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Zinc improves the immune function and the proliferation of lymphocytes in Cadmium-treated rats
The effects of Cadmium (Cd) exposure and the treatment with Zinc (Zn) on immune functions of splenocytes and cultured lymphocytes of rats were studied. The exposure of rats to Cd was at a dose of 2.2 mg/kg CdCl(2), injected subcutaneously four times weekly for 2 months. Rats were supplemented with Z...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Polish Society of Experimental and Clinical Immunology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439953/ https://www.ncbi.nlm.nih.gov/pubmed/26155160 http://dx.doi.org/10.5114/ceji.2014.47726 |
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author | Ebaid, Hossam Hassan, Iftekhar Bashandy, Samir Taha, Nael Abu Mahmood, Amer Alomar, Suliman Alhazza, Iibrahim Mashaly, Ashraf Rady, Ahmed |
author_facet | Ebaid, Hossam Hassan, Iftekhar Bashandy, Samir Taha, Nael Abu Mahmood, Amer Alomar, Suliman Alhazza, Iibrahim Mashaly, Ashraf Rady, Ahmed |
author_sort | Ebaid, Hossam |
collection | PubMed |
description | The effects of Cadmium (Cd) exposure and the treatment with Zinc (Zn) on immune functions of splenocytes and cultured lymphocytes of rats were studied. The exposure of rats to Cd was at a dose of 2.2 mg/kg CdCl(2), injected subcutaneously four times weekly for 2 months. Rats were supplemented with Zn (2.2 mg/kg ZnCl(2), injected subcutaneously four times weekly for 2 months) one hour prior to Cd exposure. Spleens were removed and splenocytes were isolated and cultured. The proliferation capacity of lymphocytes and their homing to the spleen were studied. Ribonucleic acid (RNA) was extracted from stimulated lymphocytes in order to analyse gene expressions using RT-PCR. Accordingly, proliferation of lymphocytes was found to be suppressed in Cd-treated rats, both in vivo and in vitro. Zinc served to activate the proliferation of B and T lymphocytes in Cd-treated rats both in vivo and in vitro. Antigen-activated lymphocytes showed that Cd impaired the mRNA expression of CD68, Ccl22 and CXCL10. Zinc was not found to restore mRNA expression of these genes to the normal levels. Zinc was found to decrease the MDA level with replenishment of activity of key antioxidant enzymes and proteins in Cd-pre-treated animals significantly. Moreover, the histopathological examination of spleen samples also agreed with the molecular, immunological and redox findings. Hence, Zn is able to restore the normal structure, redox status and immunity in Cd-induced damage in the rat model system. |
format | Online Article Text |
id | pubmed-4439953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Polish Society of Experimental and Clinical Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-44399532015-07-07 Zinc improves the immune function and the proliferation of lymphocytes in Cadmium-treated rats Ebaid, Hossam Hassan, Iftekhar Bashandy, Samir Taha, Nael Abu Mahmood, Amer Alomar, Suliman Alhazza, Iibrahim Mashaly, Ashraf Rady, Ahmed Cent Eur J Immunol Original Article The effects of Cadmium (Cd) exposure and the treatment with Zinc (Zn) on immune functions of splenocytes and cultured lymphocytes of rats were studied. The exposure of rats to Cd was at a dose of 2.2 mg/kg CdCl(2), injected subcutaneously four times weekly for 2 months. Rats were supplemented with Zn (2.2 mg/kg ZnCl(2), injected subcutaneously four times weekly for 2 months) one hour prior to Cd exposure. Spleens were removed and splenocytes were isolated and cultured. The proliferation capacity of lymphocytes and their homing to the spleen were studied. Ribonucleic acid (RNA) was extracted from stimulated lymphocytes in order to analyse gene expressions using RT-PCR. Accordingly, proliferation of lymphocytes was found to be suppressed in Cd-treated rats, both in vivo and in vitro. Zinc served to activate the proliferation of B and T lymphocytes in Cd-treated rats both in vivo and in vitro. Antigen-activated lymphocytes showed that Cd impaired the mRNA expression of CD68, Ccl22 and CXCL10. Zinc was not found to restore mRNA expression of these genes to the normal levels. Zinc was found to decrease the MDA level with replenishment of activity of key antioxidant enzymes and proteins in Cd-pre-treated animals significantly. Moreover, the histopathological examination of spleen samples also agreed with the molecular, immunological and redox findings. Hence, Zn is able to restore the normal structure, redox status and immunity in Cd-induced damage in the rat model system. Polish Society of Experimental and Clinical Immunology 2014-12-15 2014 /pmc/articles/PMC4439953/ /pubmed/26155160 http://dx.doi.org/10.5114/ceji.2014.47726 Text en Copyright © Central European Journal of Immunology 2014 http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ebaid, Hossam Hassan, Iftekhar Bashandy, Samir Taha, Nael Abu Mahmood, Amer Alomar, Suliman Alhazza, Iibrahim Mashaly, Ashraf Rady, Ahmed Zinc improves the immune function and the proliferation of lymphocytes in Cadmium-treated rats |
title | Zinc improves the immune function and the proliferation of lymphocytes in Cadmium-treated rats |
title_full | Zinc improves the immune function and the proliferation of lymphocytes in Cadmium-treated rats |
title_fullStr | Zinc improves the immune function and the proliferation of lymphocytes in Cadmium-treated rats |
title_full_unstemmed | Zinc improves the immune function and the proliferation of lymphocytes in Cadmium-treated rats |
title_short | Zinc improves the immune function and the proliferation of lymphocytes in Cadmium-treated rats |
title_sort | zinc improves the immune function and the proliferation of lymphocytes in cadmium-treated rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439953/ https://www.ncbi.nlm.nih.gov/pubmed/26155160 http://dx.doi.org/10.5114/ceji.2014.47726 |
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