Results 131 to 140 of about 915 (177)
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Trimethaphan as a glutamate inhibitor at the Crayfish neuromuscular junction
Brain Research, 1983At the crayfish neuromuscular junction trimethaphan reduced the amplitude of both the glutamate-induced synaptic current and the excitatory junctional current in a dose-dependent manner at concentrations greater than 5 microM. These effects were dependent on membrane potential.
H, Shinozaki, M, Ishida
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[Neuromuscular blocking action of trimethaphan camsylate and cholinesterase].
Y Tsukawaki, Mizuo Miyazaki
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Trimethaphan camsylate (Arfonad) and human plasma cholinesterase.
Research communications in chemical pathology and pharmacology, 1979These results for the first time document that the brief duration of action of the ganglionic blocker, Arfonad (trimethaphan camsylate), is not due to inactivation by plasma cholinesterase. Inhibition of the enzyme in vitro by Arfonad was not altered by prior incubation of the drug in plasma at 37 degrees C for up to 16 hours nor by treatment with ...
A H, Anton +4 more
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Ultra-high Dose Trimethaphan in an Infant with Severe Hypertension
Journal of Toxicology: Clinical Toxicology, 1996Trimethaphan camsylate is a potent antihypertensive drug used to induce systemic arterial hypotension in patients undergoing major surgery and to treat severe systemic hypertension. The pharmacokinetics and pharmacodynamics of trimethaphan administered in the usual clinical dosages have been previously reported.
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Cerebral function during trimethaphanâinduced hypotension
Neurology, 1973A, Magness +4 more
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The Prognostic Value of the Trimethaphan Test
Southern Medical Journal, 1967J F, Patterson +2 more
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TRIMETHAPHAN IS NOT INACTIVATED BY PSEUDOCHOLINESERASE
Anesthesiology, 1989T. A. Alston, F. M. deBros
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Aminoglycoside antibiotics: interaction with trimethaphan at the neuromuscular junctions.
Drugs under experimental and clinical research, 1987Trimethaphan, a ganglionic blocking agent which is administered by intravenous drip to produce controlled hypotension during surgery, produces a complete neuromuscular blockade at the isolated phrenic nerve-hemidiaphragm preparation of the rat at a concentration of 0.3 mmol X l-1. This blockade is not reversed by neostigmine, a cholinesterase inhibitor,
A G, Paradelis +3 more
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