High-Cholesterol Diet Increases Xanthine Oxidase and Decreases Nitric Oxide Synthase Activities in Erythrocytes From Rats

dc.contributor.author Devrim, Erdinc
dc.contributor.author Erguder, Imge B.
dc.contributor.author Ozbek, Hanefi
dc.contributor.author Durak, Iiker
dc.date.accessioned 2025-05-10T17:26:59Z
dc.date.available 2025-05-10T17:26:59Z
dc.date.issued 2008
dc.description Devrim, Erdinc/0000-0001-7326-5104; Erguder, Berrin Imge/0000-0002-7945-3074 en_US
dc.description.abstract The aim of this study was to investigate the effects of a high-cholesterol diet on oxidant/antioxidant status and nitric oxide synthase (NOS) activity in erythrocytes from rats. Sixteen Sprague-Dawley-type albino male rats were used in the study. The rats were randomly divided into 2 groups: the control group (group 1) was fed a standard rat diet, and the treated group (group 2) was fed a high-cholesterol diet (4% cholesterol, 1% cholic acid, and 0.5% thiouracil) in addition to standard pellet rat diet for 3 months. At the end of the study period, blood samples were obtained from the rats under ether anesthesia. Oxidant (malondialdehyde level, sensitivity to oxidation value, and xanthine oxidase [XO] activity) and antioxidant parameters (antioxidant potential value, superoxide dismutase, catalase, and glutathione peroxidase activities) were studied in erythrocyte preparations. Activities of erythrocyte NOS and arginase enzymes and serum total cholesterol levels were also measured. We observed that serum total cholesterol levels, erythrocyte XO activities, and sensitivity to oxidation values significantly increased in group 2 (cholesterol fed) compared with the control group (group 1). Erythrocyte NOS activities were also found to decrease in group 2. In conclusion, our results suggest that cholesterol feeding causes an increase in XO activity and a decrease in NOS activity in the erythrocytes from rats. The increase in XO activity may render the erythrocyte membranes sensitive to oxidant stress, and the decrease in NOS activity in the erythrocytes may increase cardiovascular disease risk via reduced endothelial relaxation. (c) 2008 Elsevier Inc. All rights reserved. en_US
dc.identifier.doi 10.1016/j.nutres.2008.01.006
dc.identifier.issn 0271-5317
dc.identifier.issn 1879-0739
dc.identifier.scopus 2-s2.0-41349101095
dc.identifier.uri https://doi.org/10.1016/j.nutres.2008.01.006
dc.identifier.uri https://hdl.handle.net/20.500.14720/11843
dc.language.iso en en_US
dc.publisher Pergamon-elsevier Science Ltd en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Erythrocytes en_US
dc.subject Hypercholesterolemia en_US
dc.subject Oxidant/Antioxidant Status en_US
dc.subject Nitric Oxide Synthase (Nos) en_US
dc.subject Rat en_US
dc.title High-Cholesterol Diet Increases Xanthine Oxidase and Decreases Nitric Oxide Synthase Activities in Erythrocytes From Rats en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Devrim, Erdinc/0000-0001-7326-5104
gdc.author.id Erguder, Berrin Imge/0000-0002-7945-3074
gdc.author.scopusid 6506342253
gdc.author.scopusid 8505581400
gdc.author.scopusid 7005912992
gdc.author.scopusid 7005916873
gdc.author.wosid Erguder, Imge/Aaz-5673-2020
gdc.author.wosid Ozbek, Hanefi/O-3472-2019
gdc.author.wosid Devrim, Erdinc/F-7511-2019
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Devrim, Erdinc; Erguder, Imge B.; Durak, Iiker] Ankara Univ, Fac Med, Dept Biochem, TR-06100 Ankara, Turkey; [Ozbek, Hanefi] Yuzuncu Yil Univ, Fac Med, Dept Pharmacol, TR-65080 Van, Turkey en_US
gdc.description.endpage 215 en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 212 en_US
gdc.description.volume 28 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 19083410
gdc.identifier.wos WOS:000255051300012
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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