Abstract
Nitroprusside (NP) and D-600 effects on norepinephrine (NE)- and KCl-induced maximal contractions and unstimulated 45Ca uptake and efflux were delineated in canine renal vein (CRV) and compared with results in renal artery. In CRV, but not in renal artery, NE-induced contractions are usually associated with rhythmic oscillations in developed tension. Corresponding KCl-induced contractions are not associated with rhythmic activity and are depressed by 57% in the presence of phentolamine (PA). The Ca channel blocker, D-600, rapidly and extensively relaxed NE-induced contractions (86%) in CRV, but slowly and moderately relaxed similar responses in artery (46%). PA-resistant, KCl-induced contractions were equally sensitive to the relaxant effects of D-600 in CRV (73%) or artery (72%), but the relaxation rate was more rapid in CRV. Prior exposure to D-600 inhibited KCl-induced contractions in CRV and artery (99 vs. 91%, respectively). Similar prior treatment reduced NE-induced contractions (60%) in CRV, and prevented the development of NE-dependent rhythmic activity. In renal artery, NE-induced contractions were unaffected by prior D-600 exposure. NP relaxed KCl-induced contractions 32% in the presence of PA in CRV, but had little effect on KCl-induced response in artery (6%). Prior exposure to NP inhibited KCl-induced contractions 60-67% in CRV, which is approximately twice the inhibition seen in artery (31%). Relaxation of NE-induced contractions with NP and CRV and renal artery are (43% and 38%, respectively). In renal artery, responses to NE are less sensitive (1.6-fold) to prior NP exposure than in CRV. Prior exposure to NP or NP plus D-600 reduced NE-induced contractions in CRV 37% and 96%, respectively. NP and D-600 were without effect on unstimulated 45Ca uptake in CRV. In CRV, D-600 had no effect on 45Ca efflux into a O-Ca2+ solution, whereas NP decreased 45Ca efflux rate in a maintained manner. NP and D-600 appear to interfere with differing components in the release and entry of Ca2+ in CRV. These components are less readily differentiated and more interdependent than similar, well-defined and characterized components in arterial smooth muscle, and appear to be convergent.