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N(G)-nitro-L-arginine Methyl Ester Protects Against Hormonal Imbalances Associated with Nicotine Administration in Male Rats
BACKGROUND: The administration of nicotine is associated with altered hormonal imbalances and increased serum and testicular nitric oxide (NO) level. AIM: This study sought to investigate the effects of NO inhibition with N(G)-nitro-L-arginine methyl ester (L-NAME) on altered hormonal imbalance in a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358050/ https://www.ncbi.nlm.nih.gov/pubmed/25789250 http://dx.doi.org/10.4103/1947-2714.152080 |
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author | Oyeyipo, Ibukun P. Raji, Y. Bolarinwa, Adeyombo F. |
author_facet | Oyeyipo, Ibukun P. Raji, Y. Bolarinwa, Adeyombo F. |
author_sort | Oyeyipo, Ibukun P. |
collection | PubMed |
description | BACKGROUND: The administration of nicotine is associated with altered hormonal imbalances and increased serum and testicular nitric oxide (NO) level. AIM: This study sought to investigate the effects of NO inhibition with N(G)-nitro-L-arginine methyl ester (L-NAME) on altered hormonal imbalance in adult male albinorats. MATERIALS AND METHODS: Rats were administered with 0.5 mg/kg body weight (BW) and 1.0 mg/kg BW nicotine and were treated with L-NAME in the drinking water or drinking water alone for 30 days. Serum was analyzed for testosterone, luteinizing hormone (LH), follicle stimulating hormone (FSH), and prolactin using radioimmunoassay. RESULTS: Nicotine administration significantly decreased (P < 0.05) testosterone in the low and high dose treated groups and FSH in the high dose treated group when compared with the control group. There was a significant increase (P < 0.05) in mean LH and prolactin level in the high dose treated group when compared with the control. Concomitant treatment with nicotine and L-NAME produced significant increases in testosterone and FSH, and a decrease in prolactin in 1.0 mg/kg BW. L-NAME alone did not lead to a significant increase in testosterone when compared with control. CONCLUSION: These data demonstrate that the suppressive effects of nicotine on testosterone level of the adult male rat can be prevented by NOS blockade with L-NAME. It appears that these beneficial effects are mediated primarily within the gonad; however, the involvement of the pituitary cannot be totally ruled out. |
format | Online Article Text |
id | pubmed-4358050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43580502015-03-18 N(G)-nitro-L-arginine Methyl Ester Protects Against Hormonal Imbalances Associated with Nicotine Administration in Male Rats Oyeyipo, Ibukun P. Raji, Y. Bolarinwa, Adeyombo F. N Am J Med Sci Original Article BACKGROUND: The administration of nicotine is associated with altered hormonal imbalances and increased serum and testicular nitric oxide (NO) level. AIM: This study sought to investigate the effects of NO inhibition with N(G)-nitro-L-arginine methyl ester (L-NAME) on altered hormonal imbalance in adult male albinorats. MATERIALS AND METHODS: Rats were administered with 0.5 mg/kg body weight (BW) and 1.0 mg/kg BW nicotine and were treated with L-NAME in the drinking water or drinking water alone for 30 days. Serum was analyzed for testosterone, luteinizing hormone (LH), follicle stimulating hormone (FSH), and prolactin using radioimmunoassay. RESULTS: Nicotine administration significantly decreased (P < 0.05) testosterone in the low and high dose treated groups and FSH in the high dose treated group when compared with the control group. There was a significant increase (P < 0.05) in mean LH and prolactin level in the high dose treated group when compared with the control. Concomitant treatment with nicotine and L-NAME produced significant increases in testosterone and FSH, and a decrease in prolactin in 1.0 mg/kg BW. L-NAME alone did not lead to a significant increase in testosterone when compared with control. CONCLUSION: These data demonstrate that the suppressive effects of nicotine on testosterone level of the adult male rat can be prevented by NOS blockade with L-NAME. It appears that these beneficial effects are mediated primarily within the gonad; however, the involvement of the pituitary cannot be totally ruled out. Medknow Publications & Media Pvt Ltd 2015-02 /pmc/articles/PMC4358050/ /pubmed/25789250 http://dx.doi.org/10.4103/1947-2714.152080 Text en Copyright: © North American Journal of Medical 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 Oyeyipo, Ibukun P. Raji, Y. Bolarinwa, Adeyombo F. N(G)-nitro-L-arginine Methyl Ester Protects Against Hormonal Imbalances Associated with Nicotine Administration in Male Rats |
title | N(G)-nitro-L-arginine Methyl Ester Protects Against Hormonal Imbalances Associated with Nicotine Administration in Male Rats |
title_full | N(G)-nitro-L-arginine Methyl Ester Protects Against Hormonal Imbalances Associated with Nicotine Administration in Male Rats |
title_fullStr | N(G)-nitro-L-arginine Methyl Ester Protects Against Hormonal Imbalances Associated with Nicotine Administration in Male Rats |
title_full_unstemmed | N(G)-nitro-L-arginine Methyl Ester Protects Against Hormonal Imbalances Associated with Nicotine Administration in Male Rats |
title_short | N(G)-nitro-L-arginine Methyl Ester Protects Against Hormonal Imbalances Associated with Nicotine Administration in Male Rats |
title_sort | n(g)-nitro-l-arginine methyl ester protects against hormonal imbalances associated with nicotine administration in male rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358050/ https://www.ncbi.nlm.nih.gov/pubmed/25789250 http://dx.doi.org/10.4103/1947-2714.152080 |
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