MODULATION OF KV4 CHANNELS, KEY COMPONENTS OF RAT VENTRICULAR TRANSIENT OUTWARD K+ CURRENT, BY PKC

Current evidence suggests that members of the Kv4 subfamily may encode native cardiac transient outward current (I-to). Antisense hybrid-arr est with oligonucleotides targeted to Kv4 mRNAs specifically inhibited rat ventricular I-to, supporting this hypothesis. To determine whethe r protein kinase C (PKC) affects I-to by an action on these molecular components, we compared the effects of PKC activation on Kv4.2 and Kv4 .3 currents expressed in Xenopus oocytes and rat ventricular I-to. Pho rbol 12-myristate 13-acetate (PMA) suppressed both Kv4.2 and Kv4.3 cur rents as well as native I-to, but not after preincubation with PKC inh ibitors (e.g., chelerythrine). An inactive stereoisomer of PMA had no effect. Phenylephrine or carbachol inhibited Kv4 currents only when co expressed, respectively, with alpha(1C)-adrenergic or M-1 muscarinic r eceptors (this inhibition was also prevented by chelerythrine). The vo ltage dependence and inactivation kinetics of Kv4.2 were unchanged by PKC, but small effects on the rates of inactivation and recovery from inactivation of native I-to were observed. Thus Kv4.2 and Kv4.3 protei ns are important subunits of native rat ventricular I-to, and PKC appe ars to reduce this current by affecting the molecular components of th e channels mediating I-to.