期刊论文详细信息
BMC Complementary and Alternative Medicine
Neuro-protective effect of rutin against Cisplatin-induced neurotoxic rat model
Research Article
Mashal M. Almutairi1  Mohamed M. Hafez1  Wael A. Alanazi1  Musaad A. Alshammari1  Moureq Rashed Alotaibi1  Salim Salah Al-Rejaie1  Ali R. Alhoshani1  Othman A. Al-Shabanah1 
[1] Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, P.O. Box 2457, 11451, Riyadh, Kingdom of Saudi Arabia;
关键词: Gene expression;    Real time PCR;    Cisplatin;    Oxidative stress;    Rutin;   
DOI  :  10.1186/s12906-017-1976-9
 received in 2017-05-23, accepted in 2017-09-14,  发布年份 2017
来源: Springer
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【 摘 要 】

BackgroundCisplatin 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.MethodsForty 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.ResultsCisplatin 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.ConclusionThis study showed that Rutin has neuroprotective effect and reduces cisplatin- neurotoxicity with possible mechanism via the antioxidant pathway.

【 授权许可】

CC BY   
© The Author(s). 2017

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