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Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats
BACKGROUND: The present study was in quested to study the effects of β-sitosterol on methyl nitrosourea (MNU) induced mammary gland carcinoma in albino wistar rats. METHODS: Animals were randomized and divided into four groups of eight animals each. Group I (sham control 1 % CMC in normal saline p.o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966711/ https://www.ncbi.nlm.nih.gov/pubmed/27473871 http://dx.doi.org/10.1186/s12906-016-1243-5 |
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author | Manral, Chetan Roy, Subhadeep Singh, Manjari Gautam, Swetlana Yadav, Rajnish K. Rawat, Jitendra K Devi, Uma Ansari, Md Nazam Saeedan, Abdulaziz S. Kaithwas, Gaurav |
author_facet | Manral, Chetan Roy, Subhadeep Singh, Manjari Gautam, Swetlana Yadav, Rajnish K. Rawat, Jitendra K Devi, Uma Ansari, Md Nazam Saeedan, Abdulaziz S. Kaithwas, Gaurav |
author_sort | Manral, Chetan |
collection | PubMed |
description | BACKGROUND: The present study was in quested to study the effects of β-sitosterol on methyl nitrosourea (MNU) induced mammary gland carcinoma in albino wistar rats. METHODS: Animals were randomized and divided into four groups of eight animals each. Group I (sham control 1 % CMC in normal saline p.o.); Group II (toxic control, MNU 47 mg/kg, i.v); Group III (MNU 47 mg/kg, i.v + β-sitosterol, 10 mg/kg, p.o); Group IV (MNU 47 mg/kg, i.v + β-sitosterol, 20 mg/kg, p.o). Toxicity was induced by single i.v. injection of MNU followed by β-sitosterol supplementation therapy for 115 days at the dose mentioned above. RESULTS: Treatment with β-sitosterol evidenced decrease in the alveolar bud and lobule score in the whole mount of the mammary gland. β-sitosterol exhibited diminishing effect on oxidative stress through synchronizing lipid and enzymatic antioxidant defense. A significant decrease in the saturated and unsaturated fatty acid was evident with the MNU treatment and β-sitosterol demonstrated a marked effect on it. Pgp 9.5 expression was dose dependently upregulated by β-sitosterol treatment in comparison to MNU treatment. On the contrary, downregulated NF-kB expression was perceived, when β-sitosterol was concomitantly administered with MNU. CONCLUSION: β-sitosterol afforded significant protection against the deleterious effects of MNU. |
format | Online Article Text |
id | pubmed-4966711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49667112016-07-30 Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats Manral, Chetan Roy, Subhadeep Singh, Manjari Gautam, Swetlana Yadav, Rajnish K. Rawat, Jitendra K Devi, Uma Ansari, Md Nazam Saeedan, Abdulaziz S. Kaithwas, Gaurav BMC Complement Altern Med Research Article BACKGROUND: The present study was in quested to study the effects of β-sitosterol on methyl nitrosourea (MNU) induced mammary gland carcinoma in albino wistar rats. METHODS: Animals were randomized and divided into four groups of eight animals each. Group I (sham control 1 % CMC in normal saline p.o.); Group II (toxic control, MNU 47 mg/kg, i.v); Group III (MNU 47 mg/kg, i.v + β-sitosterol, 10 mg/kg, p.o); Group IV (MNU 47 mg/kg, i.v + β-sitosterol, 20 mg/kg, p.o). Toxicity was induced by single i.v. injection of MNU followed by β-sitosterol supplementation therapy for 115 days at the dose mentioned above. RESULTS: Treatment with β-sitosterol evidenced decrease in the alveolar bud and lobule score in the whole mount of the mammary gland. β-sitosterol exhibited diminishing effect on oxidative stress through synchronizing lipid and enzymatic antioxidant defense. A significant decrease in the saturated and unsaturated fatty acid was evident with the MNU treatment and β-sitosterol demonstrated a marked effect on it. Pgp 9.5 expression was dose dependently upregulated by β-sitosterol treatment in comparison to MNU treatment. On the contrary, downregulated NF-kB expression was perceived, when β-sitosterol was concomitantly administered with MNU. CONCLUSION: β-sitosterol afforded significant protection against the deleterious effects of MNU. BioMed Central 2016-07-29 /pmc/articles/PMC4966711/ /pubmed/27473871 http://dx.doi.org/10.1186/s12906-016-1243-5 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Manral, Chetan Roy, Subhadeep Singh, Manjari Gautam, Swetlana Yadav, Rajnish K. Rawat, Jitendra K Devi, Uma Ansari, Md Nazam Saeedan, Abdulaziz S. Kaithwas, Gaurav Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats |
title | Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats |
title_full | Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats |
title_fullStr | Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats |
title_full_unstemmed | Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats |
title_short | Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats |
title_sort | effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966711/ https://www.ncbi.nlm.nih.gov/pubmed/27473871 http://dx.doi.org/10.1186/s12906-016-1243-5 |
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