TY - JOUR
T1 - DP-b99 modulates matrix metalloproteinase activity and neuronal plasticity
AU - Yeghiazaryan, Marine
AU - Rutkowska-Wlodarczyk, Izabela
AU - Konopka, Anna
AU - Wilczyński, Grzegorz M.
AU - Melikyan, Armenuhi
AU - Korkotian, Eduard
AU - Kaczmarek, Leszek
AU - Figiel, Izabela
PY - 2014/6/11
Y1 - 2014/6/11
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84903388753&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0099789
DO - 10.1371/journal.pone.0099789
M3 - Article
C2 - 24918931
AN - SCOPUS:84903388753
SN - 1932-6203
VL - 9
JO - PLoS One
JF - PLoS One
IS - 6
M1 - e99789
ER -