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BMC Complement Altern Med ; 17(1): 472, 2017 Sep 29.
Article in English | MEDLINE | ID: mdl-28962559

ABSTRACT

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.


Subject(s)
Brain/drug effects , Cisplatin/adverse effects , Neuroprotective Agents/pharmacology , Rutin/pharmacology , Animals , Body Weight/drug effects , Brain/enzymology , Brain/metabolism , Brain Chemistry/drug effects , Glutathione/metabolism , Glutathione Peroxidase/analysis , Glutathione Peroxidase/genetics , Glutathione Peroxidase/metabolism , Male , Oxidative Stress/drug effects , PPAR delta/analysis , PPAR delta/genetics , PPAR delta/metabolism , Rats , Rats, Wistar , Thiobarbituric Acid Reactive Substances/metabolism
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