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Discover Supplement-Drug Interactions

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Last Updated: 2 years ago

Possible Interaction: Papaverine and Calcium Supplement

Research Papers that Mention the Interaction

This characteristic distinguishes them from other drugs such as sodium nitroprusside, papaverine , hydralazine and diazoxide which interfere with the availability of calcium ions for their physiological functions by acting at sites other than the 'calcium channels'.
Drugs  •  1983  |  View Paper
This characteristic distinguishes them from other drugs such as sodium nitroprusside, papaverine , hydralazine and diazoxide which interfere with the availability of calcium ions for their physiological functions by acting at sites other than the ‘calcium channels’.
Drugs  •  2012  |  View Paper
These recent findings have led to the use of papaverin to reduce the level of intracellular calcium , alpha-blockers to antagonize alpha-receptor and prostaglandin to inhibit norepinephrine release.
Presse medicale  •  1994  |  View Paper
The in vitro inhibitory action of papaverine , aspirin, and TMQ was enhanced by increasing calcium concentration.
Biochemical pharmacology  •  1976  |  View Paper
Under our experimental conditions D 600, nifedipine and papaverine were found to act as antagonists against calcium and noradrenaline in a non-competitive fashion.
Naunyn-Schmiedeberg's Archives of Pharmacology  •  2004  |  View Paper
In vitro, reticuline, norarmepavine, coclaurine, and papaverine competitively antagonize the uterine muscular contractions induced by acetylcholine and calcium.
Planta medica  •  1993  |  View Paper
Calcium uptake by mitochondria, isolated from kidney cortex, was apparently decreased in the presence of 0.1 mM papaverine.
Journal of pharmacobio-dynamics  •  1986  |  View Paper
2 Pre‐incubation for 20 min with either ketamine (0.3 to 3 mM), papaverine (3 to 30 μM), theophylline (0.1 to 1 mM) or verapamil (3 to 30 nM) induced parallel, concentration‐dependent rightward displacements of the dose‐response curves to Ca2+ (0.04 to 22 mM).
British journal of pharmacology  •  1985  |  View Paper
From this the authors infer an interaction (complex formation) between papaverin and calcium at the phase boundary, which is independent of the biological medium.
When the calcium content was 1 mmol/l, papaverin increased the proneness to cramping only to a smaller degree, in agreement with the effect measured when the calcium content of the organ bath was reduced below 1 mmol/l.
Die Pharmazie  •  1984  |  View Paper
Papaverine was only slightly more active on contractions sustained by influx of extracellular Ca2+ (through potential‐dependent channels and receptor‐operated channels) than on those sustained by intracellular Ca2+.
The Journal of pharmacy and pharmacology  •  1984  |  View Paper
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