Cargando…
Metabolic Response of Human Osteoarthritic Cartilage to Biochemically Characterized Collagen Hydrolysates
The most frequent disease of the locomotor system is osteoarthritis (OA), which, as a chronic joint disease, might benefit more from nutrition than acute illnesses. Collagen hydrolysates (CHs) are peptidic mixtures that are often used as nutraceuticals for OA. Three CHs were characterized biochemica...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297837/ https://www.ncbi.nlm.nih.gov/pubmed/28117674 http://dx.doi.org/10.3390/ijms18010207 |
_version_ | 1782505794098429952 |
---|---|
author | Schadow, Saskia Simons, Viktor S. Lochnit, Guenter Kordelle, Jens Gazova, Zuzana Siebert, Hans-Christian Steinmeyer, Juergen |
author_facet | Schadow, Saskia Simons, Viktor S. Lochnit, Guenter Kordelle, Jens Gazova, Zuzana Siebert, Hans-Christian Steinmeyer, Juergen |
author_sort | Schadow, Saskia |
collection | PubMed |
description | The most frequent disease of the locomotor system is osteoarthritis (OA), which, as a chronic joint disease, might benefit more from nutrition than acute illnesses. Collagen hydrolysates (CHs) are peptidic mixtures that are often used as nutraceuticals for OA. Three CHs were characterized biochemically and pharmacologically. Our biophysical (MALDI-TOF-MS, NMR, AFM) and fluorescence assays revealed marked differences between CHs of fish (Peptan(®) F 5000, Peptan(®) F 2000) and porcine (Mobiforte(®)) origin with respect to the total number of peptides and common peptides between them. Using a novel dual radiolabeling procedure, no CH modulated collagen biosynthesis in human knee cartilage explants. Peptan(®) F 2000 enhanced the activities of the aggrecanase ADMATS4 and ADMATS5 in vitro without loss of proteoglycan from cartilage explants; the opposite effect was observed with Mobiforte(®). Interleukin (IL)-6, matrix metalloproteinase (MMP)-1, -3 and -13 levels were elevated in explants that were treated with Mobiforte(®) and Peptan(®) F 5000, but not with Peptan(®) F 2000. In conclusion, the heterogeneous peptide composition and disparate pharmacological effects between CHs suggest that the effect of a CH preparation cannot be extrapolated to other formulations. Thus, the declaration of a CH as a safe and effective nutraceutical requires a thorough examination of its pleiotropic effects. |
format | Online Article Text |
id | pubmed-5297837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-52978372017-02-10 Metabolic Response of Human Osteoarthritic Cartilage to Biochemically Characterized Collagen Hydrolysates Schadow, Saskia Simons, Viktor S. Lochnit, Guenter Kordelle, Jens Gazova, Zuzana Siebert, Hans-Christian Steinmeyer, Juergen Int J Mol Sci Article The most frequent disease of the locomotor system is osteoarthritis (OA), which, as a chronic joint disease, might benefit more from nutrition than acute illnesses. Collagen hydrolysates (CHs) are peptidic mixtures that are often used as nutraceuticals for OA. Three CHs were characterized biochemically and pharmacologically. Our biophysical (MALDI-TOF-MS, NMR, AFM) and fluorescence assays revealed marked differences between CHs of fish (Peptan(®) F 5000, Peptan(®) F 2000) and porcine (Mobiforte(®)) origin with respect to the total number of peptides and common peptides between them. Using a novel dual radiolabeling procedure, no CH modulated collagen biosynthesis in human knee cartilage explants. Peptan(®) F 2000 enhanced the activities of the aggrecanase ADMATS4 and ADMATS5 in vitro without loss of proteoglycan from cartilage explants; the opposite effect was observed with Mobiforte(®). Interleukin (IL)-6, matrix metalloproteinase (MMP)-1, -3 and -13 levels were elevated in explants that were treated with Mobiforte(®) and Peptan(®) F 5000, but not with Peptan(®) F 2000. In conclusion, the heterogeneous peptide composition and disparate pharmacological effects between CHs suggest that the effect of a CH preparation cannot be extrapolated to other formulations. Thus, the declaration of a CH as a safe and effective nutraceutical requires a thorough examination of its pleiotropic effects. MDPI 2017-01-20 /pmc/articles/PMC5297837/ /pubmed/28117674 http://dx.doi.org/10.3390/ijms18010207 Text en © 2017 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Schadow, Saskia Simons, Viktor S. Lochnit, Guenter Kordelle, Jens Gazova, Zuzana Siebert, Hans-Christian Steinmeyer, Juergen Metabolic Response of Human Osteoarthritic Cartilage to Biochemically Characterized Collagen Hydrolysates |
title | Metabolic Response of Human Osteoarthritic Cartilage to Biochemically Characterized Collagen Hydrolysates |
title_full | Metabolic Response of Human Osteoarthritic Cartilage to Biochemically Characterized Collagen Hydrolysates |
title_fullStr | Metabolic Response of Human Osteoarthritic Cartilage to Biochemically Characterized Collagen Hydrolysates |
title_full_unstemmed | Metabolic Response of Human Osteoarthritic Cartilage to Biochemically Characterized Collagen Hydrolysates |
title_short | Metabolic Response of Human Osteoarthritic Cartilage to Biochemically Characterized Collagen Hydrolysates |
title_sort | metabolic response of human osteoarthritic cartilage to biochemically characterized collagen hydrolysates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297837/ https://www.ncbi.nlm.nih.gov/pubmed/28117674 http://dx.doi.org/10.3390/ijms18010207 |
work_keys_str_mv | AT schadowsaskia metabolicresponseofhumanosteoarthriticcartilagetobiochemicallycharacterizedcollagenhydrolysates AT simonsviktors metabolicresponseofhumanosteoarthriticcartilagetobiochemicallycharacterizedcollagenhydrolysates AT lochnitguenter metabolicresponseofhumanosteoarthriticcartilagetobiochemicallycharacterizedcollagenhydrolysates AT kordellejens metabolicresponseofhumanosteoarthriticcartilagetobiochemicallycharacterizedcollagenhydrolysates AT gazovazuzana metabolicresponseofhumanosteoarthriticcartilagetobiochemicallycharacterizedcollagenhydrolysates AT sieberthanschristian metabolicresponseofhumanosteoarthriticcartilagetobiochemicallycharacterizedcollagenhydrolysates AT steinmeyerjuergen metabolicresponseofhumanosteoarthriticcartilagetobiochemicallycharacterizedcollagenhydrolysates |