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Last Updated: 3 years ago

Possible Interaction: Adenosine and Barium

supplement:

Adenosine

drug:

Barium

Research Papers that Mention the Interaction

Adenosine (0.5-100 microM) reduced the magnocellular preoptic nucleus and substantia innominata cholinergic neuronal firing rate by activating an inwardly rectifying potassium current that reversed at -82 mV and was blocked by barium (100 microM).
Neuroscience  •  2006  |  View Paper
Adenosine also partially inhibited barium current in these neurons.
British journal of pharmacology  •  2001  |  View Paper
Alphaxalone and 5 alpha-pregnan-3 alpha-ol-20-one also at low concentrations potentiated the inhibitory effect of adenosine alone and in the presence of 1 mM barium which blocked adenosine activated potassium channels.
Brain Research  •  1995  |  View Paper
Adenosine (100 microM) reduced the duration of control action potentials and action potentials prolonged by 1 mM barium.
The Journal of neuroscience : the official journal of the Society for Neuroscience  •  1994  |  View Paper
In order to eliminate effects of these agents on potassium channels, experiments were performed in the presence of barium , 1 mM. This concentration increased potential size, and reduced the inhibitory effect of adenosine on population spike size, but not synaptic potential size.
Brain Research  •  1994  |  View Paper
The ED50 was approximately 10 μM. The effect of adenosine 5′‐diphosphate (ADP) or adenosine 5′‐monophosphate (AMP), in the presence of barium , on membrane potential was less than that of ATP.
Journal of neuroscience research  •  1992  |  View Paper
Adenosine (10−5M) reduces the contractile response of the guinea‐pig isolated ileum to 5‐hydroxytryptamine or barium more than the responses to acetylcholine or histamine.
These results suggest that adenosine effects a blockade of the indirect responses to barium or 5‐hydroxytryptamine mediated through intrinsic nerves and has a weak direct inhibitory effect on the smooth muscle cells of this tissue.
The Journal of pharmacy and pharmacology  •  1971  |  View Paper