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Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis

Toxoplasmosis is a serious health problem in humans and animals resulting from obligatory intracellular invasion of reticuloendothelial tissue by Toxoplasma gondii. The profound pathologic effect of toxoplasmosis is confined to nervous tissue, but many other organs, including the liver and spleen, a...

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Autores principales: Yahia, Samah Hassan, Etewa, Samia Elsayed, Saleh, Nesreen Saeed, Mohammad, Samira Metwally, Aboulfotouh, Nora Ibrahim, Kandil, Ahmad Mansour, Sarhan, Mohamed Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225867/
https://www.ncbi.nlm.nih.gov/pubmed/35755604
http://dx.doi.org/10.1155/2022/2165205
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author Yahia, Samah Hassan
Etewa, Samia Elsayed
Saleh, Nesreen Saeed
Mohammad, Samira Metwally
Aboulfotouh, Nora Ibrahim
Kandil, Ahmad Mansour
Sarhan, Mohamed Hassan
author_facet Yahia, Samah Hassan
Etewa, Samia Elsayed
Saleh, Nesreen Saeed
Mohammad, Samira Metwally
Aboulfotouh, Nora Ibrahim
Kandil, Ahmad Mansour
Sarhan, Mohamed Hassan
author_sort Yahia, Samah Hassan
collection PubMed
description Toxoplasmosis is a serious health problem in humans and animals resulting from obligatory intracellular invasion of reticuloendothelial tissue by Toxoplasma gondii. The profound pathologic effect of toxoplasmosis is confined to nervous tissue, but many other organs, including the liver and spleen, are insulted. Many molecules like caspase-3, CD3, and CD138 are implicated in the tissue immune response in a trial to alleviate hazardous toxoplasmosis impact. This study aimed to investigate the effect of chronic toxoplasmosis on the liver and spleen tissues of mice using biochemical and histopathological techniques and to detect the activity and level of expression of caspase-3, CD3, and CD138 in these tissues using immunohistochemical labeling. Compared with normal control, altered normal histological features accompanied by inflammatory reaction were recorded in hepatosplenic reticuloendothelial tissues in chronically infected mice. The biochemical profile of the liver has been changed in the form of increased liver enzymes, and oxidative stress has been evidenced by elevated nitric oxide (NO) concentration in liver homogenate. The levels of caspase3, CD3, and CD138 were markedly expressed in the liver and spleen of infected mice. Our findings revealed the persistent effect of latent toxoplasmosis on the host's histological architecture, metabolic, and immunological profile, creating a continued challenging host-parasite relationship.
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spelling pubmed-92258672022-06-24 Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis Yahia, Samah Hassan Etewa, Samia Elsayed Saleh, Nesreen Saeed Mohammad, Samira Metwally Aboulfotouh, Nora Ibrahim Kandil, Ahmad Mansour Sarhan, Mohamed Hassan J Parasitol Res Research Article Toxoplasmosis is a serious health problem in humans and animals resulting from obligatory intracellular invasion of reticuloendothelial tissue by Toxoplasma gondii. The profound pathologic effect of toxoplasmosis is confined to nervous tissue, but many other organs, including the liver and spleen, are insulted. Many molecules like caspase-3, CD3, and CD138 are implicated in the tissue immune response in a trial to alleviate hazardous toxoplasmosis impact. This study aimed to investigate the effect of chronic toxoplasmosis on the liver and spleen tissues of mice using biochemical and histopathological techniques and to detect the activity and level of expression of caspase-3, CD3, and CD138 in these tissues using immunohistochemical labeling. Compared with normal control, altered normal histological features accompanied by inflammatory reaction were recorded in hepatosplenic reticuloendothelial tissues in chronically infected mice. The biochemical profile of the liver has been changed in the form of increased liver enzymes, and oxidative stress has been evidenced by elevated nitric oxide (NO) concentration in liver homogenate. The levels of caspase3, CD3, and CD138 were markedly expressed in the liver and spleen of infected mice. Our findings revealed the persistent effect of latent toxoplasmosis on the host's histological architecture, metabolic, and immunological profile, creating a continued challenging host-parasite relationship. Hindawi 2022-06-16 /pmc/articles/PMC9225867/ /pubmed/35755604 http://dx.doi.org/10.1155/2022/2165205 Text en Copyright © 2022 Samah Hassan Yahia et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yahia, Samah Hassan
Etewa, Samia Elsayed
Saleh, Nesreen Saeed
Mohammad, Samira Metwally
Aboulfotouh, Nora Ibrahim
Kandil, Ahmad Mansour
Sarhan, Mohamed Hassan
Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis
title Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis
title_full Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis
title_fullStr Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis
title_full_unstemmed Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis
title_short Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis
title_sort histopathological, immunohistochemical and biochemical studies of murine hepatosplenic tissues affected by chronic toxoplasmosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225867/
https://www.ncbi.nlm.nih.gov/pubmed/35755604
http://dx.doi.org/10.1155/2022/2165205
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