Oral Administration of Protease-Soluble Chicken Type II Collagen Ameliorates Anterior Cruciate Ligament Transection–Induced Osteoarthritis in Rats

Author:

Chen Nan-Fu12,Lin Yen-You3,Yao Zhi-Kang45ORCID,Tseng Chung-Chih2,Liu Yu-Wei5,Hung Ya-Ping6,Jean Yen-Hsuan7,Wen Zhi-Hong58ORCID

Affiliation:

1. Division of Neurosurgery, Department of Surgery, Kaohsiung Armed Forces General Hospital, Kaohsiung 80284, Taiwan

2. Institute of Medical Science and Technology, National Sun Yat-sen University, Kaohsiung 80424, Taiwan

3. Department of Sports Medicine, China Medical University, Taichung 40402, Taiwan

4. Department of Orthopedics, Kaohsiung Veterans General Hospital, Kaohsiung 81362, Taiwan

5. Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 80424, Taiwan

6. R&D Department, Taiyen Biotech Co., Ltd., Tainan 70263, Taiwan

7. Department of Orthopedic Surgery, Pingtung Christian Hospital, Pingtung 90059, Taiwan

8. Institute of BioPharmaceutical Sciences, National Sun Yat-sen University, Kaohsiung 80424, Taiwan

Abstract

This study investigated whether oral supplementation with protease-soluble chicken type II collagen (PSCC-II) mitigates the progression of anterior cruciate ligament transection (ACLT)–induced osteoarthritis (OA) in rats. Eight-week-old male Wistar rats were randomly assigned to the following groups: control, sham, ACLT, group A (ACLT + pepsin-soluble collagen type II collagen (C-II) with type I collagen), group B (ACLT + Amano M–soluble C-II with type I collagen), group C (ACLT + high-dose Amano M–soluble C-II with type I collagen), and group D (ACLT + unproteolyzed C-II). Various methods were employed to analyze the knee joint: nociceptive tests, microcomputed tomography, histopathology, and immunohistochemistry. Rats treated with any form of C-II had significant reductions in pain sensitivity and cartilage degradation. Groups that received PSCC-II treatment effectively mitigated the ACLT-induced effects of OA concerning cancellous bone volume, trabecular number, and trabecular separation compared with the ACLT alone group. Furthermore, PSCC-II and unproteolyzed C-II suppressed ACLT-induced effects, such as the downregulation of C-II and upregulation of matrix metalloproteinase-13, tumor necrosis factor-α, and interleukin-1β. These results indicate that PSCC-II treatment retains the protective effects of traditional undenatured C-II and provide superior benefits for OA management. These benefits encompass pain relief, anti-inflammatory effects, and the protection of cartilage and cancellous bone.

Funder

Taiyen Biotech Co., Ltd., Taiwan

Publisher

MDPI AG

Subject

Food Science,Nutrition and Dietetics

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