1. Two benzofuran-2-ethanolamines
Ro 03-5255 (1-(5-acetylamino-benzofuran-2-yl)-1-hydroxy-2-isopropylaminoethane) and
Ro 03-7894 (1-(5-chloracetyl aminobenzofuran-2-yl)-1-hydroxy-2-isopropylaminoethane) which had previously been shown to exhibit respectively competitive and irreversible beta-
adrenoceptor antagonism in guinea-pig isolated atria, were compared in vivo using
isoprenaline-induced
tachycardia of anaesthetized guinea-pigs and heart rate and contractility (dp/dtmax) of open-chest anaesthetized guinea-pigs and of conscious cats. 2. In
urethane-anaesthetized guinea-pigs doses of 3 mg/kg, s.c. of both antagonists produced significant blockade of the rate response to an 80% of maximum dose of
isoprenaline after 4 h. In other experiments, guinea-pigs were pretreated with the antagonists and the responses to
isoprenaline were then monitored. The slopes of the dose-response curves to
isoprenaline were depressed for up to 24 h by
Ro 03-7894 but this was not so with
Ro 03-5255. 3. In conscious cats the course of blockade by
Ro 03-7894 was followed in the same animals and was still evident after 48 h. In contrast, the beta-
adrenoceptor blockage produced by
Ro 03-5255 was not evident 24 h after administration. 4. The persistence of blockade by
Ro 03-7894 was consistent with the irreversible mode of action demonstrated in vitro.