The role of sirtuin 1 and its activator, resveratrol in osteoarthritis

Author:

Deng Zhenhan12ORCID,Li Yusheng13,Liu Haifeng2,Xiao Shengshi4,Li Liangjun5,Tian Jian1,Cheng Chao6,Zhang Greg7,Zhang Fangjie83

Affiliation:

1. Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha, Hunan, China

2. Department of Sports Medicine, The First Hospital Affiliated of Shenzhen University, Shenzhen Second People’s Hospital, Shenzhen, Guangdong, China

3. National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China

4. Department of Joint Surgery, Zhuzhou Central Hospital, Zhuzhou, Hunan, China

5. Department of Joint Surgery, Changsha Central Hospital, Changsha, Hunan, China

6. Department of Orthopaedics, Yiyang Central Hospital, Clinical Medical Technology Demonstration Base for Minimally Invasive and Digital Orthopaedics in Hunan Province, Yiyang, Hunan, China

7. McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, U.S.A.

8. Department of Emergency Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China

Abstract

Abstract Osteoarthitis (OA) is the most common aging-related joint pathology; the aging process results in changes to joint tissues that ultimately contribute to the development of OA. Articular chondrocytes exhibit an aging-related decline in their proliferative and synthetic capacity. Sirtuin 1 (SIRT 1), a longevity gene related to many diseases associated with aging, is a nicotinamide adenine dinucleotide (NAD+)-dependent protein deacetylase and master metabolic regulator. Along with its natural activator resveratrol, SIRT 1 actively participates in the OA pathological progress. SIRT 1 expression in osteoarthritic cartilage decreases in the disease progression of OA; it appears to play a predominantly regulatory role in OA. SIRT 1 can regulate the expression of extracellular matrix (ECM)-related proteins; promote mesenchymal stem cell differentiation; play anti-catabolic, anti-inflammatory, anti-oxidative stress, and anti-apoptosis roles; participate in the autophagic process; and regulate bone homeostasis in OA. Resveratrol can activate SIRT 1 in order to inhibit OA disease progression. In the future, activating SIRT 1 via resveratrol with improved bioavailability may be an appropriate therapeutic approach for OA.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference91 articles.

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