Jr. Cockcroft et al., EFFECT OF N-G-MONOMETHYL-L-ARGININE ON KININ-INDUCED VASODILATION IN THE HUMAN FOREARM, British journal of clinical pharmacology, 38(4), 1994, pp. 307-310
1 We compared effects of N-G-monomethyl-L-arginine (L-NMMA), an NO syn
thase inhibitor, on vasodilator responses to intra-arterial infusion o
f bradykinin and substance P in the human forearm. 2 Bradykinin (100 p
mol min(-1)) increased forearm blood flow when infused into the brachi
al artery of eight healthy male volunteers, from 2.8 +/- 0.2 (mean +/-
s.e. mean) to 9.3 +/- 1.0 ml min(-1) per 100 ml forearm volume. 3 Co-
infusion of L-NMMA (2 mu mol min(-1) and 4 mu mol min(-1)) with bradyk
inin (100 pmol min(-1)) for 6 min produced respectively a 9 +/- 14% an
d 42 +/- 14% inhibition (compared with L-NMMA vehicle) in the response
to bradykinin. 4 Substance P (1 pmol min(-1)) when infused into the b
rachial artery of a further eight male subjects increased forearm bloo
d flow from 3.4 +/- 0.2 to 6.3 +/- 0.7 ml min(-1) 100 ml(-1). 5 Co-inf
usion of L-NMMA (2 mu mol min(-1) and 4 mu mol min(-1)) with substance
P (1 pmol min(-1)) for 6 min produced respectively a 27 +/- 8% and 70
+/- 13% inhibition (compared with L-NMMA vehicle) in the response to
substance P. 6 These results demonstrate that vasodilator responses to
both bradykinin and substance P are mediated in part via the L-argini
ne/NO pathway. Bradykinin and substance P may be useful agonists with
which to study endothelial function in this vascular bed.