Joint hemorrhage accelerates cartilage degeneration in a rat immobilized knee model.


Journal

BMC musculoskeletal disorders
ISSN: 1471-2474
Titre abrégé: BMC Musculoskelet Disord
Pays: England
ID NLM: 100968565

Informations de publication

Date de publication:
19 Nov 2020
Historique:
received: 17 04 2020
accepted: 12 11 2020
entrez: 20 11 2020
pubmed: 21 11 2020
medline: 15 5 2021
Statut: epublish

Résumé

Joint hemorrhage is caused by trauma, ligament reconstruction surgery, and bleeding disorders such as hemophilia. Recurrence of hemorrhage in the joint space induces hemosiderotic synovitis and oxidative stress, resulting in both articular cartilage degeneration and arthropathy. Joint immobilization is a common treatment option for articular fractures accompanied by joint hemorrhage. Although joint hemorrhage has negative effects on the articular cartilage, there is no consensus on whether a reduction in joint hemorrhage would effectively prevent articular cartilage degeneration. The purpose of this study was to investigate the effect of joint hemorrhage combined with joint immobilization on articular cartilage degeneration in a rat immobilized knee model. The knee joints of adult male rats were immobilized at the flexion using an internal fixator from 3 days to 8 weeks. The rats were randomly divided into the following groups: immobilized blood injection (Im-B) and immobilized-normal saline injection (Im-NS) groups. The cartilage was evaluated in two areas (contact and non-contact areas). The cartilage was used to assess chondrocyte count, Modified Mankin score, and cartilage thickness. The total RNA was extracted from the cartilage in both areas, and the expression of metalloproteinase (MMP)-8, MMP-13, interleukin (IL)-1β, and tumor necrosis factor (TNF)-α was measured by quantitative real-time polymerase chain reaction. The number of chondrocytes in the Im-B group significantly decreased in both areas, compared with that in the Im-NS group. Modified Mankin score from 4 to 8 weeks of the Im-B group was significantly higher than that of the Im-NS group only in the contact area. The expression of MMP-8 and MMP-13 from 2 to 4 weeks and TNF-α from 2 to 8 weeks significantly increased in the Im-B group compared with those in the Im-NS group, but there was no significant difference in IL-1β expression. The results showed that joint hemorrhage exacerbated immobilization-induced articular cartilage degeneration. Drainage of a joint hemorrhage or avoidance of loading may help prevent cartilage degeneration during joint immobilization with a hemorrhage.

Sections du résumé

BACKGROUND BACKGROUND
Joint hemorrhage is caused by trauma, ligament reconstruction surgery, and bleeding disorders such as hemophilia. Recurrence of hemorrhage in the joint space induces hemosiderotic synovitis and oxidative stress, resulting in both articular cartilage degeneration and arthropathy. Joint immobilization is a common treatment option for articular fractures accompanied by joint hemorrhage. Although joint hemorrhage has negative effects on the articular cartilage, there is no consensus on whether a reduction in joint hemorrhage would effectively prevent articular cartilage degeneration. The purpose of this study was to investigate the effect of joint hemorrhage combined with joint immobilization on articular cartilage degeneration in a rat immobilized knee model.
METHODS METHODS
The knee joints of adult male rats were immobilized at the flexion using an internal fixator from 3 days to 8 weeks. The rats were randomly divided into the following groups: immobilized blood injection (Im-B) and immobilized-normal saline injection (Im-NS) groups. The cartilage was evaluated in two areas (contact and non-contact areas). The cartilage was used to assess chondrocyte count, Modified Mankin score, and cartilage thickness. The total RNA was extracted from the cartilage in both areas, and the expression of metalloproteinase (MMP)-8, MMP-13, interleukin (IL)-1β, and tumor necrosis factor (TNF)-α was measured by quantitative real-time polymerase chain reaction.
RESULTS RESULTS
The number of chondrocytes in the Im-B group significantly decreased in both areas, compared with that in the Im-NS group. Modified Mankin score from 4 to 8 weeks of the Im-B group was significantly higher than that of the Im-NS group only in the contact area. The expression of MMP-8 and MMP-13 from 2 to 4 weeks and TNF-α from 2 to 8 weeks significantly increased in the Im-B group compared with those in the Im-NS group, but there was no significant difference in IL-1β expression.
CONCLUSIONS CONCLUSIONS
The results showed that joint hemorrhage exacerbated immobilization-induced articular cartilage degeneration. Drainage of a joint hemorrhage or avoidance of loading may help prevent cartilage degeneration during joint immobilization with a hemorrhage.

Identifiants

pubmed: 33213419
doi: 10.1186/s12891-020-03795-0
pii: 10.1186/s12891-020-03795-0
pmc: PMC7678279
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

761

Références

Connect Tissue Res. 2013;54(3):210-7
pubmed: 23496380
Ann N Y Acad Sci. 2010 Nov;1211:37-50
pubmed: 21062294
Clin Orthop Relat Res. 2004 Oct;(427 Suppl):S27-36
pubmed: 15480070
J Orthop Res. 1989;7(5):619-36
pubmed: 2760736
Tohoku J Exp Med. 2011;224(2):77-85
pubmed: 21558763
Rheumatology (Oxford). 2003 Jun;42(6):784-90
pubmed: 12730540
J Orthop Res. 2009 Feb;27(2):236-42
pubmed: 18683886
Clin Biomech (Bristol, Avon). 1987 Nov;2(4):223-9
pubmed: 23915759
Int J Clin Exp Pathol. 2015 Apr 01;8(4):3426-40
pubmed: 26097527
Nat Rev Rheumatol. 2013 Aug;9(8):485-97
pubmed: 23689231
Curr Rheumatol Rep. 2000 Dec;2(6):459-65
pubmed: 11123098
J Clin Invest. 1997 Apr 1;99(7):1534-45
pubmed: 9119997
J Biol Chem. 2004 May 21;279(21):22158-65
pubmed: 15044466
Am J Sports Med. 2014 Nov;42(11):2741-50
pubmed: 25167994
J Thromb Haemost. 2017 Sep;15(9):1788-1798
pubmed: 28696534
Haemophilia. 2006 Jul;12 Suppl 3:117-21
pubmed: 16684006
J Thromb Haemost. 2010 Sep;8(9):1895-902
pubmed: 20586922
J Histochem Cytochem. 2002 Mar;50(3):325-32
pubmed: 11850435
Blood. 2015 Nov 5;126(19):2239-46
pubmed: 26276670
Instr Course Lect. 1998;47:487-504
pubmed: 9571450
Tohoku J Exp Med. 2008 Aug;215(4):321-31
pubmed: 18679006
J Clin Pathol. 2015 Aug;68(8):592-600
pubmed: 25897098
Immunology. 1994 Sep;83(1):140-7
pubmed: 7821959
Arthroscopy. 2003 Sep;19(7):794-8
pubmed: 12966391
Clin Orthop Relat Res. 2004 Jun;(423):17-26
pubmed: 15232421
Ann Rheum Dis. 1991 Aug;50(8):588-91
pubmed: 1888204
Arthritis Rheum. 2004 Jun;50(6):2024-31
pubmed: 15188380
Knee Surg Sports Traumatol Arthrosc. 2014 Nov;22(11):2874-83
pubmed: 24013446
Cytokine Growth Factor Rev. 2018 Feb;39:71-91
pubmed: 29153709
Nucleic Acids Res. 2001 May 1;29(9):e45
pubmed: 11328886
Connect Tissue Res. 2010;51(1):22-30
pubmed: 20067413
Clin Orthop Relat Res. 1994 Feb;(299):282-92
pubmed: 8119031
J Clin Med. 2017 Jun 25;6(7):
pubmed: 28672826
BMC Musculoskelet Disord. 2017 Dec 29;18(1):556
pubmed: 29284451
J Clin Invest. 1996 Feb 1;97(3):761-8
pubmed: 8609233
Arthritis Res. 2001;3(1):18-26
pubmed: 11178124
Tohoku J Exp Med. 2009 Apr;217(4):271-8
pubmed: 19346731
Arthritis Rheumatol. 2014 Dec;66(12):3337-48
pubmed: 25200274
Ups J Med Sci. 2006;111(3):303-13
pubmed: 17578797
Osteoarthritis Cartilage. 2009 Apr;17(4):433-40
pubmed: 18922705
J Thromb Haemost. 2013 Feb;11(2):293-306
pubmed: 23231432
J Orthop Res. 2010 Mar;28(3):315-21
pubmed: 19777487

Auteurs

Yasuhito Sogi (Y)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Yutaka Yabe (Y)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Yoshihiro Hagiwara (Y)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan. hagi@med.tohoku.ac.jp.

Masahiro Tsuchiya (M)

Department of Nursing, Faculty of Health Science, Tohoku Fukushi University, 1-8-1 Kunimi, Aoba-ku, Sendai, 981-8522, Japan.

Yoshito Onoda (Y)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Takuya Sekiguchi (T)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Nobuyuki Itaya (N)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Shinichiro Yoshida (S)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Toshihisa Yano (T)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Kazuaki Suzuki (K)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Takahiro Onoki (T)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Eiji Itoi (E)

Department of Orthopaedic Surgery, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH