Role of protein kinase C in the endothelin-induced contraction in the rabbit saphenous vein

The roie of protein kinase C in the endothelin-induced contraction was examined in the isolated rabbit saphenous vein in which endothelin-1, endothelin-3, sarafotoxin S6c and IRL 1620 (succinyl-[Glu⁹,Ala^11,15]endothelin-1-(8-21))-induced contraction at the threshold concentrations of 0.1-1 pM. A selective inhibitor of protein kinase C, 500 nM calphostin C (2-[12-[2-(benzyloxy)propyl]-3, 10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl]-1-methylethyl carbonic acid 4-hydroxyphenyl ester), shifted the concentration-response curves for these agonists to the right 7.4- to 109-fold. In the vein in which the endothelin ET_B receptor was desensitized, sarafotoxin S6c and IRL 1620 were ineffective whereas endothelin-1 and higher concentrations of endothelin-3 induced contractions by activating the endothelin ET_A receptor. Caiphostin C (500 nM) shifted the concentration-response curves for endothelin-1 and endothelin-3 to the right more than 155-fold. Down-regulation of protein kinase C (by treatment with phorbol 12-myristate 13-acetate for 20 h) shifted the concentration-response curves for these agonists to the right before and after desensitization of the endothelin ET_B receptor 3.7- to 59-fold. In the permeabilized smooth muscle, Ca²⁺-induced contraction was enhanced by endothelin-1, endothelin-3 and sarafotoxin S6c at concentrations much higher than those needed to induce contraction (threshold concentration was 3 nM). Caiphostin C and down-regulation of protein kinase C shifted the concentration-response curves for endothelin-1 and endothelin-3 to the right and downwards without changing the effect of sarafotoxin S6c. In the permeabilized muscle in which the endothelin ET_B receptor was desensitized, endothelin-1 and endothelin-3 still augmented the Ca²⁺-induced contraction. Calphostin C and down-regulation of protein kinase C shifted the concentration-response curves for endothelin-1 and endothelin-3 to the right and downwards. These results suggest that protein kinase C is involved in the contraction mediated by the endothelin ET_A and ET_B receptors; and Ca²⁺ sensitization mediated by the endothelin ET_A receptor is due to activation of protein kinase C whereas Ca²⁺ sensitization mediated by the endothelin ET_B receptor may be due not only to the activation of protein kinase C but also to other mechanisms.