A scavenger peptide prevents methylglyoxal induced pain in mice
The reactive metabolite methylglyoxal (MG) has been identified as mediator of pain. Scavenging of free MG and the prevention of MG-derived post-translational modifications may provide a useful therapeutic treatment. An arginine-rich, fatty acid coupled, cyclic peptide (CycK(Myr)R4E) with high proteo...
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2017
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| In: |
Biochimica et biophysica acta. Molecular basis of disease
Year: 2017, Jahrgang: 1863, Heft: 3, Pages: 654-662 |
| ISSN: | 1879-260X |
| DOI: | 10.1016/j.bbadis.2016.12.001 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1016/j.bbadis.2016.12.001 Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S0925443916303295 
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| Verfasserangaben: | Sebastian Brings, Thomas Fleming, Svenja De Buhr, Barbro Beijer, Thomas Lindner, Artjom Wischnjow, Zoltan Kender, Verena Peters, Stefan Kopf, Uwe Haberkorn, Walter Mier, Peter P. Nawroth |
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| 520 | |a The reactive metabolite methylglyoxal (MG) has been identified as mediator of pain. Scavenging of free MG and the prevention of MG-derived post-translational modifications may provide a useful therapeutic treatment. An arginine-rich, fatty acid coupled, cyclic peptide (CycK(Myr)R4E) with high proteolytic stability and prolonged circulation was developed for the scavenging of MG. It was shown to reduce the formation of albumin-MG adducts in vitro and prevented MG-induced pain by reducing plasma MG levels through the formation of peptide-MG adducts in vivo. CycK(Myr)R4E therefore presents a promising option for the treatment of pain and other diabetic complications associated with high MG levels. | ||
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