Fisetin suppresses chondrocyte senescence and attenuates osteoarthritis progression by targeting SIRT6 DOI Creative Commons
Xuezhong Wang, Xuyang Li, Jianlin Zhou

et al.

Research Square (Research Square), Journal Year: 2023, Volume and Issue: unknown

Published: Nov. 20, 2023

Abstract Background Osteoarthritis (OA), the most common type of arthritis, is a highly prevalent age-related joint disease particularly in subjects over 65 years old. The chronic rise senescent cells closely correlates with diseases including OA, and senescence-associated secretory phenotype (SASP) implicated pathogenesis OA cartilage degeneration. Sirtuin 6 (SIRT6) probable to be key senescence-related regulator. Fisetin (FST), natural flavonol flavonoid family, recommended senolytic that extends health lifespan. However, potential chondroprotective effects FST on rats remain largely unclarified. This study aimed investigate ameliorative relationship SIRT6, detailed mechanisms from both anti-inflammatory anti-senescent perspectives. Methods Rats were subjected destabilization medial meniscus (DMM) surgery induce experimental model vivo. Chondrocytes treated IL-1β utilized mimic cell vitro. Intra-articular injection FST, OSS_128167 (OSS, SIRT6 inhibitor), MDL800 (MDL, agonist) vivo or incubation IL-1β-induced rat chondrocytes vitro performed determine link SIRT6. Results level was negatively correlated severity. downregulation validated cartilages DMM IL-1β-treated chondrocytes. Of note, We demonstrated could activate Both administration activation using MDL rescued erosion, decreased extracellular matrix (ECM) degradation, prevented apoptosis, improved detrimental phenotype. alleviative against inflammation, ECM senescence also confirmed IL-1β-stimulated Conclusion loss occurs articular which linked aging. attenuates injury-induced aging-related changes by targeting

Language: Английский

Long COVID as a Disease of Accelerated Biological Aging: An Opportunity to Translate Geroscience Interventions DOI
Areez Shafqat, Mary Clare Masters, Utkarsh Tripathi

et al.

Ageing Research Reviews, Journal Year: 2024, Volume and Issue: 99, P. 102400 - 102400

Published: June 28, 2024

Language: Английский

Citations

3

Immunomodulation: A new approach to cancer cachexia, potentially suitable for aging DOI Creative Commons
Fabio Penna,

Giacomo Rubini,

Paola Costelli

et al.

Molecular Aspects of Medicine, Journal Year: 2024, Volume and Issue: 100, P. 101318 - 101318

Published: Sept. 10, 2024

Language: Английский

Citations

2

The mechanisms, hallmarks, and therapies for brain aging and age-related dementia DOI Creative Commons
Shiyun Jin, Wenping Lü,

Juan Zhang

et al.

Science Bulletin, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 1, 2024

Language: Английский

Citations

2

Adenovirus-mediated Sirt1 and Tgfbr2 gene therapy improves fertility in natural ovarian aging and doxorubicin-induced premature ovarian insufficiency mice DOI Creative Commons
Lingwei Ma, Huan Lu,

Xiaofan Gao

et al.

Materials & Design, Journal Year: 2024, Volume and Issue: 238, P. 112693 - 112693

Published: Jan. 25, 2024

Premature ovarian insufficiency (POI) may lead to early menopause, fertility loss and birth defects without effective treatment. Here, we explored the efficacy safety of gene therapy rescue function in both natural aging doxorubicin (Dox) induced POI mice. Sirt1 Tgfbr2 were screened out identified as key genes murine human tissues. Then, adenovirus (AdV) was selected a suited carrier for infection after comparison multiple viral vectors. In two models, significantly improved AdV-Sirt1 AdV-Tgfbr2 invention individually or combination, obvious side effects themselves their offspring. Compared with control group, successful pregnancy rate 9-month-old-AdV-Sirt1 group increased by 60 % (67 vs 42 %). Meanwhile, + Dox 85 (55.6 20 The biological process follicle development fibrosis rescued. Our work demonstrated that alleviates Dox-associated POI, which be potentially applicable female protection.

Language: Английский

Citations

1

Cellular Senescence and Anti-Aging Strategies in Aesthetic Medicine: A Bibliometric Analysis and Brief Review DOI Creative Commons

Huilan Zheng,

Jingping Wu,

Jinhong Feng

et al.

Clinical Cosmetic and Investigational Dermatology, Journal Year: 2024, Volume and Issue: Volume 17, P. 2243 - 2259

Published: Oct. 1, 2024

Background: Skin aging is the most obvious feature of human aging, and delaying has become a hot difficult research topic in aesthetic medicine. The accumulation dysfunctional senescent cells one important mechanisms skin based on which series anti-aging strategies have been generated. In this paper, from perspective cellular senescence, we utilize bibliometrics review to explore hotspots trends field, with view providing references for health Methods: We obtained literature related field Web Science Core Collection database 1994 2024. Bibliometrix packages R, CiteSpace, VOSviewer, Origin, Scimago Graphica were utilized data mining visualization. Results: A total 2,796 documents included analysis. overall trend publications showed continuous rapid increase 2016– 2023, but citations improved poorly over time. Journal Cosmetic Dermatology, Investigative Experimental Gerontology are core journals. Kim J, Lee JH, S, Rattan SIS, Chung JH authors field. Seoul National University first terms publications. Korea country publications, USA citations. Top 10 keywords include: gene-expression, skin, cell, oxidative stress, antioxidants, vitro, fibroblasts, mechanism, cancer. Current focused neurodegeneration, rejuvenation, molecular docking, fibrosis, wound healing, SASP, barrier, antioxidants. reflect topics such as major pathways process, relationship tumors. Conclusion: This rapidly rising recent years. Relevant focus senescence-associated secretory phenotype. Anti-aging targeting senescence hold great promise, including removal or attenuation SASP factors, corresponding senolytics senomorphics therapies, respectively. Keywords: medicine, senolytic,

Language: Английский

Citations

1

Effect of physical activity in lymphocytes senescence burden in COPD patients DOI
Enrique Alfaro, Elena Díaz‐García,

Sara García-Tovar

et al.

AJP Lung Cellular and Molecular Physiology, Journal Year: 2024, Volume and Issue: 327(4), P. L464 - L472

Published: Aug. 6, 2024

Chronic obstructive pulmonary disease (COPD) is regarded as an accelerated-age in which chronic inflammation, maladaptive immune responses, and senescence cell burden coexist. Accordingly, cellular has emerged a potential mechanism involved COPD pathophysiology. In this study, 25 stable patients with underwent daily physical activity promotion program for 6 mo. We reported that increase of was related to reduction the senescent circulating lymphocytes COPD. Senescent T-lymphocyte population, characterized by absence surface expression CD28, reduced after intervention, associated level. addition, mRNA cyclin-dependent kinase inhibitors, hallmark senescence, and, accordance, proliferative capacity improved postintervention. Moreover, we observed functionality T cells from including markers activation, enhanced cytotoxicity, altered cytokine secretions response viral challenge. Lastly, intervention lymphocytes' secretome induce human primary fibroblasts. conclusion, our study provides, first time, evidence reduce cells.

Language: Английский

Citations

0

Identication and validation of cell senescence biomarkers in idiopathic pulmonary hypertension via integrated transcriptome analyses and machine learning DOI Creative Commons
Wenzhang Lu, Jiayi Xu, Yanrong Chen

et al.

Experimental Gerontology, Journal Year: 2023, Volume and Issue: 182, P. 112303 - 112303

Published: Sept. 30, 2023

Idiopathic pulmonary hypertension (IPAH) is a rare and severe disease that affects the vasculature. As diagnosis of IPAH requires invasive right heart catheterization surgery, early detection this condition notoriously challenging. Therefore, it utmost importance to investigate biomarkers present in peripheral blood could aid physicians identification management IPAH.We speculate cellular senescence may be involved occurrence development through various pathways. In study, we utilized integrated transcriptome analyses machine learning-based approach develop diagnostic model for cell senescence. To select genetic features, employed two learning algorithms: Least Absolute Shrinkage Selection Operator (LASSO) Random Forest (RF). Additionally, validated our findings both external data sets qRT-PCR experiments.The resulting nomogram was able identify five important can IPAH, including TNFRSF1B, CCL16, GCLM, IL15, SOD1. These genes are primarily associated with immune system, as well apoptosis.Our study demonstrates utility algorithms making accurate diagnoses providing clinicians more directed treatment disease.

Language: Английский

Citations

0

Fisetin suppresses chondrocyte senescence and attenuates osteoarthritis progression by targeting SIRT6 DOI Creative Commons
Xuezhong Wang, Xuyang Li, Jianlin Zhou

et al.

Research Square (Research Square), Journal Year: 2023, Volume and Issue: unknown

Published: Nov. 20, 2023

Abstract Background Osteoarthritis (OA), the most common type of arthritis, is a highly prevalent age-related joint disease particularly in subjects over 65 years old. The chronic rise senescent cells closely correlates with diseases including OA, and senescence-associated secretory phenotype (SASP) implicated pathogenesis OA cartilage degeneration. Sirtuin 6 (SIRT6) probable to be key senescence-related regulator. Fisetin (FST), natural flavonol flavonoid family, recommended senolytic that extends health lifespan. However, potential chondroprotective effects FST on rats remain largely unclarified. This study aimed investigate ameliorative relationship SIRT6, detailed mechanisms from both anti-inflammatory anti-senescent perspectives. Methods Rats were subjected destabilization medial meniscus (DMM) surgery induce experimental model vivo. Chondrocytes treated IL-1β utilized mimic cell vitro. Intra-articular injection FST, OSS_128167 (OSS, SIRT6 inhibitor), MDL800 (MDL, agonist) vivo or incubation IL-1β-induced rat chondrocytes vitro performed determine link SIRT6. Results level was negatively correlated severity. downregulation validated cartilages DMM IL-1β-treated chondrocytes. Of note, We demonstrated could activate Both administration activation using MDL rescued erosion, decreased extracellular matrix (ECM) degradation, prevented apoptosis, improved detrimental phenotype. alleviative against inflammation, ECM senescence also confirmed IL-1β-stimulated Conclusion loss occurs articular which linked aging. attenuates injury-induced aging-related changes by targeting

Language: Английский

Citations

0