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Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model
BACKGROUND: Cisplatin is widely used chemotherapeutic agent for cancer treatment with limited uses due to its neurotoxic side effect. The aim of this study was to determine the potential preventive effects of rutin on the brain of cisplatin- neurotoxic rat model. METHODS: Forty rats were divided int...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622464/ https://www.ncbi.nlm.nih.gov/pubmed/28962559 http://dx.doi.org/10.1186/s12906-017-1976-9 |
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author | Almutairi, Mashal M. Alanazi, Wael A. Alshammari, Musaad A. Alotaibi, Moureq Rashed Alhoshani, Ali R. Al-Rejaie, Salim Salah Hafez, Mohamed M. Al-Shabanah, Othman A. |
author_facet | Almutairi, Mashal M. Alanazi, Wael A. Alshammari, Musaad A. Alotaibi, Moureq Rashed Alhoshani, Ali R. Al-Rejaie, Salim Salah Hafez, Mohamed M. Al-Shabanah, Othman A. |
author_sort | Almutairi, Mashal M. |
collection | PubMed |
description | BACKGROUND: Cisplatin is widely used chemotherapeutic agent for cancer treatment with limited uses due to its neurotoxic side effect. The aim of this study was to determine the potential preventive effects of rutin on the brain of cisplatin- neurotoxic rat model. METHODS: Forty rats were divided into four groups. Group-1 (control group) was intra-peritoneal (IP) injected with 2.5 ml/kg saline. Group-2 (rutin group) was orally administrated 30 mg/kg rutin dissolved in water for 14 days. Group-3 (cisplatin group) was IP received 5 mg/kg cisplatin single dose. Group-4 (rutin and cisplatin group) was orally administrated 30 mg/kg rutin dissolved in water for 14 days with a single dose of 5 mg/kg cisplatin IP on day ten. Brain tissues from frontal cortex was used to extract RNA, the gene expression levels of paraoxonase-1 (PON-1), PON-2, PON-3, peroxisome proliferator-activated receptor delta (PPAR-δ), and glutathione peroxidase (GPx) was investigated by Real-time PCR. RESULTS: Cisplatin significantly decreased the expression levels of PON-1, PON-3, PPAR-δ and GPX whereas significantly increased PON-2 expression levels. Co-administration of Rutin prevented the cisplatin-induced toxicity by restoring the alteration in the studied genes to normal values as in the control group. CONCLUSION: This study showed that Rutin has neuroprotective effect and reduces cisplatin- neurotoxicity with possible mechanism via the antioxidant pathway. |
format | Online Article Text |
id | pubmed-5622464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56224642017-10-11 Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model Almutairi, Mashal M. Alanazi, Wael A. Alshammari, Musaad A. Alotaibi, Moureq Rashed Alhoshani, Ali R. Al-Rejaie, Salim Salah Hafez, Mohamed M. Al-Shabanah, Othman A. BMC Complement Altern Med Research Article BACKGROUND: Cisplatin is widely used chemotherapeutic agent for cancer treatment with limited uses due to its neurotoxic side effect. The aim of this study was to determine the potential preventive effects of rutin on the brain of cisplatin- neurotoxic rat model. METHODS: Forty rats were divided into four groups. Group-1 (control group) was intra-peritoneal (IP) injected with 2.5 ml/kg saline. Group-2 (rutin group) was orally administrated 30 mg/kg rutin dissolved in water for 14 days. Group-3 (cisplatin group) was IP received 5 mg/kg cisplatin single dose. Group-4 (rutin and cisplatin group) was orally administrated 30 mg/kg rutin dissolved in water for 14 days with a single dose of 5 mg/kg cisplatin IP on day ten. Brain tissues from frontal cortex was used to extract RNA, the gene expression levels of paraoxonase-1 (PON-1), PON-2, PON-3, peroxisome proliferator-activated receptor delta (PPAR-δ), and glutathione peroxidase (GPx) was investigated by Real-time PCR. RESULTS: Cisplatin significantly decreased the expression levels of PON-1, PON-3, PPAR-δ and GPX whereas significantly increased PON-2 expression levels. Co-administration of Rutin prevented the cisplatin-induced toxicity by restoring the alteration in the studied genes to normal values as in the control group. CONCLUSION: This study showed that Rutin has neuroprotective effect and reduces cisplatin- neurotoxicity with possible mechanism via the antioxidant pathway. BioMed Central 2017-09-29 /pmc/articles/PMC5622464/ /pubmed/28962559 http://dx.doi.org/10.1186/s12906-017-1976-9 Text en © The Author(s). 2017 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 Almutairi, Mashal M. Alanazi, Wael A. Alshammari, Musaad A. Alotaibi, Moureq Rashed Alhoshani, Ali R. Al-Rejaie, Salim Salah Hafez, Mohamed M. Al-Shabanah, Othman A. Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model |
title | Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model |
title_full | Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model |
title_fullStr | Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model |
title_full_unstemmed | Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model |
title_short | Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model |
title_sort | neuro-protective effect of rutin against cisplatin-induced neurotoxic rat model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622464/ https://www.ncbi.nlm.nih.gov/pubmed/28962559 http://dx.doi.org/10.1186/s12906-017-1976-9 |
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