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dc.contributor.authorRønning, Sissel Beate
dc.contributor.authorCarlsen, Harald
dc.contributor.authorRocha, Sergio Domingos Cardoso
dc.contributor.authorRud, Ida
dc.contributor.authorSolberg, Nina
dc.contributor.authorHøst, Vibeke
dc.contributor.authorVeiseth-Kent, Eva
dc.contributor.authorArnesen, Henriette
dc.contributor.authorBergum, Silje
dc.contributor.authorKirkhus, Bente
dc.contributor.authorBöcker, Ulrike
dc.contributor.authorAbedali, Nada
dc.contributor.authorRundblad, Amanda
dc.contributor.authorBålsrud, Pia
dc.contributor.authorMåge, Ingrid
dc.contributor.authorHolven, Kirsten Bjørklund
dc.contributor.authorUlven, Stine Marie
dc.contributor.authorPedersen, Mona Elisabeth
dc.date.accessioned2024-01-23T10:03:46Z
dc.date.available2024-01-23T10:03:46Z
dc.date.created2024-01-17T14:42:31Z
dc.date.issued2024
dc.identifier.citationFrontiers in Nutrition. 2024, 10 1-19.
dc.identifier.issn2296-861X
dc.identifier.urihttps://hdl.handle.net/11250/3113283
dc.description.abstractIntroduction: Avian eggshell membrane (ESM) is a complex extracellular matrix comprising collagens, glycoproteins, proteoglycans, and hyaluronic acid. We have previously demonstrated that ESM possesses anti-inflammatory properties in vitro and regulates wound healing processes in vivo. The present study aimed to investigate if oral intake of micronized ESM could attenuate skeletal muscle aging associated with beneficial alterations in gut microbiota profile and reduced inflammation. Methods: Elderly male C57BL/6 mice were fed an AIN93G diet supplemented with 0, 0.1, 1, or 8% ESM. Young mice were used as reference. The digestibility of ESM was investigated using the static in vitro digestion model INFOGEST for older people and adults, and the gut microbiota profile was analyzed in mice. In addition, we performed a small-scale pre-clinical human study with healthy home-dwelling elderly (>70 years) who received capsules with a placebo or 500 mg ESM every day for 4 weeks and studied the effect on circulating inflammatory markers. Results and discussion: Intake of ESM in elderly mice impacted and attenuated several well-known hallmarks of aging, such as a reduction in the number of skeletal muscle fibers, the appearance of centronucleated fibers, a decrease in type IIa/IIx fiber type proportion, reduced gene expression of satellite cell markers Sdc3 and Pax7 and increased gene expression of the muscle atrophy marker Fbxo32. Similarly, a transition toward the phenotypic characteristics of young mice was observed for several proteins involved in cellular processes and metabolism. The digestibility of ESM was poor, especially for the elderly condition. Furthermore, our experiments showed that mice fed with 8% ESM had increased gut microbiota diversity and altered microbiota composition compared with the other groups. ESM in the diet also lowered the expression of the inflammation marker TNFA in mice and in vitro in THP-1 macrophages. In the human study, intake of ESM capsules significantly reduced the inflammatory marker CRP. Altogether, our results suggest that ESM, a natural extracellular biomaterial, may be attractive as a nutraceutical candidate with a possible effect on skeletal muscle aging possibly through its immunomodulating effect or gut microbiota.
dc.language.isoeng
dc.titleDietary intake of micronized avian eggshell membrane in aged mice reduces circulating inflammatory markers, increases microbiota diversity, and attenuates skeletal muscle aging
dc.title.alternativeDietary intake of micronized avian eggshell membrane in aged mice reduces circulating inflammatory markers, increases microbiota diversity, and attenuates skeletal muscle aging
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber1-19
dc.source.volume10
dc.source.journalFrontiers in Nutrition
dc.identifier.doi10.3389/fnut.2023.1336477
dc.identifier.cristin2228763
dc.relation.projectNorges forskningsråd: 314599
dc.relation.projectNofima AS: 202101
dc.relation.projectNorges forskningsråd: 314111
dc.relation.projectNorges forskningsråd: 282247
dc.relation.projectNofima AS: 202102
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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