Allen Institute for Artificial Intelligence
supp.ai logo
supp.ai

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 years ago

Possible Interaction: Glutathione and Probenecid

supplement:

Glutathione

Research Papers that Mention the Interaction

GSH release in Jurkat cells undergoing apoptosis was inhibited by the organic anion transport inhibitors MK571, sulfinpyrazone, and probenecid , supporting a role for the MRP transporters in this process.
Journal of Biological Chemistry  •  2007  |  View Paper
Two organic anion transporter inhibitors, probenecid and dibromosulfophthalein (DBSP), were effective in inhibiting Fas-stimulated GSH release.
Toxicology and applied pharmacology  •  2004  |  View Paper
However, probenecid caused a clear decrease in release of GSH from resistant cells into the medium.
International journal of cancer  •  1995  |  View Paper
At 24 h, both probenecid and NAC inhibited trauma-induced intracellular GSH depletion, lactate dehydrogenase (LDH) release, and propidium iodide (PI) uptake in both XY- and XX-neurons.
Journal of neurotrauma  •  2016  |  View Paper
Probenecid (1 mM) blocked resting or nifedipine-stimulated GSH secretion but only weakly inhibited BSP excretion.
American journal of physiology. Gastrointestinal and liver physiology  •  2001  |  View Paper
However, S-alkyl glutathiones (hexyl and octyl), sulfobromophthalein-glutathione, glutathione monoethyl ester, probenecid (5 mM) and ophthalmic acid (10 mM) inhibited GSH uptake significantly.
The Journal of pharmacology and experimental therapeutics  •  1992  |  View Paper
Probenecid prevented Cld accumulation, tubule injury, ATP depletion, and lipid peroxidation and markedly attenuated the GSH depletion.
Toxicology and applied pharmacology  •  1991  |  View Paper
Addition of inhibitors of this transport system, gamma-glutamyl-glutamate and probenecid , prevented the protection against injury afforded by GSH.
Biochemical pharmacology  •  1986  |  View Paper
The rate of GSH uptake by the vesicles was enhanced by valinomycin-induced K+-diffusion potential (vesicle inside-positive) and was inhibited by probenecid , indicating that GSH transport across the canalicular membranes is electrogenic and involves the transfer of negative charge.
European journal of biochemistry  •  1983  |  View Paper
Abstract Cephalothin, penicillin G and probenecid inhibited GSH organic nitrate ester reductase (ONER) and several other enzymatic activities of GSH- S -transferases (EC 2.5.1.18) from rat and guinea pig liver.
Biochemical pharmacology  •  1980  |  View Paper
Show More