In 1943 Swan and White (1) studied a series of choline esters with atropine-like properties. The dibutyl urethane of choline, and a closely related compound, the dibutyl urethane of dimethylethyl-$-hydroxyethyl ammonium sulfate, were selected for clinical trial as mydriatic and cycloplegic agents. In a pharmacologi-cal study of the actions of the latter compound (“Dibutoline”), Peterson and Peterson (2) demonstrated blockade of the actions of acetyicholine and para-sympathetic nerve stimulation on cholinergic effector organs, but stated that the drug possessed no “nicotinic paralyzing ” action. Some of the characteristics of the cardiovascular responses to Dibutoline, however, suggested that blockade of autonomic ganglia was produced by the...
It has been long accepted that the anti-curare action of neostigmine is at-tributable to its strong ...
Under controlled conditions the effects of various "sympatholytic " agents on the cardiova...
In man, C6, a new ganglionic blocking agent (50 mg. intravenously) produced inhibition of the Valsal...
Although the powerful parasympathetic action of acetyl choline was discovered more than thirty years...
As a result of the classic studies of Langley and Dickinson (1889), it was estab-lished that nicotin...
Experiments were performed in animals to evaluate 4,5,6,7-tetrachloro-2-(2 dimethylaminoethyl)-isoin...
CARBAMINOYLCHOLINE, known popularly as Doryl, is one of the most powerful parasympathomimetic drugs ...
In 1914 Dale published his now famous paper on â€oe¿ The action of certain esters and ethers of chol...
THE well known role of the sympathetic nervous system in hypertension has led to search for sympatho...
Dale (1933) defined a cholinergic nerve as one whose impulses are mediated by an acetylcholine-like ...
The two marjor properties to be considered are: - the degree of paralysis, which depends on the aff...
The intense pharmacological activity of acetyicholine and its physiological significance as the chem...
A peripheral atropine-like action of certain choline esters which were recently synthesized by the a...
From results of pharmacological tests on the neuromuscular and autonomic blocking actions of a serie...
The work of Dale in 1914 to a great extent characterized the action of acetyicholine. This investiga...
It has been long accepted that the anti-curare action of neostigmine is at-tributable to its strong ...
Under controlled conditions the effects of various "sympatholytic " agents on the cardiova...
In man, C6, a new ganglionic blocking agent (50 mg. intravenously) produced inhibition of the Valsal...
Although the powerful parasympathetic action of acetyl choline was discovered more than thirty years...
As a result of the classic studies of Langley and Dickinson (1889), it was estab-lished that nicotin...
Experiments were performed in animals to evaluate 4,5,6,7-tetrachloro-2-(2 dimethylaminoethyl)-isoin...
CARBAMINOYLCHOLINE, known popularly as Doryl, is one of the most powerful parasympathomimetic drugs ...
In 1914 Dale published his now famous paper on â€oe¿ The action of certain esters and ethers of chol...
THE well known role of the sympathetic nervous system in hypertension has led to search for sympatho...
Dale (1933) defined a cholinergic nerve as one whose impulses are mediated by an acetylcholine-like ...
The two marjor properties to be considered are: - the degree of paralysis, which depends on the aff...
The intense pharmacological activity of acetyicholine and its physiological significance as the chem...
A peripheral atropine-like action of certain choline esters which were recently synthesized by the a...
From results of pharmacological tests on the neuromuscular and autonomic blocking actions of a serie...
The work of Dale in 1914 to a great extent characterized the action of acetyicholine. This investiga...
It has been long accepted that the anti-curare action of neostigmine is at-tributable to its strong ...
Under controlled conditions the effects of various "sympatholytic " agents on the cardiova...
In man, C6, a new ganglionic blocking agent (50 mg. intravenously) produced inhibition of the Valsal...