Acute lipopolysaccharide exposure facilitates epileptiform activity via enhanced excitatory synaptic transmission and neuronal excitability in vitro
被引:30
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作者:
Gao, Fei
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机构:
Fourth Mil Med Univ, Xijing Hosp, Dept Neurol, Xian 710032, Peoples R China
Xian Med Univ, Affiliated Hosp 1, Dept Neurol, Xian 710077, Peoples R ChinaFourth Mil Med Univ, Xijing Hosp, Dept Neurol, Xian 710032, Peoples R China
Gao, Fei
[1
,2
]
Liu, Zhiqiang
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机构:
Shaanxi Normal Univ, Coll Life Sci, Xian 710062, Peoples R ChinaFourth Mil Med Univ, Xijing Hosp, Dept Neurol, Xian 710032, Peoples R China
Liu, Zhiqiang
[3
]
Ren, Wei
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机构:
Shaanxi Normal Univ, Coll Life Sci, Xian 710062, Peoples R ChinaFourth Mil Med Univ, Xijing Hosp, Dept Neurol, Xian 710032, Peoples R China
Ren, Wei
[3
]
Jiang, Wen
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机构:
Fourth Mil Med Univ, Xijing Hosp, Dept Neurol, Xian 710032, Peoples R ChinaFourth Mil Med Univ, Xijing Hosp, Dept Neurol, Xian 710032, Peoples R China
Jiang, Wen
[1
]
机构:
[1] Fourth Mil Med Univ, Xijing Hosp, Dept Neurol, Xian 710032, Peoples R China
[2] Xian Med Univ, Affiliated Hosp 1, Dept Neurol, Xian 710077, Peoples R China
[3] Shaanxi Normal Univ, Coll Life Sci, Xian 710062, Peoples R China
来源:
NEUROPSYCHIATRIC DISEASE AND TREATMENT
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2014年
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10卷
Growing evidence indicates brain inflammation has been involved in the genesis of seizures. However, the direct effect of acute inflammation on neuronal circuits is not well known. Lipopolysaccharide (LPS) has been used extensively to stimulate brain inflammatory responses both in vivo and in vitro. Here, we observed the contribution of inflammation induced by 10 mu g/mL LPS to the excitability of neuronal circuits in acute hippocampal slices. When slices were incubated with LPS for 30 minutes, significant increased concentration of tumor necrosis factor a and interleukin 1 beta were detected by enzyme-linked immunosorbent assay. In electrophysiological recordings, we found that frequency of epileptiform discharges and spikes per burst increased 30 minutes after LPS application. LPS enhanced evoked excitatory postsynaptic currents but did not modify evoked inhibitory postsynaptic currents. In addition, exposure to LPS enhanced the excitability of CA1 pyramidal neurons, as demonstrated by a decrease in rheobase and an increase in action potential frequency elicited by depolarizing current injection. Our observations suggest that acute inflammation induced by LPS facilitates epileptiform activity in vitro and that enhancement of excitatory synaptic transmission and neuronal excitability may contribute to this facilitation. These results may provide new clues for treating seizures associated with brain inflammatory disease.
机构:
Univ Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, NetherlandsUniv Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, Netherlands
van Melis, Lennart V. J.
Peerdeman, Anneloes M.
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Univ Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, NetherlandsUniv Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, Netherlands
Peerdeman, Anneloes M.
Huiberts, Eva H. W.
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Univ Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, NetherlandsUniv Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, Netherlands
Huiberts, Eva H. W.
van Kleef, Regina G. D. M.
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机构:
Univ Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, NetherlandsUniv Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, Netherlands
van Kleef, Regina G. D. M.
de Groot, Aart
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Univ Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, NetherlandsUniv Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, Netherlands
de Groot, Aart
Westerink, Remco H. S.
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Univ Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, NetherlandsUniv Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, Div Toxicol,Neurotoxicol Res Grp, POB 80 177, NL-3508 TD Utrecht, Netherlands