Objective To determine the subset of alpha(1)-adrenoceptors mediating
the functional abstraction of the prostate to noradrenaline. Materials
and methods Radioligand experiments were performed with membranes pre
pared from rat 1 fibroblasts transfected with rat alpha(1a), hamster a
lpha(1b) or bovine alpha(1c) adrenoceptor cDNA. Human prostatic tissue
obtained from transurethral resection of the prostate with full infor
med consent was submitted to functional in vitro muscle strip experime
nts. Results The binding experiments defined the potential subtype sel
ectivity of various antagonists. Using this information, it was possib
le to define the functionally important alpha(1)-adrenoceptor subtype
in the human prostate. Conclusion This work reports the results of the
first functional characterization of the alpha(1c)-adrenoceptor subty
pe. The most functionally important alpha(1)-adrenoceptor type in the
human prostate appears to be the alpha(1c) subtype. This finding may a
id the development of prostate-selective adrenoceptor pharmacotherapy.