Mechanisms of T-type calcium channel blockade by zonisamide
نویسندگان
چکیده
We investigated the effects of zonisamide, a new antiepileptic drug, on voltage-dependent T-type calcium current (ICa) in cultured neuroblastoma cells of human origin (NB-I). Zonisamide reduced T-type ICa in a concentration-dependent manner without evoking any change in its inactivation kinetics or voltage dependence of action. The mean percent reduction was 38.3 +/- 5.8% at 50 microM. Further, zonisamide shifted the inactivation curve approximately 20 mV negative compared to the control. These resting blocking actions suggest that zonisamide shifts the channel population toward the inactivation state, allowing fewer channels to open during membrane depolarization. The blockade of T-type calcium channels by zonisamide could suppress an important component of inward current that underlies epileptiform cellular bursting, thereby inhibiting the spread of seizure activity.
منابع مشابه
Zonisamide – a review of experience and use in partial seizures
Zonisamide is a modern antiepileptic drug (AED) that is distinguished from other AEDs by its unique structure and broad mechanistic profile. Preclinical studies have reported a range of potential mechanisms of action for zonisamide, such as blocking voltage-gated sodium channels, reduction of T-type calcium channel currents, and enhancement of gamma-aminobutyric acid (GABA)-mediated inhibition,...
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Dr. Leppik raised some important issues regarding the mechanism of action of zonisamide. There is a great deal of interest in the impact of zonisamide on the T-type calcium channel. However, the relevance of that mechanism to the clinical experience is not known. The drug’s impact on the sodium channel is one that is not unique to this antiepilepsy drug (AED). There is some unpublished scientif...
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عنوان ژورنال:
- Seizure
دوره 5 شماره
صفحات -
تاریخ انتشار 1996