Yeghiazaryan Marine, Rutkowska-Wlodarczyk Izabela, Konopka Anna, Wilczyński Grzegorz M, Melikyan Armenuhi, Korkotian Eduard, Kaczmarek Leszek, Figiel Izabela
Department of Neurophysiology, The Nencki Institute of Experimental Biology, Warsaw, Poland.
Department of Molecular and Cellular Neurobiology, The Nencki Institute of Experimental Biology, Warsaw, Poland.
PLoS One. 2014 Jun 11;9(6):e99789. doi: 10.1371/journal.pone.0099789. eCollection 2014.
DP-b99 is a membrane-activated chelator of zinc and calcium ions, recently proposed as a therapeutic agent. Matrix metalloproteinases (MMPs) are zinc-dependent extracellularly operating proteases that might contribute to synaptic plasticity, learning and memory under physiological conditions. In excessive amounts these enzymes contribute to a number of neuronal pathologies ranging from the stroke to neurodegeneration and epileptogenesis. In the present study, we report that DP-b99 delays onset and severity of PTZ-induced seizures in mice, as well as displays neuroprotective effect on kainate excitotoxicity in hippocampal organotypic slices and furthermore blocks morphological reorganization of the dendritic spines evoked by a major neuronal MMP, MMP-9. Taken together, our findings suggest that DP-b99 may inhibit neuronal plasticity driven by MMPs, in particular MMP-9, and thus may be considered as a therapeutic agent under conditions of aberrant plasticity, such as those subserving epileptogenesis.
DP-b99是一种膜激活的锌离子和钙离子螯合剂,最近被提议作为一种治疗剂。基质金属蛋白酶(MMPs)是锌依赖性的细胞外蛋白酶,在生理条件下可能有助于突触可塑性、学习和记忆。这些酶过量时会导致从中风到神经退行性变和癫痫发生等多种神经元病变。在本研究中,我们报告DP-b99可延迟小鼠戊四氮诱导癫痫发作的起始和严重程度,并且对海马器官型切片中的红藻氨酸兴奋性毒性具有神经保护作用,此外还可阻断主要神经元MMP即MMP-9诱发的树突棘形态重组。综上所述,我们的研究结果表明DP-b99可能抑制由MMPs尤其是MMP-9驱动的神经元可塑性,因此在异常可塑性条件下,如那些支持癫痫发生的条件下,可被视为一种治疗剂。