Results 131 to 140 of about 13,717 (182)
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Facile synthesis of functionalized 4-aminopyridines
Chemical Communications, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Nagatoshi, Nishiwaki +5 more
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Effects of 4-aminopyridine on saxitoxin intoxication
Toxicology and Applied Pharmacology, 1996Effects of 4-aminopyridine (4-AP) on neurotoxicity induced by saxitoxin (STX) are investigated in this study. In vitro, twitch tension evoked by nerve stimulation was depressed by STX (1.35 nM) in rat phrenic nerve-diaphragm preparations, and this inhibition was antagonized by 4-AP (0.1 mM).
H M, Chen, C H, Lin, T M, Wang
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Determination of 4-aminopyridine in plasma
Analytical Biochemistry, 1981Abstract Gas-liquid chromatographic procedures for the determination of 4-aminopyridine in human and animal plasma are reported. The procedures involve the addition of an internal standard 3-methyl-4-aminopyridine to plasma followed by extraction into methylene chloride/isopropranol under alkaline conditions.
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4‐Aminopyridine in multiple sclerosis
Neurology, 1991In an earlier study, we demonstrated efficacy of single oral doses of 4-aminopyridine (4-AP) in improving motor and visual signs in multiple sclerosis (MS) patients for a mean of 4.97 hours. We attempted to determine whether efficacy could safely be prolonged using multiple daily doses over several days by administering 7.5 to 52.5 mg 4-AP to 17 ...
D, Stefoski +5 more
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Action of 4-aminopyridine on the cerebral circulation
Acta Neurologica Scandinavica, 20094-Aminopyridine (4-AP) facilitates both inhibitory and excitatory synaptic activity in the central nervous system, and may, therefore, be a drug of potential therapeutic use in brain diseases with a disturbed synaptic transmission. In the present study the vasomotor effects upon isolated feline brain vessels, and regional cerebral blood flow and brain ...
L, Edvinsson, J E, Hardebo, H, Lundh
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4-Aminopyridine derivatives with antiamnesic activity
European Journal of Medicinal Chemistry, 2000Acetylcholine (Ach) enhancement, useful in the treatment of Alzheimer's disease (AD), may be obtained by means of ion channel modulators such as 4-aminopyridine (4-AP). 4-AP is also the central ring of tacrine, the first drug approved for the treatment of AD. The synthesis and pharmacological activity of three 4-AP derivatives, prepared with the aim of
A, Andreani +6 more
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4-Aminopyridine in the treatment of alzheimer's disease
Biological Psychiatry, 1988The cognitive and behavioral effect of 4-aminopyridine (4-AP) was examined in Alzheimer's disease (AD) using a dose finding/replication study design. Fourteen inpatients, aged 54-89 years (mean 66.1 +/- 10.6 SD), meeting NINCDS criteria for probable AD, were studied.
M, Davidson +6 more
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Pharmacokinetics of 4‐aminopyridine derivatives in dogs
Journal of Veterinary Pharmacology and Therapeutics, 2009Blockade of potassium channels with 4‐aminopryidine (4‐AP) restores conduction to demyelinated axons and improves function. Unfortunately, 4‐AP causes adverse effects and its clinical effects are unpredictable and limited. Derivatives of 4‐AP have been tested in models of spinal cord injury in guinea pigs; three derivatives (methyl‐, ethyl‐ and t‐butyl
N J, Olby +7 more
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Long-term potentiation and 4-aminopyridine
Cellular and Molecular Neurobiology, 1985Long-term potentiation (LTP) of excitatory postsynaptic potentials (epsp's) was investigated with extracellular field potential recording in hippocampal slices from rats. In the presence of 100 microM 4-aminopyridine (4-AP) the probability of eliciting LTP was unchanged or increased; the extent of potentiation was not significantly different from ...
H L, Haas, R W, Greene
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The effect of 4-aminopyridine on acetylcholine release
Journal of Neural Transmission, 1977The effect of 2-, and 4-aminopyridine (4-APYR) on the release mechanism of acetylcholine (ACh) from the nerve terminals of the Auerbach plexus-longitudinal muscle preparation of the guinea-pig ileum, suspended in eserinized Krebs' solution, was investigated. 2- and 4-APYR increased the release of ACh from the nerve terminals at rest and at both low and
E S, Vizi, J, van Dijk, F F, Foldes
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