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Last Updated: 3 years ago

Possible Interaction: 4-Aminopyridine and Potassium

supplement:

Potassium

Research Papers that Mention the Interaction

4-AP application (0,2 mM) reduced potassium current amplitude of the retinal neurons.
Fiziolohichnyi zhurnal  •  2010  |  View Paper
The potassium current was inhibited by 4-AP and by Heteropodatoxin, a specific blocker of Kv4.2 and Kv4.3 channels, but not by Stromatoxin, a blocker of Kv4.2 channels.
Brain Research  •  2006  |  View Paper
Transient potassium currents were reduced by 4-aminopyridine and sodium currents were blocked by tetrodotoxin.
Neuroscience  •  1999  |  View Paper
Tetraethylammonium-sensitive … the transient potassium … 4-aminopyridine increased only about 2.5-fold from 174 pA/pF to 442 pA/pF. The Ba2(+)-sensitive current increased simultaneously from … cell differentiation accounted for the changes in decay kinetics of Ca2(+)-independent voltage-activated potassium current observed in later postnatal stages.
Neuroscience  •  1999  |  View Paper
Application of 4-aminopyridine , an antagonist of the rapidly inactivating potassium current IA, reduced the threshold for dendritic spikes in slices from naive animals to levels found in slices from trained animals.
Journal of neurophysiology  •  1997  |  View Paper
The potassium current was blocked by tetraethylammonium, 4-aminopyridine , barium and cobalt.
Biochemical and biophysical research communications  •  1996  |  View Paper
A transient potassium current was activated by depolarizations positive to -20 mV. This current was blocked by 4-aminopyridine (2 mM) and inactivated with a time constant of approximately 500 ms.
Journal of neurophysiology  •  1994  |  View Paper
The potassium current was blocked by 4-AP.
Journal of neurophysiology  •  1994  |  View Paper
4-aminopyridine is a pharmacological blocker that reduces potassium conductance through potassium channels in nerve and muscle.
Brain Research  •  1993  |  View Paper
Tetraethylammonium and 4-aminopyridine effectively blocked potassium outward currents but failed to distinguish this calcium-dependent potassium channel from the other two potassium channels in this preparation.
Journal of neurophysiology  •  1993  |  View Paper
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