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Int. J. Mol. Sci. 2014, 15(5), 7475-7484; doi:10.3390/ijms15057475
Article

The Minor Structural Difference between the Antioxidants Quercetin and 4'O-Methylquercetin Has a Major Impact on Their Selective Thiol Toxicity

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Received: 19 March 2014; in revised form: 16 April 2014 / Accepted: 21 April 2014 / Published: 30 April 2014
(This article belongs to the Section Molecular Toxicology)
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Abstract: Antioxidants act as intermediates by picking up the high unselective reactivity of radicals and transferring it to other molecules. In this process the reactivity is reduced and becomes selective. This channeling of the reactivity can cause selective toxicity. The antioxidant quercetin is known to channel the reactivity towards thiol groups. The present study compares the thiol reactivity of quercetin with that of 4'O-methylquercetin (tamarixetin) towards creatine kinase (CK), a vital protein that contains a critical thiol moiety. Our results showed that oxidized quercetin and oxidized tamarixetin both adduct CK, which then loses its enzymatic function. Ascorbate, an important representative of the antioxidant network, is able to prevent adduction to and thus the inhibition of the enzyme by tamarixetin but not by quercetin. Apparently, tamarixetin is less thiol toxic than quercetin, because—rather than adduction to CK—tamarixetin quinone prefers to pass reactivity to the antioxidant network, i.e., to ascorbate. The findings exemplify that radical scavenging flavonoids pick up the reactivity of radicals and act as a pivot in directing the way the reactivity is channeled. A mere minor structural difference of only one methyl moiety between quercetin and tamarixetin appears to have a high impact on the selective, thiol toxicity.
Keywords: quercetin; tamarixetin; thiol reactivity; creatine kinase; antioxidant quercetin; tamarixetin; thiol reactivity; creatine kinase; antioxidant
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

Lemmens, K.J.A.; Vrolijk, M.F.; Bouwman, F.G.; van der Vijgh, W.J.F.; Bast, A.; Haenen, G.R.M.M. The Minor Structural Difference between the Antioxidants Quercetin and 4'O-Methylquercetin Has a Major Impact on Their Selective Thiol Toxicity. Int. J. Mol. Sci. 2014, 15, 7475-7484.

AMA Style

Lemmens KJA, Vrolijk MF, Bouwman FG, van der Vijgh WJF, Bast A, Haenen GRMM. The Minor Structural Difference between the Antioxidants Quercetin and 4'O-Methylquercetin Has a Major Impact on Their Selective Thiol Toxicity. International Journal of Molecular Sciences. 2014; 15(5):7475-7484.

Chicago/Turabian Style

Lemmens, Kristien J.A.; Vrolijk, Misha F.; Bouwman, Freek G.; van der Vijgh, Wim J.F.; Bast, Aalt; Haenen, Guido R.M.M. 2014. "The Minor Structural Difference between the Antioxidants Quercetin and 4'O-Methylquercetin Has a Major Impact on Their Selective Thiol Toxicity." Int. J. Mol. Sci. 15, no. 5: 7475-7484.



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