Attenuative effects of collagen peptide from milkfish (Chanos chanos) scales on ovariectomy‐induced osteoporosis

Author:

Chuu Jiunn‐Jye1,Lu Jeng‐Wei23,Chang Hung‐Ju1,Chu You‐Hsiang4,Peng Yi‐Jen4,Ho Yi‐Jung56,Shen Pei‐Hung7,Cheng Yu‐Shuan1,Cheng Chia‐Hui1,Liu Yi‐Chien1,Wang Chih‐Chien7ORCID

Affiliation:

1. Department of Biotechnology and Food Technology College of Engineering, Southern Taiwan University of Science Tainan Taiwan

2. Biotech Research and Innovation Centre University of Copenhagen Copenhagen Denmark

3. The Finsen Laboratory Rigshospitalet/National University Hospital, Faculty of Health and Medical Sciences, University of Copenhagen Copenhagen Denmark

4. Department of Pathology Tri‐Service General Hospital, National Defense Medical Center Taipei Taiwan

5. Graduate Institute of Life Sciences, National Defense Medical Center Taipei Taiwan

6. School of Pharmacy, National Defense Medical Center Taipei Taiwan

7. Department of Orthopedics Tri‐Service General Hospital, National Defense Medical Center Taipei Taiwan

Abstract

AbstractOsteoporosis is characterized by low bone mass, bone microarchitecture disruption, and collagen loss, leading to increased fracture risk. In the current study, collagen peptides were extracted from milkfish scales (MS) to develop potential therapeutic candidates for osteoporosis. MS was used to synthesize a crude extract of fish scales (FS), collagen liquid (COL), and hydroxyapatite powder (HA). COL samples were further categorized according to the peptide size of total COL (0.1 mg/mL), COL < 1 kDa (0.1 mg/mL), COL: 1–10 kDa (0.1 mg/mL), and COL > 10 kDa (0.1 mg/mL) to determine it. Semi‐quantitative reverse transcription polymerase chain reaction (sqRT‐PCR) and immunofluorescence labeling were used to assess the expression levels of specific mRNA and proteins in vitro. For in vivo studies, mice ovariectomy (OVX)‐induced postmenopausal osteoporosis were developed, while the sham surgery (Sham) group was treated as a control. Collagen peptides (CP) from MS inhibited osteoclast differentiation in RAW264.7 cells following an insult with nuclear factor kappa‐B ligand (RANKL). CP also enhanced osteoblast proliferation in MG‐63 cells, possibly through downregulating NFATc1 and TRAP mRNA expression and upregulating ALP and OPG mRNA levels. Furthermore, COL1 kDa also inhibited bone density loss in osteoporotic mice. Taken together, CP may reduce RANKL‐induced osteoclast activity while promoting osteoblast synthesis, and therefore may act as a potential therapeutic agent for the prevention and control of osteoporosis.

Funder

Ministry of Science and Technology, Taiwan

Publisher

Wiley

Subject

Food Science

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