Results 141 to 150 of about 2,992 (170)
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The uptake of decamethonium and hexamethonium by slices of mouse kidney.
Acta Pharmacologica et Toxicologica, 2009The renal uptake of decamethonium was studied and compared to that of hexamethonium. Incubations were carried out at 37° in a medium with pH 7.4 containing 14C-decamethonium (1.8 μM) and the uptake expressed as the slice-to-medium concentration ratio (S ...
J. Holm
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, 1955
Summary. The neuromuscular block produced in frog muscle by acetylcholine, nicotine, decamethonium and succinylcholine has been investigated with extracellular and intracellular recording electrodes.
S. Thesleff
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Summary. The neuromuscular block produced in frog muscle by acetylcholine, nicotine, decamethonium and succinylcholine has been investigated with extracellular and intracellular recording electrodes.
S. Thesleff
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Acta Physiologica Scandinavica, 1955
Summary. The neuromuscular block produced in the isolated nerve-diaphragm preparation of the rat by acetylcholine, decamethonium and succinylcholine has been investigated with intracellular recording electrodes.
S. Thesleff
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Summary. The neuromuscular block produced in the isolated nerve-diaphragm preparation of the rat by acetylcholine, decamethonium and succinylcholine has been investigated with intracellular recording electrodes.
S. Thesleff
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Activation of muscle spindles by succinylcholine and decamethonium, the effects of curare.
Acta Physiologica Scandinavica, 1953Summary. The effect of the neuromuscular blocking agent succinylcholine-iodide (Sch) was studied, by intraarterial injection, on single muscle spindles in cats. Spindle afferents were isolated in the dorsal roots.
R. Granit, S. Skoglund, S. Thesleff
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Acta Pharmacologica et Toxicologica, 2009
The accumulation of decamethonium by mouse kidney slices was investigated with particular reference to the possibility that this agent uses a choline transport system. Slices of mice kidneys were incubated (1 hour) in Krebs-Ringer bicarbonate medium (37°,
J. Holm
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The accumulation of decamethonium by mouse kidney slices was investigated with particular reference to the possibility that this agent uses a choline transport system. Slices of mice kidneys were incubated (1 hour) in Krebs-Ringer bicarbonate medium (37°,
J. Holm
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Acta Pharmacologica et Toxicologica, 2009
An investigation was performed to determine whether decamethonium and carbamoylcholine share a common transport mechanism with tetraethyl-ammonium and N1-methylnicotinamide in mouse kidney slices.
J. Holm
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An investigation was performed to determine whether decamethonium and carbamoylcholine share a common transport mechanism with tetraethyl-ammonium and N1-methylnicotinamide in mouse kidney slices.
J. Holm
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The effect of d-tubocurarine on the kinetics of decamethonium uptake by mouse kidney slices.
Acta Pharmacologica et Toxicologica, 2009The effect of d-tubocurarine on the kinetics of the decamethonium uptake by mouse kidney slices was studied. Slices were incubated (1 hour) in a Krebs-Ringer bicarbonate medium (37°, pH 7.4) in the presence of 14C-decame-thonium and d-tubocurarine.
J. Holm
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Journal of Medicinal Chemistry, 1975
Spin-labeled analogs of biotin (vitamin H), hexamethonium, decamethonium, dichlorisoproterenol, propranolol, and primaquine containing the nitroxide free radical have been synthesized and tested for biological activity.
B. Sinha, C. Chignell
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Spin-labeled analogs of biotin (vitamin H), hexamethonium, decamethonium, dichlorisoproterenol, propranolol, and primaquine containing the nitroxide free radical have been synthesized and tested for biological activity.
B. Sinha, C. Chignell
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Journal of Medicinal Chemistry, 1994
Symmetrically bis-catechol-substituted analogues (1 and 2, respectively) of hexamethonium and decamethonium were synthesized and investigated as redox-activated affinity reagents toward the neurotoxin-binding sites of the nicotinic acetylcholine receptor
Y. Gu, H. Lee, R. A. Hudson
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Symmetrically bis-catechol-substituted analogues (1 and 2, respectively) of hexamethonium and decamethonium were synthesized and investigated as redox-activated affinity reagents toward the neurotoxin-binding sites of the nicotinic acetylcholine receptor
Y. Gu, H. Lee, R. A. Hudson
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