Delphinidin Prevents Muscle Atrophy and Upregulates miR-23a Expression

Untitled work

Bartel (2004) · doi:10.1016/s0092-8674(04)00045-5 · Cited by 34,714 · 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

Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy.

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 regulation by calcium, calcineurin, and NFAT

Hogan, P. G., Chen, L., Nardone, J., & Rao, A. (2003) · Genes & Development · doi:10.1101/gad.1102703 · Cited by 1,991 · see citing works

The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors.

Stitt, T. N., Drujan, D., Clarke, B. A., Panaro, F., Timofeyva, Y., Kline, W. O., Gonzalez, M., Yancopoulos, G. D., & Glass, D. J. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00211-4 · Cited by 1,964 · see citing works

Analysis and biological activities of anthocyanins

Kong, J.-M., Chia, L. S., Goh, N.-K., Chia, T., & Brouillard, R. (2003) · Phytochemistry · doi:10.1016/s0031-9422(03)00438-2 · Cited by 1,689 · see citing works

Oxygen Radical Absorbing Capacity of Anthocyanins

Wang, H., Cao, G., & Prior, R. L. (1997) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf960421t · Cited by 1,368 · see citing works

Anthocyanins in fruits, vegetables and grains

Brouillard, R. (1993) · Food Research International · doi:10.1016/0963-9969(93)90093-x · Cited by 746 · 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

During muscle atrophy, thick, but not thin, filament components are degraded by MuRF1-dependent ubiquitylation

Cohen, S., Brault, J. J., Gygi, S. P., Glass, D. J., Valenzuela, D. M., Gartner, C. A., Latres, E., & Goldberg, A. L. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200901052 · Cited by 584 · see citing works

Skeletal Muscle FOXO1 (FKHR) Transgenic Mice Have Less Skeletal Muscle Mass, Down-regulated Type I (Slow Twitch/Red Muscle) Fiber Genes, and Impaired Glycemic Control

Kamei, Y., Miura, S., SUZUKI, M. T., Kai, Y., Mizukami, J., Taniguchi, T., Mochida, K., Tomoko, H. A. T. A., Matsuda, J., Aburatani, H., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m400674200 · Cited by 574 · see citing works

Crosstalk between Glucocorticoid Receptor and Nutritional Sensor mTOR in Skeletal Muscle

Shimizu, N., Yoshikawa, N., Ito, N., Maruyama, T., Suzuki, Y., Takeda, S.-I., Nakae, J., Tagata, Y., Nishitani, S., Takehana, K., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.01.001 · Cited by 498 · see citing works

Absorption of anthocyanins from blueberries and serum antioxidant status in human subjects

Mazza, G., Kay, C. D., Cottrell, T., & Holub, B. J. (2002) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf020690l · Cited by 484 · see citing works

Protecting muscle mass and function in older adults during bed rest

English, K. L., & Paddon-Jones, D. (2010) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0b013e328333aa66 · Cited by 477 · see citing works

Induction of Apoptosis in Cancer Cells by Bilberry ( Vaccinium myrtillus ) and the Anthocyanins

Katsube, N., Iwashita, K., Tsushida, T., Yamaki, K., & Kobori, M. (2002) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf025781x · Cited by 442 · see citing works

Metabolic acidosis stimulates muscle protein degradation by activating the adenosine triphosphate-dependent pathway involving ubiquitin and proteasomes.

Mitch, W. E., Medina, R., Grieber, S., May, R. C., England, B. K., Price, S. R., Bailey, J. L., & Goldberg, A. L. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117208 · Cited by 405 · see citing works

miR-23a functions downstream of NFATc3 to regulate cardiac hypertrophy

Lin, Z., Murtaza, I., Wang, K., Jiao, J., Gao, J., & Li, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811371106 · Cited by 360 · see citing works

Tart cherry anthocyanins inhibit tumor development in ApcMin mice and reduce proliferation of human colon cancer cells

Kang, S.-Y., Seeram, N. P., Nair, M. G., & Bourquin, L. D. (2003) · Cancer Letters · doi:10.1016/s0304-3940(02)00583-9 · Cited by 350 · see citing works

Muscle wasting in insulinopenic rats results from activation of the ATP-dependent, ubiquitin-proteasome proteolytic pathway by a mechanism including gene transcription.

Price, S. R., Bailey, J. L., Wang, X., Jurkovitz, C. T., England, B. K., Ding, X., Phillips, L. S., & Mitch, W. E. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118968 · Cited by 348 · see citing works

Orally Administered Delphinidin 3-Rutinoside and Cyanidin 3-Rutinoside Are Directly Absorbed in Rats and Humans and Appear in the Blood as the Intact Forms

Matsumoto, H., Inaba, H., Kishi, M., Tominaga, S., Hirayama, M., & Tsuda, T. (2001) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf001246q · Cited by 342 · see citing works

Potential role of dietary flavonoids in reducing microvascular endothelium vulnerability to oxidative and inflammatory insults ☆ ☆Mention of trade name, proprietary product, or specific equipment does not constitute a guarantee by the US Department of Agriculture and does not imply its approval to the exclusion of other products that may be suitable.

Youdim, K. A., McDonald, J., Kalt, W., & Joseph, J. A. (2002) · The Journal of Nutritional Biochemistry · doi:10.1016/s0955-2863(01)00221-2 · Cited by 319 · see citing works

Increase in levels of polyubiquitin and proteasome mRNA in skeletal muscle during starvation and denervation atrophy

Medina, R., Wing, S. S., & Goldberg, A. L. (1995) · Biochemical Journal · doi:10.1042/bj3070631 · Cited by 294 · see citing works

Suppression of Tumor Cell Growth by Anthocyanins In Vitro

Kamei, H., Kojima, T., Hasegawa, M., et al. (1995) · Cancer Investigation · doi:10.3109/07357909509024927 · Cited by 282 · see citing works

Regulation of miRNAs in human skeletal muscle following acute endurance exercise and short‐term endurance training

Russell, A. P., Lamon, S., Boon, H., Wada, S., Güller, I., Brown, E. L., Chibalin, A., Zierath, J. R., Snow, R. J., Stepto, N. K., et al. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.255695 · Cited by 272 · see citing works

Coordinate activation of lysosomal, Ca2+-activated and ATP-ubiquitin-dependent proteinases in the unweighted rat soleus muscle

Taillandier, D., AUROUSSEAU, E., Meynial‐Denis, D., Béchet, D., Ferrara, M., Cottin, P., Ducastaing, A., Bigard, X. A., Guezennec, C. Y., Schmid, H.-P., et al. (1996) · Biochemical Journal · doi:10.1042/bj3160065 · Cited by 272 · see citing works

Sepsis is associated with increased mRNAs of the ubiquitin-proteasome proteolytic pathway in human skeletal muscle.

Tiao, G. M., Hobler, S. C., Wang, J. J., Meyer, T. A., Luchette, F. A., Fischer, J. E., & Hasselgren, P.-O. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119143 · Cited by 264 · see citing works

Effects of Anthocyanins and Other Phenolic Compounds on the Production of Tumor Necrosis Factor α in LPS/IFN-γ-Activated RAW 264.7 Macrophages

Wang, J., & Mazza, G. (2002) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf011613d · Cited by 246 · see citing works

Muscle wasting in a rat model of long-lasting sepsis results from the activation of lysosomal, Ca2+ -activated, and ubiquitin-proteasome proteolytic pathways.

Voisin, L., Breuillé, D., Combaret, L., Pouyet, C., Taillandier, D., AUROUSSEAU, E., Obled, C., & Attaix, D. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118586 · Cited by 225 · see citing works

Disruption of skeletal muscle mitochondrial network genes and miRNAs in amyotrophic lateral sclerosis

Russell, A. P., Wada, S., Vergani, L., Hock, M. B., Lamon, S., Léger, B., Ushida, T., Cartoni, R., Wadley, G. D., Hespel, P., et al. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.08.015 · Cited by 224 · see citing works

Increased ATP-ubiquitin-dependent proteolysis in skeletal muscles of tumor-bearing rats.

Temparis, S., Asensi, M., Taillandier, D., AUROUSSEAU, E., Larbaud, D., Obled, A., Béchet, D., Ferrara, M., Estrela, J. M., & Attaix, D. (1994) · PubMed · Cited by 214 · see citing works

Translational Suppression of Atrophic Regulators by MicroRNA-23a Integrates Resistance to Skeletal Muscle Atrophy

Wada, S., Kato, Y., Okutsu, M., Miyaki, S., Suzuki, K., Yan, Z., Schiaffino, S., Asahara, H., Ushida, T., & Akimoto, T. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.271270 · Cited by 200 · see citing works

Fruit Polyphenolics and Brain Aging

Galli, R. L., Shukitt‐Hale, B., Youdim, K. A., & Joseph, J. A. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb02089.x · Cited by 199 · see citing works

Short-Term Dietary Supplementation of Blueberry Polyphenolics: Beneficial Effects on Aging Brain Performance and Peripheral Tissue Function

Youdim, K. A., Shukitt‐Hale, B., Martin-Marco, A., Wang, H., Denisova, N., Bickford, P. C., & Joseph, J. A. (2000) · Nutritional Neuroscience · doi:10.1080/1028415x.2000.11747338 · Cited by 148 · see citing works

Dietary cyanidin 3‐O‐β‐ d ‐glucoside increases ex vivo oxidation resistance of serum in rats

Tsuda, T., Horio, F., & Osawa, T. (1998) · Lipids · doi:10.1007/s11745-998-0243-5 · Cited by 143 · see citing works

miR-23a is decreased during muscle atrophy by a mechanism that includes calcineurin signaling and exosome-mediated export

Hudson, M. B., Woodworth-Hobbs, M. E., Zheng, B., Rahnert, J. A., Blount, M. A., Gooch, J. L., Searles, C. D., & Price, S. R. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00266.2013 · Cited by 137 · see citing works

Muscle-specific MicroRNA1 (miR1) Targets Heat Shock Protein 70 (HSP70) during Dexamethasone-mediated Atrophy*

Kukreti, H., Amuthavalli, K., Harikumar, A., Sathiyamoorthy, S., Feng, P. Z., Anantharaj, R., Tan, S. L. K., Lokireddy, S., Bonala, S., Sriram, S., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.390369 · Cited by 121 · see citing works

Decreased miR-29 Suppresses Myogenesis in CKD

Wang, X. H., Hu, Z., Klein, J. D., Zhang, L., Fang, F., & Mitch, W. E. (2011) · Journal of the American Society of Nephrology · doi:10.1681/asn.2010121278 · Cited by 110 · see citing works

Quercetin Prevents Unloading-Derived Disused Muscle Atrophy by Attenuating the Induction of Ubiquitin Ligases in Tail-Suspension Mice

Mukai, R., Nakao, R., Yamamoto, H., Nikawa, T., Takeda, E., & Terao, J. (2010) · Journal of Natural Products · doi:10.1021/np100240y · Cited by 66 · 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

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

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

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

Testosterone reduced methylprednisolone-induced muscle atrophy in spinal cord-injured rats

Wu, Y., Collier, L., Pan, J., et al. (2011) · Spinal Cord · doi:10.1038/sc.2011.91 · Cited by 16 · see citing works

Muscle Atrophy Classification: The Need for a Pathway-Driven Approach

Zizzo, J. (2021) · Current Pharmaceutical Design · doi:10.2174/1381612824666210316102413 · Cited by 9 · see citing works

Molecular Nutritional Study on Prevention of Muscle Atrophy

Hirasaka, K. (2014) · Nippon Eiyo Shokuryo Gakkaishi · doi:10.4327/jsnfs.67.291 · Cited by 1 · see citing works

Cold-induced muscle atrophy in zebrafish: Insights from swimming activity and gene expression analysisPreprint

Ikeda, D., Fujita, S., Toda, K., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.03.553941 · Cited by 1 · see citing works

Exercise and Muscle Atrophy

He, N., & Ye, H. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-1792-1_17 · Cited by 47 · see citing works