Results 161 to 170 of about 6,413 (205)
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A Method for Detecting Tubocurarine in Tissue
Journal of the Forensic Science Society, 1971A method is described by which d-tubocurarine can be extracted from liver tissue. Proteins are first removed, and the solution made alkaline; interfering bases are removed by shaking with dichloromethane. The tubocurarine can then be extracted, and is estimated by ultraviolet spectrophotometry.
H M, Stevens, R H, Fox
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Nitroprusside and the duration of tubocurarine and pancuronium
Anaesthesia, 1979Seventy-six patients in whom sodium nitroprusside was administered in order to induce hypotension received either 0.2 mg/kg tubocurarine or 0.04 mg/kg pancuronium bromide. The duration of action of these two drugs was assessed. In contrast to previous studies in the dog, sodium nitroprusside, given concurrently with either tubocurarine or pancuronium ...
C W, Graham, L F, Walts
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THE TOXICITY OF d‐TUBOCURARINE TO RATS
Australian Journal of Experimental Biology and Medical Science, 1962SUMMARYFemale Wistar rats were found to be more susceptible to the lethal effect of d‐tubocurarine than were male rats of the same strain and age. The LD50 of d‐tubocurarine administered intraperitoneally was estimated as 0·256 mg./kg. body weight for female rats and 0·328 mg./kg.
C H, GALLAGHER, J H, KOCH
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THE DISTRIBUTION AND FATE OF d-TUBOCURARINE
The Journal of Pharmacology and Experimental Therapeutics, 1965The distribution and elimination of d -tubocurarine were investigated in 30 dogs at a minimal paralyzing dose and at a second higher concentration sufficient to produce saturation of depots. The concentration of d -tubocurarine in the muscle tissue closely paralleled that found in the plasma.
E N, COHEN, A, CORBASCIO, G, FLEISCHLI
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Binding of d-Tubocurarine by Gangliosides
Hoppe-Seyler´s Zeitschrift für physiologische Chemie, 1979The binding of d-tubocurarine by ganglioside mixtures from chicken and bovine brain as well as by the single gangliosides GGtet1-NeuAc, GGtet2aNeuAc and GGtet3aNeuAc was demonstrated by means of equilibrium gel filtration. The sialyl-oligosaccharide derivatives of GGtet1NeuAc and GGtet2aNeuAc, however, did not bind any d-tubocurarine. A lack of binding
H, Rösner, G, Merz, H, Rahmann
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2000
Abstract Valproic acid is a branched-chain fatty acid. It is structurally similar to the inhibitory neurotransmitter y-aminobutyric acid (GABA). Valproic acid, an antiepileptic drug, was approved for prescribed use by the U.S. Food and Drug Administration in 1978; therapeutic use may be associated with significant adverse effects on ...
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Abstract Valproic acid is a branched-chain fatty acid. It is structurally similar to the inhibitory neurotransmitter y-aminobutyric acid (GABA). Valproic acid, an antiepileptic drug, was approved for prescribed use by the U.S. Food and Drug Administration in 1978; therapeutic use may be associated with significant adverse effects on ...
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