Results 141 to 150 of about 13,554 (179)
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4-Aminopyridine in the treatment of alzheimer's disease

Biological Psychiatry, 1988
The 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
openaire   +2 more sources

Long-term potentiation and 4-aminopyridine

Cellular and Molecular Neurobiology, 1985
Long-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
openaire   +2 more sources

The effect of 4-aminopyridine on acetylcholine release

Journal of Neural Transmission, 1977
The 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
openaire   +2 more sources

An unusual case of 4-aminopyridine toxicity

The Journal of Emergency Medicine, 2006
4-aminopyridine (4-AP) is an orphan drug in the United States. It enhances neuronal conduction at synapses and is indicated in the treatment of selected neuromuscular disorders, including multiple sclerosis and myasthenia gravis, among others. Its documented toxicity generally has been limited to central nervous system (CNS) hyperexcitation and ...
Nicholas C, Johnson, Matthew W, Morgan
openaire   +2 more sources

Atypical Presentation of 4-Aminopyridine Overdose

Annals of Emergency Medicine, 1996
4-Aminopyridine (4-AP) is an investigational drug for the treatment of neurologic disorders including multiple sclerosis (MS). Until recently, relatively little was known about 4-AP toxicity in overdose; the only recorded cases involved neurologic symptoms ranging from mild parasthesias to tonic-clonic seizures.
T A, Pickett, R, Enns
openaire   +2 more sources

4-Aminopyridine and Haemodialysis in the Treatment of Verapamil Intoxication

Human Toxicology, 1985
Verapamil, a calcium antagonist, is used as an antianginal, antidysrhythmic and antihypertensive agent. Fatal intoxications with this commonly used drug have been described. We report the effects of 4-aminopyridine and haemodialysis in a patient with severe verapamil intoxication.
TERWEE, PM   +3 more
openaire   +3 more sources

4-Aminopyridine derivatives with anticholinesterase and antiamnesic activity

Bioorganic & Medicinal Chemistry Letters, 2008
Several carbamate derivatives of 4-aminopyridine were synthesized and their anticholinesterase activity was evaluated. Compound 4d showed the highest inhibitory effect blocking non-competitively acetylcholinesterase and competitively butyrylcholinesterase.
SCIPIONE, Luigi   +5 more
openaire   +2 more sources

Distribution of the 4-aminopyridine derivative 3-methoxy-4-aminopyridime in mice

Neuropharmacology, 1989
The tissue distribution of [14C]3-Methoxy-4-aminopyridine was studied after intravenous administration in mice using whole body and microautoradiography. Dense accumulation was found in cholinergically innervated, secretory organs. High radioactivity was detected in the adrenal medulla suggesting that the observed excitement and hyperglycemia are due ...
Berger SG, Waser PG, Chang Sin-Ren A
openaire   +3 more sources

Effects of 4-aminopyridine on neuromuscular transmission

Brain Research, 1978
4-Aminopyridine (4-AP) powerfully increases transmitter release from motor nerve terminals of rat and frog skeletal muscle in response to single nerve impulses. The drug also enhances transmitter release during repetitive nerve activity but, at D-tubocurarine-blocked endplates, only the first impulses cause increased transmitter release at stimulation ...
openaire   +2 more sources

4-Aminopyridine

Drugs of the Future, 1980
J. CastaƱer, D.M. Paton
openaire   +1 more source

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