Comparison of University of Wisconsin and St. Thomas' Hospital solutions on endothelium-derived hyperpolarizing factor-mediated function in coronary micro-arteries
Zd. Ge et Gw. He, Comparison of University of Wisconsin and St. Thomas' Hospital solutions on endothelium-derived hyperpolarizing factor-mediated function in coronary micro-arteries, TRANSPLANT, 70(1), 2000, pp. 22-31
Background. It is controversial whether coronary endothelial function is im
paired after cold exposure to University of Wisconsin (UW) or St. Thomas' H
ospital (ST) solution during heart transplantation, We therefore examined t
he effects of cold storage of coronary micro-arteries with UW or ST solutio
n on endothelium-derived hyperpolarizing factor (EDHF)-mediated function.
Methods. Porcine and human coronary arteries were immersed in either UW or
ST solution at 4 degrees C for 4 hr and then normalized in a wire myograph,
Results. In the rings (normalized diameter: 200-500 mu M) precontracted by
U-46619, EDHF-mediated relaxation and hyperpolarization were initiated by b
radykinin (BK) or A(23187) in the presence of indomethacin and N-G-nitro-L-
arginine. In the human coronary arteries, the EDHF-mediated relaxation to B
K was reduced by UW solution from 53.2+/-5.6% to 24.0+/-2.7% (P=0.006), The
reduced EDHF-mediated relaxation occurred concurrently with the decreased
hyperpolarization to BK (17.0+/-1.5 vs. 10.5+/-1.1 mV, n=10, P=0.004) or A(
23187) in porcine coronary arteries. In the control arteries, K+ channel bl
ockers, either glybenclamide or tetraethylammonium reduced the EDHF-mediate
d relaxation, After exposure to UW solution, the EDHF-mediated relaxation w
as further significantly inhibited. In contrast, ST solution did not affect
, these responses.
Conclusions. These results show that in coronary micro-arteries, UW, but no
t ST, solution impairs the EDHF-mediated function and inhibits the Ca2+-act
ivated and ATP-sensitive K+ channels. Our comparative study suggests that S
T solution may be superior to Um solution in preserving the EDHF-related en
dothelial function of coronary micro-arteries.