The neuromuscular block induced in cats by depolarizing drugs was intensified and the effect of tubocurarine was reduced by intravenous infusions of propranolol, although by themselves they did not affect contraction of skeletal muscle. The use of propranolol in the treatment of ar-rhythmias during anaesthesia has recently been discussed by Vickers (1966). After intra-arterial injection of comparatively large doses, proprano-lol, like the structurally related pronethalol (Tiirker and Kiran, 1965), augments the action of neuromuscular blocking agents (Wislicki and Rosenblum, 1967). It has been shown that pro-pranolol not only blocks adrenergic beta-receptors but that it also has a sympathomimetic effect, apparently by inducing a release of c...
With pronethalol, quinidine, and reserpine it was necessary to increase the dose of acetylstrophanth...
1 A new in vivo experimental method is described whereby the neuromuscular blocking effects of muscl...
PURPOSE: Sugammadex is a selective relaxant binding agent designed to encapsulate the aminosteroidal...
SUMMARY The influence of /3-adrenergic receptor blockade on the impulse activity of 21 cardio-vascul...
The influence of beta-adrenergic receptor blockade on the impulse activity of 21 cardiovascular symp...
Summary: The effects of an alpha2 adrenoceptor blocker, yohimbine, and an alpha1 adrenoceptor blocke...
The present study was carried out in order to investigate the effects of alpha and beta adrenoceptor...
KATZ, RONALD L., CLYDE 0. Low) AND KENNETH E. EAKINS: Anesthetic-dopamine cardiac arrhythmias and th...
Cr.itvoux, PETER AND ERNEST REIT: Interaction between angiotensin and neurally released norepinephri...
Item does not contain fulltextThis study was undertaken to investigate the neuromuscular blocking pr...
The interaction of ORG 9426, a new non-depolarizing neuromuscular blocking agent, with intravenous a...
Summary: The possible involvement of an adrenergic-endorphin system in the mediation of the pressor ...
While pronethalol ’ possesses significant beta-adrenergic receptor blocking actions (Black and Steph...
Typescript.Bibliography: leaves 132-142.xii, 142 l illusStudies were performed to assess the role of...
의학과/박사[한글] [영문] Accumulated evidences indicated that the administration of epinephrine causes ...
With pronethalol, quinidine, and reserpine it was necessary to increase the dose of acetylstrophanth...
1 A new in vivo experimental method is described whereby the neuromuscular blocking effects of muscl...
PURPOSE: Sugammadex is a selective relaxant binding agent designed to encapsulate the aminosteroidal...
SUMMARY The influence of /3-adrenergic receptor blockade on the impulse activity of 21 cardio-vascul...
The influence of beta-adrenergic receptor blockade on the impulse activity of 21 cardiovascular symp...
Summary: The effects of an alpha2 adrenoceptor blocker, yohimbine, and an alpha1 adrenoceptor blocke...
The present study was carried out in order to investigate the effects of alpha and beta adrenoceptor...
KATZ, RONALD L., CLYDE 0. Low) AND KENNETH E. EAKINS: Anesthetic-dopamine cardiac arrhythmias and th...
Cr.itvoux, PETER AND ERNEST REIT: Interaction between angiotensin and neurally released norepinephri...
Item does not contain fulltextThis study was undertaken to investigate the neuromuscular blocking pr...
The interaction of ORG 9426, a new non-depolarizing neuromuscular blocking agent, with intravenous a...
Summary: The possible involvement of an adrenergic-endorphin system in the mediation of the pressor ...
While pronethalol ’ possesses significant beta-adrenergic receptor blocking actions (Black and Steph...
Typescript.Bibliography: leaves 132-142.xii, 142 l illusStudies were performed to assess the role of...
의학과/박사[한글] [영문] Accumulated evidences indicated that the administration of epinephrine causes ...
With pronethalol, quinidine, and reserpine it was necessary to increase the dose of acetylstrophanth...
1 A new in vivo experimental method is described whereby the neuromuscular blocking effects of muscl...
PURPOSE: Sugammadex is a selective relaxant binding agent designed to encapsulate the aminosteroidal...