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The alpha1G subunit (CaV3.1) is the pore-forming component of T-type voltage-gated calcium channels. These channels are characterized by low-voltage activation thresholds and transient currents due to rapid inactivation. They play critical roles in pacemaking activity in the heart, thalamic relay, and generating rhythmic burst firing patterns. Dysfunction of CACNA1G has been implicated in absence epilepsy, sleep disorders, pain syndromes, Parkinson’s disease, some cancers, and endocrine disorders. It is a primary pharmacological target for anti-seizure drugs used to treat absence epilepsy, such as ethosuximide.
Inhibition of T-type calcium channels, blocking burst mode activation.
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