Al. Garciavillalon et al., ROLE OF NA+ K+ ATPASE ON THE RELAXATION OF RABBIT EAR AND FEMORAL ARTERIES/, Journal of Pharmacy and Pharmacology, 48(10), 1996, pp. 1057-1062
The role of Na+/K+ ATPase in vascular relaxation has been studied by d
etermining its inhibitory effects on 2-mm segments from rabbit central
ear and femoral arteries, mounted for isometric tension recording. Ac
etylcholine (10(-8)-10(-4) M), the nitric oxide donor sodium nitroprus
side (10(-8)-3 x 10(-4) M), the potassium channel agonist cromakalim (
10(-8)-3 x 10(-5) M), histamine (10(-8)-10(-4) M) in the presence of t
he H-1 antagonist chlorpheniramine (10(-5) M), and papaverine (10(-6)-
3 x 10(-4) M) all produced arterial relaxation in ear and femoral arte
ries precontracted with endothelin 1. Addition of potassium (6 x 10(-3
) 1 . 2 x 10(-2) M) caused relaxation of the same arteries preincubate
d in potassium-free medium. Ouabain (10(-5) M) an inhibitor of Na+/KATPase, reduced the relaxation of ear arteries, but not of femoral art
eries, in response to acetylcholine; it also reduced the response to s
odium nitroprusside, cromakalim or histamine, and abolished the relaxa
tion to potassium, but did not modify the response to papaverine, in b
oth types of artery. These results suggest that Na+/K+ ATPase might pl
ay a role in the relaxation of ear and femoral arteries to nitrovasodi
lators, to potassium channel openers and to activation of histamine re
ceptors, and that Na+/K+ ATPase might play a role in the cholinergic r
elaxation of ear, but not femoral arteries, suggesting that the mechan
ism of cholinergic relaxation might differ in each type of artery.