Human Enriched Serum Following Hydrolysed Collagen Absorption Modulates Bone Cell Activity: from Bedside to Bench and Vice Versa.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
31 May 2019
Historique:
received: 24 04 2019
revised: 27 05 2019
accepted: 28 05 2019
entrez: 5 6 2019
pubmed: 5 6 2019
medline: 7 1 2020
Statut: epublish

Résumé

Collagen proteins are crucial components of the bone matrix. Since collagen-derived products are widely used in the food and supplement industry, one may raise the question whether collagen-enriched diets can provide benefits for the skeleton. In this study, we designed an innovative approach to investigate this question taking into account the metabolites that are formed by the digestive tract and appear in the circulation after ingestion of hydrolysed collagen. Blood samples collected in clinical and pre-clinical trials following ingestion and absorption of hydrolysed collagen were processed and applied on bone-related primary cell cultures. This original ex vivo methodology revealed that hydrolysed collagen-enriched serum had a direct impact on the behaviour of cells from both human and mouse origin that was not observed with controls (bovine serum albumin or hydrolysed casein-enriched serum). These ex vivo findings were fully in line with in vivo results obtained from a mouse model of post-menopausal osteoporosis. A significant reduction of bone loss was observed in mice supplemented with hydrolysed collagen compared to a control protein. Both the modulation of osteoblast and osteoclast activity observed upon incubation with human or mouse serum ex vivo and the attenuation of bone loss in vivo, clearly indicates that the benefits of hydrolysed collagen for osteoporosis prevention go beyond the effect of a simple protein supplementation.

Identifiants

pubmed: 31159319
pii: nu11061249
doi: 10.3390/nu11061249
pmc: PMC6627680
pii:
doi:

Substances chimiques

RANK Ligand 0
Collagen 9007-34-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Association Nationale de la Recherche et de la Technologie
ID : COLOS

Déclaration de conflit d'intérêts

Fabien Wauquier, Henri Granel, Audrey Daneault, Gael Rochefort, Jérome Guicheux, Adeline Blot, Nathalie Meunier and Yohann Wittrant have no conflict of interest to declare. Janne Prawitt and Véronique Fabien-Soulé work for Rousselot and provided the hydrolysed collagens.

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Auteurs

Fabien Wauquier (F)

INRA, UMR 1019, UNH, CRNH Auvergne, F-63009 Clermont-Ferrand, France. Fabien_Wauquier@gmx.fr.
Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000 Clermont-Ferrand, France. Fabien_Wauquier@gmx.fr.

Audrey Daneault (A)

INRA, UMR 1019, UNH, CRNH Auvergne, F-63009 Clermont-Ferrand, France. audrey.daneault@gmail.com.
Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000 Clermont-Ferrand, France. audrey.daneault@gmail.com.

Henri Granel (H)

INRA, UMR 1019, UNH, CRNH Auvergne, F-63009 Clermont-Ferrand, France. henri.granel@inra.fr.
Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000 Clermont-Ferrand, France. henri.granel@inra.fr.

Janne Prawitt (J)

Rousselot BVBA, Meulestedekaai 81, 9000 Gent, Belgium. janne.prawitt@rousselot.com.

Véronique Fabien Soulé (V)

Rousselot SAS, 4 rue de l'abreuvoir, 92400 Courbevoie, France. vfabiensoule@syndifrais.com.

Juliette Berger (J)

CRB Auvergne, 1 place Lucie et Raymond Aubrac, 63003 Clermont-Ferrand Cedex 1, France CHUClermont-Ferrand, CHU Estaing, Hématologie Biologique, 1 place Lucie et Raymond Aubrac,63003 Clermont-Ferrand Cedex 1, CHU Clermont-Ferrand, CHU Estaing, Université Clermont Auvergne,Equipe d'Accueil 7453 CHELTER, CHU Estaing, 1 place Lucie et Raymond Aubrac,F-63003 Clermont-Ferrand Cedex 1, France. jberger@chu-clermontferrand.fr.

Bruno Pereira (B)

University hospital Clermont-Ferrand, Biostatistics Unit (DRCI), 58 rue Montalembert, 63000 Clermont-Ferrand, France. bpereira@chu-clermontferrand.fr.

Jérôme Guicheux (J)

Inserm, UMR 1229, RMeS, Regenerative Medicine and Skeleton, Université de Nantes, ONIRIS, 44000 Nantes, France. jerome.guicheux@inserm.fr.
Université de Nantes, UFR Odontologie, 44000 Nantes, France. jerome.guicheux@inserm.fr.
CHU Nantes, PHU4 OTONN, 44000 Nantes, France. jerome.guicheux@inserm.fr.

Gael Y Rochefort (GY)

Inserm, UMR 1229, RMeS, Regenerative Medicine and Skeleton, Université de Nantes, ONIRIS, 44000 Nantes, France. gael.rochefort@gmail.com.

Nathalie Meunier (N)

Chu Clermont-Ferrand, Centre De Recherche En Nutrition Humaine Auvergne, 58 rue Montalembert, 63000 Clermont-Ferrand, France. nmeunier@chu-clermontferrand.fr.

Adeline Blot (A)

Chu Clermont-Ferrand, Centre De Recherche En Nutrition Humaine Auvergne, 58 rue Montalembert, 63000 Clermont-Ferrand, France. ablot@chu-clermontferrand.fr.

Yohann Wittrant (Y)

INRA, UMR 1019, UNH, CRNH Auvergne, F-63009 Clermont-Ferrand, France. yohann.wittrant@inra.fr.
Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000 Clermont-Ferrand, France. yohann.wittrant@inra.fr.

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