Polyphenols and Their Potential Role in Preventing Skeletal Muscle Atrophy

mTOR Signaling in Growth Control and Disease

Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509 · see citing works

Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1

Bodine, S. C., & Baehr, L. M. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00204.2014 · Cited by 1,117 · see citing works

Metabolism and roles of stilbenes in plants

Chong, J., Poutaraud, A., & Hugueney, P. (2009) · Plant Science · doi:10.1016/j.plantsci.2009.05.012 · Cited by 664 · see citing works

Oxidative stress: role of physical exercise and antioxidant nutraceuticals in adulthood and aging

Simioni, C., Zauli, G., Martelli, A. M., Vitale, M., Sacchetti, G., Gonelli, A., & Neri, L. M. (2018) · Oncotarget · doi:10.18632/oncotarget.24729 · Cited by 518 · see citing works

mTOR as a key regulator in maintaining skeletal muscle mass

Yoon, M.-S. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00788 · Cited by 495 · see citing works

Therapeutic applications of compounds in the Magnolia family

Lee, Y., Lee, Y. M., Lee, C., Jung, J., Han, S., & Hong, J. T. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.01.010 · Cited by 490 · see citing works

Quercetin increases brain and muscle mitochondrial biogenesis and exercise tolerance

Davis, J. M., Murphy, E. A., Carmichael, M. D., & Davis, B. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.90925.2008 · Cited by 486 · see citing works

Oxidative stress and disuse muscle atrophy

Powers, S. K., Kavazis, A. N., & McClung, J. M. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01202.2006 · Cited by 471 · see citing works

Oxidative stress, consequences and ROS mediated cellular signaling in rheumatoid arthritis

Phull, A. R., Nasir, B., Haq, I. U., & Kim, S. J. (2017) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2017.12.024 · Cited by 460 · see citing works

Interplay of IKK/NF-κB signaling in macrophages and myofibers promotes muscle degeneration in Duchenne muscular dystrophy

Acharyya, S., Villalta, S. A., Bakkar, N., Bupha‐Intr, T., Janssen, P. M. L., Carathers, M., Li, Z.-W., Beg, A. A., Ghosh, S., Sahenk, Z., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30556 · Cited by 436 · see citing works

Oxidative Stress, Chronic Disease, and Muscle Wasting

Moylan, J. S., & Reid, M. B. (2007) · Muscle & Nerve · doi:10.1002/mus.20743 · Cited by 416 · see citing works

Role of resveratrol in regulation of cellular defense systems against oxidative stress

Truong, V., Jun, M., & Jeong, W. (2017) · BioFactors · doi:10.1002/biof.1399 · Cited by 397 · see citing works

A Review on Free Radicals and Antioxidants

Alkadi, H. (2018) · Infectious Disorders - Drug Targets · doi:10.2174/1871526518666180628124323 · Cited by 318 · see citing works

The pharmacology of resveratrol in animals and humans

Park, E.-J., & Pezzuto, J. M. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.01.014 · Cited by 302 · see citing works

Molecular Targets Underlying the Anticancer Effects of Quercetin: An Update

Khan, F., Niaz, K., Maqbool, F., Hassan, F. I., Abdollahi, M. R., Venkata, K. C. N., Nabavi, S. M., & Bishayee, A. (2016) · Nutrients · doi:10.3390/nu8090529 · Cited by 287 · see citing works

Genomic and proteomic profiling reveals reduced mitochondrial function and disruption of the neuromuscular junction driving rat sarcopenia

Ibebunjo, C., Chick, J. M., Kendall, T., Eash, J. K., Li, C., Zhang, Y., Vickers, C., Wu, Z., Clarke, B. A., Shi, J., et al. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.01036-12 · Cited by 267 · see citing works

Oxidative stress and disuse muscle atrophy

Powers, S. K., Smuder, A. J., & Judge, A. R. (2012) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e328352b4c2 · Cited by 234 · see citing works

Sex Differences in Muscle Wasting

Anderson, L. J., Liu, H. M., & Garcia, J. M. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-70178-3_9 · Cited by 222 · see citing works

Redox control of skeletal muscle atrophy.

Powers, S. K., Morton, A. B., Ahn, B., & Smuder, A. J. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.021 · Cited by 207 · see citing works

Redox Control of Skeletal Muscle Regeneration

Moal, E. L., Pialoux, V., Juban, G., Groussard, C., Zouhal, H., Chazaud, B., & Mounier, R. (2016) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6782 · Cited by 197 · see citing works

Hydroxytyrosol prevents diet-induced metabolic syndrome and attenuates mitochondrial abnormalities in obese mice

Cao, K. J., Xu, J., Zou, X., Li, Y., Chen, C., Zheng, A., Li, H., Li, H., Szeto, I. M., Shi, Y., et al. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.11.029 · Cited by 192 · see citing works

Induction of ferroptosis and mitochondrial dysfunction by oxidative stress in PC12 cells

Wu, C., Zhao, W., Yu, J. Z., Li, S., Lin, L., & Chen, X. (2018) · Scientific Reports · doi:10.1038/s41598-017-18935-1 · Cited by 192 · see citing works

Induction of proteasome expression in skeletal muscle is attenuated by inhibitors of NF-κB activation

Wyke, S. M., Russell, S. T., & Tisdale, M. J. (2004) · British Journal of Cancer · doi:10.1038/sj.bjc.6602165 · Cited by 184 · see citing works

Phenolic compounds and antioxidant capacity of virgin olive oil

Franco, M. N., Díaz, T. G., López, Ó., Fernández‐Bolaños, J. G., Sánchez, J., Miguel, C. D., Gil, M. V., & Martín‐Vertedor, D. (2014) · Food Chemistry · doi:10.1016/j.foodchem.2014.04.091 · Cited by 184 · see citing works

Reduction of low grade inflammation restores blunting of postprandial muscle anabolism and limits sarcopenia in old rats

Rieu, I., Magne, H., Savary‐Auzeloux, I., Avérous, J., Bos, C., Peyron, M., Combaret, L., & Dardevet, D. P. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.178319 · Cited by 182 · see citing works

Resveratrol prevents the wasting disorders of mechanical unloading by acting as a physical exercise mimetic in the rat

Momken, I., Stevens, L., Bergouignan, A., Desplanches, D., Rudwill, F., Chery, I., Zahariev, A., Zahn, S., Stein, T. P., Sebedio, J. L., et al. (2011) · The FASEB Journal · doi:10.1096/fj.10-177295 · Cited by 181 · see citing works

Resveratrol Ameliorates Muscular Pathology in the Dystrophic mdx Mouse, a Model for Duchenne Muscular Dystrophy

Hori, Y. S., Kuno, A., Hosoda, R., Tanno, M., Miura, T., Shimamoto, K., & Horio, Y. (2011) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.111.183210 · Cited by 165 · see citing works

ER stress in skeletal muscle remodeling and myopathies

Afroze, D., & Kumar, A. (2017) · FEBS Journal · doi:10.1111/febs.14358 · Cited by 162 · see citing works

Ghrelin enhances gastric motility through direct stimulation of intrinsic neural pathways and capsaicin-sensitive afferent neurones in rats

Fukuda, H., Mizuta, Y., Isomoto, H., Takeshima, F., Ohnita, K., Ohba, K., Omagari, K., Taniyama, K., & KOHNO, S. (2004) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365520410007908 · Cited by 157 · see citing works

Mitochondrial Dysfunction Launches Dexamethasone-Induced Skeletal Muscle Atrophy via AMPK/FOXO3 Signaling

Liu, J., Peng, Y., Wang, X., Fan, Y., Qin, C., Shi, L., Tang, Y., Cao, K., Li, H., Long, J., et al. (2016) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.5b00516 · Cited by 133 · see citing works

MUSCLE DISUSE AS A PIVOTAL PROBLEM IN SARCOPENIA-RELATED MUSCLE LOSS AND DYSFUNCTION

Bell, K. E., von Allmen, M., Devries, M. C., & Phillips, S. M. (2016) · The Journal of Frailty & Aging · doi:10.14283/jfa.2016.78 · Cited by 127 · see citing works

The Pivotal Role of Copper in Neurodegeneration: A New Strategy for the Therapy of Neurodegenerative Disorders

Giampietro, R., Spinelli, F., Contino, M., & Colabufo, N. A. (2018) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.7b00841 · Cited by 124 · see citing works

p-Coumaric acid modulates glucose and lipid metabolism via AMP-activated protein kinase in L6 skeletal muscle cells

Yoon, S., Kang, S., Shin, H., Kang, S.-W., Kim, J., Ko, H., & Kim, S. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.02.067 · Cited by 120 · see citing works

Muscle-specific and age-related changes in protein synthesis and protein degradation in response to hindlimb unloading in rats

Baehr, L. M., West, D. W. D., Marshall, A. G., Marcotte, G. R., Baar, K., & Bodine, S. C. (2017) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00703.2016 · Cited by 119 · see citing works

Mitochondrial dynamic remodeling in strenuous exercise-induced muscle and mitochondrial dysfunction: Regulatory effects of hydroxytyrosol

Feng, Z., Bai, L., Yan, J., Li, Y., Shen, W., Wang, Y., Wertz, K., Weber, P., Zhang, Y., Chen, Y., et al. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.03.001 · Cited by 111 · see citing works

A Green Tea-Derived Polyphenol, Epigallocatechin-3-Gallate, Inhibits IκB Kinase Activation and IL-8 Gene Expression in Respiratory Epithelium

Chen, P. C., Wheeler, D. S., Malhotra, V., Odoms, K., Denenberg, A. G., & Wong, H. R. (2002) · Inflammation · doi:10.1023/a:1019718718977 · Cited by 109 · see citing works

Ubiquitin-Proteasome Pathway and Muscle Atrophy

Khalil, R. M. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-1435-3_10 · Cited by 108 · see citing works

Dihydromyricetin modulates p62 and autophagy crosstalk with the Keap-1/Nrf2 pathway to alleviate ethanol-induced hepatic injury

Qiu, P., Dong, Y. H., Li, B., Kang, X., Gu, C., Zhu, T., Luo, Y., Pang, M.-X., Du, W., & Ge, W. (2017) · Toxicology Letters · doi:10.1016/j.toxlet.2017.04.009 · Cited by 105 · see citing works

Muscle redox signalling pathways in exercise. Role of antioxidants

Mason, S. A., Morrison, D., McConell, G. K., & Wadley, G. D. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.022 · Cited by 103 · see citing works

Mechanistic Role of Reactive Oxygen Species and Therapeutic Potential of Antioxidants in Denervation- or Fasting-Induced Skeletal Muscle Atrophy

Qiu, J., Fang, Q., Xu, T., Wu, C., Xu, L., Wang, L., Yang, X., Yu, S., Zhang, Q., Ding, F., et al. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00215 · Cited by 103 · see citing works

The effect of exercise, resveratrol or their combination on Sarcopenia in aged rats via regulation of AMPK/Sirt1 pathway

Liao, Z.-Y., Chen, J.-L., Xiao, M.-H., Sun, Y., Zhao, Y.-X., Pu, D., Lv, A.-K., Wang, M.-L., Zhou, J., Zhu, S.-Y., et al. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.08.032 · Cited by 102 · see citing works

Can Antioxidants Protect Against Disuse Muscle Atrophy?

Powers, S. K. (2014) · Sports Medicine · doi:10.1007/s40279-014-0255-x · Cited by 101 · see citing works

Curcumin Ameliorates Skeletal Muscle Atrophy in Type 1 Diabetic Mice by Inhibiting Protein Ubiquitination

Ono, T., Takada, S., Kinugawa, S., & Tsutsui, H. (2015) · Experimental Physiology · doi:10.1113/ep085049 · Cited by 99 · see citing works

Oral resveratrol therapy inhibits cancer-induced skeletal muscle and cardiac atrophy in vivo.

Shadfar, S., Couch, M. E., McKinney, K. A., Weinstein, L. J., Yin, X., Rodríguez, J. E., Guttridge, D. C., & Willis, M. (2011) · Nutrition and Cancer · doi:10.1080/01635581.2011.563032 · Cited by 98 · see citing works

Resveratrol prevents dexamethasone-induced expression of the muscle atrophy-related ubiquitin ligases atrogin-1 and MuRF1 in cultured myotubes through a SIRT1-dependent mechanism

Alamdari, N., Aversa, Z., Castillero, E., Gurav, A., Petkova, V., Tizio, S., & Hasselgren, P.-O. J. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.11.154 · Cited by 97 · see citing works

Key Markers of mTORC1-Dependent and mTORC1-Independent Signaling Pathways Regulating Protein Synthesis in Rat Soleus Muscle During Early Stages of Hindlimb Unloading

Mirzoev, T., Tyganov, S., Vilchinskaya, N., Lomonosova, Y., & Shenkman, B. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000447808 · Cited by 92 · see citing works

Dietary resveratrol supplementation prevents transport-stress-impaired meat quality of broilers through maintaining muscle energy metabolism and antioxidant status

Zhang, C., Wang, L., Zhao, X. H., Chen, X. Y., Yang, L., & Geng, Z. (2017) · Poultry Science · doi:10.3382/ps/pex004 · Cited by 86 · see citing works

The Molecular Mechanisms of Calpains Action on Skeletal Muscle Atrophy

HUANG, J., & Zhu, X. (2016) · Physiological Research · doi:10.33549/physiolres.933087 · Cited by 84 · see citing works

Physical Exercise Positively Influences Breast Cancer Evolution

Adraskela, K., Veisaki, E., Koutsilieris, M., & Philippou, Α. (2017) · Clinical Breast Cancer · doi:10.1016/j.clbc.2017.05.003 · Cited by 83 · see citing works

Curcumin ameliorates palmitate-induced inflammation in skeletal muscle cells by regulating JNK/NF-kB pathway and ROS production

Sadeghi, A., Rostamirad, A., Seyyedebrahimi, S., & Meshkani, R. (2018) · Inflammopharmacology · doi:10.1007/s10787-018-0466-0 · Cited by 82 · see citing works

Ampelopsin Attenuates the Atrophy of Skeletal Muscle from D-Gal-Induced Aging Rats through Activating AMPK/SIRT1/PGC-1α Signaling Cascade

Kou, X., Li, J., Liu, X., Yang, X., Fan, J., & Chen, N. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.03.070 · Cited by 81 · see citing works

Apigenin Ameliorates the Obesity-Induced Skeletal Muscle Atrophy by Attenuating Mitochondrial Dysfunction in the Muscle of Obese Mice

Choi, W. H., Son, H. J., Jang, Y. J., Ahn, J., Jung, C. H., & Ha, T. Y. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201700218 · Cited by 81 · see citing works

Magnolol suppresses hypoxia-induced angiogenesis via inhibition of HIF-1α/VEGF signaling pathway in human bladder cancer cells

Chen, M., Lee, C.-F., Huang, W., & Chou, T. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.02.009 · Cited by 80 · see citing works

Curcumin attenuates skeletal muscle mitochondrial impairment in COPD rats: PGC-1α/SIRT3 pathway involved

Zhang, M., Tang, J., Li, Y., Xie, Y., Hu, S., Chen, M., Zhang, J., Yang, X., Zhang, Q., & Yang, X. (2017) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2017.09.018 · Cited by 80 · see citing works

Schisandrin A prevents oxidative stress-induced DNA damage and apoptosis by attenuating ROS generation in C2C12 cells

Choi, Y. H. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.07.035 · Cited by 77 · see citing works

Natural Polyphenols and their Synthetic Analogs as Emerging Anticancer Agents

Colomer, R., Sarrats, A., Lupu, R., & Puig, T. (2016) · Current Drug Targets · doi:10.2174/1389450117666160112113930 · Cited by 76 · see citing works

Resveratrol and/or exercise training counteract aging-associated decline of physical endurance in aged mice; targeting mitochondrial biogenesis and function

Muhammad, M. H., & Allam, M. M. (2017) · The Journal of Physiological Sciences · doi:10.1007/s12576-017-0582-4 · Cited by 76 · see citing works

Preventive effect of dietary quercetin on disuse muscle atrophy by targeting mitochondria in denervated mice

Mukai, R., Matsui, N., Fujikura, Y., Matsumoto, N., Hou, D., Kanzaki, N., Shibata, H., Horikawa, M., Iwasa, K., Hirasaka, K., et al. (2016) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2016.02.001 · Cited by 75 · see citing works

Redox regulation of autophagy in skeletal muscle

Rodney, G. G., Pal, R., & Abo‐Zahrah, R. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.05.010 · Cited by 72 · see citing works

Caffeic acid phenethyl ester alleviates asthma by regulating the airway microenvironment via the ROS-responsive MAPK/Akt pathway

Ma, Y., Zhang, J., Liu, Y., Ge, A., Gu, H., Zha, W., Zeng, X., & Huang, M. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.09.012 · Cited by 71 · see citing works

Mitochondrial dysfunction-associated OPA1 cleavage contributes to muscle degeneration: preventative effect of hydroxytyrosol acetate

Wang, X., Li, H., Zheng, A., Yang, L., Liu, J., Chen, C., Tang, Y., Zou, X., Li, Y., Long, J., et al. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.473 · Cited by 69 · see citing works

Prenylation Enhances Quercetin Uptake and Reduces Efflux in Caco-2 Cells and Enhances Tissue Accumulation in Mice Fed Long-Term

Mukai, R., Fujikura, Y., Murota, K., Uehara, M., Minekawa, S., Matsui, N., Kawamura, T., Nemoto, H., & Terao, J. (2013) · Journal of Nutrition · doi:10.3945/jn.113.176818 · Cited by 69 · see citing works

THE GREEN TEA POLYPHENOL EPIGALLOCATECHIN-3-GALLATE (EGCG) ATTENUATES SKELETAL MUSCLE ATROPHY IN A RAT MODEL OF SARCOPENIA

Meador, B. M., Mirza, K. A., Tian, M., Skelding, M. B., Reaves, L. A., Edens, N. K., Tisdale, M. J., & Pereira, S. L. (2015) · The Journal of Frailty & Aging · doi:10.14283/jfa.2015.58 · Cited by 69 · see citing works

Quercetin Reduces Tumor Necrosis Factor Alpha-Induced Muscle Atrophy by Upregulation of Heme Oxygenase-1

Kim, Y., Kim, C.-S., Joe, Y., Chung, H. T., Ha, T. Y., & Yu, R. (2018) · Journal of Medicinal Food · doi:10.1089/jmf.2017.4108 · Cited by 69 · see citing works

Muscle redox disturbances and oxidative stress as pathomechanisms and therapeutic targets in early-onset myopathies

Moulin, M., & Ferreiro, A. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.08.003 · Cited by 65 · see citing works

Anti-apoptotic activity of hydroxytyrosol and hydroxytyrosyl laurate

Burattini, S., Salucci, S., Baldassarri, V., Accorsi, A., Piatti, E., Madrona, A., Espartero, J. L., Candiracci, M., Zappia, G., & Falcieri, E. (2013) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.12.049 · Cited by 64 · see citing works

Dihydromyricetin Attenuates Dexamethasone-Induced Muscle Atrophy by Improving Mitochondrial Function Via the PGC-1α Pathway

Huang, Y., Chen, K., Ren, Q., Yi, L., Zhu, J., Zhang, Q., & Mi, M. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000493040 · Cited by 64 · see citing works

Effect of lifelong resveratrol supplementation and exercise training on skeletal muscle oxidative capacity in aging mice; impact of PGC-1α

Ringholm, S., Olesen, J., Pedersen, J. T., Brandt, C. T., Halling, J. F., Hellsten, Y., Prats, C., & Pilegaard, H. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.08.012 · Cited by 61 · see citing works

The paradoxical role of thioredoxin on oxidative stress and aging

Cunningham, G. M., Roman, M. G., Flores, L. C., Hubbard, G. B., Salmon, A. B., Zhang, Y., Gelfond, J., & Ikeno, Y. (2015) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2015.02.025 · Cited by 60 · see citing works

Redox Characterization of Functioning Skeletal Muscle

Zuo, L., & Pannell, B. K. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00338 · Cited by 60 · see citing works

Reloading Functionally Ameliorates Disuse-Induced Muscle Atrophy by Reversing Mitochondrial Dysfunction, and Similar Benefits Are Gained by Administering a Combination of Mitochondrial Nutrients

Liu, J., Peng, Y., Feng, Z., Shi, W., Qu, L., Li, Y., Liu, J., & Long, J. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.01.003 · Cited by 55 · see citing works

Creatine Prevents the Structural and Functional Damage to Mitochondria in Myogenic, Oxidatively Stressed C2C12 Cells and Restores Their Differentiation Capacity

Barbieri, E., Guescini, M., Calcabrini, C., Vallorani, L., Diaz, A. R., Fimognari, C., Canonico, B., Luchetti, F., Papa, S., Battistelli, M., et al. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/5152029 · Cited by 55 · see citing works

Green tea extracts ameliorate high-fat diet–induced muscle atrophy in senescence-accelerated mouse prone-8 mice

Onishi, S., Ishino, M., Kitazawa, H., Yoto, A., Shimba, Y., Mochizuki, Y., Unno, K., Meguro, S., Tokimitsu, I., & Miura, S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0195753 · Cited by 53 · see citing works

Dihydromyricetin Improves Hypobaric Hypoxia-Induced Memory Impairment via Modulation of SIRT3 Signaling

Liu, P., Zou, D., Chen, K., Zhou, Q., Gao, Y., Huang, Y., Zhu, J., Zhang, Q., & Mi, M. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9627-y · Cited by 52 · see citing works

Role of E2-Ub-conjugating enzymes during skeletal muscle atrophy

Polge, C., Attaix, D., & Taillandier, D. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00059 · Cited by 51 · see citing works

Gallic acid provokes DNA damage and suppresses DNA repair gene expression in human prostate cancer PC‐3 cells

Liu, K.-C., Ho, H.-C., Huang, A., Ji, B., Lin, H., Chueh, F., Yang, J., Lu, C., Chiang, J., Meng, M., et al. (2011) · Environmental Toxicology · doi:10.1002/tox.20752 · Cited by 48 · see citing works

Delphinidin Prevents Muscle Atrophy and Upregulates miR-23a Expression

Murata, M., Nonaka, H., Komatsu, S., Goto, M., Morozumi, M., Yamada, S., Lin, I.-C., Yamashita, S., & Tachibana, H. (2017) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.6b03661 · Cited by 47 · see citing works

Oligonol, a Low-Molecular Weight Polyphenol Derived from Lychee, Alleviates Muscle Loss in Diabetes by Suppressing Atrogin-1 and MuRF1

Liu, H.-W., Chen, Y.-J., Chang, Y.-C., & Chang, S.-J. (2017) · Nutrients · doi:10.3390/nu9091040 · Cited by 47 · see citing works

Protection by extra virgin olive oil against oxidative stress in vitro and in vivo. Chemical and biological studies on the health benefits due to a major component of the Mediterranean diet

Rossi, M., Caruso, F., Kwok, L., Lee, G., Caruso, A., Gionfra, F., Candelotti, E., Belli, S. L., Molasky, N., Raley‐Susman, K. M., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0189341 · Cited by 47 · see citing works

Green Tea Extract Preserves Neuromuscular Activation and Muscle Damage Markers in Athletes Under Cumulative Fatigue

Machado, Á. S., da Silva, W., Souza, M. A., & Carpes, F. P. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01137 · Cited by 47 · see citing works

Dihydromyricetin Improves Physical Performance under Simulated High Altitude

Zou, D., Chen, K., Liu, P., Chang, H., Zhu, J., & Mi, M. (2014) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000336 · Cited by 46 · see citing works

Ameliorative effect of p-coumaric acid, a common dietary phenol, on adjuvant-induced arthritis in rats

Pragasam, S. J., Murunikkara, V., Prince, S. E., & Rasool, M. (2012) · Rheumatology International · doi:10.1007/s00296-012-2394-4 · Cited by 45 · see citing works

Supplementation of Magnolol Attenuates Skeletal Muscle Atrophy in Bladder Cancer-Bearing Mice Undergoing Chemotherapy via Suppression of FoxO3 Activation and Induction of IGF-1

Chen, M.-C., Chen, Y.-L., Lee, C.-F., Hung, C.-H., & Chou, T.-C. (2015) · PLOS ONE · doi:10.1371/journal.pone.0143594 · Cited by 45 · see citing works

Anti-fatigue effect of green tea polyphenols (-)-Epigallocatechin-3-Gallate (EGCG)

Teng, Y.-S., & Wu, D. (2017) · Pharmacognosy Magazine · doi:10.4103/0973-1296.204546 · Cited by 44 · see citing works

Potential Application of p-Coumaric Acid on Differentiation of C2C12 Skeletal Muscle and 3T3-L1 Preadipocytes—An in Vitro and in Silico Approach

Soundharrajan, I., Kim, D., Srigopalram, S., Arasu, M. V., Lee, K., Lee, J. W., Lee, J., Senthil, R., & Choi, K. C. (2016) · Molecules · doi:10.3390/molecules21080997 · Cited by 43 · see citing works

Hydrogen Sulfide Donor NaHS Improves Metabolism and Reduces Muscle Atrophy in Type 2 Diabetes: Implication for Understanding Sarcopenic Pathophysiology

Bitar, M. S., Nader, J., Al-Ali, W., Madhoun, A. S. A., Arefanian, H., & Al‐Mulla, F. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/6825452 · Cited by 42 · see citing works

Epigallocatechin-3-gallate inhibits bladder cancer cell invasion via suppression of NF-κB-mediated matrix metalloproteinase-9 expression

Qin, J., Wang, Y., Bai, Y., Yang, K. G., Mao, Q., LIN, Y., Kong, D., Zheng, X., & Xie, L. (2012) · Molecular Medicine Reports · doi:10.3892/mmr.2012.1054 · Cited by 39 · see citing works

Licorice flavonoid oil enhances muscle mass in KK-A mice

Yoshioka, Y., Yamashita, Y., Kishida, H., Nakagawa, K., & Ashida, H. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.05.024 · Cited by 39 · see citing works

An olive oil-derived antioxidant mixture ameliorates the age-related decline of skeletal muscle function

Pierno, S., Tricarico, D., Liantonio, A., Mele, A., Digennaro, C., Rolland, J., Bianco, G., Villanova, L., Merendino, A., Camerino, G. M., et al. (2013) · AGE · doi:10.1007/s11357-013-9544-9 · Cited by 38 · see citing works

Tetramethylpyrazine ameliorated disuse-induced gastrocnemius muscle atrophy in hindlimb unloading rats through suppression of Ca2+/ROS-mediated apoptosis

Hu, N.-F., Chang, H., Du, B., Zhang, Q.-W., Arfat, Y., Dang, K., & Gao, Y. (2016) · Applied Physiology Nutrition and Metabolism · doi:10.1139/apnm-2016-0363 · Cited by 38 · see citing works

Schisandrin C enhances mitochondrial biogenesis and autophagy in C2C12 skeletal muscle cells: potential involvement of anti-oxidative mechanisms

Kim, J.-S., & Yi, H. (2017) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-017-1449-1 · Cited by 37 · see citing works

Pyrroloquinoline quinone attenuates cachexia-induced muscle atrophy via suppression of reactive oxygen species

Xu, T., Yang, X., Wu, C., Qiu, J., Fang, Q., Wang, L., Yu, S. Y., & Sun, H. (2018) · Journal of Thoracic Disease · doi:10.21037/jtd.2018.04.112 · Cited by 37 · see citing works

Epigallocatechin-3-gallate increases autophagy signaling in resting and unloaded plantaris muscles but selectively suppresses autophagy protein abundance in reloaded muscles of aged rats

Takahashi, H., Suzuki, Y., Mohamed, J. S., Gotoh, T., Pereira, S. L., & Alway, S. E. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.02.075 · Cited by 36 · see citing works

High Altitude Mediated Skeletal Muscle Atrophy: Protective Role of Curcumin

Chaudhary, P., Sharma, Y. K., Sharma, S., Singh, S. N., & Suryakumar, G. (2019) · Biochimie · doi:10.1016/j.biochi.2018.10.012 · Cited by 35 · see citing works

Mechanisms of skeletal muscle ageing; avenues for therapeutic intervention

Lightfoot, A. P., McCormick, R., Nye, G. A., & McArdle, A. (2014) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2014.05.005 · Cited by 33 · see citing works

Nutraceuticals and Their Potential to Treat Duchenne Muscular Dystrophy: Separating the Credible from the Conjecture

Woodman, K. G., Coles, C. A., Lamandé, S. R., & White, J. D. (2016) · Nutrients · doi:10.3390/nu8110713 · Cited by 33 · see citing works

Resveratrol Attenuates Denervation-Induced Muscle Atrophy Due to the Blockade of Atrogin-1 and p62 Accumulation

Asami, Y., Aizawa, M., Kinoshita, M., Ishikawa, J., & Sakuma, K. (2018) · International Journal of Medical Sciences · doi:10.7150/ijms.22723 · Cited by 33 · see citing works

Effects of long-term resveratrol-induced SIRT1 activation on insulin and apoptotic signalling in aged skeletal muscle

Sin, T. K., Yu, A. P., Yung, B. Y., Yip, S. P., Chan, L., Wong, S. C. C., Rudd, J. A., & Siu, P. M. (2015) · Acta Diabetologica · doi:10.1007/s00592-015-0767-3 · Cited by 32 · see citing works

Protective Effect of Different Antioxidant Agents in UVB-Irradiated Keratinocytes

Salucci, S., Burattini, S., Buontempo, F., Martelli, A. M., Falcieri, E., & Battistelli, M. (2017) · European Journal of Histochemistry · doi:10.4081/ejh.2017.2784 · Cited by 32 · see citing works

Oxidative Stress in Muscle Diseases: Current and Future Therapy

Serra, A. J., Prokić, M. D., Vasconsuelo, A., & Pinto, J. R. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/6439138 · Cited by 32 · see citing works

Olive Oil by Capillary Electrophoresis: Characterization and Genuineness

Monasterio, R. P., Fernández, M. D. L. Á., & Silva, M. F. (2013) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf400864q · Cited by 30 · see citing works

Resveratrol and Myopathy

Bastin, J., & Djouadi, F. (2016) · Nutrients · doi:10.3390/nu8050254 · Cited by 30 · see citing works

Long-Term Quercetin Dietary Enrichment Partially Protects Dystrophic Skeletal Muscle

Spaulding, H. R., Ballmann, C. G., Quindry, J. C., & Selsby, J. T. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168293 · Cited by 30 · see citing works

Stilbenes: Chemistry and Molecular Mechanisms of Anti-obesity

Chou, Y.-C., Ho, C., & Pan, M. (2018) · Current Pharmacology Reports · doi:10.1007/s40495-018-0134-5 · Cited by 30 · see citing works

A randomised controlled intervention study investigating the efficacy of carotenoid-rich fruits and vegetables and extra-virgin olive oil on attenuating sarcopenic symptomology in overweight and obese older adults during energy intake restriction: protocol paper

Villani, A. M., Wright, H. H., Slater, G., & Buckley, J. D. (2018) · BMC Geriatrics · doi:10.1186/s12877-017-0700-4 · Cited by 27 · see citing works

Melatonin behavior in restoring chemical damaged C2C12 myoblasts

Salucci, S., Baldassarri, V., Canonico, B., Burattini, S., Battistelli, M., Guescini, M., Papa, S., Stocchi, V., & Falcieri, E. (2016) · Microscopy Research and Technique · doi:10.1002/jemt.22663 · Cited by 26 · see citing works

Quercetin enhances the antitumor effect of trichostatin A and suppresses muscle wasting in tumor-bearing mice

Chan, S.-T., Chuang, C., Lin, Y., Liao, J., Lii, C., & Yeh, S.-L. (2017) · Food & Function · doi:10.1039/c7fo01444a · Cited by 26 · see citing works

Oral quercetin administration transiently protects respiratory function in dystrophin‐deficient mice

Selsby, J. T., Ballmann, C. G., Spaulding, H. R., Ross, J. W., & Quindry, J. C. (2016) · The Journal of Physiology · doi:10.1113/jp272057 · Cited by 25 · see citing works

Melatonin prevents mitochondrial dysfunctions and death in differentiated skeletal muscle cells

Salucci, S., Battistelli, M., Baldassarri, V., Burini, D., Falcieri, E., & Burattini, S. (2017) · Microscopy Research and Technique · doi:10.1002/jemt.22914 · Cited by 25 · see citing works

Further Highlighting on the Prevention of Oxidative Damage by Polyphenol-Rich Wine Extracts

Salucci, S., Burattini, S., Giordano, F. M., Lucarini, S., Diamantini, G., & Falcieri, E. (2017) · Journal of Medicinal Food · doi:10.1089/jmf.2016.0153 · Cited by 24 · see citing works

Nutraceutical Properties of Chestnut Flours: Beneficial Effects on Skeletal Muscle Atrophy

Frati, A., Landi, D., Marinelli, C., Gianni, G., Fontana, L., Migliorini, M., Pierucci, F., Garcia-Gil, M., & Meacci, E. (2014) · Food Funct. · doi:10.1039/c4fo00353e · Cited by 23 · see citing works

The Proteolytic Systems of Muscle Wasting

Scicchitano, B. M., Faraldi, M., & Musarò, A. (2016) · Recent Advances in DNA & Gene Sequences (Formerly Recent Patents on DNA & Gene Sequences) · doi:10.2174/2352092209999150911121502 · Cited by 21 · see citing works

Panduratin A Prevents Tumor Necrosis Factor-Alpha-Induced Muscle Atrophy in L6 Rat Skeletal Muscle Cells

Sa, B.-K., Kim, C., Kim, M., & Hwang, J. (2017) · Journal of Medicinal Food · doi:10.1089/jmf.2017.3970 · Cited by 20 · see citing works

Dysfonctions mitochondriales et vieillissement musculaire

Faitg, J., Reynaud, O., Leduc‐Gaudet, J., & Gouspillou, G. (2017) · médecine/sciences · doi:10.1051/medsci/20173311012 · Cited by 20 · see citing works

Protective effect of Rhus coriaria fruit extracts against hydrogen peroxide-induced oxidative stress in muscle progenitors and zebrafish embryos

Najjar, F., Rizk, F., Carnac, G., Nassar, R., Jabak, S., Sobolev, A. P., Saada, Y. B., El-Sabban, M. E., & Hamadé, A. (2017) · PeerJ · doi:10.7717/peerj.4144 · Cited by 19 · see citing works

Nutrition Strategies to Improve Physical Capabilities in Duchenne Muscular Dystrophy

Davoodi, J., Markert, C. D., Voelker, K. A., Hutson, S. M., & Grange, R. W. (2011) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/j.pmr.2011.11.010 · Cited by 18 · see citing works

3-n-Butylphthalide reduces the oxidative damage of muscles in an experimental autoimmune myositis animal model

Chen, J., Wang, J., Zhang, J., & Pu, C. (2017) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2017.4766 · Cited by 16 · see citing works

Nutritional Support to Counteract Muscle Atrophy

Owens, D. J. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-1435-3_22 · Cited by 16 · see citing works

Carboxylic acid derivatives of histone deacetylase inhibitors induce full length SMN2 transcripts: a promising target for spinal muscular atrophy therapeutics

Erden, D. D., Bora, G., Dalkara, S., DEMİR, A. S., & Erdem‐Yurter, H. (2011) · Archives of Medical Science · doi:10.5114/aoms.2011.22072 · Cited by 15 · see citing works

Further considerations on in vitro skeletal muscle cell death

Battistelli, M., Salucci, S., Burattini, S., & Falcieri, E. (2019) · Muscles Ligaments and Tendons Journal · doi:10.32098/mltj.04.2013.06 · Cited by 13 · see citing works

Diet Modulation Restores Autophagic Flux in Damaged Skeletal Muscle Cells

Giordano, F. M., Burattini, S., Buontempo, F., Canonico, B., Martelli, A. M., Papa, S., Sampaolesi, M., Falcieri, E., & Salucci, S. (2019) · The journal of nutrition health & aging · doi:10.1007/s12603-019-1245-3 · Cited by 13 · see citing works

Effects of Coenzyme Q10 on Skeletal Muscle Oxidative Metabolism in Statin Users Assessed Using 31P Magnetic Resonance Spectroscopy: a Randomized Controlled Study.

Buettner, C., Greenman, R. L., Ngo, L. H., & Wu, J. S. (2016) · PubMed · Cited by 11 · see citing works

Effect of Hazelnut Oil on Muscle Cell Signalling and Differentiation

Terruzzi, I. M., Vacante, F., Senesi, P., Montesano, A., Codella, R., & Luzi, L. (2018) · Journal of Oleo Science · doi:10.5650/jos.ess18086 · Cited by 11 · see citing works

MIP/MTMR14 and muscle aging

Powers, S. K., & Reid, M. B. (2010) · Aging · doi:10.18632/aging.100193 · Cited by 10 · see citing works

Flavan 3-ol Delays the Progression of Disuse Atrophy Induced by Hindlimb Suspension in Mice

Ito, M., Kudo, N., Miyake, Y., Imai, T., Unno, T., Yamashita, Y., Hirota, Y., Ashida, H., & Osakabe, N. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.07.010 · Cited by 10 · see citing works

Isoflavin-β Modifies Muscle Oxidative Stress and Prevents a Thyrotoxicosis-Induced Loss of Muscle Mass in Rats

Marinello, P. C., Bernardes, S. S., Guarnier, F. A., Da Silva, T. N. X., Borges, F. H., Lopes, N. M. D., Simão, A. N. C., Armani, A., Cecchini, R., & Cecchini, A. L. (2017) · Muscle & Nerve · doi:10.1002/mus.25546 · Cited by 9 · see citing works

Physical exercise and oxidative stress in muscular dystrophies: is there a good balance?

Simoncini, C., Chico, L., Ricci, G., & Cosci, M. (2017) · ARCHIVES ITALIENNES DE BIOLOGIE · doi:10.12871/000398292017122 · Cited by 8 · see citing works

A Review On Free Radicals And Antioxidants

R, D. A. S. W. A. S. R. S. (2018) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.1479233 · Cited by 8 · see citing works

Effects of Antioxidant on Reduction of Hindlimb Muscle Atrophy Induced by Cisplatin in Rats

Kim, J. I., & Choe, M. (2014) · Journal of Korean Academy of Nursing · doi:10.4040/jkan.2014.44.4.371 · Cited by 3 · see citing works

Mitochondrial dysfunction: roles in skeletal muscle atrophy

Chen, X., Ji, Y., Liu, R., Zhu, X., Wang, K., Yang, X., Liu, B., Gao, Z., Huang, Y. H., Shen, Y., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04369-z · Cited by 340 · see citing works

Skeletal muscle oxidative stress and inflammation in aging: Focus on antioxidant and anti-inflammatory therapy

Chen, M., Wang, Y., Deng, S., Lian, Z., & Yu, K. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.964130 · Cited by 187 · see citing works

Disuse-induced skeletal muscle atrophy in disease and nondisease states in humans: mechanisms, prevention, and recovery strategies

Nunes, E. A., Stokes, T., McKendry, J., Currier, B. S., & Phillips, S. M. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00425.2021 · Cited by 183 · see citing works

Polyphenols and Their Effects on Muscle Atrophy and Muscle Health

Nikawa, T., Ulla, A., & Sakakibara, I. (2021) · Molecules · doi:10.3390/molecules26164887 · Cited by 140 · see citing works

Potential Therapeutic Strategies for Skeletal Muscle Atrophy

Huang, L. T., Li, M., Deng, C., Qiu, J., Wang, K., Chang, M., Zhou, S., Gu, Y., Shen, Y., Wang, W., et al. (2022) · Antioxidants · doi:10.3390/antiox12010044 · Cited by 111 · see citing works

Isoquercitrin Delays Denervated Soleus Muscle Atrophy by Inhibiting Oxidative Stress and Inflammation

Shen, Y., Zhang, Q., Huang, Z., Zhu, J., Qiu, J., Ma, W., Yang, X., Ding, F., & Sun, H. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00988 · Cited by 95 · see citing works

Microencapsulation as a tool to counteract the typical low bioavailability of polyphenols in the management of diabetes

Annunziata, G., Jiménez‐García, M., Capó, X., Moranta, D., Arnone, A., Tenore, G. C., Sureda, A., & Tejada, S. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111248 · Cited by 86 · see citing works

Microalgae Produce Antioxidant Molecules with Potential Preventive Effects on Mitochondrial Functions and Skeletal Muscular Oxidative Stress

Vignaud, J., Loiseau, C., Hérault, J., Mayer, C., Côme, M., Martin, I., & Ulmann, L. (2023) · Antioxidants · doi:10.3390/antiox12051050 · Cited by 72 · see citing works

Nutraceuticals in the Prevention and Treatment of the Muscle Atrophy

Wang, Y., Liu, Q., Quan, H., Kang, S.-G., Huang, K., & Tong, T. (2021) · Nutrients · doi:10.3390/nu13061914 · Cited by 61 · see citing works

Mitochondrial involvement in sarcopenia

Affourtit, C., & Carré, J. E. (2024) · Acta Physiologica · doi:10.1111/apha.14107 · Cited by 58 · see citing works

Flavonoids: Nutraceutical Potential for Counteracting Muscle Atrophy

Kim, C., & Hwang, J.-K. (2020) · Food Science and Biotechnology · doi:10.1007/s10068-020-00816-5 · Cited by 45 · see citing works

High Adherence to the Mediterranean Diet is Associated with Higher Physical Fitness in Adults: a Systematic Review and Meta-Analysis

Bizzozero‐Peroni, B., Brazo‐Sayavera, J., Martínez‐Vizcaíno, V., Fernández-Rodríguez, R., López‐Gil, J. F., Goñi, V. D., Cavero‐Redondo, I., & Mesas, A. E. (2022) · Advances in Nutrition · doi:10.1093/advances/nmac104 · Cited by 43 · see citing works

Phenolic Compounds from Apples: Reviewing their Occurrence, Absorption, Bioavailability, Processing, and Antioxidant Activity – a Review

Starowicz, M., Piskuła, M. K., Achrem–Achremowicz, B., & Zieliński, H. (2020) · Polish Journal of Food and Nutrition Sciences · doi:10.31883/pjfns/127635 · Cited by 42 · see citing works

Phenolic Compounds Profile and Antioxidant Capacity of Plant-Based Protein Supplements

Sawicki, T., Jabłońska, M., Danielewicz, A., & Przybyłowicz, K. E. (2024) · Molecules · doi:10.3390/molecules29092101 · Cited by 39 · see citing works

Resveratrol-based compounds and neurodegeneration: Recent insight in multitarget therapy

Fantacuzzi, M., Amoroso, R., Carradori, S., & Filippis, B. D. (2022) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2022.114242 · Cited by 36 · see citing works

Sarcopenia: Current Insights into Molecular Mechanisms, Diagnostics, and Emerging Interventional Approaches

Tu, S., Hao, X., Xu, S., Jin, X., Liao, W., Xia, H., Wang, S., & Sun, G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26146740 · Cited by 35 · see citing works

Polyphenols as Potential Geroprotectors

Николаевна, П. Е., Koval, L. A., Platonova, E. Y., Golubev, D., Ulyasheva, N. S., Babak, T. V., Shaposhnikov, M. V., & Moskalev, A. (2024) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0247 · Cited by 34 · see citing works

Quercetin Modulates IGF-I and IGF-II Levels After Eccentric Exercise-Induced Muscle-Damage: A Placebo-Controlled Study

Sgrò, P., Ceci, R., Lista, M., Patrizio, F., Sabatini, S., Felici, F., Sacchetti, M., Bazzucchi, I., Duranti, G., & Luigi, L. D. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.745959 · Cited by 33 · see citing works

Quercetin Supplementation Improves Neuromuscular Function Recovery from Muscle Damage

Bazzucchi, I., Patrizio, F., Ceci, R., Duranti, G., Sabatini, S., Sgrò, P., Luigi, L. D., & Sacchetti, M. (2020) · Nutrients · doi:10.3390/nu12092850 · Cited by 32 · see citing works

Recent Advances in Nutraceuticals for the Treatment of Sarcopenic Obesity

Kim, Y.-C., Ki, S.-W., Kim, H., Kang, S., Kim, H., & Go, G. (2023) · Nutrients · doi:10.3390/nu15173854 · Cited by 33 · see citing works

Extra Virgin Olive Oil (EVOO), a Mediterranean Diet Component, in the Management of Muscle Mass and Function Preservation

Salucci, S., Bartoletti‐Stella, A., Bavelloni, A., Aramini, B., Blalock, W. L., Fabbri, F., Vannini, I., Sambri, V., Stella, F., & Faenza, I. (2022) · Nutrients · doi:10.3390/nu14173567 · Cited by 30 · see citing works

The Effect of Mediterranean Diet on Body Composition, Inflammatory Factors, and Nutritional Status in Patients with Cachexia Induced by Colorectal Cancer: A Randomized Clinical Trial

Bagheri, A., Asoudeh, F., Rezaei, S., Babaei, M., & Esmaillzadeh, A. (2023) · Integrative Cancer Therapies · doi:10.1177/15347354231195322 · Cited by 26 · see citing works

How Inflammation Pathways Contribute to Cell Death in Neuro-Muscular Disorders

Salucci, S., Stella, A. B., Battistelli, M., Burattini, S., Bavelloni, A., Cocco, L., Gobbi, P., & Faenza, I. (2021) · Biomolecules · doi:10.3390/biom11081109 · Cited by 24 · see citing works

Effects of Dietary Chlorogenic Acid Supplementation Derived from Lonicera macranthoides Hand‐Mazz on Growth Performance, Free Amino Acid Profile, and Muscle Protein Synthesis in a Finishing Pig Model

Wang, W., Li, F., Duan, Y., Guo, Q., Zhang, L., Yang, Y., Yin, Y., Han, M., Gong, S., Li, J., et al. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/6316611 · Cited by 23 · see citing works

The polyphenols profile of co-fermented quinoa and black barley with Lactobacillus kisonensis and its in vitro bioactivities

Jiang, H.-B., Nie, P., Lin, Z.-H., Zhu, C., Zhong, L., Wei, F.-F., Wu, Y., & Song, L. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.103712 · Cited by 23 · see citing works

Polyphenol Supplementation and Sarcopenia: A Systematic Review and Meta-Analysis of Clinical Trials

Medoro, A., Scapagnini, G., & Davinelli, S. (2024) · The Journal of Frailty & Aging · doi:10.14283/jfa.2024.73 · Cited by 26 · see citing works

Effect of Epicatechin on Skeletal Muscle

Zbinden‐Foncea, H., Castro‐Sepúlveda, M., Fuentes, J., & Speisky, H. (2021) · Current Medicinal Chemistry · doi:10.2174/0929867329666211217100020 · Cited by 20 · see citing works

Polyphenol content and bioactivity of Achillea moschata from the Italian and Swiss Alps

Argentieri, M. P., Madeo, M., Avato, P., Iriti, M., & Vitalini, S. (2020) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2019-0214 · Cited by 19 · see citing works

Plant-based polyphenol rich protein supplementation attenuated skeletal muscle loss and lowered the LDL level via gut microbiota remodeling in Taiwan's community-dwelling elderly

Chang, S.-S., Chen, L., Huang, K., Huang, S.-W., Chang, C., Liao, K., Hu, E.-C., Chen, Y., Chen, Y., Hsu, P.-C., et al. (2023) · Food & Function · doi:10.1039/d3fo02766j · Cited by 20 · see citing works

Nutritional and Behavioral Approaches to Body Composition and Low-Grade Chronic Inflammation Management for Older Adults in the Ordinary and COVID-19 Times

Ilich, J. Z. (2020) · Nutrients · doi:10.3390/nu12123898 · Cited by 19 · see citing works

Quercetin supplementation promotes recovery after exercise-induced muscle damage: a systematic review and meta-analysis of randomized controlled trials

Ortega, D. R., Peña, J., Berral-Aguilar, A. J., & de la Rosa, F. J. B. (2022) · Biology of Sport · doi:10.5114/biolsport.2023.121320 · Cited by 17 · see citing works

Phytochemicals: A potential therapeutic intervention for the prevention and treatment of cachexia

Zarifi, S. H., Bagherniya, M., Banach, M., Johnston, T. P., & Sahebkar, A. (2022) · Clinical Nutrition · doi:10.1016/j.clnu.2022.11.009 · Cited by 17 · see citing works

Role for Plant-Derived Antioxidants in Attenuating Cancer Cachexia

Li, W., Swiderski, K., Murphy, K. T., & Lynch, G. S. (2022) · Antioxidants · doi:10.3390/antiox11020183 · Cited by 16 · see citing works

A Comprehensive Review of Essential Aspects of Molecular Pathophysiological Mechanisms with Emerging Interventions for Sarcopenia in Older People

Prajapati, P., Kumar, A., Chaudary, R., Mangrulkar, S. V., Arya, M., & Kushwaha, S. (2023) · Current Molecular Pharmacology · doi:10.2174/1874467216666230308142137 · Cited by 17 · see citing works

Attenuation of Skeletal Muscle Atrophy Induced by Dexamethasone in Rats by Teaghrelin Supplementation

Jhuo, C., Hsieh, S., Chen, W., & Tzen, J. T. C. (2023) · Molecules · doi:10.3390/molecules28020688 · Cited by 15 · see citing works

Hydroxytyrosol-rich extract from olive juice as an additive in gilthead sea bream juveniles fed a high-fat diet: Regulation of somatic growth

Balbuena-Pecino, S., Montblanch, M., García-Meilán, I., Fontanillas, R., Gallardo, Á., Gutiérrez, J., Navarro, I., & Capilla, E. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.966175 · Cited by 14 · see citing works

Nutritional support in a comprehensive program of prevention and treatment of sarcopenia

Kurmaev, D. P., Bulgakova, S. V., Treneva, E. V., Kosareva, O. V., Dolgikh, Y. A., Sharonova, L. A., & Сергеевна, Ч. И. (2023) · Russian Journal of Geriatric Medicine · doi:10.37586/2686-8636-1-2023-29-38 · Cited by 13 · see citing works

Synthesis and Biological Evaluation of Halogenated E-Stilbenols as Promising Antiaging Agents

Filippo, E. S. D., Giampietro, L., Filippis, B. D., Balaha, M. F., Ferrone, V., Locatelli, M., Pietrangelo, T., Tartaglia, A., Amoroso, R., & Fulle, S. (2020) · Molecules · doi:10.3390/molecules25235770 · Cited by 13 · see citing works

Effects of marine oligomeric polyphenols on body composition and physical ability of elderly individuals with sarcopenia: a pilot study

Kwon, I.-S., Park, D.-S., Shin, H., Seok, M.-G., & Oh, J. (2021) · Physical Activity and Nutrition · doi:10.20463/pan.2021.0014 · Cited by 12 · see citing works

Nutritional approaches targeting mitochondria for the prevention of sarcopenia

Hahm, J., Nirmala, F. S., Ha, T. Y., & Ahn, J. (2023) · Nutrition Reviews · doi:10.1093/nutrit/nuad084 · Cited by 12 · see citing works

Effect of Tomato Peel Extract Grown under Drought Stress Condition in a Sarcopenia Model

Felice, F., Cesare, M. M., Fredianelli, L., Leo, M. D., Conti, V., Braca, A., & Stefano, R. D. (2022) · Molecules · doi:10.3390/molecules27082563 · Cited by 11 · see citing works

Rodent model intervention for prevention and optimal management of sarcopenia: A systematic review on the beneficial effects of nutrients & non-nutrients and exercise to improve skeletal muscle health

Vijayakumar, M., Kannappan, P., Janani, B., & Kim, C. Y. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102543 · Cited by 10 · see citing works

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Xiao, Y., Li, X., Zhang, H., Zhu, Y., Gao, W., Jiang, S., Ru, G., & Sun, A. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.106783 · Cited by 9 · see citing works

Dietary polyphenols and sarcopenia: epigenetic mechanisms and geroscience perspectives for muscle health in aging

Rodrigues, G. D. S., da Silva, L. S. L., Sobrinho, A. C. D. S., Benjamim, C. J. R., Abud, G. F., Ortiz, G. U., de Freitas, E. C., & Júnior, C. R. B. (2026) · Frontiers in Aging · doi:10.3389/fragi.2025.1696473 · Cited by 9 · see citing works

Next-Generation Ultrasol Curcumin Boosts Muscle Endurance and Reduces Muscle Damage in Treadmill-Exhausted Rats

Şahin, E., Orhan, C., Erten, F., Er, B., Acharya, M., Morde, A. A., Padigaru, M., & Şahin, K. (2021) · Antioxidants · doi:10.3390/antiox10111692 · Cited by 9 · see citing works

Functional characterization of GNE mutations prevalent in Asian subjects with GNE myopathy, an ultra-rare neuromuscular disorder

Sharma, S., Chanana, P., Bharadwaj, R., Bhattacharya, S., & Arya, R. (2022) · Biochimie · doi:10.1016/j.biochi.2022.03.014 · Cited by 9 · see citing works

Functional Nutrients to Ameliorate Neurogenic Muscle Atrophy

Moresi, V., Renzini, A., Cavioli, G., Seelaender, M. C. L., Coletti, D., Gigli, G., & Cedola, A. (2022) · Metabolites · doi:10.3390/metabo12111149 · Cited by 9 · see citing works

Effect of oligonol, a lychee‐derived polyphenol, on skeletal muscle in ovariectomized rats by regulating body composition, protein turnover, and mitochondrial quality signaling

Kim, J. H., Lee, H., Kim, J. M., Lee, B., Kim, I., Pak, K., Jeon, Y. K., & Keun-young Kim, A. (2022) · Food Science & Nutrition · doi:10.1002/fsn3.2750 · Cited by 7 · see citing works

Soy Food Consumption Is Inversely Associated with Handgrip Strength: Results from the TCLSIH Cohort Study

Wu, H., Quan, J., Wang, X., Gu, Y., Zhang, S., Meng, G., Zhang, Q., Liu, L., Wang, X., Sun, S., et al. (2023) · Nutrients · doi:10.3390/nu15020391 · Cited by 8 · see citing works

The polyphenol metabolite urolithin A suppresses myostatin expression and augments glucose uptake in human skeletal muscle cells

Wilhelmsen, A., Karagounis, L. G., Bennett, A. J., D'Amico, D. F., Fouassier, A. M., Jones, S. W., & Tsintzas, K. (2025) · Nutrition & Metabolism · doi:10.1186/s12986-025-00909-0 · Cited by 6 · see citing works

Postbiotics derived from wine grape seed extract and whey with lactic acid bacteria alleviate muscle atrophy by modulating genes involved in inflammation, myogenesis, and bone metabolism

Jeong, Y., Seo, K., Hwang, S.-B., Park, Y., & Kim, H. (2025) · Journal of Dairy Science · doi:10.3168/jds.2024-26229 · Cited by 6 · see citing works

Chitosan nanoparticles loaded with Foeniculum vulgare extract regulate retrieval of sensory and motor functions in mice

Bajaber, M. A., Hameed, A., Hussain, G., Noreen, R., Ibrahim, M., Batool, S., Qayyum, M. A., Farooq, T., Parveen, B., Khalid, T., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e25414 · Cited by 6 · see citing works

3-(4-Hydroxy-3-methoxyphenyl) propionic acid mitigates dexamethasone-induced muscle atrophy by attenuating Atrogin-1 and MuRF-1 expression in mouse C2C12 skeletal myotubes

Ulla, A., Rahman, M. M., Uchida, T., Kayaki, H., Nishitani, Y., Yoshino, S., Kuwahara, H., & Nikawa, T. (2024) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.23-70 · Cited by 4 · see citing works

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Wal, P., Kaushal, S., Dwivedi, J., Patel, P., Sachan, P., & Srivastava, P. (2025) · Russian Journal of Bioorganic Chemistry · doi:10.1134/s1068162025120015 · Cited by 4 · see citing works

Nanosuspension of Foeniculum Vulgare Promotes Accelerated Sensory and Motor Function Recovery after Sciatic Nerve Injury

Bajaber, M. A., Hussain, G., Farooq, T., Noreen, R., Ibrahim, M., Umbreen, H., Batool, S., Rehman, K., Hameed, A., Farid, M. F., et al. (2023) · Metabolites · doi:10.3390/metabo13030391 · Cited by 4 · see citing works

Effects of two weeks of daily consumption of (poly)phenol-rich red berry fruit juice, with and without high-intensity physical training, on health outcomes in individuals with pre-diabetes mellitus

Valder, S., Schick, F., Pietsch, N., Wagner, T., Urban, H., Lindemann, P., Riemer, L., Quenzer, S., Herdegen, V., Diel, P. R., et al. (2025) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2025.104121 · Cited by 3 · see citing works

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Peng, L., Lin, M., Lee, H., Hsu, C., Chang, S.-J., & Chen, L. (2022) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2022.104784 · Cited by 3 · see citing works

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Pereira, S. D. C., Manhães‐de‐Castro, R., Souza, V. D. S., Calado, C. M. S. D. S., de Silveira, B. S., Barbosa, L. N. F., Torner, L., Guzmán‐Quevedo, O., & Toscano, A. E. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114835 · Cited by 3 · see citing works

Physiological and morphological impact of physical activity and nutritional interventions to offset disuse-induced skeletal muscle atrophy

Arif, I., Rasheed, A., Nazeer, S., & Shahid, F. (2025) · European Journal of Translational Myology · doi:10.4081/ejtm.2025.13177 · Cited by 2 · see citing works

Muscle Disuse Atrophy

Yeo, D. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-88361-3_8 · Cited by 3 · see citing works

From molecular mechanisms to nutritional applications: protein and polyphenol interventions in sarcopenia

Aragón-Espinosa, P., Pérez, C., Bompart, C., Gueugneau, M., Capel, F., Arbonés-Mainar, J. M., Gómez-Zorita, S., Mas‐Capdevila, A., Escoté, X., Pinent, M., et al. (2026) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-026-01154-6 · Cited by 2 · see citing works

Cachexia and phytonutrients

Fakhri, S., Piri, S., & Khan, H. Z. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-824356-5.00007-2 · Cited by 2 · see citing works

Nutrition and Exercise to Maintain Physical Functioning During Ageing

Grootswagers, P., Mensink, M., & de Groot, C. P. G. M. (2021) · Healthy ageing and longevity · doi:10.1007/978-3-030-83017-5_14 · Cited by 2 · see citing works

Differences in mediterranean diet adherence on bmi, waist circumference, fat percentage, muscle mass in obesity

Septiadi, E., Mutiara, D., Juliastuti, H., Rakhmat, I. I., & Handayani, D. R. (2022) · ACTA Medical Health Sciences · doi:10.35990/amhs.v1n1.p28-37 · Cited by 2 · see citing works

Decrease in Muscle Mass in Diet-Induced Visceral Obesity in Male Wistar Rats: Relationship with Hormonal and Metabolic Parameters

Mityukova, T. A., Басалай, А. А., Chudilovskaya, K. N., Poluliakh, O. Y., Shcherbakov, Y. V., & Kastsiuchenko, M. S. (2023) · Российский физиологический журнал им  И  М  Сеченова · doi:10.31857/s0869813923070099 · Cited by 2 · see citing works

Inhibitory effect of standardized Kaempferia parviflora extract on sarcopenia by improving protein metabolism pathways in aged C57BL/6J mice

Kim, C., Kang, M., Kim, Y., & Hwang, J. (2025) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2025.03.007 · Cited by 1 · see citing works

Effect of Continuous Intake of Onion Powder on Oxidative Stress Biomarkers and Skeletal Muscle Maintenance in Elderly Bedridden Individuals:A Pilot Study

Mukai, R., Kondo-Kawai, A., Nakamura, T., Noboritama, Y., Otsuka, A., Sakai, A., Yasui, N., Inatsugi, M., Doi, D., Nikawa, T., et al. (2025) · The Journal of Medical Investigation · doi:10.2152/jmi.72.324 · Cited by 1 · see citing works

Effect of Polyphenol-Rich Diet Combined with Leucine, Vitamin D3, and Magnesium Supplementation on Self-Reported Mobility and Health Perception in Adults at Risk of Sarcopenia: A 3-Months Quasi-Experimental Study

Tache-Codreanu, D.-L., Tache-Codreanu, A.-M., Ștefan, G., Trăistaru, M. R., Rusu, E., Tache-Codreanu, A., & Sporea, C. (2026) · Life · doi:10.3390/life16040554 · Cited by 1 · see citing works

From Growth Trajectory to Functional Decline: Age-Contextualized Nutritional Strategies for Muscle Vulnerability. A Narrative Review

Malaguarnera, L., Sortino, V., Surdo, S., & Piro, S. (2026) · Nutrients · doi:10.3390/nu18091437 · Cited by 1 · see citing works

Effects of Blackcurrant Extract on H2O2-Induced Oxidative Stress in C2C12 Myotubes

Kim, J., Nam, Y. R., Kim, Y., & Kim, K. (2024) · Journal of the Korean Society of Food Science and Nutrition · doi:10.3746/jkfn.2024.53.12.1259 · Cited by 1 · see citing works

The Effect of Feeding with Resveratrol on Myogenin and mTOR Levels in Mice

ÖZTÜRK, S. A., Kızıltan, G., Yurtçu, E., Bacanlı, D., Kasap, Y. K., & Köse, B. (2020) · Journal of Nutrition and Dietetics · doi:10.33076/2020.bdd.1351

Supplementation of Rhodomyrtus tomentosa fruit polyphenols improved dextran sulfate induced colitis in mice by regulating gut microbiota

Zhang, J., Chai, S., Jia, X., Han, Y., Liu, Y., He, X., Li, Y., & Yuan, F. (2020) · E3S Web of Conferences · doi:10.1051/e3sconf/202018902023

Recent Development of Hybrids and Derivatives of Resveratrol in Neurodegenerative Diseases

Filippis, B. D., & Fantacuzzi, M. (2022) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815079098122010005

Decrease in Muscle Mass in Diet-Induced Visceral Obesity in Male Wistar Rats: Relationship with Hormonal and Metabolic Parameters

Mityukova, T. A., Басалай, А. А., Chudilovskaya, K. N., Poluliakh, O. Y., Shcherbakov, Y. V., & Kastiuchenka, M. S. (2023) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093023040208

Bénéfices et risques de la végétalisation de l’alimentation pour les personnes âgées

Bompart, C., & Gueugneau, M. (2024) · Médecine des Maladies Métaboliques · doi:10.1016/j.mmm.2024.10.003

Polyphenols-Enriched Diet Prevents Muscle Atrophy in an Inflamed Zebrafish (Danio Rerio) ModelPreprint

Orso, G., Matuozzo, M., Rocco, M., Hoseinifar, S. H., Ashouri, G., Scaloni, A., Paolucci, M., DˈAmbrosio, C., & Imperatore, R. (2025) · Preprints.org · doi:10.20944/preprints202508.1585.v1

Neonatal quercetin exposure reduces motor impairments and cerebellar damage in cerebral palsy rats, with different effects on males and females

de Albuquerque, G. L., Manhães-de-Castro, R., Paz, I. A. A. D. S. G., da Silva‐Araújo, E. R., Gouveia, H. J. C. B., Tenório, M. L. F., Araújo, M. A. D. S., & Toscano, A. E. (2026) · Neuroscience · doi:10.1016/j.neuroscience.2026.01.023

Dietary Leucine and Total Polyphenol Intake and Their Associations with Sarcopenia Indicators Among Older People Participating in the Program for Complementary Food in Older People (PACAM) in the Metropolitan Region, Santiago de Chile

Bustos-Arriagada, E., Arazo-Rusindo, M. C., Calderón-Herrera, J., Pérez‐Bravo, F., Castillo, O., Barros‐Velázquez, J., & Mariotti‐Celis, M. S. (2026) · Nutrients · doi:10.3390/nu18142237

Shanyu Wan attenuates age-related muscle alterations in SAMP8 mice with improved mitochondrial function

Hu, Y., Xiang, Q., Jiang, C., Huang, C., Zhou, H., Lan, Y., Wu, H., Li, Z., Wang, X., Chen, C., et al. (2026) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2026.07.002

Polyphenol dietary supplementation prevents inflammation‐induced muscle atrophy in a zebrafish ( Danio rerio ) model

Orso, G., Matuozzo, M., Rocco, M., Hoseinifar, S. H., Ashouri, G., Scaloni, A., Paolucci, M., DˈAmbrosio, C., & Imperatore, R. (2026) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.70932

Beer consumption: Effects on motor performance, recovery, and injury in exercise and sports

Rodrigues, R., Pompeo, K. D., & da Rocha, E. S. (2026) · Beer in Health and Disease Prevention · doi:10.1016/b978-0-443-22332-7.00006-4

(Poly)phenol intake and mental health: a scoping review

Kamarunzaman, N. N. Z., Campbell, L., Astarcioglu, T., Bajka, B. H., Gibson, R., & Rodriguez‐Mateos, A. (2026) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2026.2742757

BindingDB Entry 50016445: Resveratrol-based compounds and neurodegeneration: Recent insight in multitarget therapy.

BindingDB (2023) · UC San Diego · doi:10.7270/q2445rhz

Polyphenols and Their Effects on Muscle Atrophy and Muscle Health

Nikawa, T., Ulla, A., & Sakakibara, I. (2021) · Molecules · doi:10.3390/molecules26164887 · Cited by 140 · see citing works

Polyphenols as Therapeutic Approach to High Altitude Mediated Skeletal Muscle Impairments

Kushwaha, A. D., Bhardwaj, V., & Saraswat, D. (2021) · Defence Life Science Journal · doi:10.14429/dlsj.6.16344

Effects of polyphenols on skeletal muscle cells and underlying molecular mechanisms

Nakazato, K., Tsutaki, A., & Min, S.-K. (2012) · Physical Activity and Nutrition · doi:10.5717/jenb.2012.16.3.127

Using polyphenol derivatives to prevent muscle wasting

Francaux, M., & Deldicque, L. (2018) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000455 · Cited by 21 · see citing works

Polyphenols prevent ageing‐related impairment in skeletal muscle mitochondrial function through decreased reactive oxygen species production

Charles, A., Meyer, A., Dal-Ros, S., Auger, C., Keller, N., Ramamoorthy, T. G., Zoll, J., METZGER, D., Schini‐Kerth, V. B., & Gény, B. (2012) · Experimental Physiology · doi:10.1113/expphysiol.2012.067496 · Cited by 53 · see citing works