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Brunet A, Rovira A, Quer M, Sanabria A, Guntinas-Lichius O, Zafereo ME , Hartl DM, Coca-Pelaz A, Shaha AR, Marie JP, Vander Poorten V, Piazza C, Kowalski LP, Randolph GW, Shah JP, Rinaldo A, Simo R

The induction (or inhibition) of hepatic and intestinal drug-metabolizing enzymes, specifically cytochrome P450 (CYP) and/or drug transporters like P-glycoprotein, as well as pharmacokinetic interactions, which have been more thoroughly studied, maybe the cause of the altered drug concentrations caused by co-administration of herbs (147)

By far, none of these agents have been approved for the treatment of GBS by FDA

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In many organisms, there exists another important thiol, ergothioneine, which is a thio-imidazole containing amino acid ( 5 , Fig