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持续性血脑屏障破坏可能是α干扰素诱导癫痫发作的潜在原因。

Persistent BBB disruption may underlie alpha interferon-induced seizures.

作者信息

Pavlovsky Lev, Seiffert Ernst, Heinemann Uwe, Korn Akiva, Golan Haim, Friedman Alon

机构信息

Laboratory of Experimental Neurosurgery, Soroka University Hospital and Zlotowski Center of Neuroscience, Ben-Gurion University, Beersheva 84105, Israel.

出版信息

J Neurol. 2005 Jan;252(1):42-6. doi: 10.1007/s00415-005-0596-3.

Abstract

Generalized seizures during Interferon-alpha (IFN-alpha) therapy have been repeatedly described in about 1%-4% of patients. However, the mechanisms underlying IFN-alpha induced seizures are not known. We describe a patient who developed partial and secondary generalized seizures during IFN-alpha therapy while displaying a focal disruption of her blood-brain barrier (BBB) corresponding with pathological electroencephalography (EEG). To test our hypothesis that IFN-alpha induces seizure activity, we exposed rat somatosensory cortices to clinically relevant concentrations of IFN-alpha in the acute in-vitro slice preparation or in-vivo. While acute exposure did not induce epileptic activity, recordings from slices exposed to IFN-alpha in-vivo one week prior to recordings revealed pronounced epileptiform activity in > 80% of the slices. We propose that cortical exposure to IFN-alpha leads to the generation of an epileptic cortex, which explains the weeks of latency in patients from initial treatment to seizures, and stressing the importance of identifying possible BBB disruption among high-risk patients administered peripherally acting drugs.

摘要

在接受α-干扰素(IFN-α)治疗的患者中,约1%-4%会反复出现全身性癫痫发作。然而,IFN-α诱发癫痫发作的机制尚不清楚。我们报告了一名患者,在接受IFN-α治疗期间出现部分性发作和继发性全身性发作,同时其血脑屏障(BBB)出现局灶性破坏,伴有病理性脑电图(EEG)表现。为了验证我们关于IFN-α诱发癫痫活动的假设,我们在急性体外脑片制备或体内实验中,将大鼠体感皮层暴露于临床相关浓度的IFN-α。虽然急性暴露未诱发癫痫活动,但在记录前一周体内暴露于IFN-α的脑片记录显示,超过80%的脑片出现明显的癫痫样活动。我们认为,皮层暴露于IFN-α会导致癫痫皮层的产生,这解释了患者从初始治疗到癫痫发作之间数周的潜伏期,并强调了在接受外周作用药物治疗的高危患者中识别可能的血脑屏障破坏的重要性。

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