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Subacute Testicular Toxicity to Cadmium Exposure Intraperitoneally and Orally
The toxic effects of cadmium (Cd) on reproductive parameters are widely described in the literature. Experimental models often make use of the intraperitoneal route (i.p.), although human intoxication occurs preferentially by the oral route and can be continuous. However, little is known about the e...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899267/ https://www.ncbi.nlm.nih.gov/pubmed/31885783 http://dx.doi.org/10.1155/2019/3429635 |
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author | Mouro, Viviane G. S. Martins, Ana L. P. Silva, Janaina Menezes, Tatiana P. Gomes, Marcos L. M. Oliveira, Juraci A. Melo, Fabiana C. S. A. Matta, Sérgio L. P. |
author_facet | Mouro, Viviane G. S. Martins, Ana L. P. Silva, Janaina Menezes, Tatiana P. Gomes, Marcos L. M. Oliveira, Juraci A. Melo, Fabiana C. S. A. Matta, Sérgio L. P. |
author_sort | Mouro, Viviane G. S. |
collection | PubMed |
description | The toxic effects of cadmium (Cd) on reproductive parameters are widely described in the literature. Experimental models often make use of the intraperitoneal route (i.p.), although human intoxication occurs preferentially by the oral route and can be continuous. However, little is known about the effect of Cd administration routes on the testicular structure. Thus, this study investigated the testicular impact of Cd exposure comparing both i.p. and oral routes, both single dose (SD), in addition to the oral route in fractional doses (FD). Swiss adult male mice received CdCl(2) 1.5 mg/kg i.p., 30 mg/kg oral SD, and 4.28 mg/kg oral FD for 7 consecutive days. The Cd bioaccumulation was observed in all routes, mainly in the oral FD route. The concentrations of testicular Ca and Cu decreased in all animals exposed to Cd, while Zn and Mn decreased only in the i.p. route. Testicular SOD activity was reduced in both routes of oral administration, while CAT increased in the i.p. route, and GST increased in all animals exposed to Cd. Changes in the tubular parameters and cell viability were observed in both routes of Cd administration but were more intense in the oral route, mainly in the FD. Serum testosterone concentration was reduced in both routes of oral administration. Tubular damage, such as the vacuolization of the seminiferous epithelium, germ cell detachment, and seminiferous tubule degeneration, occurred in all groups exposed to Cd. Therefore, the oral Cd administration presented greater potential to promote testicular damage, mainly when the metal was given in a fractionated way. |
format | Online Article Text |
id | pubmed-6899267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-68992672019-12-29 Subacute Testicular Toxicity to Cadmium Exposure Intraperitoneally and Orally Mouro, Viviane G. S. Martins, Ana L. P. Silva, Janaina Menezes, Tatiana P. Gomes, Marcos L. M. Oliveira, Juraci A. Melo, Fabiana C. S. A. Matta, Sérgio L. P. Oxid Med Cell Longev Research Article The toxic effects of cadmium (Cd) on reproductive parameters are widely described in the literature. Experimental models often make use of the intraperitoneal route (i.p.), although human intoxication occurs preferentially by the oral route and can be continuous. However, little is known about the effect of Cd administration routes on the testicular structure. Thus, this study investigated the testicular impact of Cd exposure comparing both i.p. and oral routes, both single dose (SD), in addition to the oral route in fractional doses (FD). Swiss adult male mice received CdCl(2) 1.5 mg/kg i.p., 30 mg/kg oral SD, and 4.28 mg/kg oral FD for 7 consecutive days. The Cd bioaccumulation was observed in all routes, mainly in the oral FD route. The concentrations of testicular Ca and Cu decreased in all animals exposed to Cd, while Zn and Mn decreased only in the i.p. route. Testicular SOD activity was reduced in both routes of oral administration, while CAT increased in the i.p. route, and GST increased in all animals exposed to Cd. Changes in the tubular parameters and cell viability were observed in both routes of Cd administration but were more intense in the oral route, mainly in the FD. Serum testosterone concentration was reduced in both routes of oral administration. Tubular damage, such as the vacuolization of the seminiferous epithelium, germ cell detachment, and seminiferous tubule degeneration, occurred in all groups exposed to Cd. Therefore, the oral Cd administration presented greater potential to promote testicular damage, mainly when the metal was given in a fractionated way. Hindawi 2019-11-25 /pmc/articles/PMC6899267/ /pubmed/31885783 http://dx.doi.org/10.1155/2019/3429635 Text en Copyright © 2019 Viviane G. S. Mouro et al. http://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 Mouro, Viviane G. S. Martins, Ana L. P. Silva, Janaina Menezes, Tatiana P. Gomes, Marcos L. M. Oliveira, Juraci A. Melo, Fabiana C. S. A. Matta, Sérgio L. P. Subacute Testicular Toxicity to Cadmium Exposure Intraperitoneally and Orally |
title | Subacute Testicular Toxicity to Cadmium Exposure Intraperitoneally and Orally |
title_full | Subacute Testicular Toxicity to Cadmium Exposure Intraperitoneally and Orally |
title_fullStr | Subacute Testicular Toxicity to Cadmium Exposure Intraperitoneally and Orally |
title_full_unstemmed | Subacute Testicular Toxicity to Cadmium Exposure Intraperitoneally and Orally |
title_short | Subacute Testicular Toxicity to Cadmium Exposure Intraperitoneally and Orally |
title_sort | subacute testicular toxicity to cadmium exposure intraperitoneally and orally |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899267/ https://www.ncbi.nlm.nih.gov/pubmed/31885783 http://dx.doi.org/10.1155/2019/3429635 |
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