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Immunochemical detection of oxalate monoalkylamide, an ascorbate-derived Maillard reaction product in the human lens.
Nagaraj, R H; Shamsi, F A; Huber, B; Pischetsrieder, M.
Affiliation
  • Nagaraj RH; Center for Vision Research, Department of Ophthalmology, Case Western Reserve University and University Hospitals of Cleveland, OH 44106, USA.
FEBS Lett ; 453(3): 327-30, 1999 Jun 25.
Article in En | MEDLINE | ID: mdl-10405169
ABSTRACT
Carbohydrates with reactive aldehyde and ketone groups can undergo Maillard reactions with proteins to form advanced glycation end products. Oxalate monoalkylamide was identified as one of the advanced glycation end products formed from the Maillard reaction of ascorbate with proteins. In these experiments, we have analyzed human lens proteins immunochemically for the presence of oxalate monoalkylamide. Oxalate monoalkylamide was absent in most of the very young lenses but was present in old and cataractous lenses. The highest levels were found in senile brunescent lenses. Incubation experiments using bovine lens proteins revealed that oxalate monoalkylamide could form from the ascorbate degradation products, 2,3-diketogulonate and L-threose. These data provide the first evidence for oxalate monoalkylamide in vivo and suggest that ascorbate degradation and its binding to proteins are enhanced during lens aging and cataract formation.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Oxalates / Ascorbic Acid / Cataract / Aging / Maillard Reaction / Glycation End Products, Advanced / Lens, Crystalline Type of study: Diagnostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Animals / Child / Humans / Middle aged Language: En Journal: FEBS Lett Year: 1999 Document type: Article Affiliation country: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Oxalates / Ascorbic Acid / Cataract / Aging / Maillard Reaction / Glycation End Products, Advanced / Lens, Crystalline Type of study: Diagnostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Animals / Child / Humans / Middle aged Language: En Journal: FEBS Lett Year: 1999 Document type: Article Affiliation country: United States