Apigenin Ameliorates the Obesity-Induced Skeletal Muscle Atrophy by Attenuating Mitochondrial Dysfunction in the Muscle of Obese Mice
Abstract
SCOPE: It was investigated whether apigenin (AP) protected against skeletal muscle atrophy induced by obesity. METHODS AND RESULTS: Mice were fed a high-fat diet (HFD) for 9 weeks to induce obesity, and then were assigned to two groups; the HFD group received a high-fat diet, and the HFD+AP group received a 0.1% AP-containing HFD. After additional feeding of the experimental diet for 8 weeks, mice in the HFD group were highly obese compared with the mice in the standard diet fed mice group. The mice in the AP-treated group showed less fat pad accumulation and less inflammatory cytokines without body weight reduction. The weight of skeletal muscle in the AP group tended to increase as compared with that of the HFD group. Furthermore, AP reduced the expression of atrophic genes, including MuRF1 and Atrogin-1, but increased the exercise capacity. The mitochondrial function and mitochondrial biogenesis were enhanced by AP. In cultured C2C12 cells, AP also suppressed palmitic acid-induced muscle atrophy and mitochondrial dysfunction. In addition, AP activated AMP-activated protein kinase (AMPK) in the C2C12 and the muscle of HFD-induced obese mice. CONCLUSION: The results suggested that AP ameliorated the obesity-induced skeletal muscle atrophy by attenuating mitochondrial dysfunction.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In C2C12 myotubes, apigenin suppresses muscle atrophy and mitochondrial dysfunction induced by palmitic acid.
“The group also reported that in C2C12 myotubes, apigenin suppresses muscle atrophy and mitochondrial dysfunction induced by palmitic acid [110].”
From Nutraceuticals in the Prevention and Treatment of the Muscle Atrophy (2021) · cites this paper as [110]
The positive effect of apigenin is related to upregulation of mitochondrial content and downregulation of gene expression of MuRF1 and MAFbx in skeletal muscle of C57BL/6 mice.
“The positive effect of apigenin is related to the upregulation of mitochondrial content and downregulation of gene expression of MuRF1 and MAFbx in skeletal muscle of C57BL/6 mice [110].”
From Nutraceuticals in the Prevention and Treatment of the Muscle Atrophy (2021) · cites this paper as [110]
Dietary supplementation of apigenin ameliorates obesity-induced skeletal muscle atrophy and increases exercise capacity.
“Choi et al. reported that dietary supplementation of apigenin ameliorates the obesity-induced skeletal muscle atrophy and increases the exercise capacity.”
From Nutraceuticals in the Prevention and Treatment of the Muscle Atrophy (2021) · cites this paper as [110]
Cites
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 · see citing works
Identification of ubiquitin ligases required for skeletal muscle atrophy.
Bodine, S. C., Latres, E., Baumhueter, S., Lai, V. K.-M., Nunez, L., Clarke, B. A., Poueymirou, W. T., Panaro, F. J., Na, E., Dharmarajan, K., et al. (2001) · Science · doi:10.1126/science.1065874 · Cited by 3,521 · see citing works
Sandri, M., Sandri, C., Gilbert, A., Skurk, C., Calabria, E., Picard, A., Walsh, K., Schiaffino, S., Lecker, S. H., & Goldberg, A. L. (2004) · Cell · doi:10.1016/s0092-8674(04)00400-3 · Cited by 3,012 · see citing works
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
Lin, J., Wu, H., Tarr, P. T., Zhang, C.-Y., Wu, Z., Boss, O., Michael, L. F., Puigserver, P., Isotani, E., Olson, E. N., et al. (2002) · Nature · doi:10.1038/nature00904 · Cited by 2,546 · see citing works
Dysfunction of Mitochondria in Human Skeletal Muscle in Type 2 Diabetes
Kelley, D. E., He, J., Menshikova, E. V., & Ritov, V. B. (2002) · Diabetes · doi:10.2337/diabetes.51.10.2944 · Cited by 2,321 · see citing works
Mitochondrial dysfunction in the elderly: possible role in insulin resistance
Petersen, K. F., Befroy, D., Dufour, S., Dziura, J., Ariyan, C., Rothman, D. L., DiPietro, L., Cline, G. W., & Shulman, G. I. (2003) · Science · doi:10.1126/science.1082889 · Cited by 2,107 · see citing works
Patti, M. E., Butte, A. J., Crunkhorn, S., Cusi, K., Berria, R., Kashyap, S., Miyazaki, Y., Kohane, I., Costello, M., Saccone, R., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1032913100 · Cited by 1,952 · see citing works
Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice
Larsson, N.-G., Wang, J., Wilhelmsson, H., Oldfors, A., Rustin, P., Lewandoski, M., Barsh, G. S., & Clayton, D. A. (1998) · Nature Genetics · doi:10.1038/ng0398-231 · Cited by 1,594 · see citing works
Zong, H., Ren, J. M., Young, L. H., Pypaert, M., Mu, J., Birnbaum, M. J., & Shulman, G. I. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.252625599 · Cited by 1,036 · see citing works
Bonnard, C., Durand, A., Peyrol, S., Chanseaume, E., Chauvin, M.-A., Morio, B., Vidal, H., & Rieusset, J. (2008) · Journal of Clinical Investigation · doi:10.1172/jci32601 · Cited by 819 · see citing works
Mitochondrial control of apoptosis: the role of cytochrome c.
Cai, J.-Y., Yang, J., & Jones, D. P. (1998) · Biochimica et Biophysica Acta · doi:10.1016/s0005-2728(98)00109-1 · Cited by 777 · see citing works
The E3 Ligase MuRF1 Degrades Myosin Heavy Chain Protein in Dexamethasone-Treated Skeletal Muscle
Clarke, B. A., Drujan, D., Willis, M. S., Murphy, L. O., Corpina, R. A., Burova, E., Rakhilin, S. V., Stitt, T. N., Patterson, C., Latres, E., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.09.009 · Cited by 683 · see citing works
Sparks, L. M., Xie, H., Koza, R. A., Mynatt, R., Hulver, M. W., Bray, G. A., & Smith, S. R. (2005) · Diabetes · doi:10.2337/diabetes.54.7.1926 · Cited by 629 · see citing works
Handschin, C., Chin, S., Li, P., Liu, F., Maratos-Flier, E., LeBrasseur, N. K., Yan, Z., & Spiegelman, B. M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m704817200 · Cited by 611 · see citing works
He, J., Watkins, S., & Kelley, D. E. (2001) · Diabetes · doi:10.2337/diabetes.50.4.817 · Cited by 518 · see citing works
Age Changes in Body Composition Revealed by Computed Tomography
Borkan, G. A., Hults, D. E., Gerzof, S. G., Robbins, A. H., & Silbert, C. K. (1983) · Journal of Gerontology · doi:10.1093/geronj/38.6.673 · Cited by 460 · see citing works
Oberbach, A., Bossenz, Y., Lehmann, S., Niebauer, J., Adams, V., Paschke, R., Schön, M. R., Blüher, M., & Punkt, K. (2006) · Diabetes Care · doi:10.2337/diacare.29.04.06.dc05-1854 · Cited by 384 · see citing works
Flavonoid Apigenin Is an Inhibitor of the NAD+ase CD38
Escande, C., Nin, V., Price, N. L., Capellini, V., Gomes, A. P., Barbosa, M. T., O’Neil, L., White, T. A., Sinclair, D. A., & Chini, E. N. (2013) · Diabetes · doi:10.2337/db12-1139 · Cited by 332 · see citing works
Lipid modulation of skeletal muscle mass and function
Lipina, C., & Hundal, H. S. (2017) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12144 · Cited by 247 · see citing works
Perry, B. D., Caldow, M. K., Brennan‐Speranza, T. C., Sbaraglia, M., Jerums, G., GARNHAM, A. P., Wong, C. Y., Levinger, P., Haq, M. A. U., Hare, D. L., et al. (2016) · PubMed · Cited by 239 · see citing works
Ectopic lipid storage and insulin resistance: a harmful relationship
Borén, J., Taskinen, M., Olofsson, S. ‐., & Levin, M. C. (2013) · Journal of Internal Medicine · doi:10.1111/joim.12071 · Cited by 230 · see citing works
Varma, V., Yao-Borengasser, A., Rasouli, N., Nolen, G. T., Phanavanh, B., Starks, T., Gurley, C., Simpson, P., McGehee, R. E., Kern, P. A., et al. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.90885.2008 · Cited by 229 · see citing works
Exercise capacity in lean versus obese women
Hulens, M., Vansant, G. A. A. M., Lysens, R., Claessens, A., & Muls, E. (2001) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1034/j.1600-0838.2001.110509.x · Cited by 223 · see citing works
Decline in isokinetic force with age: muscle cross-sectional area and specific force
Jubrias, S. A., Odderson, I. R., Esselman, P. C., & Conley, K. E. (1997) · Pfl�gers Archiv European Journal of Physiology · doi:10.1007/s004240050392 · Cited by 222 · see citing works
Lee, J., Zhou, H. Y., Cho, S. Y., Kim, Y. S., Lee, Y. S., & Jeong, C. S. (2007) · Archives of Pharmacal Research · doi:10.1007/bf02980273 · Cited by 220 · see citing works
Tardif, N., Salles, J., Guillet, C., Tordjman, J., Reggio, S., Landrier, J., Giraudet, C., Patrac, V., Bertrand‐Michel, J., Migne, C., et al. (2014) · Aging Cell · doi:10.1111/acel.12263 · Cited by 186 · see citing works
Measurement of Fatty Acid Oxidation Rates in Animal Tissues and Cell Lines
Huynh, F. K., Green, M. F., Koves, T. R., & Hirschey, M. D. (2014) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-416618-9.00020-0 · Cited by 154 · see citing works
Dyle, M. C., Ebert, S. M., Cook, D. P., Kunkel, S. D., Fox, D. K., Bongers, K. S., Bullard, S. A., Dierdorff, J. M., & Adams, C. M. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.556241 · Cited by 138 · see citing works
Regulation of skeletal muscle fiber size, shape and function
Edgerton, V. R., & Roy, R. R. (1991) · Journal of Biomechanics · doi:10.1016/0021-9290(91)90383-x · Cited by 104 · see citing works
Prmt7 Deficiency Causes Reduced Skeletal Muscle Oxidative Metabolism and Age-Related Obesity
Jeong, H.-J., Lee, H.-J., Vuong, T. A., Choi, K.-S., Choi, D., Koo, S.-H., Cho, S. C., Cho, H., & Kang, J.-S. (2016) · Diabetes · doi:10.2337/db15-1500 · Cited by 101 · see citing works
Coen, P. M., Hames, K. C., Leachman, E. M., DeLany, J. P., Ritov, V. B., Menshikova, E. V., Dubé, J. J., Stefanović-Račić, M., Toledo, F. G. S., & Goodpaster, B. H. (2013) · Obesity · doi:10.1002/oby.20381 · Cited by 97 · see citing works
Fibre size and metabolic properties of myosin heavy chain-based fibre types in rat skeletal muscle
Rivero, J. L. L., Talmadge, R. J., & Edgerton, V. R. (1998) · Journal of Muscle Research and Cell Motility · doi:10.1023/a:1005482816442 · Cited by 96 · see citing works
Diet-induced obesity alters skeletal muscle fiber types of male but not female mice
DeNies, M. S., Johnson, J., Maliphol, A. B., Bruno, M., Kim, A., Rizvi, A., Rustici, K., & Medler, S. (2014) · Physiological Reports · doi:10.1002/phy2.204 · Cited by 94 · see citing works
Jeong, G., Lee, S., Jeong, S., Kim, Y., & Kim, E.-C. (2009) · International Immunopharmacology · doi:10.1016/j.intimp.2009.08.015 · Cited by 86 · see citing works
Satellite cell proliferation is reduced in muscles of obese Zucker rats but restored with loading
Peterson, J. M., Bryner, R. W., & Alway, S. E. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00073.2008 · Cited by 81 · see citing works
Skeletal Muscle Metabolic Dysfunction in Obesity and Metabolic Syndrome
Wells, G. D., Noseworthy, M. D., Hamilton, J. K., Tarnopolski, M., & Tein, I. (2008) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100007538 · Cited by 78 · see citing works
Kim, M. A., Kang, K., Lee, H.-J., Kim, M., Kim, C. Y., & Nho, C. W. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.02.012 · Cited by 70 · see citing works
Warmington, S. A., Tolan, R., & McBennett, S. (2000) · International Journal of Obesity · doi:10.1038/sj.ijo.0801357 · Cited by 66 · see citing works
Han, L., Sumiyoshi, M., Zheng, Y., Okuda, H., & Kimura, Y. (2003) · Phytotherapy Research · doi:10.1002/ptr.1405 · Cited by 59 · see citing works
Flavones Inhibit LPS-Induced Atrogin-1/MAFbx Expression in Mouse C2C12 Skeletal Myotubes
SHIOTA, C., ABE, T., KAWAI, N., OHNO, A., TESHIMA-KONDO, S., MORI, H., TERAO, J., TANAKA, E., & NIKAWA, T. (2015) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.61.188 · Cited by 46 · see citing works
Toledo, F. G. S., & Kelley, D. E. (2005) · Current Opinion in Endocrinology & Diabetes · doi:10.1097/01.med.0000155365.26870.64 · Cited by 10 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Kashyap, P., Shikha, D., Thakur, M., & Aneja, A. (2021) · Journal of Food Biochemistry · doi:10.1111/jfbc.13950 · Cited by 182 · see citing works
Nutritional Modulation of AMPK-Impact upon Metabolic-Inflammation
Lyons, C. L., & Roche, H. M. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103092 · Cited by 165 · 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
Therapeutical properties of apigenin: a review on the experimental evidence and basic mechanisms
Mushtaq, Z., Sadeer, N., Hussain, M., Mahwish, Alsagaby, S., Imran, M., Mumtaz, T., Umar, M., Tauseef, A., Abdulmonem, W. A., et al. (2023) · International Journal of Food Properties · doi:10.1080/10942912.2023.2236329 · Cited by 102 · see citing works
Guo, A., Li, K., Tian, H., Fan, Z., Chen, Q., Yang, Y., Yu, J., Wu, Y., & Xiao, Q. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16448 · Cited by 112 · see citing works
Apigenin prevents metabolic syndrome in high-fructose diet-fed mice by Keap1-Nrf2 pathway
Yang, M. H., Jiang, Z., Li, C.-G., Zhu, Y., Li, Z., Tang, Y., & Ni, C. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.06.108 · Cited by 88 · see citing works
Wang, D., Yang, Y., Zou, X., Zhang, J., Zheng, Z., & Wang, Z. (2020) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaa214 · Cited by 87 · see citing works
Polyphenols and Their Potential Role in Preventing Skeletal Muscle Atrophy
Salucci, S., & Falcieri, E. (2020) · Nutrition Research · doi:10.1016/j.nutres.2019.11.004 · Cited by 83 · see citing works
Kim, C., & Hwang, J.-K. (2020) · Nutrients · doi:10.3390/nu12041079 · Cited by 80 · see citing works
Pan, F., Shao, J., Shi, C.-J., Li, Z., Fu, W.-M., & Zhang, J. (2021) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00543.2019 · Cited by 77 · 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
Sharma, A., Chabloz, S., Lapides, R. A., Roider, E., & Ewald, C. Y. (2023) · Nutrients · doi:10.3390/nu15020445 · Cited by 60 · see citing works
Protective Roles of Apigenin Against Cardiometabolic Diseases: A Systematic Review
Xu, Y., Li, X., & Wang, H. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.875826 · Cited by 55 · see citing works
Apigenin ameliorates hepatic lipid accumulation by activating the autophagy-mitochondria pathway
Hsu, M., Guo, B. C., Hu, P.-A., Chen, C. H., & Lee, T. (2021) · Journal of Food and Drug Analysis · doi:10.38212/2224-6614.3269 · Cited by 56 · see citing works
Natural products: Potential therapeutic agents to prevent skeletal muscle atrophy.
Yadav, A., Yadav, S., Singh, S., & Dabur, R. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.174995 · Cited by 45 · see citing works
DHA alleviates diet-induced skeletal muscle fiber remodeling via FTO/m6A/DDIT4/PGC1α signaling
Chen, W., Chen, Y., Wu, R., Guo, G., Liu, Y., Zeng, B., Liao, X., Wang, Y., & Wang, X. (2022) · BMC Biology · doi:10.1186/s12915-022-01239-w · Cited by 45 · 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
Cheng, K., Song, Z., Chen, Y., Li, S., Zhang, Y., Zhang, H., Zhang, L., Wang, C., & Wang, T. Z. (2018) · Inflammation · doi:10.1007/s10753-018-0948-7 · Cited by 43 · see citing works
Sarcopenic Obesity: Involvement of Oxidative Stress and Beneficial Role of Antioxidant Flavonoids
Jung, U. J. (2023) · Antioxidants · doi:10.3390/antiox12051063 · Cited by 41 · see citing works
Targeting Mitochondria and Oxidative Stress in Cancer- and Chemotherapy-Induced Muscle Wasting
Huot, J. R., Baumfalk, D. R., Resendiz, A., Bonetto, A., Smuder, A. J., & Penna, F. (2022) · Antioxidants and Redox Signaling · doi:10.1089/ars.2022.0149 · Cited by 35 · see citing works
Down syndrome is an oxidative phosphorylation disorder
Bayona‐Bafaluy, M. P., Garrido-Pérez, N., Meade, P., Iglesias, E., Jiménez-Salvador, I., Montoya, J., Martínez‐Cué, C., & Ruiz‐Pesini, E. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101871 · Cited by 33 · see citing works
Targeting CD38 to Suppress Osteoarthritis Development and Associated Pain After Joint Injury in Mice
Alabarse, P. V. G., Chen, L.-Y., Oliveira, P., Qin, H., & Liu‐Bryan, R. (2022) · Arthritis & Rheumatology · doi:10.1002/art.42351 · Cited by 31 · see citing works
Yoo, A., Jang, Y. J., Ahn, J., Jung, C. H., Seo, H., & Ha, T. Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21082811 · Cited by 29 · see citing works
Modeling Diet‐Induced Metabolic Syndrome in Rodents
Leonardi, B. F., Gosmann, G., & Zimmer, A. R. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000249 · Cited by 26 · see citing works
Bai, C., Alizargar, J., Peng, C.-Y., & Wu, J. (2020) · The Chinese Journal of Physiology · doi:10.4103/cjp.cjp_95_19 · Cited by 26 · see citing works
Dupuit, M., Chavanelle, V., Chassaing, B., Pérrière, F., Etienne, M., Plissonneau, C., Boscaro, A., Barnich, N., Pialoux, V., Maugard, T., et al. (2021) · Nutrients · doi:10.3390/nu13051569 · Cited by 25 · see citing works
Tong, T., Kim, M., & Park, T. (2019) · Food & Function · doi:10.1039/c8fo01992d · Cited by 23 · see citing works
Liu, Y., Elangovan, P., Bi, X., Wang, Y., & Ding, W. Q. (2020) · International Urology and Nephrology · doi:10.1007/s11255-020-02508-9 · Cited by 23 · see citing works
Zhang, W., You, B., Qi, D., Qiu, L., Ripley-Gonzalez, J. W., Zheng, F., Fu, S., Li, C., Dun, Y., & Liu, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-98771-6 · Cited by 22 · see citing works
Beneficial Effects of Flavonoids on Skeletal Muscle Health: A Systematic Review and Meta-Analysis
Munguía, L., Ortíz-Flores, M., González, C., Portilla, A., Meaney, E., Villarreal, F. J., Nájera, N., & Ceballos, G. M. (2022) · Journal of Medicinal Food · doi:10.1089/jmf.2021.0054 · Cited by 22 · see citing works
Xie, B., Pan, D., Liu, H., Liu, M., Shi, X., Chu, X., Lu, J. F., Zhu, M., Xia, B., & Wu, J. W. (2021) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202100070 · Cited by 22 · see citing works
Guo, Y., Wang, M., Liu, Y., Pang, Y., Tian, L., Zhao, J., Liu, M., Shen, C., Yuan, M., Wang, Y.-F., et al. (2023) · Chinese Medicine · doi:10.1186/s13020-023-00738-4 · Cited by 21 · see citing works
Molecular targets of exercise mimetics and their natural activators
Jang, Y. J., & Byun, S. (2021) · BMB Reports · doi:10.5483/bmbrep.2021.54.12.151 · Cited by 16 · see citing works
Wang, Z., Li, Q., Hao, Y., Wang, Z., Yang, H., Liu, J., & Wang, J. (2022) · Journal of Functional Foods · doi:10.1016/j.jff.2022.105178 · Cited by 13 · see citing works
Canfora, I., Tarantino, N., & Pierno, S. (2022) · Cells · doi:10.3390/cells11162566 · Cited by 15 · see citing works
Dysfunction of Akt/FoxO3a/Atg7 regulatory loop magnifies obesity-regulated muscular mass decline
Yu, Y., Yang, J., Zheng, L., Su, H., Cao, S., Jiang, X., Liu, X., Liu, W., Wang, Z., Meng, F., et al. (2024) · Molecular Metabolism · doi:10.1016/j.molmet.2024.101892 · Cited by 11 · see citing works
Kaempferol as a phytochemical increases ATP content in C2C12 myotubes under hypoxic conditions
Mizokami, T., Akiyama, M., & Ikeda, Y. (2021) · Journal of Functional Foods · doi:10.1016/j.jff.2021.104510 · Cited by 10 · see citing works
Hydrangea serrata Tea Enhances Running Endurance and Skeletal Muscle Mass
Jang, Y. J., Ahn, J., Son, H. J., Jung, C. H., Ahn, J., & Ha, T. Y. (2019) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201801149 · Cited by 10 · see citing works
Liu, S., Chen, Y., Tzeng, H.-P., & Chiang, M. (2021) · Journal of Functional Foods · doi:10.1016/j.jff.2021.104755 · Cited by 10 · see citing works
Kim, J., Park, E., & Lee, H. (2023) · Journal of Applied Phycology · doi:10.1007/s10811-023-03111-y · Cited by 9 · see citing works
Truong, T. M. T., Jang, H., Ghosh, M., Son, Y., & Kang, I. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105979 · Cited by 9 · see citing works
Lee, J., Kim, C., Lee, H., & Hwang, J. (2020) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2005.05023 · Cited by 9 · see citing works
Caenorhabditis elegans as a model organism in obesity research
Dyczkowska, A., & Chabowska-Kita, A. (2021) · Biotechnologia · doi:10.5114/bta.2021.109094 · Cited by 9 · see citing works
Potential of Laurel (Laurus nobilis L.) Leaf Polyphenols for Modulation of Body Composition
Dobroslavić, E., Garofulić, I. E., & Ilich, J. Z. (2023) · Applied Sciences · doi:10.3390/app13042275 · Cited by 9 · see citing works
Park, K.-S., Kim, H. J., Hwang, J. T., & Ko, B. S. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.104109 · Cited by 8 · see citing works
Meng, X., Tian, C., Xie, C., Zhang, H., Wang, H., Zhang, M., Lu, Z., Li, D., Chen, L., & Gao, T. (2023) · Food & Function · doi:10.1039/d2fo03926e · Cited by 8 · see citing works
Kwak, H. J., Kim, J., Kim, S., Park, S., Choi, J., & Kim, S. H. (2023) · Scientific Reports · doi:10.1038/s41598-023-47411-2 · Cited by 8 · see citing works
Hu, Y., Hu, Y., Li, T., & Shi, R. (2025) · Clinical Interventions in Aging · doi:10.2147/cia.s539923 · Cited by 7 · see citing works
Dietary Plant Extracts in Improving Skeletal Muscle Development and Metabolic Function
Xiang, J., Du, ., & Wang, H. (2022) · Food Reviews International · doi:10.1080/87559129.2022.2087669 · Cited by 8 · see citing works
Shaikh, S., Ahmad, K., Lim, J. H., Ahmad, S. S., Lee, E. J., & Choi, I. (2025) · Pharmaceuticals · doi:10.3390/ph18091407 · Cited by 6 · see citing works
Akpulat, U., Çetiz, M. V., Baloğlu, M. C., Altunoğlu, Y. Ç., & Zengin, G. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.106000 · Cited by 6 · see citing works
Kim, Y. I., Kim, J., Lee, H., Jung, C. H., & Ahn, J. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105624 · Cited by 6 · see citing works
Eleazu, C. O., Suleiman, J. B., Othman, Z. A., Zakaria, Z., Nna, V. U., & Mohamed, M. (2021) · Journal of Food Biochemistry · doi:10.1111/jfbc.13626 · Cited by 6 · see citing works
Lee, S. R., Jo, S. L., Heo, J. H., Kim, T., Lee, K. P., & Hong, E. (2022) · Phytomedicine · doi:10.1016/j.phymed.2022.153974 · Cited by 6 · see citing works
Kim, J., Lee, H., Yoo, A., Jeong, H. Y., Jung, C. H., Ahn, J., & Ha, T. Y. (2023) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2311.11034 · Cited by 5 · see citing works
Equisetum arvense standardized dried extract hinders age-related osteosarcopenia
Salvadori, L., Paiella, M., Castiglioni, B., Belladonna, M. L., Manenti, T., Ercolani, C., Cornioli, L., Clemente, N., Scircoli, A., Sardella, R., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116517 · Cited by 5 · see citing works
Kim, J., Yoon, Y. E., Shin, J., Lee, S. J., & Lee, S. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106174 · Cited by 5 · see citing works
A Microfluidic Stretch System Upregulates Resistance Exercise-Related Pathway
Ahn, J., Kim, J.-S., Jeon, J. S., & Jang, Y. J. (2022) · BioChip Journal · doi:10.1007/s13206-022-00051-6 · Cited by 5 · see citing works
Bai, C., Alizargar, J., & Wu, J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/823088 · Cited by 4 · see citing works
Sun, C., Xu, Y., Du, H., Chen, Y., Qu, W., He, M., Liu, Z., Huang, J. J., Huo, J., Yin, J., et al. (2025) · Antioxidants · doi:10.3390/antiox14030315 · Cited by 3 · see citing works
Lyu, R., Shi, J., Xiao, X., Gu, W., Chen, J., Wu, X., Wang, J., & Liu, C. (2025) · Fitoterapia · doi:10.1016/j.fitote.2025.106643 · Cited by 3 · see citing works
de Castro, J. M., Melo, A. D. S., Silveira, B. L., Martins, I. A. S., Marçal, M., Bosco, T. D., Keingeski, M. B., de Oliveira, E. C. L., Álvares‐da‐Silva, M. R., Türck, P., et al. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118342 · Cited by 3 · see citing works
Skeletal Muscle as a Therapeutic Target for Natural Products to Reverse Metabolic Syndrome
Mazibuko-Mbeje, S. E., Dludla, P. V., Nkambule, B. B., Obonye, N., & Louw, J. (2018) · InTech eBooks · doi:10.5772/intechopen.78687 · Cited by 3 · see citing works
Li, M., Qin, Y., Geng, R., Fang, J., Kang, S., Huang, K., & Tong, T. (2025) · Food Innovation and Advances · doi:10.48130/fia-0025-0009 · Cited by 2 · see citing works
Krill oil attenuates obesity-induced skeletal muscle atrophy in mice
Zhou, M., Yang, Y., Zheng, Y., Wu, Z., Chen, C., Liang, Q., Yang, Y., Wu, H., Guo, X., & Du, L. (2024) · Food Science and Human Wellness · doi:10.26599/fshw.2024.9250018 · Cited by 2 · see citing works
Poblete-Aro, C., Gasaly, N., Asenjo-Paredes, D., Cadagan, C., López, P. R., Flores-Lucero, F., García‐Díaz, D. F., & Rodrigo, R. (2023) · Revista chilena de nutrición · doi:10.4067/s0717-75182023000600691 · Cited by 2 · see citing works
Apigenin as a promising myocyte protectant against damage and degradation
Huang, X. Y., Yu, Z., NING, L., LEI, Y., ZHANG, X., & WANG, Z. (2021) · Biocell · doi:10.32604/biocell.2021.015651 · Cited by 2 · see citing works
Chen, M., Ling, C., Chen, Y., Wang, H.-P., Qin, Y., Xu, J.-Y., Chen, G.-C., Shi, B.-M., Qin, L.-Q., & Yang, J. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106114 · Cited by 2 · see citing works
Kim, D. Y., & Kang, M. (2024) · Journal of Nutrition and Health · doi:10.4163/jnh.2024.57.5.469 · Cited by 1 · see citing works
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
Jiang, H., Inoue, S., Hatakeyama, J., & Moriyama, H. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104186 · Cited by 1 · see citing works
Le-Chan, G., Amoah, N. Q., Sofia, H. M., Quee, A. H., Chan, S. S. K., & Thomas-Charles, C. A. (2026) · Pharmaceuticals · doi:10.3390/ph19060905 · Cited by 1 · see citing works
Role of Polyphenols from Polygonum Multiflorum Caulis in Obesity-Related DisordersPreprint
Shen, C., Lang, D.-Q., Hao, Y.-F., & Jiang, J. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4006000
Saha, M., & Chatterjee, S. (2023) · Oriental Journal Of Chemistry · doi:10.13005/ojc/390517
Suzuki, S., Otsuka, A., Kurata, E., Mio, K., Inaba, T., Yoshida, K., Kinoshita, S., Hamaguchi, T., Sangsoo, E., & Abo, M. (2025) · Cureus · doi:10.7759/cureus.82774
Zhao, R., Jiang, N., Ding, J., Ji, Y., Zhong, H., & Wang, Y. (2025) · Precision Nutrition · doi:10.1097/pn9.0000000000000122
Zhong, Y., Chen, S., Pan, J., Niu, R., Du, J., Dong, Q., Liu, Y., Yao, Y., Lin, Y., Fang, H., et al. (2025) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2025.110223
Herbal Bioactives and Their Role in Modulating Inflammation and Oxidative Stress in Skeletal Muscle
Karim, A., Mharchi, S., & Marghich, M. (2026) · Physiology · doi:10.5772/intechopen.1014219
Kim, M., Kim, C., Kang, J., Han, S., Kim, Y., Kang, H., & Hwang, J.-K. (2026) · Nutrition Research · doi:10.1016/j.nutres.2026.06.007
Kim, T., Seo, J., Kang, S., Kim, H. K., Lee, B., Lee, J., & Go, G. (2026) · Food Science and Biotechnology · doi:10.1007/s10068-026-02259-w
Shin, S., Jeong, J., Kim, M.-J., Jang, M. J., Park, C. L., Kim, S., & Kwon, E. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1861420
- Authors
- Choi, W. H., Son, H. J., Jang, Y. J., Ahn, J., Jung, C. H., & Ha, T. Y.
- Affiliations
- Korea Food Research Institute (KR)
- Corresponding author
- Ha, Tae Youl
- Venue
- Molecular Nutrition & Food Research
- Publisher
- Wiley
- Published
- 2017-11-02
- Volume
- 61
- Issue
- 12
- ISSN
- 1613-4125 (ISSN-L)
- 1613-4133
- OpenAlex
- W2761348958
- Cited by
- 81
- References
- 41
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 6 · 2023: 13 · 2022: 12 · 2021: 16 · 2020: 9 · 2019: 4 · 2018: 4
- FWCI
- 1.90
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Molecular Nutrition & Food Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Korea Food Research Institute (E0160500)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Pharmacology › Flavonoids in Medical Research
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Keywords
- apigenin, skeletal muscle atrophy, obesity, mitochondrial dysfunction, mitochondrial biogenesis, AMPK, high-fat diet, MuRF1, atrogin-1, muscle protein degradation, exercise capacity, palmitic acid, C2C12 myocytes, dietary flavonoids
- MeSH terms
- Animals, Cell Line, Male, Mice, Inbred C57BL, Mice, Obese, Mitochondria, Muscle, Muscular Atrophy, Obesity, Muscle, Skeletal, Palmitic Acid, Apigenin, AMP-Activated Protein Kinases, Diet, High-Fat
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review