Gorji A, Scheld H H, Speckmann E-J
Institut für Physiologie, Universität Münster, Robert-Koch-Strasse 27a, 48149, Münster, Germany.
Neuroscience. 2002;115(4):993-7. doi: 10.1016/s0306-4522(02)00507-9.
Cyclosporine A (CsA) neurotoxicity is a common cause of seizures in transplant patients and others receiving immunosuppressive therapy. CsA at concentrations higher than the levels estimated for cerebrospinal fluid of the patients suffering from seizure attacks was ineffective to induce epileptiform field potentials (EFP) in in vitro brain-slice preparation. The aim of this study was to test the effect of CsA at lower concentrations on neuronal activity. Guinea-pig hippocampal slices were exposed to artificial cerebrospinal fluid containing CsA (0.1-2 microM). Furthermore, the effects of CsA (0.25-10 microM) were tested on EFP elicited by omission of Mg2+ from superfusate. Low concentrations of CsA (0.1-0.25 microM) induced EFP while higher doses (0.5-2 microM) failed to decrease the seizure threshold. CsA at concentrations of 0.25 and 1 microM had no significant effect on the low Mg2+-induced EFP. Higher CsA concentration (10 microM) strongly suppressed EFP. The results indicate that CsA at doses that are probably clinically relevant increases the neuronal excitability.
环孢素A(CsA)神经毒性是移植患者及其他接受免疫抑制治疗者癫痫发作的常见原因。在体外脑片制备中,浓度高于癫痫发作患者脑脊液估计水平的CsA无法诱导癫痫样场电位(EFP)。本研究的目的是测试较低浓度的CsA对神经元活动的影响。将豚鼠海马切片暴露于含CsA(0.1 - 2微摩尔)的人工脑脊液中。此外,测试了CsA(0.25 - 10微摩尔)对因超滤液中Mg2+缺失而引发的EFP的影响。低浓度的CsA(0.1 - 0.25微摩尔)可诱导EFP,而高剂量(0.5 - 2微摩尔)未能降低癫痫阈值。浓度为0.25和1微摩尔的CsA对低Mg2+诱导的EFP无显著影响。较高浓度的CsA(10微摩尔)强烈抑制EFP。结果表明,可能具有临床相关性剂量的CsA会增加神经元兴奋性。