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Despite the pathophysiological similarities with SeD, ID was not associated with new-onset AFib

The predicted binding position of GSH in the P-pocket of rat Mrp1 is similar to those found by Johnson and Chen [12] for the GS-moiety of LTC4 in bovine Mrp1 resolved by cryo-EM experiments, including hydrogen bond formation to residues R1198 and R1250

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This increase in absorption suggests that quercetin glucoside facilitates interaction with epithelial glucose transporters, leading to a more rapid uptake and improved bioavailability of glucosides following ingestion (Gee et al., 1998)

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