appeared normal. Tartrazine had deleterious effects on the cerebellar cytoarchitecture, and riboflavin co-administration alleviated these neurotoxic effects. Nature Publishing Group UK 2022-11-11 /pmc/articles/PMC9652251/ /pubmed/36369258 http://dx.doi.org/10.1038/s41598-022-23894-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Ismail, Omnia I.
Rashed, Noha A.
Riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat
title Riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat
title_full Riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat
title_fullStr Riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat
title_full_unstemmed Riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat
title_short Riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat
title_sort riboflavin attenuates tartrazine toxicity in the cerebellar cortex of adult albino rat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652251/
https://www.ncbi.nlm.nih.gov/pubmed/36369258
http://dx.doi.org/10.1038/s41598-022-23894-3
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