The bacterial endotoxin lipopolysaccharide enhances seizure susceptibility in mice: Involvement of proinflammatory factors: Nitric oxide and prostaglandins

被引:130
作者
Sayyah, M [1 ]
Javad-Pour, M
Ghazi-Khansari, M
机构
[1] Inst Pasteur Iran, Dept Physiol & Pharmacol, Tehran 13164, Iran
[2] Univ Tehran, Sch Med, Dept Pharmacol, Tehran, Iran
关键词
epilepsy; microglia; naloxone; neuroinflammation; pentylenetetrazole;
D O I
10.1016/j.neuroscience.2003.08.043
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Central nervous system (CNS) inflammation in cases such as head trauma, infection and stroke has been associated with the occurrence of epileptic seizures. Microglia, the principal immune cells in the brain, readily become activated in response to injury, infection or inflammation. The bacterial endotoxin lipopolysaccharide (LPS) induces the activation of microglia and the production of proinflammatory factors including nitric oxide (NO) and Prostaglandins (PGs). We examined the effect of LPS on seizure susceptibility of mice, by using the sensitive test, threshold of clonic seizures induced by i.v. infusion of pentylenetetrazole. LPS decreased the seizure threshold in a dose- and time-dependent manner. Pretreatment of mice with the NO synthase inhibitor, N(G)-nitro-L-arginine methyl ester or cyclooxygenase inhibitor, piroxicam or the opioid receptor antagonist, (-)-naloxone completely reversed the proconvulsant effect of LPS. These results indicate that NO, PGs and endogenous opioid peptides seem to be involved in LPS-induced decrease in seizure threshold. (C) 2003 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1073 / 1080
页数:8
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