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Pathological changes in platelet histamine oxidases in atopic eczema
Increased plasma histamine levels were associated with significantly lowered diamine and type B monoamine oxidase activities in platelet-rich plasma of atopic eczema (AE) patients. The diamine oxidase has almost normal cofactor levels (pyridoxal phosphate and Cu(2+)) but the cofactor levels for type...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
1993
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365432/ https://www.ncbi.nlm.nih.gov/pubmed/18475554 http://dx.doi.org/10.1155/S0962935193000560 |
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author | Kiehl, Reinhold Ionescu, Gruia |
author_facet | Kiehl, Reinhold Ionescu, Gruia |
author_sort | Kiehl, Reinhold |
collection | PubMed |
description | Increased plasma histamine levels were associated with significantly lowered diamine and type B monoamine oxidase activities in platelet-rich plasma of atopic eczema (AE) patients. The diamine oxidase has almost normal cofactor levels (pyridoxal phosphate and Cu(2+)) but the cofactor levels for type B monoamine oxidase (flavin adenine dinucleotide and Fe(2+)) are lowered. The biogenic amines putrescine, cadaverine, spermidine, spermine, tyramine and serotonin in the sera, as well as dopamine and epinephrine in EDTA-plasma were found to be normal. It is unlikely, therefore, that these amines are responsible for the decreased activities of monoamine and diamine oxidase in these patients. The most likely causative factors for the inhibition of the diamine oxidase are nicotine, alcohol, food additives and other environmental chemicals, or perhaps a genetic defect of the diamine oxidase. |
format | Text |
id | pubmed-2365432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-23654322008-05-12 Pathological changes in platelet histamine oxidases in atopic eczema Kiehl, Reinhold Ionescu, Gruia Mediators Inflamm Research Article Increased plasma histamine levels were associated with significantly lowered diamine and type B monoamine oxidase activities in platelet-rich plasma of atopic eczema (AE) patients. The diamine oxidase has almost normal cofactor levels (pyridoxal phosphate and Cu(2+)) but the cofactor levels for type B monoamine oxidase (flavin adenine dinucleotide and Fe(2+)) are lowered. The biogenic amines putrescine, cadaverine, spermidine, spermine, tyramine and serotonin in the sera, as well as dopamine and epinephrine in EDTA-plasma were found to be normal. It is unlikely, therefore, that these amines are responsible for the decreased activities of monoamine and diamine oxidase in these patients. The most likely causative factors for the inhibition of the diamine oxidase are nicotine, alcohol, food additives and other environmental chemicals, or perhaps a genetic defect of the diamine oxidase. Hindawi Publishing Corporation 1993 /pmc/articles/PMC2365432/ /pubmed/18475554 http://dx.doi.org/10.1155/S0962935193000560 Text en Copyright © 1993 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kiehl, Reinhold Ionescu, Gruia Pathological changes in platelet histamine oxidases in atopic eczema |
title | Pathological changes in platelet histamine oxidases in atopic eczema |
title_full | Pathological changes in platelet histamine oxidases in atopic eczema |
title_fullStr | Pathological changes in platelet histamine oxidases in atopic eczema |
title_full_unstemmed | Pathological changes in platelet histamine oxidases in atopic eczema |
title_short | Pathological changes in platelet histamine oxidases in atopic eczema |
title_sort | pathological changes in platelet histamine oxidases in atopic eczema |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365432/ https://www.ncbi.nlm.nih.gov/pubmed/18475554 http://dx.doi.org/10.1155/S0962935193000560 |
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