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Protective Effects of Thymoquinone against Methotrexate-Induced Germ Cell Apoptosis in Male Mice
BACKGROUND: Toxic effects of anti-cancer and other drugs on the normal tissues could be reduced by the herbal plants and their fractions. This study investigated the protective effect of thymoquinone (TQ) as a fraction of Nigella sativa on methotrexate (MTX)- induced germ cell apoptosis in male mice...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793176/ https://www.ncbi.nlm.nih.gov/pubmed/26985343 |
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author | Sheikhbahaei, Fatemeh Khazaei, Mozafar Rabzia, Arezou Mansouri, Kamran Ghanbari, Ali |
author_facet | Sheikhbahaei, Fatemeh Khazaei, Mozafar Rabzia, Arezou Mansouri, Kamran Ghanbari, Ali |
author_sort | Sheikhbahaei, Fatemeh |
collection | PubMed |
description | BACKGROUND: Toxic effects of anti-cancer and other drugs on the normal tissues could be reduced by the herbal plants and their fractions. This study investigated the protective effect of thymoquinone (TQ) as a fraction of Nigella sativa on methotrexate (MTX)- induced germ cell apoptosis in male mice. MATERIALS AND METHODS: In this experimental study, thirty male Balb/c mice were divided randomly into 5 groups (n=6). A single dose of MTX (20 mg/kg) and different concentrations of TQ were administrated for 4 consecutive days. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay was performed on paraffin embedded tissue sections to analysis the occurrence of apoptosis in the testis. Reverse transcription polymerase chain reaction (RT-PCR) of apoptosis-related genes was performed with RNA extracted from testes of the mice. Statistical analysis was done using one-way ANOVA. RESULTS: In the MTX group, there was a significant increase in morphologic sign of germ cell degeneration of tubules (48 ± 0.6%), apoptotic index (AI; 2.3 ± 0.6%), as well as mRNA expression of p53 (P=0.008), caspase 8 (P=0.002), caspase 3 (P=0.005), caspase 9 (P=0.000), bax (P=0.004) and the ratio of bax/bcl-2 (P=0.000), whereas there was an decrease in the expression of bcl-2 (P=0.003), as compared to control group. In MTX+TQ groups, the data showed that different concentrations of TQ could improve the harmful effects caused by the MTX. The best protective effects were achieved in MTX+TQ (10 mg/kg). CONCLUSION: TQ protects testicular germ cell against MTX-induced apoptosis by affecting related genes regulation. |
format | Online Article Text |
id | pubmed-4793176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-47931762016-03-16 Protective Effects of Thymoquinone against Methotrexate-Induced Germ Cell Apoptosis in Male Mice Sheikhbahaei, Fatemeh Khazaei, Mozafar Rabzia, Arezou Mansouri, Kamran Ghanbari, Ali Int J Fertil Steril Original Article BACKGROUND: Toxic effects of anti-cancer and other drugs on the normal tissues could be reduced by the herbal plants and their fractions. This study investigated the protective effect of thymoquinone (TQ) as a fraction of Nigella sativa on methotrexate (MTX)- induced germ cell apoptosis in male mice. MATERIALS AND METHODS: In this experimental study, thirty male Balb/c mice were divided randomly into 5 groups (n=6). A single dose of MTX (20 mg/kg) and different concentrations of TQ were administrated for 4 consecutive days. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay was performed on paraffin embedded tissue sections to analysis the occurrence of apoptosis in the testis. Reverse transcription polymerase chain reaction (RT-PCR) of apoptosis-related genes was performed with RNA extracted from testes of the mice. Statistical analysis was done using one-way ANOVA. RESULTS: In the MTX group, there was a significant increase in morphologic sign of germ cell degeneration of tubules (48 ± 0.6%), apoptotic index (AI; 2.3 ± 0.6%), as well as mRNA expression of p53 (P=0.008), caspase 8 (P=0.002), caspase 3 (P=0.005), caspase 9 (P=0.000), bax (P=0.004) and the ratio of bax/bcl-2 (P=0.000), whereas there was an decrease in the expression of bcl-2 (P=0.003), as compared to control group. In MTX+TQ groups, the data showed that different concentrations of TQ could improve the harmful effects caused by the MTX. The best protective effects were achieved in MTX+TQ (10 mg/kg). CONCLUSION: TQ protects testicular germ cell against MTX-induced apoptosis by affecting related genes regulation. Royan Institute 2016 2015-12-23 /pmc/articles/PMC4793176/ /pubmed/26985343 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sheikhbahaei, Fatemeh Khazaei, Mozafar Rabzia, Arezou Mansouri, Kamran Ghanbari, Ali Protective Effects of Thymoquinone against Methotrexate-Induced Germ Cell Apoptosis in Male Mice |
title | Protective Effects of Thymoquinone against
Methotrexate-Induced Germ Cell
Apoptosis in Male Mice |
title_full | Protective Effects of Thymoquinone against
Methotrexate-Induced Germ Cell
Apoptosis in Male Mice |
title_fullStr | Protective Effects of Thymoquinone against
Methotrexate-Induced Germ Cell
Apoptosis in Male Mice |
title_full_unstemmed | Protective Effects of Thymoquinone against
Methotrexate-Induced Germ Cell
Apoptosis in Male Mice |
title_short | Protective Effects of Thymoquinone against
Methotrexate-Induced Germ Cell
Apoptosis in Male Mice |
title_sort | protective effects of thymoquinone against
methotrexate-induced germ cell
apoptosis in male mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793176/ https://www.ncbi.nlm.nih.gov/pubmed/26985343 |
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