Protective effect of melatonin on oxidative damage by deltamethrin in rat brain.
- Author:
Min SUN
1
;
Pei-pei XU
;
Yong REN
;
Yuan-feng LI
;
Yu-fang ZHONG
;
Hong YAN
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Brain; drug effects; metabolism; Cerebellum; drug effects; metabolism; Cerebral Cortex; drug effects; metabolism; Glutathione; metabolism; Glutathione Peroxidase; metabolism; Hippocampus; drug effects; metabolism; Lipid Peroxidation; drug effects; Male; Malondialdehyde; metabolism; Melatonin; pharmacology; Nitriles; toxicity; Oxidative Stress; Pyrethrins; toxicity; Rats; Rats, Wistar; Superoxide Dismutase; metabolism
- From: Chinese Journal of Industrial Hygiene and Occupational Diseases 2007;25(3):155-158
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the potential protective effect of melatonin on the oxidative damage induced by deltamethrin in cerebral cortex, hippocampus and cerebellum of rats.
METHODS35 male wistar rats were randomly divided into five groups(seven rats per group): olive oil control, deltamethrin-treated (12.5 mg/kg), melatonin(25.0 mg/kg) and deltamethrin plus melatonin (25.0 mg/kg , 2.5 mg/kg respectively) group. Levels of malondialdehyde (MDA) and the activity of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), glutathione (GSH) in cerebral cortex, hippocampus and cerebellum were determined after 5 days of DM treatments.
RESULTSMDA content in cerebral cortex, hippocampus and cerebellum tissue of the DM-treated rats were significantly higher than those in control group, and compared with DM-treated group, MDA content in those tissue of MT + DM-treated group have significantly decreased after 5 days of DM exposure (P < 0.05). Activities of GSH-Px in DM-treated group were significantly lower than those in control group, and those in the MT + DM group were significantly higher than DM group(P < 0.05).
CONCLUSIONDM can induce the oxidative damage in rat brain and melatonin has protective effects on deltamethrin-induced oxidative damage in hippocampus, cerebral cortex and cerebellum of rats.
