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Selected Publication:

Malle, E; Leis, HJ; Steinmetz, A; Paschke, E; Hoefler, G.
Cyclooxygenase pathway in dermal fibroblasts from patients with metabolic disorders of peroxisomal origin.
CLIN CHIM ACTA. 1993; 217(2): 205-212. Doi: 10.1016/0009-8981(93)90167-3
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Leading authors Med Uni Graz
Malle Ernst
Co-authors Med Uni Graz
Höfler Gerald
Leis Hans-Joerg
Paschke Eduard
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Abstract:
Cyclooxygenase metabolism was studied in fibroblasts from patients with metabolic disorders of peroxisomal origin (adrenomyeloneuropathy, X-linked adrenoleukodystrophy, cerebrohepatorenal syndrome of Zellweger and rhizomelic chondrodysplasia punctata). In response to arachidonic acid (6.25-100 microM) or calcium ionophore A23187 (2.5-20 microM) prostaglandin E2 and 6-keto-prostaglandin F1 alpha are the main cyclooxygenase metabolites formed. No formation of thromboxane B2 or 2,3-dinor-thromboxane B2 was found. Apparently due to the heterogeneous nature of peroxisomal disorders no uniform pattern of cyclooxygenase metabolism and eicosanoid concentrations in cell lines from patients with peroxisomal defects was found.
Find related publications in this database (using NLM MeSH Indexing)
6-Ketoprostaglandin F1 alpha - biosynthesis
Adrenoleukodystrophy - enzymology
Cells, Cultured - enzymology
Chondrodysplasia Punctata - enzymology
Dinoprostone - biosynthesis
Fibroblasts - enzymology
Humans - enzymology
Linkage (Genetics) - enzymology
Microbodies - metabolism
Prostaglandin-Endoperoxide Synthases - metabolism
Skin - cytology
X Chromosome - cytology
Zellweger Syndrome - enzymology

Find related publications in this database (Keywords)
Peroxisomal Disease Fibroblasts
Eicosanoids
Arachidonic Acid Metabolism
Gas Chromatography Mass Spectrometry
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