K. Yano et al., CARDIOVASCULAR ACTIONS OF FROG UROTENSIN-II IN THE FROG, RANA-CATESBEIANA, General and comparative endocrinology, 97(1), 1995, pp. 103-110
The effects of synthetic frog urotensin II on cardiac output and arter
ial blood pressure and on the motility of isolated vascular smooth mus
cle were investigated in the bullfrog, Rana catesbeiana. Bolus injecti
ons of frog urotensin II (100 nmol/kg) into the left systemic arch pro
duced a rapid and sustained fall in blood flow through the right branc
h of the truncus arteriosus (to 62 +/- 5% of preinjection values; n =
8). The response exhibited strong tachyphylaxis. There were no signifi
cant effects on heart rate and central arterial blood pressure but the
fact that a fall in cardiac output was not accompanied by a fall in p
ressure suggests that the peptide produced an increase in peripheral v
ascular resistance. Rings of vascular smooth muscle from the proximal
and distal regions of the left and right systemic arches responded to
urotensin II with sustained and concentration-dependent contractions.
The tissues from the different regions did not significantly differ in
their maximum response and sensitivity to the peptide (EC(50) values
from 4.6 x 10(-9) to 6.5 x 10(-9) M; n = 6). Acetylcholine (3 x 10(-8)
to 3 x 10(-6) M) significantly (P < 0.05) relaxed the rings in an end
othelium-dependent manner but urotensin II did not produce relaxation
at any concentration tested. The contractile effect of urotensin II (1
0(-7) M) was not affected by preincubation of the rings with atropine,
tetrodotoxin, and somatostatin-14 but indomethacin produced a signifi
cant (P < 0.05) decrease in the amplitude of the contractions of the s
ystemic arch (to 18 +/- 2% of control values; n = 6). Arachidonic acid
(10(-5) M) also produced a sustained contraction of the rings. The da
ta suggest an involvement of prostaglandin synthesis in the contractil
e action of urotensin II on isolated frog vascular smooth muscle but,
unlike in mammals, urotensin II does not stimulate nitric oxide synthe
sis in this tissue. (C) 1995 Academic Press, Inc.