S. Alaranta et al., RELAXATION OF THE BOVINE RETRACTOR PENIS MUSCLE BY A SMALL K+ EXCESS AND THE ROLE OF K+ IN ITS NEUROGENIC RELAXATION, European journal of pharmacology, 259(2), 1994, pp. 203-209
The mechanism of the relaxation of the bovine retractor penis muscle i
nduced by 6.7 mM Kf as well as the role of K+ in the neurogenic relaxa
tion of this muscle induced by nicotine, acetylcholine or electrical f
ield stimulation, was studied. The relaxation induced by 6.7 mM K+ was
, contrary to that induced by nicotine or electrical field stimulation
, abolished by 10(-7) M ouabain. 15 min exposure to 10(-5) M N-G-nitro
-L-arginine, 3.2 x 10(-6) M tetrodotoxin, 5.0 x 10(-4) M hexamethonium
, 5.3 x 10(-4) M methylene blue or hypoxia, all known to inhibit the n
eurogenic relaxation, did not affect the relaxation induced by 6.7 mM
K+ which was also unaffected by 10(-5) M apamin, 3 X 10(-3) M 4-aminop
yridine, 2.6 x 10(-2) M tetraethylammonium and 7.3 x 10(-4) M Ba2+. Ex
posure to K+-free solution reversibly abolished the neurogenic relaxat
ions. The relaxations caused by 5.0 X 10(-7) M cromakalim and 2.0 x 10
(-6) M pinacidil were totally blocked by 10(-5) M glibenclamide. Glibe
nclamide and apamin did not affect the tone of the muscle or its neuro
genic relaxations. 4-Aminopyridine 4.0 X 10(-5) to 3.0 X 10(-3) M and
tetraethylammonium 10(-4) to 2.6 x 10(-2) M raised the tone and enhanc
ed the relaxations elicited by electrical field stimulation. The resul
ts indicate that the relaxation induced by 6.7 mM K+ is partly mediate
d by activation of Na+-K+ ATPase and that its mechanism is thoroughly
different from that of the neurogenic relaxations. K-f channels sensit
ive to cromakalim and pinacidil exist in the smooth muscle cells of th
e bovine retractor penis, but they or small conductance K+ channels ar
e not involved in its neurogenic relaxation. The effects of the inhibi
tory neurotransmitter(s) on the smooth muscle cells are not mediated b
y K+ channels sensitive to 4-aminopyridine or tetraethylammonium, but
such neuronal K+ channels may participate in the regulation of release
of the inhibitory transmitter(s).