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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Papavasiliou, E. C. | en |
| dc.contributor.author | Gouva, C. | en |
| dc.contributor.author | Siamopoulos, K. C. | en |
| dc.contributor.author | Tselepis, A. D. | en |
| dc.date.accessioned | 2015-11-24T16:43:50Z | - |
| dc.date.available | 2015-11-24T16:43:50Z | - |
| dc.identifier.issn | 0931-0509 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/8744 | - |
| dc.rights | Default Licence | - |
| dc.subject | chronic kidney disease | en |
| dc.subject | epoetin | en |
| dc.subject | lipoproteins | en |
| dc.subject | monocytes | en |
| dc.subject | paf-acetylhydrolase | en |
| dc.subject | paraoxonase-1 | en |
| dc.subject | platelet-activating-factor | en |
| dc.subject | coronary-heart-disease | en |
| dc.subject | lipoprotein-associated phospholipase-a2 | en |
| dc.subject | recombinant-human-erythropoietin | en |
| dc.subject | blood cell-cultures | en |
| dc.subject | renal-failure | en |
| dc.subject | hemodialysis-patients | en |
| dc.subject | inflammation | en |
| dc.subject | atherosclerosis | en |
| dc.subject | a(2) | en |
| dc.title | PAF-acetylhydrolase activity in plasma of patients with chronic kidney disease. Effect of long-term therapy with erythropoietin | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | Doi 10.1093/Ndt/Gfk043 | - |
| heal.identifier.secondary | <Go to ISI>://000237004900021 | - |
| heal.identifier.secondary | http://ndt.oxfordjournals.org/content/21/5/1270.full.pdf | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.publicationDate | 2006 | - |
| heal.abstract | Background. Platelet activating factor acetylhydrolase (PAF-AH) is a Ca2+-independent phospholipase A(2) that is secreted mainly from monocytes/macrophages. In human plasma, PAF-AH is associated primarily with low-density lipoprotein (LDL), while a small proportion of enzyme is associated with high-density lipoprotein (HDL). The ratio of HDL-PAF-AH to total plasma enzyme activity may represent a potential marker of atherogenicity. We evaluated possible alterations of lipoprotein-associated enzyme activity in Chronic Kidney Disease (CKD) patients, stages 3-4, and further investigated whether long-term therapy with recombinant human erythropoietin (epoetin) has any influence on the plasma PAF-AH activity in vivo or on the enzyme activity secreted from peripheral blood monocytes (PBMs), in vitro. Methods. Forty-eight patients, 28 men and 20 women, with CKD (stages 3-4) participated in the study. Patients were randomized into groups I and II. Patients of group I (n = 28) were administered subcutaneously epoetin, 50 units/kg once per week. The Hb target was 13 g/dl. In group II (n = 20), epoetin was initiated only when the Hb levels decreased during follow-up to less than 9 g/dl. All patients were seen on an outpatient basis at 2, 4 and 6 months. Twenty-two normolipidemic age- and sex-matched healthy volunteers also participated in the study and were used as controls. Results. The PAF-AH activity in plasma of both patient groups at baseline was higher compared to controls, whereas no difference in the HDL-PAF-AH activity was observed among the studied groups. Thus, the ratio of HDL-PAF-AH to the plasma enzyme activity was significantly lower in both patient groups compared to controls. Epoetin administration in the patients of group I was associated with a significant increase in the plasma PAF-AH and in HDL-PAF-AH activities 2 months after treatment, which remained stable for up to 6 months of therapy, a phenomenon not observed in untreated patients of group II. Thus, the ratio of HDL-PAF-AH to the plasma enzyme activity was significantly increased in patients of group I compared to the baseline values, a phenomenon not observed in patients of group II. In vitro treatment with epoetin of PBMs from patients of group I (undergoing therapy with epoetin) resulted in a dose-dependent increase in total and secreted enzyme activity, a phenomenon not observed in patients of group II who did not receive therapy with epoetin. This suggests that the in vivo increase in lipoprotein-associated PAF-AH observed in patients treated with epoetin may be attributed to the drug-induced enhanced secretion of PAF-AH from PBMs of these patients. Conclusions. CKD patients of stages 3-4 are characterized by an increase in plasma PAF-AH activity and a low ratio of HDL-PAF-AH to total plasma enzyme activity. Long-term therapy with epoetin may improve this atherogenic ratio thus this drug may play an important antiatherogenic role in CKD. | en |
| heal.journalName | Nephrology Dialysis Transplantation | en |
| heal.journalType | peer reviewed | - |
| heal.fullTextAvailability | TRUE | - |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Papavasiliou-2006-PAF-acetylhydrolase.pdf | 140.89 kB | Adobe PDF | View/Open Request a copy |
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