ABSTRACT-We investigated the effect of black currant (BC) concentrate on smooth muscle in rat thoracic aorta. BC concentrate dose-dependently relaxed the norepinephrine (0.1 mM)-precontracted aorta, and the response was abolished after endothelium removal. Both oxyhemoglobin (1 mM), a nitric oxide (NO) scavenger, and 1H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one (ODQ, 0.5 mM), an inhibitor of guanylyl cyclase (GC), inhibited the relaxing effect of BC concentrate. N G -nitro-L-arginine methyl ester (L-NAME, 10 mM), a nitric oxide synthase (NOS) inhibitor, inhibited the relaxation, and the subsequent addition of L-arginine (1 mM), a NOS substrate, reversed the inhibitory effects of L-NAME. Neither indomethacin (10 mM), an inhibitor of cyclooxygenase, nor atropine (1 mM), an antagonist of muscarinic receptors, modified the effect of BC concentrate. Diphenhydramine (3 m M) and chlorpheniramine (2 mM), selective antagonists of H1-receptors, inhibited the relaxation, but cimetidine (0.3 mM), a selective antagonist of H2-receptors, did not affect the relaxation. These results indicate that, in the rat aorta, BC concentrate enhances synthesis of NO, which subsequently induces the endothelium-dependent vasorelaxation via the H1-receptors on the endothelium.