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Krel 2013
Krel 2013
Krel 2013
not NMDA or AMPA mediated currents in cortical neu- patient’s pain scale was assessed at 6 and 12week follow-
rons cell culture. SPD had no effect on voltage dependent up sessions.
sodium channel currents.
Results: Despite multiple trials of medical and surgical
Conclusions: SPD, a novel amide analogue of valproic management patient developed substantial relief with the
acid, robustly suppresses CSD frequency and elevates use of onobotuIinumtoxin A. Due to development of
the threshold of both NTG induced mechanical allodynia onobotuIinumtoxin A resistance in the form of shortened
and heat hyperalgesia. SPD may exert its anti-migraine duration of therapeutic activity, patient was transitioned to
effects through enhancing cortical inhibition. As a promis- incobotuIinumtoxin A with a beneficial result for a 12
ing novel anti-migraine compound further evaluation of week period of time. In the second patient an improve-
SPD’s specific mechanism of action is warranted. ment in patient symptoms were seen with injections of
incobotulinumtoxin A.