3-Hydroxykynurenine and 3-Hydroxyanthranilic Acid Generate Hydrogen Peroxide and Promote α-Crystallin Cross-Linking by Metal Ion Reduction
- 26 May 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 39 (24), 7266-7275
- https://doi.org/10.1021/bi992997s
Abstract
The kynurenine pathway catabolite 3-hydroxykynurenine (3HK) and redox-active metals such as copper and iron are implicated in cataractogenesis. Here we investigate the reaction of kynurenine pathway catabolites with copper and iron, as well as interactions with the major lenticular structural proteins, the α-crystallins. The o-aminophenol kynurenine catabolites 3HK and 3-hydroxyanthranilic acid (3HAA) reduced Cu(II)>Fe(III) to Cu(I) and Fe(II), respectively, whereas quinolinic acid and the nonphenolic kynurenine catabolites kynurenine and anthranilic acid did not reduce either metal. Both 3HK and 3HAA generated superoxide and hydrogen peroxide in a copper-dependent manner. In addition, 3HK and 3HAA fostered copper-dependent α-crystallin cross-linking. 3HK- or 3HAA-modifed α-crystallin showed enhanced redox activity in comparison to unmodified α-crystallin or ascorbate-modified α-crystallin. These data support the possibility that 3HK and 3HAA may be cofactors in the oxidative damage of proteins, such as α-crystallin, through interactions with redox-active metals and especially copper. These findings may have relevance for understanding cataractogenesis and other degenerative conditions in which the kynurenine pathway is activated.Keywords
This publication has 26 references indexed in Scilit:
- The kynurenine metabolic pathway in the eye: studies on 3‐hydroxykynurenine, a putative cataractogenic compoundFEBS Letters, 1999
- Neurotoxin Quinolinic Acid Is Selectively Elevated in Spinal Cords of Rats with Experimental Allergic EncephalomyelitisJournal of Neurochemistry, 1995
- Increased Concentrations of the Neurotoxin 3‐Hydroxykynurenine in the Frontal Cortex of HIV‐1‐Positive PatientsJournal of Neurochemistry, 1995
- Structure and Modifications of the Junior Chaperone α‐CrystallinEuropean Journal of Biochemistry, 1994
- Intact human ceruloplasmin oxidatively modifies low density lipoprotein.Journal of Clinical Investigation, 1994
- α-Crystallin: molecular chaperone and protein surfactantBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1994
- Role of trace elements in senile cataractActa Ophthalmologica, 1992
- Copper levels in human mixed, nuclear brunescence, and posterior subcapsular cataract.British Journal of Ophthalmology, 1992
- A possible structure for α‐crystallinFEBS Letters, 1987
- Superoxide dismutase, catalase and glutathione peroxidase in the human cataractous lensExperimental Eye Research, 1983