Pentoxyphylline and propentophylline are inhibitors of TNF-? release in monocytes activated by advanced glycation endproducts

Non-enzymatic glycation of proteins with reducing sugars and subsequent transition metal-catalyzed oxidation leads to the formation of protein-bound "advanced glycation endproducts" (AGEs). They accumulate on long-lived protein deposits inducing senile plaques in Alzheimer's disease....

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Bibliographic Details
Published inJournal of Neural Transmission Vol. 111; no. 3; pp. 441 - 447
Main Authors Meiners, I., Hauschildt, S., Nieber, K., M nch, G.
Format Journal Article
LanguageEnglish
Published Wien Springer Nature B.V 01.03.2004
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Summary:Non-enzymatic glycation of proteins with reducing sugars and subsequent transition metal-catalyzed oxidation leads to the formation of protein-bound "advanced glycation endproducts" (AGEs). They accumulate on long-lived protein deposits inducing senile plaques in Alzheimer's disease. AGE-modified proteins are able to activate microglia and astroglia and can cause chronic inflammation. The aim of the present study was to confirm the stimulatory effect of different AGEs on TNF-[alpha] release in human monocytes. Furthermore, the effects of four xanthine derivatives on AGE-induced TNF-[alpha] release were investigated. We show that chicken egg albumin-AGEs prepared with glucose and chicken egg albumin-AGEs prepared with methylglyoxal dose-dependently induce TNF-[alpha] release. The xanthine derivatives pentoxyphylline and propentophylline attenuate AGE-induced TNF-[alpha] release in a dose-dependent manner. Theophylline at low concentrations slightly stimulated TNF-[alpha] release whereas caffeine had no effect. The inhibition of the AGE-induced TNF-[alpha] release by pentoxyphylline and propentophylline provides interesting pharmacological strategies for diseases with local neuroinflammation such as Alzheimer's disease.
ISSN:0300-9564
1435-1463
DOI:10.1007/s00702-003-0066-y