The ability of members of the Dibenamine series of adrenergic blocking agents (13-haloalkylamines) to inhibit or “reverse ” vasopressor responses to a variety of sympathomimetic agents has been repeatedly demonstrated. With different stimulating agents the responses obtained after blockade vary from easily elicited, complete reversals of the pressor response (epinephrine, Kephrine, etc.) to re-sponses which usually retain a pressor component and in which a significant depressor phase can be demonstrated only under special conditions (aliphatic amines, norepinephrine, etc.). Because the pressor response to epinephrine is readily reversed whereas that to norepinephrine is usually only partially inhibited (Barger and Dale, 1910; Greer et al., ...
THE purpose of this paper is to present the re-sults of an investigation of the therapeutic use of a...
The literature contains indications that adrenaline antagonists inhibit muscarinic actions of acetyl...
Numerous reports have described enhancement or potentiation by cocaine, ephedrine, anti-histaminic a...
The recent demonstration of the high potency and specificity of the adrenergic blocking action of N,...
Under controlled conditions the effects of various "sympatholytic " agents on the cardiova...
Previously reported studies of the structural requirements for activity in the f-haloaikylamine (Dib...
THE well known role of the sympathetic nervous system in hypertension has led to search for sympatho...
The mechanism of the pressor response to ephedrine is con-troversial. In the present study. i.v. inj...
The mode of action of clonidine and norepinephnne (NE) has concentration-effect curve to NE remainin...
Studies performed and published from this laboratory in 1953 by Lanier et al. demonstrated that the ...
The forearm vasoconstrictor response to lower body negative pressure (LBNP), a reflex stimulus to no...
In experiments carried out to develop an orally active beta-haloamine adren-ergic blocking agent (Fe...
It is frequently stated or implied that the domestic rabbit is devoid of adrener-gic vascular inhibi...
<p>Blockade of alpha2 (yohimbine) and beta (propranolol) but not of alpha1 (benoxathian) receptors p...
β-Haloalkylamines are a series of sympathetic blocking compounds. Phenoxybenzamine, the only commerc...
THE purpose of this paper is to present the re-sults of an investigation of the therapeutic use of a...
The literature contains indications that adrenaline antagonists inhibit muscarinic actions of acetyl...
Numerous reports have described enhancement or potentiation by cocaine, ephedrine, anti-histaminic a...
The recent demonstration of the high potency and specificity of the adrenergic blocking action of N,...
Under controlled conditions the effects of various "sympatholytic " agents on the cardiova...
Previously reported studies of the structural requirements for activity in the f-haloaikylamine (Dib...
THE well known role of the sympathetic nervous system in hypertension has led to search for sympatho...
The mechanism of the pressor response to ephedrine is con-troversial. In the present study. i.v. inj...
The mode of action of clonidine and norepinephnne (NE) has concentration-effect curve to NE remainin...
Studies performed and published from this laboratory in 1953 by Lanier et al. demonstrated that the ...
The forearm vasoconstrictor response to lower body negative pressure (LBNP), a reflex stimulus to no...
In experiments carried out to develop an orally active beta-haloamine adren-ergic blocking agent (Fe...
It is frequently stated or implied that the domestic rabbit is devoid of adrener-gic vascular inhibi...
<p>Blockade of alpha2 (yohimbine) and beta (propranolol) but not of alpha1 (benoxathian) receptors p...
β-Haloalkylamines are a series of sympathetic blocking compounds. Phenoxybenzamine, the only commerc...
THE purpose of this paper is to present the re-sults of an investigation of the therapeutic use of a...
The literature contains indications that adrenaline antagonists inhibit muscarinic actions of acetyl...
Numerous reports have described enhancement or potentiation by cocaine, ephedrine, anti-histaminic a...