Infrared spectrochemical findings on intermittent fasting-associated gross molecular modifications in rat myocardium

dc.authorscopusid56520257000
dc.authorscopusid57223288724
dc.authorscopusid57844989100
dc.authorscopusid36866012100
dc.authorscopusid57204017980
dc.authorscopusid57202468006
dc.contributor.authorArdahanlı, İ.
dc.contributor.authorÖzkan, H.İ.
dc.contributor.authorÖzel, F.
dc.contributor.authorGurbanov, R.
dc.contributor.authorTeker, Hikmet Taner
dc.contributor.authorCeylani, Taha
dc.date.accessioned2022-09-04T10:27:13Z
dc.date.available2022-09-04T10:27:13Z
dc.date.issued2022
dc.departmentMeslek Yüksekokulları, Teknik Bilimler Meslek Yüksekokulu, Gıda İşleme Bölümüen_US
dc.departmentMeslek Yüksekokulları, Teknik Bilimler Meslek Yüksekokulu, Gıda İşleme Bölümüen_US
dc.description.abstractCardiovascular diseases are among the primary life-threatening conditions affecting human society. Intermittent fasting is shown to be functional in the prevention of cardiovascular diseases, however, the information on fasting-associated modifications in myocardial biomolecules is limited. This study aimed to determine the impact of 18-h intermittent fasting administered for five weeks on 12 months-old rats using supervised linear discriminant analysis and support vector machine algorithms constructed on spectrochemical data obtained from myocardial tissues. These algorithms revealed gross biomolecular modifications, while quantitative analyses demonstrated higher amounts of saturated lipids (19%), triglycerides (11%), and lipids (56%), in addition to enhancement in membrane dynamics (18%). The concentrations of nucleic acids and glucose are increased by 52%, while the glycogen content is diminished by 61%. The protein carbonylation/oxidation is reduced by 38%, whereas a 35% increase in protein content was measured. Phosphorylated proteins have been calculated to be at higher concentrations in the 13–62% range. The study findings demonstrated significant molecular changes in the myocardium of rats subjected to intermittent fasting. © 2022 Elsevier B.V.en_US
dc.description.sponsorshipNo financial support was requested from any institution or organization for this study.en_US
dc.identifier.doi10.1016/j.bpc.2022.106873
dc.identifier.issn0301-4622
dc.identifier.pmid35964448
dc.identifier.scopus2-s2.0-85135911230
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://hdl.handle.net/20.500.12639/4762
dc.identifier.volume289en_US
dc.identifier.wosWOS:000863266200003
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorCeylani, Taha
dc.language.isoen
dc.publisherElsevier B.V.en_US
dc.relation.ispartofBiophysical Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCardiovascular diseasesen_US
dc.subjectInfrared spectroscopyen_US
dc.subjectIntermittent fastingen_US
dc.subjectLinear Discriminant Analysisen_US
dc.subjectSupport Vector Machineen_US
dc.titleInfrared spectrochemical findings on intermittent fasting-associated gross molecular modifications in rat myocardiumen_US
dc.typeArticle

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