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The calcium channel protein subunit alpha1 (CaVα1) is the primary pore-forming component of voltage-gated calcium channels. These channels mediate calcium influx into cells upon membrane depolarization, crucial for processes like muscle contraction, neurotransmitter release, and hormone secretion. Multiple isoforms (CaV1.x, CaV2.x, CaV3.x) exist with distinct tissue distributions and functions. The α₁ subunit forms the central pore, while auxiliary subunits (β, α₂δ, γ) modulate channel properties. Dysregulation or mutations in α₁ genes cause various diseases, including cardiac arrhythmias and periodic paralysis. Dihydropyridines block L-type channels and are used clinically for treating hypertension and arrhythmias.
Block calcium influx through voltage-gated calcium channels.
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