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Evaluation of the Effect of Two Systemic Doses of HESA-A on Prevention of Induced Tongue Neoplasm in Rats

Background and aims. The aim of the present study was to compare the inhibitory effects of two systemic doses of HESA-A on prevention of 4-NQO-induced tongue neoplasms in rats. This study evaluated weight and histopathological changes. Materials and methods. Forty-eight male Sprague Dawley rats were...

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Autores principales: Mehdipour, Masoumeh, Taghavi Zenouz, Ali, Mesgari Abbasi, Mehran, Mohajeri, Daryoush, Damghani, Hossein, Helli, Sanaz, Abdollahi, Bita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935553/
https://www.ncbi.nlm.nih.gov/pubmed/24578820
http://dx.doi.org/10.5681/joddd.2013.035
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author Mehdipour, Masoumeh
Taghavi Zenouz, Ali
Mesgari Abbasi, Mehran
Mohajeri, Daryoush
Damghani, Hossein
Helli, Sanaz
Abdollahi, Bita
author_facet Mehdipour, Masoumeh
Taghavi Zenouz, Ali
Mesgari Abbasi, Mehran
Mohajeri, Daryoush
Damghani, Hossein
Helli, Sanaz
Abdollahi, Bita
author_sort Mehdipour, Masoumeh
collection PubMed
description Background and aims. The aim of the present study was to compare the inhibitory effects of two systemic doses of HESA-A on prevention of 4-NQO-induced tongue neoplasms in rats. This study evaluated weight and histopathological changes. Materials and methods. Forty-eight male Sprague Dawley rats were divided into four groups of A, B, C and D of each 12 rats. The rats in groups B to D received 30 ppm of 4-Nitroquinoline-1-oxide (4-NQO) in drinking water for 12 weeks.  When feeding with 4-NQO was initiated, the rats in groups B and C received HESA-A at doses of 250 and 500 mg/kg, respectively, 3 times a week. Body weights were measured three times a week. At the end, the rats were euthanized and the tongue was removed. Histological evaluations for carcinogenesis were carried out under a light microscope. Results. The mean body weights of rats in groups B, C and D were significantly lower than that in group A (P < 0.05). There were no significant differences in weight changes between groups B, C and D. In the present study, after 12 weeks of treatment, Tongue specimens in groups B and C did not exhibit severe dysplastic changes; however, concurrent hyperplasia, without atypia and mild-to-moderate dysplastic changes were detected. These changes were significantly less than those in group D, with significant differences between group D and groups A, B and C (P<0.001, P<0.01 and P<0.05, respectively). Conclusion. HESA-A has dose-dependent inhibitory effects on the development of neoplasms of the tongue.
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spelling pubmed-39355532014-02-26 Evaluation of the Effect of Two Systemic Doses of HESA-A on Prevention of Induced Tongue Neoplasm in Rats Mehdipour, Masoumeh Taghavi Zenouz, Ali Mesgari Abbasi, Mehran Mohajeri, Daryoush Damghani, Hossein Helli, Sanaz Abdollahi, Bita J Dent Res Dent Clin Dent Prospects Original Article Background and aims. The aim of the present study was to compare the inhibitory effects of two systemic doses of HESA-A on prevention of 4-NQO-induced tongue neoplasms in rats. This study evaluated weight and histopathological changes. Materials and methods. Forty-eight male Sprague Dawley rats were divided into four groups of A, B, C and D of each 12 rats. The rats in groups B to D received 30 ppm of 4-Nitroquinoline-1-oxide (4-NQO) in drinking water for 12 weeks.  When feeding with 4-NQO was initiated, the rats in groups B and C received HESA-A at doses of 250 and 500 mg/kg, respectively, 3 times a week. Body weights were measured three times a week. At the end, the rats were euthanized and the tongue was removed. Histological evaluations for carcinogenesis were carried out under a light microscope. Results. The mean body weights of rats in groups B, C and D were significantly lower than that in group A (P < 0.05). There were no significant differences in weight changes between groups B, C and D. In the present study, after 12 weeks of treatment, Tongue specimens in groups B and C did not exhibit severe dysplastic changes; however, concurrent hyperplasia, without atypia and mild-to-moderate dysplastic changes were detected. These changes were significantly less than those in group D, with significant differences between group D and groups A, B and C (P<0.001, P<0.01 and P<0.05, respectively). Conclusion. HESA-A has dose-dependent inhibitory effects on the development of neoplasms of the tongue. Tabriz University of Medical Sciences 2013 2013-12-18 /pmc/articles/PMC3935553/ /pubmed/24578820 http://dx.doi.org/10.5681/joddd.2013.035 Text en © 2013 The Authors; Tabriz University of Medical Sciences http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mehdipour, Masoumeh
Taghavi Zenouz, Ali
Mesgari Abbasi, Mehran
Mohajeri, Daryoush
Damghani, Hossein
Helli, Sanaz
Abdollahi, Bita
Evaluation of the Effect of Two Systemic Doses of HESA-A on Prevention of Induced Tongue Neoplasm in Rats
title Evaluation of the Effect of Two Systemic Doses of HESA-A on Prevention of Induced Tongue Neoplasm in Rats
title_full Evaluation of the Effect of Two Systemic Doses of HESA-A on Prevention of Induced Tongue Neoplasm in Rats
title_fullStr Evaluation of the Effect of Two Systemic Doses of HESA-A on Prevention of Induced Tongue Neoplasm in Rats
title_full_unstemmed Evaluation of the Effect of Two Systemic Doses of HESA-A on Prevention of Induced Tongue Neoplasm in Rats
title_short Evaluation of the Effect of Two Systemic Doses of HESA-A on Prevention of Induced Tongue Neoplasm in Rats
title_sort evaluation of the effect of two systemic doses of hesa-a on prevention of induced tongue neoplasm in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935553/
https://www.ncbi.nlm.nih.gov/pubmed/24578820
http://dx.doi.org/10.5681/joddd.2013.035
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