Key result
Celiprolol exhibits weak postsynaptic alpha2-blocking effects in isolated rat tail arteries.
Why the study?
The alpha-adrenoceptor blocking effects of the cardioselective beta-blocker celiprolol were not fully characterized, particularly its action on alpha2-receptors.
Answers are grounded in this paper and cite their sources.
alpha-Adrenoceptor blocking effects of the cardioselective beta-blocker celiprolol were tested. 1. Celiprolol antagonized the contractions induced by UK-14304, but not those by phenylephrine, in isolated rat tail arteries with a pA2 value of 4.95. 2. In the isolated rat vas deferens, twitch contractions elicited by the transmural electrical stimulation (TS) were almost blocked by TTX (10(-7) M). Clonidine inhibited the TTX-sensitive contraction in a concentration-dependent manner. Celiprolol produced little effect on the inhibitory effects of clonidine. The concentration-inhibition curve of clonidine was shifted to the right by yohimbine (10(-8) M), but not by prazosin (10(-8) M). 3. Although celiprolol slightly increased the 3H-efflux to TS from the [3H]-norepinephrine-loaded rat vas deferens, the increment was not significant. Yohimbine (10(-7) M) significantly increased the 3H-efflux. TTX (10(-7) M) and bretylium (3 x 10(-5) M) blocked the 3H-efflux. 4. In the spinal rat treated with propranolol (3 mg/kg, i.v.) and prazosin (0.1 mg/kg, i.v.), celiprolol (30 and 100 mg/kg, i.v.) and yohimbine (0.1-1 mg/kg, i.v.) inhibited the pressor response to clonidine. 5. These results indicate that celiprolol may have a weak alpha 2-blocking effect which was more effective on postsynaptic alpha 2-receptors than presynaptic ones.
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Ukai et al. (1990) studied Healthy (preclinical animal model). Celiprolol vs. Control (vehicle) and other antagonists (yohimbine, prazosin) was evaluated on Antagonism of UK-14304-induced contractions in isolated rat tail arteries (pA2 value of 4.95). Celiprolol competitively antagonized contractions induced by the alpha2-agonist UK-14304 in isolated rat tail arteries with a pA2 value of 4.95, indicating a weak postsynaptic alpha2-blocking effect.
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