Sirt1 and the Mitochondria

Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α

Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057

Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan

Howitz, K. T., Bitterman, K. J., Cohen, H. Y., Lamming, D. W., Lavu, S., Wood, J. G., Zipkin, R. E., Chung, P., Kisielewski, A., Zhang, L.-L., et al. (2003) · Nature · doi:10.1038/nature01960 · Cited by 3,796

AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity

Cantó, C., Gerhart-Hines, Z., Feige, J. N., Lagouge, M., Noriega, L., Milne, J. C., Elliott, P. J., Puigserver, P., & Auwerx, J. (2009) · Nature · doi:10.1038/nature07813 · Cited by 3,300

Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase

Brunet, A., Sweeney, L. B., Sturgill, J. F., Chua, K. F., Greer, P. L., Lin, Y., Tran, H., Ross, S. E., Mostoslavsky, R., Cohen, H. Y., et al. (2004) · Science · doi:10.1126/science.1094637 · Cited by 3,239

Multiple Wearable Sensors in Parkinson and Huntington Disease Individuals: A Pilot Study in Clinic and at Home

Adams, J., Dinesh, K., Xiong, M., Tarolli, C. G., Sharma, S., Sheth, N., Aranyosi, A. J., Zhu, W. Y., Goldenthal, S. B., Biglan, K., et al. (2017) · Digital Biomarkers · doi:10.1159/000479018 · Cited by 3,190

Nutrient control of glucose homeostasis through a complex of PGC-1α and SIRT1

Rodgers, J. T., Lerin, C., Haas, W., Gygi, S. P., Spiegelman, B. M., & Puigserver, P. (2005) · Nature · doi:10.1038/nature03354 · Cited by 3,160

Modulation of NF‐κB‐dependent transcription and cell survival by the SIRT1 deacetylase

Yeung, F., Hoberg, J. E., Ramsey, C. S., Keller, M. D., Jones, D. R., Frye, R. A., & Mayo, M. W. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600244 · Cited by 2,750

hSIR2SIRT1 Functions as an NAD-Dependent p53 Deacetylase

Vaziri, H., Dessain, S. K., Eaton, E. N., Imai, S., Frye, R. A., Pandita, T. K., Guarente, L., & Weinberg, R. A. (2001) · Cell · doi:10.1016/s0092-8674(01)00527-x · Cited by 2,690

AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1α

Jäger, S., Handschin, C., St.-Pierre, J., & Spiegelman, B. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705070104 · Cited by 2,491

[Resveratrol alleviates hyperglycemia-induced cardiomyocyte hypertrophy by maintaining mitochondrial homeostasis via enhancing SIRT1 expression].

Ye, H., Zhang, Y., Yun, Q., DU, R., Li, L., Li, Y., & Gao, Q. F. (2024) · PubMed Central · doi:10.12122/j.issn.1673-4254.2024.01.06 · Cited by 2

Beneficial effects of Tteokbokki sauce meeting the functional labeling system claim on dexamethasone-induced C2C12 myotube and hindlimb immobilization-induced C57BL/6J mice

Oh, G., Han, X., Men, X., Im, J., Fu, X., Lim, J.-S., Lee, L., Kwon, M. H., Lee, H. S., Ra, M., et al. (2024) · Food Science and Biotechnology · doi:10.1007/s10068-024-01675-0 · Cited by 2

Temporal expression of mitochondrial life cycle markers during acute and chronic overload of rat plantaris muscles

Hyatt, J. K., Lu, E. J., & McCall, G. E. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1420276 · Cited by 2

Molecular etiopathogenesis of neurodegenerative diseases

Divya, D., Thekkekkara, D., Sai, T. E., Ramakrishna, D., Manjula, S. N., & Goswami, S. K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-28822-7.00002-7 · Cited by 2

Alterations in ether phospholipids metabolism activate the conserved UPR-Xbp1- PDIA3/ERp60 signaling to maintain intestinal homeostasis

Makdissi, S., Loudhaief, R., George, S., Weller, T., Salim, M., Malick, A., Mu, Y., Parsons, B., & Cara, F. D. (2025) · iScience · doi:10.1016/j.isci.2025.111946 · Cited by 2

Agomelatine alleviates palmitic acid-induced mouse oocyte meiosis defects by restoring mitochondrial function

Zhao, R., Tang, Y., Zhang, Y., Liu, J., Zhong, C., Ji, B., Song, W., Zhang, C., & Su, J. (2025) · International Journal of Obesity · doi:10.1038/s41366-025-01825-2 · Cited by 2

Cross-sensitizing effects of Resveratrol and Astaxanthin

Kipshidze, M., Mazanashvili, V., & Gorgaslidze, N. (2023) · JUNIOR RESEARCHERS · doi:10.52340/2023.01.01.16 · Cited by 4

Micro-RNAs differentially expressed in comparative analysis of sperm samples with high and low efficiency in the in vitro production of bovine (Bos Taurus) embryos

da Silva, R. T., Gomes, M. D. S., Fujimura, P. T., Ueira-Vieira, C., do Amaral, L. R., & Beletti, M. E. (2019) · Bioscience Journal · doi:10.14393/bj-v35n1a2019-42257 · Cited by 2

Targeting Reductive Metabolic Shifts by T315I Mutation in BCR-ABL Myeloid Leukemia for TherapyPreprint

Huang, C.-Y., Chung, Y.-H., Wu, S.-Y., Wang, H.-Y., Lin, Z., Yang, T.-J., Feng, J.-M., Hu, C., & Chang, Z.-F. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.22.485260 · Cited by 2

Mitochondrial Function and Dysfunction in White Adipocytes and Therapeutic Implications

Wang, F., Huynh, P. M., & An, Y. (2024) · Comprehensive physiology · doi:10.1002/cphy.c230009 · Cited by 10

NAD+ Metabolism in Aging

Palikhe, S., & Nakagawa, T. (2022) · Springer eBooks · doi:10.1007/978-981-16-7977-3_8 · Cited by 1

Regulatory signaling pathways of osteoblast autophagy in periprosthetic osteolysis

Gu, Y., Wu, Z., Xie, H., Fang, T., Wang, Q., & Gu, Y. (2024) · Frontiers in Cell Death · doi:10.3389/fceld.2024.1337724 · Cited by 1

Role of polyphenols in epilepsy: from the perspective of gut microbiota

Xu, X., Shi, J., Cai, G., Ma, C., Wang, W., Feng, R., Boczek, T., Tang, Y., He, Z., & Guo, F. (2024) · Food Science and Human Wellness · doi:10.26599/fshw.2024.9250303 · Cited by 1

Circular RNA circVAPA mediates alveolar macrophage activation by modulating miR-212-3p/Sirt1 axis in acute respiratory distress syndrome

Bao, L., Li, M., Li, J., & Gao, J. (2024) · Journal of Molecular Histology · doi:10.1007/s10735-024-10312-3 · Cited by 1

A tale of two endothelins: the rise and fall of the corpus luteum

Szymańska, M., Basavaraja, R., & Meidan, R. (2024) · Reproduction Fertility and Development · doi:10.1071/rd24158 · Cited by 1

Model systems informing mechanisms and drug discovery: a review of POLG-related disease models

Meyrick, J., Stefanetti, R. J., Errington, L., McFarland, R., Gorman, G. S., & Lax, N. Z. (2025) · Wellcome Open Research · doi:10.12688/wellcomeopenres.18637.2 · Cited by 1

Daqinjiao Decoction Ameliorates CSVD via RXR‐γ/PPAR‐γ/VEGF‐α Pathway: Insights From Transcriptome Sequencing and Network Pharmacology

Lv, M., Yang, X.-L., Shi, X., Cao, S., Li, W., Zhou, M., Gou, X., & Huang, Y. (2025) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70712 · Cited by 1

Mammalian Sterile 20-Like Kinase 2 Knockdown Alleviates Neuropathic Pain in Rats by Mitochondrial Protection

Zeng, Q., Huang, B.-X., Liu, C., Liang, N., Yu, J., & Liao, S. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05202-y · Cited by 1

Unlocking Hopeaphenol: A Potent Ally Against Cardiac Hypertrophy via AMPK Activation

Chen, J., Wang, M., Zhang, Z., Fang, C., Zhuang, H., Zhao, J., Wang, T., Wang, J., Li, C., & Fang, C. (2025) · Nutrients · doi:10.3390/nu17183025 · Cited by 1

Agomelatine alleviates hypoxia-induced pulmonary arterial hypertension by activating mitophagy via the SIRT1/FoxO1/ULK1 signaling pathway

Zhang, J., Zhang, R., Liu, J., Chen, L., Sun, Y., He, Y., Xie, W., Wang, L., Kong, H., & He, M. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117624 · Cited by 1

The roles of RNA-binding proteins in ovarian aging

Zhang, H., Pan, H., Zheng, T., Dou, C., Geng, Y., & Chen, J. (2025) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-025-03765-2 · Cited by 1

ENPP2 Protects Mouse Myocardium from Ischemia-Reperfusion-Induced Ferroptosis Injury Via the SIRT1/PGC-1α/NRF1 Pathway

Liao, D., wang, Z., Tian, G., Wang, H., & Fang, G. (2026) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-025-05494-9 · Cited by 1

Targeting the SARM1-NAD⁺ axis: A review of new strategy for reversing the imbalance of energy and mitochondrial homeostasis in metabolic diseases

Xiong, A., Lv, W., Shao, X., Lv, Y., & Zhang, Y. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108128 · Cited by 1

Therapeutic Potential of HDAC Inhibitors in Neurodegenerative Diseases

Singh, A. K., Sudhan, Y. G., Chandana, S. L., Iyaswamy, A., & Durairajan, S. S. K. (2026) · Springer eBooks · doi:10.1007/978-981-95-6099-8_14 · Cited by 2

Changed Serum Levels of Sirtuin1 and Sirtuin3 and Their Correlations with Sleep Quality and Cognitive Function in Patients with Chronic Insomnia Disorder

Liu, G.-X., Zhang, Y. H., Song, Y., Yang, S., Su, A.-X., Feng, Y.-Z., Zhou, Y.-S., Ma, Z.-J., Xia, L., & Chen, G. (2026) · Nature and Science of Sleep · doi:10.2147/nss.s518388 · Cited by 1

Resolvin D1 alleviates liver inflammation and fibrosis through SIRT1-mediated NF-κB and TGF-β1/Smads pathways

Li, J., Zhao, L., Xi, Y., & Xiaoling, D. (2026) · Journal of Inflammation · doi:10.1186/s12950-026-00492-y · Cited by 1

Rhodiola sacra Protects Against Hippocampal Neuronal Apoptosis in Chronic Cerebral Ischemia via SIRT1-Driven Mitochondrial Biogenesis

Zhou, L., Jia, J., Li, J., Yao, Z., Fu, Z., & Wang, S. (2026) · Current Neuropharmacology · doi:10.2174/011570159x417392251118050138 · Cited by 1

Preclinical evaluation of puerarin for the treatment of non-alcoholic fatty liver disease: a systematic review and meta-analysis

Li, J., Li, M., Meng, R., An, S., Zhang, X., Shang, Z., Chen, Y. A., Qi, Y., & Su, C. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1795374 · Cited by 1

Sirtuin 1 as an emerging exerkine in the aging process: unveiling its multifaceted biological roles

Leite, P. L. D. A., Maciel, L. A., Patricio, R. C. B., Pereira, G. L. C., Lamounier, A. S. D. O., Aguiar, S. D. S., Sousa, C. V., Neto, I. V. D. S., & Simões, H. G. (2026) · Biogerontology · doi:10.1007/s10522-026-10442-z · Cited by 1

Oxidative Damage Induced Disruption of Mitochondrial Quality Control Underlying Abnormal Energy Metabolism in Peripheral Leukocytes of Schizophrenia Patients

Li, S., Zhu, W., Jiang, J., Bu, Y., Wang, Q. M., Li, M., Dm, W., Gao, Y., Wang, J., Wang, T., et al. (2026) · Schizophrenia Bulletin Open · doi:10.1093/schizbullopen/sgag029 · Cited by 1

A Function-Centric Framework for Mitochondrial Quality Control

Ozcan, F., Vujovic, F., & Farahani, R. H. (2026) · Biomolecules · doi:10.3390/biom16081116 · Cited by 1

Redox-sensitive coordination of mitochondrial quality control: Integrating ROS, NAD+, and Ca2+ signaling in disease

Marcondes‐de‐Castro, I. A., Sales, T. A., Marinho, T. D. S., Águila, M. B., & Mandarim‐de‐Lacerda, C. A. (2026) · Life Sciences · doi:10.1016/j.lfs.2026.124642 · Cited by 1

Therapeutic Effects of Sirtuin 1 Activator on Glaucoma Mice and the Regulation Mechanism of Mitogen-Activated Protein Kinase Pathway

Zhao, Y., Yu, S., Huang, Z., Chen, J., Zhang, X., & Qu, C. (2021) · Journal of Biomaterials and Tissue Engineering · doi:10.1166/jbt.2022.2874 · Cited by 1

Features Neurohumoral and Immune Profile in Children with Functional Disorders of the Autonomic Nervous System Associated with Sirtuin Gene SIRT1 (rs7069102) Polymorphism

Dolgikh, О. V., Зайцева, Н. В., & Алексеевна, Н. Н. (2022) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-022-05439-w · Cited by 1

Correlation between serum SIRT1 and EZH2 expressions and peritoneal function in patients with diabetic nephropathy undergoing peritoneal dialysis

Zhu, Q., Hu, H., & Xia, F. (2022) · Pakistan Journal of Medical Sciences · doi:10.12669/pjms.38.8.5527 · Cited by 1

Circadian Clocks and Metabolism

Challet, É., & Vuillez, P. (2024) · Royal Society of Chemistry eBooks · doi:10.1039/bk9781839167553-00476 · Cited by 2

mTOR-related linc-PMB promotes mitochondrial biogenesis via stabilizing SIRT1 mRNA through binding to the HuR protein

Chen, Q., Zhang, H., Wang, D., Liao, W., Liu, Y., Cai, Y., Wang, S., & Yu, M. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024236 · Cited by 2

HSF1 Regulates Cellular Senescence: Role of the DHRS2-MDM2-p53 Pathway

Yamashita, T. (2020) · Heat shock proteins · doi:10.1007/7515_2020_17 · Cited by 1

Dihydroartemisinin ameliorates palmitate-induced apoptosis in cardiomyocytes via regulation on miR-133b/Sirt1 axis

Qi, L., Xu, X., LI, B., CHANG, B., WANG, S., Liu, C., Wu, L., Zhou, X., & WANG, Q. (2021) · Biocell · doi:10.32604/biocell.2022.018014 · Cited by 1

Proteoma nuclear e micro-RNAs de espermatozoides de bovinos férteis e subférteis

da Silva, R. T. (2018) · doi:10.14393/ufu.te.2018.457 · Cited by 1

The Anti-Senescence Effect and Mechanism of 17β-estradiol on Pelvic Organ Prolapse Derived FibroblastsPreprint

Cheng, J., Zhao, Z., Wang, L., Wen, J., Miao, Y., & Wu, J. (2023) · Research Square · doi:10.21203/rs.3.rs-2469297/v1 · Cited by 1

An overview of biological functions of natural polysaccharides: influence factors, mitochondria and signaling pathwaysPreprint

Du, J., Li, L., Guo, X., Tong, X., Xu, W., Ye, H., Li, D., & Li, J. (2023) · Research Square · doi:10.21203/rs.3.rs-2672467/v1 · Cited by 1

Sirtuin 1 Activation Mitigates Murine Vasculitis Severity by Promoting Autophagy and MitophagyPreprint

Atici, A. E., Jena, P. K., de Carvalho, T. T., Ross, B. L., Aubuchon, E. A., Lane, M. E., Gomez, A. C., Lee, Y., Chen, S., Crother, T. R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.04.671113 · Cited by 1

Hydrolyzed Pearl Improves Mitochondrial Function in Rats with Diminished Ovarian Reserve via Regulation of the AMPK/SIRT1/PGC-1α Signaling PathwayPreprint

Liu, Y. Y., Ni, Z., Fan, Y., Wei, M., Han, J., Wei, M., & Lin, J. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5570323 · Cited by 1

Synchronization of biological oscillators : modeling, analysis and coupling of the mammalian cell cycle and circadian clock

Almeida, S. J. F. (2018) · theses.fr (ABES) · doi:10.70675/d7f43940zfb09z447az8fcez09de3d68881f · Cited by 1

The Evolving Concept of Mitochondrial Dynamics in Heart: Interventional Opportunities

Ashok, S., Ganjoo, M., Panicker, V. T., Pillai, V. V., & Gopala, S. (2019) · Springer eBooks · doi:10.1007/978-981-13-8946-7_25

Pathological Interaction between DNA Repair and Mitochondrial Dysfunction in ALS

Bermúdez-Guzmán, L., & Leal, A. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.90217

Effects of Baicalin on the ATP Levels in the Prefrontal Cortex in Mice Exposed to Chronic Unpredictable Mild StressPreprint

Lu, S., Jin, X., Zhu, L., Shen, J.-D., Bai, M., Li, Y., & Xu, E. (2021) · Research Square · doi:10.21203/rs.3.rs-793924/v1

Des outils issus de la didactique pour une analyse réflexive des pratiques.

Roditi, É. (2003) · HAL

A Novel Caenorhabditis elegans Gene Network Uncovers Mechanisms of Mitochondrial MaintenancePreprint

Moreno, A., Taffet, A., Tjahjono, E., & Kirienko, N. V. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.06.487352

Sirtuins and Metabolic Health

Xu, J., & Kitada, M. (2022) · Springer eBooks · doi:10.1007/978-981-16-7977-3_10

Papel da Sirtuina 1 na ativação e diferenciação das células T CD4>sup<+>/sup< em um modelo murino de obesidade e transplante

Domínguez-Amorocho, O. A. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2022.tde-16052022-092324

Mitokondriyal Disfonksiyonun Koroner Arter Hastalığı Üzerine Etkisi - Bölüm II

Doğan, N. (2023) · Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology · doi:10.5543/tkda.2022.07282

Downregulation of SIRT1, SIRT3, and IGF-1 in ApoE-deficient mice exacerbates neuronal damage induced by chronic cerebral hypoperfusion

Harmatina, O. Y., Rozova, K. V., Voznesenska, T. Y., Vasylenko, M., Lapikova-Bryhinska, T., & Portnychenko, A. G. (2023) · Regulatory Mechanisms in Biosystems · doi:10.15421/10.15421/022350

Bases moleculares del efecto la restricción calórica sobre la activación de sirtuina-1 y la longevidad. Una revisión narrativa

Cortés-Palma, F., Tehozol-Limón, D., & Juárez, R. G. (2023) · Casos y Revisiones de Salud · doi:10.22201/fesz.26831422e.2023.5.2.6

IL-37 ameliorates myocardial fibrosis by regulating mtDNA-enriched vesicle release in diabetic cardiomyopathy micePreprint

Wu, B., Huang, Q., Chen, T., Li, J. H., Wang, Y., Shi, H., Yu, Y., Ji, Q., Shen, X. X., Sun, T., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-3728567/v1

Uncarboxylated Osteocalcin Inhibits De Novo Lipogenesis and Promotes Fatty Acid Oxidation via SIRT1 to Alleviate Hepatocyte Lipid AccumulationPreprint

Chen, L., Zhang, M., Xu, J., & Yang, J. (2024) · Research Square · doi:10.21203/rs.3.rs-3856420/v1

Sirtuins in the pathogenetic therapy of neurodegenerative diseases

Samoilova, E. M., Ivanova, A. A., Laktionov, P. P., Анатольевич, К. В., & Romanov, S. E. (2024) · Journal of clinical practice · doi:10.17816/clinpract624496

Antifreeze Protein Type I in the Vitrification Solution Improves the Cryosurvival of Immature Cat OocytesPreprint

Leal, G. R., Prellwitz, L., Correia, L. L. R., Oliveira, T. A., Guimarães, M. P. D. P., Xavier-Getirana, B. R., Dias, Â. J. B., Batista, R. I. T. P., & Souza‐Fabjan, J. M. G. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4829592

SIRT1 Controls Lipid Metabolism Under Physiological and Pathological Conditions: Implications in Atherosclerosis

Poznyak, A. V., Недосугова, Л. В., Khotina, V. A., Beloyartsev, D. F., Golovyuk, A. L., Sukhorukov, V. N., Sukhorukov, V. N., Melnichenko, A. A., & Orekhov, A. N. (2024) · OnLine Journal of Biological Sciences · doi:10.3844/ojbsci.2024.584.596

Kai Yu Zhong Yu recipe mitigates stress-induced accelerated follicle loss in mice by regulating the interplay between apoptosis and autophagy via the SIRT1/FOXO1/3 pathway

Zhao, X., Rong, B., Dou, Z., Dong, R., Jiang, N., Chen, M., Feng, W., Li, H., & Xia, T. (2024) · Phytomedicine Plus · doi:10.1016/j.phyplu.2024.100623

Revealing the Complex Interaction of Noncoding RNAs, Sirtuin Family, and Mitochondrial Function

Yuan, L., Yin, L., Lin, X., Li, J., Liang, P., & Jiang, B. (2025) · The Journal of Gene Medicine · doi:10.1002/jgm.70007

Pre-clinical evidence for mitochondria as a therapeutic target for luteolin: A mechanistic view

de Oliveira, M. R. (2025) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2025.111492

Homocysteine Disrupts Cerebral Ischemia-Reperfusion Outcomes Through Sirt1-Regulated Crosstalk between Mitochondrial Dynamics and FerroptosisPreprint

Li, S., Hou, C., Yang, L., He, W., & Zhang, W. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5222385

Repositioning of a nutraceutical, scoparone, in the management of MK-801-induced schizophrenia-like behavior in Mice: An insight into SIRT1/PGC-1α/TFAM pathway

Rabie, M. A., Marcus, W. H., Sadek, M. A., Ruby, H. A., Emam, K. A. F., Budzyńska, B., Skalicka‐Woźniak, K., Sayed, R. H., Ahmed, L. A., & Sayed, N. S. E. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177981

Protein Kinase C θ Deletion Ameliorates Bleomycin-Induced Pulmonary Fibrosis Via the Improvement of SIRT1/AMPK Signaling on Autophagy and SenescencePreprint

Li, W., Zhao, X., Wang, M., Wang, H., Rongyu, L. I., & Guoguang, W. A. N. G. (2025) · Research Square · doi:10.21203/rs.3.rs-7015361/v1

Aging of the vascular system: proposal of preventive intervention with known natural substances

Fazio, S., Fazio, V., & Affuso, F. (2025) · Exploration of Cardiology · doi:10.37349/ec.2025.101268

Endogenous Upstream Bioelectrical Modulation of Inflammatory, Angiogenic, and Anti- Senescent Pathways in Human Dermal Fibroblasts Using the REAC-ACT ProtocolPreprint

Cruciani, S., Fontani, V., Rinaldi, A., Rinaldi, S., & Maioli, M. (2025) · Research Square · doi:10.21203/rs.3.rs-6701676/v1

CCAR2 Drives Glioma Cell Survival by Positively Regulating SIRT1 and Activating the Notch1/c‐Myc Pathway

Ma, L., Liu, C., Zhang, Y., & Chen, Z.-J. (2025) · Drug Development Research · doi:10.1002/ddr.70159

Small molecular therapeutic targets for neurodegenerative diseases

Rangappa, N., Upadhyay, R., Lakshman, N., Ramasamy, S., Sevanan, M., Justin, A., & Chinnathambi, S. (2025) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2025.10.012

Additional file 1 of SIRT1 activation promotes energy homeostasis and reprograms liver cancer metabolism

Varghese, B., Chianese, U., Capasso, L., Sian, V., Bontempo, P., Conte, M., Benedetti, R., Altucci, L., Carafa, V., & Nebbioso, A. (2023) · Figshare · doi:10.6084/m9.figshare.24151221

Additional file 1 of Ginsenoside Rg3 alleviates septic liver injury by regulating the lncRNA TUG1/miR-200c-3p/SIRT1 axis

Wu, P., Yu, X., Peng, Y., Wang, Q.-L., Longtian, D., & Xing, W. (2021) · Figshare · doi:10.6084/m9.figshare.17304890

Additional file 1 of Neospora caninum infection induced mitochondrial dysfunction in caprine endometrial epithelial cells via downregulating SIRT1

Tao, D.-L., Zhao, S.-S., Chen, J.-M., Chen, X., Yang, X., Song, J., Liu, Q., & Zhao, G. (2022) · Figshare · doi:10.6084/m9.figshare.20416528

Additional file 2 of Neospora caninum infection induced mitochondrial dysfunction in caprine endometrial epithelial cells via downregulating SIRT1

Tao, D.-L., Zhao, S.-S., Chen, J.-M., Chen, X., Yang, X., Song, J., Liu, Q., & Zhao, G. (2022) · Figshare · doi:10.6084/m9.figshare.20416531

Additional file 1 of Bifidobacterium bifidum and Lactobacillus paracasei alleviate sarcopenia and cognitive impairment in aged mice by regulating gut microbiota-mediated AKT, NF-κB, and FOXO3a signaling pathways

Baek, J.-S., Shin, Y.-J., Ma, X., Park, H.-S., Hwang, Y.-H., & Kim, D.-H. (2024) · Figshare · doi:10.6084/m9.figshare.26630455

Additional file 5 of SIRT1-mediated deacetylation of FOXO3 enhances mitophagy and drives hormone resistance in endometrial cancer

Wei, X., Xiong, X., Wang, P., Zhang, S., & Peng, D. (2024) · Figshare · doi:10.6084/m9.figshare.27012195

Additional file 2 of SIRT1-mediated deacetylation of FOXO3 enhances mitophagy and drives hormone resistance in endometrial cancer

Wei, X., Xiong, X., Wang, P., Zhang, S., & 彭冬先 (2024) · Figshare · doi:10.6084/m9.figshare.27012180

Additional file 1 of SIRT1-mediated deacetylation of FOXO3 enhances mitophagy and drives hormone resistance in endometrial cancer

Wei, X., Xiong, X., Wang, P., Zhang, S., & Peng, D. (2024) · Figshare · doi:10.6084/m9.figshare.27012177

Additional file 1 of IL-37 ameliorates myocardial fibrosis by regulating mtDNA-enriched vesicle release in diabetic cardiomyopathy mice

Huang, Q., Chen, T., Li, J., Wang, Y., Shi, H., Yu, Y., Ji, Q., Shen, X., Sun, T., Shi, H., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25902317

Additional file 3 of SIRT1-mediated deacetylation of FOXO3 enhances mitophagy and drives hormone resistance in endometrial cancer

Wei, X., Xiong, X., Wang, P., Zhang, S., & Peng, D. (2024) · Figshare · doi:10.6084/m9.figshare.27012186

Additional file 1 of Puerarin ameliorates metabolic dysfunction-associated fatty liver disease by inhibiting ferroptosis and inflammation

Yang, M., Xia, L., Song, J., Hu, H., Zang, N., Yang, J., Zou, Y., Wang, L., Zheng, X., He, Q., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26644786

Additional file 4 of SIRT1-mediated deacetylation of FOXO3 enhances mitophagy and drives hormone resistance in endometrial cancer

Wei, X., Xiong, X., Wang, P., Zhang, S., & 彭冬先 (2024) · Figshare · doi:10.6084/m9.figshare.27012192

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AAV-mediated surtuin 1 overexpression in the cochlear inner hair cells protects ribbon synapses of D-galactose-induced aging mice

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Therapeutic Potential of Spermidine in Rheumatoid Arthritis: Mechanisms and Future Directions

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Metabolic reprogramming in Alzheimer’s disease: Interaction between receptor tyrosine kinase signaling, noncoding RNAs, and Neuron–Glia energy networks

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A proteomic approach for understanding the metabolic adaptations in non-small cell lung cancer

Martín-Bernabé, A. (2018) · theses.fr (ABES) · doi:10.70675/426e7b40z057az4326z8cfez7da3a5c12c7e

Influence de la méthionine synthase sur la neurogenèse postnatale & conséquences ophtalmologiques de l’invalidation de la méthionine synthase

Matmat, K. (2022) · theses.fr (ABES) · doi:10.70675/0f7203adze1a2z4ab8za1adz2ee0b5b7c94f

Effects of early-life and chronic exposure to dietary advanced glycation end-products on chronic low-grade inflammation and age-associated disorders

Lima, M. T. N. S. (2023) · theses.fr (ABES) · doi:10.70675/aaf90876z1a0cz4bdbzb765zd592559927f8

The expression levels of SIRT1 splicing isoforms and genes regulating mitochondrial homeostasis in the liver of patients with type 2 diabetes mellitus and obesity

Voronova, S. S., Bograya, M., Bograya, A. M., Vulf, M., Газатова, Н. Д., & Litvinova, L. S. (2026) · Bulletin of Siberian Medicine · doi:10.20538/1682-0363-2026-1-32-42

Öregedésgátló mechanizmusok és potenciális beavatkozási lehetőségek a gammopátiák progressziójának lassítására

Veronika Urbán, S., Balázs, V., Kocsis, L., Ceglédi, A., & Mikala, G. (2026) · Hematológia–Transzfuziológia · doi:10.1556/2068.2026.00238

Oxymatrine alleviates cognitive dysfunction in mice caused by chronic cerebral hypoperfusion by promoting SIRT1/ PINK1-mediated mitophagy

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Cynandione A improves white adipose tissue homeostasis in high-fat diet-fed mice

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SIRT1 Functionally Interacts with the Metabolic Regulator and Transcriptional Coactivator PGC-1α

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The deacetylase enzyme SIRT1 is not associated with oxidative capacity in rat heart and skeletal muscle and its overexpression reduces mitochondrial biogenesis

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Relationship between Sirt1 expression and mitochondrial proteins during conditions of chronic muscle use and disuse

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