Subtypes of muscarinic receptors in rat duodenum - A comparison with rabbit vas deferens, rat atria, guinea-pig ileum and gallbladder by using imperialine
H. Akbulut et al., Subtypes of muscarinic receptors in rat duodenum - A comparison with rabbit vas deferens, rat atria, guinea-pig ileum and gallbladder by using imperialine, GEN PHARM, 32(4), 1999, pp. 505-511
The specific binding of [H-3]QNB to rat duodenum smooth muscle membranes wa
s a saturable process and Scatchard transformation of the saturation curves
indicated a linear plot (n(H) = 1.017 +/- 0.071). The K-D and B-max values
were 0.168 +/- 0.025 nM and 46.7 +/- 8.6 fmol/mg protein, respectively. An
alyses of competition curves using pirenzepine and guanylpirenzepine indica
ted more than one class of binding site. A minor population of muscarinic b
inding sites showed high affinity (M-1) for both pirenzepine (19.3 +/- 1.2%
; pK(i) = 8.29 +/- 0.36) and guanylpirenzepine (29.4 +/- 2.0%; pK(i) = 7.28
+/- 0.11). The antagonistic affinity values of pirenzepine and guanylpiren
zepine for the remaining low affinity binding sites, and that of methoctram
ine indicated the presence of both M-2 and M-3 subtypes. McN-A-343 produced
relaxations in rat duodenum and inhibited twitch contractions of rabbit va
s deferens induced by electrical stimulation in a concentration dependent m
anner. Carbachol (Cch) exerted concentration-dependent negative inotropic e
ffect in rat atria and contractile effects in guinea-pig gallbladder and il
eum longitudinal muscle-myenteric plexus preparation. Imperaline displaced
the concentration-response curves to McN-A-343 and Cch to the right in para
llel, without affecting the maximum responses in all tissues studied. The r
ank order of the pA(2) values was rabbit vas deferens > rat atria > guinea-
pig gallbladder = guinea-pig ileum > rat duodenum. The presynaptic muscarin
ic receptors at the rat duodenum and rabbit vas deferens were concluded to
be of M-1 and M-2 subtypes, respectively. (C) 1999 Elsevier Science Inc. Al
l rights reserved.