Allen Institute for Artificial Intelligence logo

Discover Supplement-Drug Interactions

Disclaimer: The information contained herein should NOT be used as a substitute for the advice of an appropriately qualified and licensed physician or other health care provider. The tool is not a substitute for the care provided… (more)
Last Updated: 3 months ago

Possible Interaction: Hexachlorocyclohexane and Calcium Supplement

Research Papers that Mention the Interaction

Conclusion: A correlation between CA frequency and exposure to benzene hexachloride ( BHC ) pesticide residue was observed.
Human & experimental toxicology  •  2012  |  View Paper
Since lindane interacts specifically with calcium transport and can induce an increase in cytoplasmic calcium , the strong effect of lindane on ciliary beat is probably correlated with a modification of the calcium balance of the cell.
Biology of the cell  •  1988  |  View Paper
HCH inhibited Na(+),K(+)-ATPase, which could be involved in raising the intracellular calcium and increased Ca(2+),Mg(2+)-ATPase activity.
Chemico-biological interactions  •  2010  |  View Paper
In the presence of 100 microM calcium, gamma-HCCH induced a calcium influx into the two subpopulations, but the calcium oscillations appeared only in small macrophages.
gamma-HCCH induced a transient calcium entry which triggered phospholipase C activation and the associated [Ca2+]i oscillations.
Journal de la Societe de biologie  •  2001  |  View Paper
Lindane significantly decreased urinary calcium concentration, serum alkaline phosphatase concentration and the cross-sectional medullary area of the bone.
Toxicology  •  1990  |  View Paper
Lindane inhibited the ACh-dependent contracture (I50 less than 10(-5) M) and suppressed the histochemical localizations of calcium.
Toxicology and applied pharmacology  •  1984  |  View Paper
It is suggested that lindane is able to promote both Ca 2+ -influx and the release of Ca 2+ from intracellular sites in the muscle.
Comparative biochemistry and physiology. C: Comparative pharmacology  •  1979  |  View Paper