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The role of Allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models
AIM: Reproductive toxicity is a major challenge associated with aluminum (Al) exposure. Studies that associated Al with reproductive dysfunction did not account for the possible influence of Allium cepa extract. This study, therefore, investigates the influence of A. cepa on aluminum-induced reprodu...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493836/ https://www.ncbi.nlm.nih.gov/pubmed/23162360 http://dx.doi.org/10.4103/0974-1208.101022 |
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author | Ige, Serah F Akhigbe, Roland E |
author_facet | Ige, Serah F Akhigbe, Roland E |
author_sort | Ige, Serah F |
collection | PubMed |
description | AIM: Reproductive toxicity is a major challenge associated with aluminum (Al) exposure. Studies that associated Al with reproductive dysfunction did not account for the possible influence of Allium cepa extract. This study, therefore, investigates the influence of A. cepa on aluminum-induced reproductive dysfunction. MATERIALS AND METHODS: Six male rats per group were assigned to one of the following four treatment groups: The control animals were on control diet. A. cepa-treated rats received 1 ml of the extract/100 g body weight (BW), Al-treated rats received 100 mg AlCl(3) /kg BW, and A.cepa+Al received 1 ml of the extract/100 g BW plus 100 mg AlCl(3) /kg BW. Rats were orally administered their respective doses. A. cepa treatment was for 8 weeks, while Al treatment was for the last 3 days of the experimental period. RESULTS: Results obtained showed that Al significantly decreased (P < 0.05) plasma testosterone, follicular stimulating hormone (FSH), luteinizing hormone (LH), sperm count, motility, morphology and viability, superoxide dismutase (SOD) and catalase (CAT) activities, while lipid peroxidation index [malondialdehyde (MDA)] was significantly (P < 0.05) increased. Reproductive hormones (except testosterone), sperm qualities, and enzymatic antioxidants were significantly (P < 0.05) increased in A. cepa-treated rats and A. cepa plus Al-treated rats, while MDA was significantly (P < 0.05) improved. Weights of testes were comparable in all groups. CONCLUSION: It is thus suggested that Al exerts reproductive dysfunction by oxidative damage. A. cepa antagonizes the toxic effects of AlCl(3) and improves the antioxidant status and sperm quality of male rat. However, testosterone level did not increase with A. cepa treatment. |
format | Online Article Text |
id | pubmed-3493836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-34938362012-11-16 The role of Allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models Ige, Serah F Akhigbe, Roland E J Hum Reprod Sci Original Article AIM: Reproductive toxicity is a major challenge associated with aluminum (Al) exposure. Studies that associated Al with reproductive dysfunction did not account for the possible influence of Allium cepa extract. This study, therefore, investigates the influence of A. cepa on aluminum-induced reproductive dysfunction. MATERIALS AND METHODS: Six male rats per group were assigned to one of the following four treatment groups: The control animals were on control diet. A. cepa-treated rats received 1 ml of the extract/100 g body weight (BW), Al-treated rats received 100 mg AlCl(3) /kg BW, and A.cepa+Al received 1 ml of the extract/100 g BW plus 100 mg AlCl(3) /kg BW. Rats were orally administered their respective doses. A. cepa treatment was for 8 weeks, while Al treatment was for the last 3 days of the experimental period. RESULTS: Results obtained showed that Al significantly decreased (P < 0.05) plasma testosterone, follicular stimulating hormone (FSH), luteinizing hormone (LH), sperm count, motility, morphology and viability, superoxide dismutase (SOD) and catalase (CAT) activities, while lipid peroxidation index [malondialdehyde (MDA)] was significantly (P < 0.05) increased. Reproductive hormones (except testosterone), sperm qualities, and enzymatic antioxidants were significantly (P < 0.05) increased in A. cepa-treated rats and A. cepa plus Al-treated rats, while MDA was significantly (P < 0.05) improved. Weights of testes were comparable in all groups. CONCLUSION: It is thus suggested that Al exerts reproductive dysfunction by oxidative damage. A. cepa antagonizes the toxic effects of AlCl(3) and improves the antioxidant status and sperm quality of male rat. However, testosterone level did not increase with A. cepa treatment. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3493836/ /pubmed/23162360 http://dx.doi.org/10.4103/0974-1208.101022 Text en Copyright: © Journal of Human Reproductive Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ige, Serah F Akhigbe, Roland E The role of Allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models |
title | The role of Allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models |
title_full | The role of Allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models |
title_fullStr | The role of Allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models |
title_full_unstemmed | The role of Allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models |
title_short | The role of Allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models |
title_sort | role of allium cepa on aluminum-induced reproductive dysfunction in experimental male rat models |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493836/ https://www.ncbi.nlm.nih.gov/pubmed/23162360 http://dx.doi.org/10.4103/0974-1208.101022 |
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