THIS WAS ORIGINALLY POSTED BY ABCESSION FROM BBX.
----------------------------------------------------------------------------------
There's been a lot of talk lately, backed up by legitimate research, proving that the R form of ALA may be more beneficial, not to mention a bit more costly than getting the R and S mix.
Maybe we should all save a bit of hard-earned cash and read this:
Combined non-enzymic and enzymic reduction favors bioactivation of racemic lipoic acid: an advantage of a racemic drug? Biewenga, Gerreke Ph.; Haenen, Guido R. M. M.; Groen, Brenda H.; Biewenga, Jeike E.; Van Grondelle, Rienk; Bast, Aalt. Department of Pharmacochemistry, Division of Molecular Pharmacology, Leiden/Amsterdam Center for Drug Research, Amsterdam, Neth. Chirality (1997), 9(4), 362-366.
Abstract
For the antioxidant effect of lipoic acid, reduction to dihydrolipoic acid is considered to be important. Dihydrolipoamide dehydrogenase (LipHD) preferentially reduces R-lipoic acid and in a subsequent reaction, and R-dihydrolipoic acid formed may non-enzymically reduce S-lipoic acid. In vitro, it was found that S-lipoic acid is reduced by LipDH using R-lipoic acid as a catalyst. The non-enzymic dithiol-disulfide reaction leads to synergistic redn. of the enantiomers which can explain the higher antioxidant activity of racemic lipoic acid found in vivo (Maitra et al. Biochem. Biophys. Res. Commun. 221:422-429, 1996) in comparison to the enantiomers. Lipoic acid is therapeutically active in several diseases via antioxidant activity. These findings suggest that racemic lipoic acid can be therapeutically more active than the separate enantiomers.
Has anyone used both the mixture and the R form separately? What kind of results did you have? Any input would be appreciated.
Abcession
----------------------------------------------------------------------------------
There's been a lot of talk lately, backed up by legitimate research, proving that the R form of ALA may be more beneficial, not to mention a bit more costly than getting the R and S mix.
Maybe we should all save a bit of hard-earned cash and read this:
Combined non-enzymic and enzymic reduction favors bioactivation of racemic lipoic acid: an advantage of a racemic drug? Biewenga, Gerreke Ph.; Haenen, Guido R. M. M.; Groen, Brenda H.; Biewenga, Jeike E.; Van Grondelle, Rienk; Bast, Aalt. Department of Pharmacochemistry, Division of Molecular Pharmacology, Leiden/Amsterdam Center for Drug Research, Amsterdam, Neth. Chirality (1997), 9(4), 362-366.
Abstract
For the antioxidant effect of lipoic acid, reduction to dihydrolipoic acid is considered to be important. Dihydrolipoamide dehydrogenase (LipHD) preferentially reduces R-lipoic acid and in a subsequent reaction, and R-dihydrolipoic acid formed may non-enzymically reduce S-lipoic acid. In vitro, it was found that S-lipoic acid is reduced by LipDH using R-lipoic acid as a catalyst. The non-enzymic dithiol-disulfide reaction leads to synergistic redn. of the enantiomers which can explain the higher antioxidant activity of racemic lipoic acid found in vivo (Maitra et al. Biochem. Biophys. Res. Commun. 221:422-429, 1996) in comparison to the enantiomers. Lipoic acid is therapeutically active in several diseases via antioxidant activity. These findings suggest that racemic lipoic acid can be therapeutically more active than the separate enantiomers.
Has anyone used both the mixture and the R form separately? What kind of results did you have? Any input would be appreciated.
Abcession