Investigation of PKC isoform‐specific translocation and targeting of the current of the late afterhyperpolarizing potential of myenteric AH neurons

AbstractAH neurons in the enteric nervous system play an essential role in initiating intestinal reflexes and factors that control AH neuron excitability therefore influence the state of the digestive system. Prominent afterhyperpolarizations that follow action potentials in these neurons strongly affect their excitability. In the present work, we have investigated the regulation of the afterhyperpolarizing current (IAHP) by protein kinase C (PKC). Electrophysiological responses and protein translocation were investigated in AH neurons of freshly dissected preparations of myenteric ganglia from the guinea‐pig ileum. The activator of conventional and novel PKCs, phorbol dibutyrate, but not the activator of novel PKCs, ingenol, blocked the IAHP. Phorbol dibutyrate had no effect on the hyperpolarization‐activated current (Ih) or on the A current (IA). Stimulation of synaptic inputs to the neurons also reduced the IAHP, and had no effect on Ih or IA. Phorbol dibutyrate also reduced a background outward current that was present after the IAHP current had been blocked by clotrimazole. Both phorbol dibutyrate and ingenol caused translocation of the novel PKC, PKCε, in these neurons. Only phorbol dibutyrate caused translocation of PKCγ, a conventional PKC. The studies thus indicate that the activation of PKC by phorbol esters and by nerve stimulation affects AH neurons in a similar way, and that PKC activation targets both the IAHP and another background K+ current. The IAHP is targeted by a conventional PKC, suggested to be PKCγ, as this is the only conventional PKC that is prominent in AH neurons.