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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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