Br. Bond et al., Differential effects of calcium channel antagonists in the amelioration ofradial artery vasospasm, ANN THORAC, 69(4), 2000, pp. 1035-1040
Citations number
24
Categorie Soggetti
Cardiovascular & Respiratory Systems","Medical Research Diagnosis & Treatment
Background. Radial artery (RA) is being used for coronary artery bypass gra
fting (CABG) with greater frequency. However, RA is prone to post-CABG vaso
spasm, which may be neurohormonally mediated. Use of the calcium channel an
tagonist diltiazem has been advocated as a strategy to reduce post-CABG RA
vasospasm. However, whether and to what degree different calcium channel an
tagonists influence neurohormonally induced RA vasoconstriction remains unk
nown.
Methods. RA segments were collected from patients undergoing elective CABG
(n = 13), and isometric tension was examined in the presence of endothelin
(10 nM) or norepinephrine (1 mu M). In matched RA, endothelin- or norepinep
hrine-induced contractions were measured in the presence of diltiazem (277
nM), amlodipine (73 nM), or nifedipine (145 nhl). These concentrations of c
alcium channel antagonists were based upon clinical plasma profiles.
Results. Endothelin and norepinephrine caused a significant increase in RA-
developed tension (0.54 +/- 0.1 and 0.68 +/- 0.1 g/mg, respectively; p < 0.
05). Amlodipine or nifedipine significantly reduced RA vasoconstriction in
the presence of endothelin (30 +/- 6% and 41 +/- 9%, respectively; p < 0.05
) or norepinephrine (27 +/- 8% and 53 +/- 9%, respectively; p < 0.05), wher
eas diltiazem did not significantly reduce RA vasoconstriction.
Conlclusions. These results demonstrate that neurohormonal factors released
post-CABG can cause RA vasoconstriction, and that calcium channel antagoni
sts are not equally effective in abrogating that response. Both amlodipine
and nifedipine, which have a higher degree of vascular selectivity, appear
to be the most effective in reducing RA vasoconstriction. (C) 2000 by The S
ociety of Thoracic Surgeons.