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Greilberger, J; Oettl, K; Cvirn, G; Reibnegger, G; Jürgens, G.
Modulation of LDL oxidation by 7,8-dihydroneopterin.
FREE RADICAL RES. 2004; 38: 9-17.
Doi: 10.1080%2F10715760310001623322
Web of Science
PubMed
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- Führende Autor*innen der Med Uni Graz
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Greilberger Joachim
- Co-Autor*innen der Med Uni Graz
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Cvirn Gerhard
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Jürgens Günther
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Öttl Karl
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Reibnegger Gilbert
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- Abstract:
- Human macrophages stimulated with interferon-gamma generate neopterin and 7,8-dihydroneopterin which interfere with reactive species involved in LDL oxidation. While neopterin was found to have pro-oxidative effects on copper-mediated LDL oxidation, the influence of 7,8-dihydroneopterin is more complex. This study provides detailed information that 7,8-dihydroneopterin reveals both pro-oxidative and anti-oxidative effects on copper mediated LDL oxidation. 7,8-dihydroneopterin inhibited the oxidation of native LDL effectively monitored by (i) formation of conjugated dienes, (ii) relative electrophoretic mobility (EM) and (iii) specific oxidized epitopes. Using minimally oxidized LDL (mi-LDL) or moderately oxidized LDL (mo-LDL) 7,8-dihydroneopterin changed its antioxidative behavior to a strongly pro-oxidative. Incubation of 7,8-dihydroneopterin with native LDL, mi-LDL or mo-LDL in the absence of copper ions showed that formation of conjugated dienes was more increased in mo-LDL than in mi-LDL while no diene formation was observed with native LDL. We suggest that 7,8-dihydroneopterin is a modulator for LDL oxidation in the presence of copper ions depending on the "oxidative status" of this lipoprotein.
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Chelating Agents - pharmacology
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Copper - metabolism
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Edetic Acid - pharmacology
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Electrophoretic Mobility Shift Assay - pharmacology
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Epitopes - metabolism
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Humans - metabolism
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Lipoproteins, LDL - chemistry
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Neopterin - analogs and derivatives
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Oxidants - metabolism
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Oxidation-Reduction - metabolism
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Pentetic Acid - pharmacology
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Research Support, Non-U.S. Gov't - pharmacology
- Find related publications in this database (Keywords)
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7
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-dihydroneopterin
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lipid hydroperoxides (LPO)
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lipid peroxidation
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electrophoretic mobility (EM)
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free radicals
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atherosclerosis