PROSTAGLANDINS AND RENIN RELEASE - EFFECT OF PGI2, PGE2, AND 13,14-DIHYDRO PGE2 ON THE BARORECEPTOR MECHANISM OF RENIN RELEASE IN THE DOG

The abilities of the vasodilator prostaglandins PGI2, PGE2 and 13,14-dihydro PGE2 to release renin were compared when infused into the denervated, nonfiltering canine kidney in vivo. Papaverine was used as a nonprostaglandin vasodilator. All prostaglandins tested were capable of stimulating renin secretion, with the scale of potency being 13,14-dihydro PGE2 > PGI2 > PGE2; papaverine had no effect on renin secretion. Apparently both PGE2 and PGI2 can stimulate renin secretion but that vasodilation per se is not a stimulus. 13,14-Dihydro PGE2 was included because it is a poorer substrate than PGE2, for transport and catabolism to inactive products, but has comparable potency to PGE2 when tested in systems with limited ability to catabolize PGE2. The fact that 13,14-dihydro PGE2 was the most potent prostaglandin tested suggests that the effects of PGE2 in our system are reduced by the kidneys'' recognized ability to extract and catabolize PGE2. Since PGI2 is less avidly metabolized when PGE2 by the kidney, the differences in observed potency between PGE2 and PGI2 could be largely the result of differences in renal catabolism of the 2 prostaglandins rather than differences in intrinsic potency. Both PGE2 and PGI2 are candidates for the endogenous prostaglandin responsible for stimulating renin secretion.