Fish oil provides protection against the oxidative stress in pilocarpine model of epilepsy

被引:8
|
作者
Nejm, Mariana B. [1 ]
Haidar, Andre A. [2 ]
Marques, Marcia J. G. [1 ]
Hirata, Aparecida E. [2 ]
Nogueira, Fernando N. [3 ]
Cavalheiro, Esper A. [1 ]
Scorza, Fulvio A. [1 ]
Cysneiros, Roberta Monterazzo [4 ]
机构
[1] Univ Fed Sao Paulo, UNIFESP EPM, Disciplina Neurol Expt, Dept Neurol & Neurocirurgia, Sao Paulo, SP, Brazil
[2] Univ Fed Sao Paulo, UNIFESP EPM, Dept Fisiol, Sao Paulo, SP, Brazil
[3] Univ Sao Paulo, Fac Odontol, Dept Biomat & Biol Oral, Sao Paulo, Brazil
[4] Univ Presbiteriana Mackenzie, Neurobiol Lab, Programa Posgrad Disturbios Denvolvimento, BR-01302907 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Oxidative stress; Fish oil; Epilepsy; Pilocarpine; INDUCED HIPPOCAMPAL DAMAGE; TEMPORAL-LOBE EPILEPSY; DOCOSAHEXAENOIC ACID; NADPH OXIDASE; SUPEROXIDE PRODUCTION; STATUS EPILEPTICUS; FATTY-ACID; BRAIN; RATS; OMEGA-3-FATTY-ACIDS;
D O I
10.1007/s11011-015-9666-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Temporal lobe epilepsy (TLE), the most common form of epilepsy is often resistant to pharmacological treatment. Neuronal loss observed in epileptic brain may be result of an overproduction of free radicals (oxidative stress). Oxidative stress is characterized by an imbalance between antioxidant defenses and oxidizing agents (free radicals), which can lead to tissue injury. The n-3 PUFAs are important for the development and maintenance of central nervous system functions. Research by our group has shown that chronic treatment with fish oil, immediately after status epilepticus (SE), exhibits both neuroprotective effects and effects on neuroplasticity. The main purpose of this research was to evaluate if fish oil exhibits a protective effect against oxidative stress. Animals were subjected to TLE model by pilocarpine administration. After 3 h of SE they were randomly divided into the following groups: control animals treated daily with vehicle or with 85 mg/kg of fish oil and animals with epilepsy treated daily with vehicle or with 85 mg/kg of fish oil. After 90 days, superoxide anion production, enzymatic activity of superoxide dismutase (SOD) and catalase (CAT) and protein expression of NAD(P)H oxidase subunits (p47(PHOX) and gp91(PHOX)) were analyzed. Our results showed evidences that reactive oxygen species are increased in animals with epilepsy and that fish oil supplementation could counteract it. Fish oil supplementation promoted protection against oxidative stress by multiple ways, which involved the reduction of activity and expression of NAD(P)H oxidase subunits and increased the activity and expression of antioxidants enzymes, contributing to well-known neuroprotective effect in epilepsy.
引用
收藏
页码:903 / 909
页数:7
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