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Last Updated: 3 years ago

Possible Interaction: Neomycin and Calcium Supplement

Research Papers that Mention the Interaction

Neomycin displayed higher blockade with a half inhibition in the nanomolar range at low calcium concentration and in the micromolar range in physiological calcium concentration but still exerted blockade below the concentration used in the clinic.
Neuroreport  •  2006  |  View Paper
In this study, we found that the store‐operated Ca2+ entry was inhibited by neomycin , an aminoglycoside that strongly binds phosphatidylinositol 4,5‐bisphosphate (PtdIns(4,5)P2).
Patch clamp recordings revealed that neomycin blocked the CRAC currents reconstituted by co‐expression of Orai1 and Stim1 in HEK293 cells.
This result suggests that PtdIns(4,5)P2 is not required for CRAC channel activity, and thereby, neomycin inhibits CRAC channels in a manner that is independent of neomycin–PtdIns(4,5)P2 binding.
Cell biochemistry and function  •  2015  |  View Paper
Neomycin , an aminoglycoside polycation, inhibited both the “transient” (ICa,t) and the “slowly-inactivating” (ICa,s) Ca currents in a dose-dependent manner (100–1,000 μM).
Pflügers Archiv - European Journal of Physiology  •  2004  |  View Paper
Consistently, neomycin time-dependently diminished the calcium current amplitude letting the channel exhibit the hallmarks of the voltage-independent regulation.
Archives of biochemistry and biophysics  •  2020  |  View Paper
In the presence of U73122 or neomycin there was a decrease in calcium with inhibition factors (I.F.) of 0.39 ± 0.09 and 0.37 ± 0.08, respectively, whereas rottlerin abolished the REV5901-induced [Ca2+]i rise.
General physiology and biophysics  •  2012  |  View Paper
Neomycin (0.5 mmol l–1) blocked inositol 1,4,5-trisphosphate-, caffeine-, and Ca2+ -induced Ca2+ release.
Journal of Comparative Physiology A  •  2000  |  View Paper
Whereas ryanodine and caffeine had no effect, both neomycin and thapsigargin significantly decreased the Ca2+i response to flow, suggesting a role for Ca2+ store release, possibly through an inositol 1,4,5‐trisphosphate (IP3)‐dependent mechanism.
Journal of cellular physiology  •  1999  |  View Paper
Moreover, in synaptosomes permeabilized with Staphylococcus aureus α‐toxin, PLD activation induced by calcium was abolished by neomycin , a PIP2 chelator.
FEBS letters  •  1999  |  View Paper
A portion of the dendritic release is calcium independent but can be inhibited partially by neomycin , which might suggest a role for inositol 4,5‐bisphosphate breakdown products.
Journal of neurochemistry  •  1998  |  View Paper
Ca2+o from 1.1 to 5 mM reversibly reduced the activity of the 70-pS K+ … to 16 +/- 2% of the control value within 300 s. In addition, 50 microM neomycin mimicked the effect of an increase in Ca2+o … cell-attached patches and completely inhibited channel activity.
The American journal of physiology  •  1996  |  View Paper
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