Dwp. Hay et al., Differential modulation of endothelin ligand-induced contraction in isolated tracheae from endothelin B (ETB) receptor knockout mice, BR J PHARM, 132(8), 2001, pp. 1905-1915
1 The role of endothelin B (ETB) receptors in mediating ET ligand-induced c
ontractions in mouse trachea was examined in ETB receptor knockout animals.
2 Autoradiographic binding studies, using [I-125]-ET-1, confirmed the prese
nce of ETA receptors in tracheal and bronchial airway smooth muscle from wi
ld-type (+/+) and homozygous recessive (-/-) ETB receptor knockout mice. In
contrast, ETB receptors were not detected in airway tissues from (-/-) mic
e.
3 In tracheas from (+/+) mice, the rank order of potencies of the ET ligand
s was sarafotoxin (Stx) S6c > ET-1 > ET-3; Stx S6c had a lower efficacy tha
n ET-1 or ET-3. In tissues from (-/-) mice there was no response to Stx S6c
(up to 0.1 muM), whereas the maximum responses and potencies of ET-1 and E
T-3 were similar to those in (+/+) tracheae. ET-3 concentration-response cu
rve was biphasic in (+/+) tissues (via ETA and ETB receptor activation), an
d monophasic in (-/-) preparations (via stimulation of only ETA receptors).
4 In (+/+) preparations SE 234551 (1 nM), an ETA receptor-selective antagon
ist, inhibited the secondary phase, but not the first phase, of the ET-3 co
ncentration-response curve, whereas A192621 (100 nM), an ETB receptor-selec
tive antagonist, had the opposite effect. In (-/-) tissues SE 234551 (1 nM)
, but not A192621 (100 nM), produced a rightward shift in ET-3 concentratio
n-response curves.
5 The results confirm the significant influence of both ETA and ETB recepto
rs in mediating ET-1-induced contractions in mouse trachea. Furthermore, th
e data do not support the hypothesis of atypical ETB receptors. In this pre
paration ET-3 is not an ETB receptor-selective ligand, producing contractio
ns via activation of both ETA and ETB receptors.