Acute induction of epileptiform discharges by pilocarpine in the in vitro isolated guinea-pig brain requires enhancement of blood-brain barrier permeability

被引:54
作者
Uva, L. [1 ]
Librizzi, L. [1 ]
Marchi, N. [2 ]
Noe, F. [3 ]
Bongiovanni, R. [4 ]
Vezzani, A. [3 ]
Janigro, D. [2 ]
De Curtis, M. [1 ]
机构
[1] Fondaz Ist Neurol, Unit Expt Neurophysiol & Epileptol, I-20133 Milan, Italy
[2] Cleveland Clin Fdn, Dept Mol Med, Cleveland, OH 44195 USA
[3] Mario Negri Inst Pharmacol Res, Lab Expt Neurol, Dept Neurosci, I-20157 Milan, Italy
[4] Case Western Reserve Univ, Dept Vet Affairs Med Ctr, Brecksville, OH 44141 USA
关键词
extracellular potassium; limbic cortex; muscarinic;
D O I
10.1016/j.neuroscience.2007.10.037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Systemic application of the muscarinic agonist, pilocarpine, is commonly utilized to induce an acute status epilepticus that evolves into a chronic epileptic condition characterized by spontaneous seizures. Recent findings suggest that the status epilepticus induced by pilocarpine may be triggered by changes in the blood-brain barrier (BBB) permeability. We tested the role of the BBB in an acute pilocarpine model by using the in vitro model brain preparation and compared our finding with in vivo data. Arterial perfusion of the in vitro isolated guinea-pig brain with <1 mM pilocarpine did not cause epileptiform activity, but rather reduced synaptic transmission and induced steady fast (20-25 Hz) oscillatory activity in limbic cortices. These effects were reversibly blocked by co-perfusion of the muscarinic antagonist atropine Sulfate (5 mu M). Brain pilocarpine measurements in vivo and in vitro suggested modest BBB penetration. Pilocarpine induced epileptiform discharges only when perfused with compounds that enhance BBB permeability, such as bradykinin (n=2) or histamine (n=10). This pro-epileptic effect was abolished when the BBB-impermeable muscarinic antagonist atropine methyl bromide (5 mu M) was co-perfused with histamine and pilocarpine. In the absence of BBB permeability enhancing drugs, pilocarpine induced epileptiform activity only after arterial perfusion at concentrations >10 mM. Ictal discharges correlated with a high intracerebral pilocarpine concentration measured by high pressure liquid chromatography. We propose that acute epileptiform discharges induced by pilocarpine treatment in the in vitro isolated brain preparation are mediated by a dose-dependent, atropine-sensitive muscarinic effect promoted by an increase in BBB permeability. Pilocarpine accumulation secondary to BBB permeability changes may contribute to in vivo ictogenesis in the pilocarpine epilepsy model. (c) 2008 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:303 / 312
页数:10
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