Caloric restriction protects mitochondrial function with aging in skeletal and cardiac muscles

Premature ageing in mice expressing defective mitochondrial DNA polymerase

Trifunovic, A., Wredenberg, A., Falkenberg, M., Spelbrink, J. N., Rovio, A. T., Bruder, C. E., Bohlooly-Y, M., Gidlöf, S., Oldfors, A., Wibom, R., et al. (2004) · Nature · doi:10.1038/nature02517 · Cited by 2,734 · see citing works

Oxidative capacity and ageing in human muscle

Conley, K. E., Jubrias, S. A., & Esselman, P. C. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-1-00203.x · Cited by 651 · see citing works

Effect of age on <i>in vivo</i> rates of mitochondrial protein synthesis in human skeletal muscle

Rooyackers, O. E., Adey, D. B., Ades, P. A., & Nair, K. S. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15364 · Cited by 564 · see citing works

Histochemical and enzymatic comparison of the gastrocnemius muscle of young and elderly men and women

Coggan, A. R., Spina, R. J., King, D. S., Rogers, M. A., Rogers, M. A., Brown, M., Nemeth, P. M., & Holloszy, J. O. (1992) · Journal of Gerontology · doi:10.1093/geronj/47.3.b71 · Cited by 456 · see citing works

Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia

WANAGAT, J., CAO, Z., PATHARE, P., & AIKEN, J. M. (2001) · The FASEB Journal · doi:10.1096/fj.00-0320com · Cited by 378 · see citing works

Caloric restriction decreases mitochondrial free radical generation at complex I and lowers oxidative damage to mitochondrial DNA in the rat heart

Gredilla, R., Sanz, A., Lopez-Torres, M., & Barja, G. (2001) · The FASEB Journal · doi:10.1096/fj.00-0764fje · Cited by 372 · see citing works

Aging Selectively Decreases Oxidative Capacity in Rat Heart Interfibrillar Mitochondria

Fannin, S. W., Lesnefsky, E. J., Slabe, T. J., Hassan, M. O., & Hoppel, C. L. (1999) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1999.1508 · Cited by 262 · see citing works

Histochemical and metabolic characteristics of human skeletal muscle in relation to age

Essén-Gustavsson, B., & Borges, O. (1986) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1986.tb07793.x · Cited by 238 · see citing works

Modulation of Lon protease activity and aconitase turnover during aging and oxidative stress

Bota, D. A., Van Remmen, H., & Davies, K. J. A. (2002) · FEBS Letters · doi:10.1016/s0014-5793(02)03638-4 · Cited by 233 · see citing works

Effects of short- and medium-term calorie restriction on muscle mitochondrial proton leak and reactive oxygen species production

Bevilacqua, L., Ramsey, J. J., Hagopian, K., Weindruch, R. H., & Harper, M. (2004) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00367.2003 · Cited by 168 · see citing works

Reduced oxidative power but unchanged antioxidative capacity in skeletal muscle from aged humans

Tonkonogi, M., Fernström, M., Walsh, B., Ji, L. L., Rooyackers, O., Hammarqvist, F., Wernerman, J., & Sahlin, K. (2003) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-003-1044-9 · Cited by 159 · see citing works

Skeletal Muscle Aging in F344BN F1-Hybrid Rats: I. Mitochondrial Dysfunction Contributes to the Age-Associated Reduction in VO2max

Hagen, J. L., Krause, D. J., Baker, D. J., Fu, M. H., Tarnopolsky, M. A., & Hepple, R. T. (2004) · The Journals of Gerontology Series A · doi:10.1093/gerona/59.11.1099 · Cited by 113 · see citing works

Influences of Age and Dietary Restriction on Gastrocnemius Electron Transport System Activities in Mice

Desai, V. G., Weindruch, R. H., Hart, R. W., & Feuers, R. J. (1996) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1996.0375 · Cited by 109 · see citing works

Changes in skeletal muscle, heart and liver mitochondrial electron transport activities in rats and dogs of various ages.

Sugiyama, S., Takasawa, M., Hayakawa, M., & Ozawa, T. (1993) · PubMed · Cited by 99 · see citing works

The effect of aging and caloric restriction on mitochondrial protein density and oxygen consumption

Lambert, A. J., Wang, B., Yardley, J., Edwards, J., & Merry, B. J. (2004) · Experimental Gerontology · doi:10.1016/j.exger.2003.12.009 · Cited by 91 · see citing works

Effects of physical training on skeletal muscle metabolism and ultrastructure in 70 to 75‐year‐old men

Örlander, J., & ANIANSSON, A. (1980) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1980.tb06580.x · Cited by 87 · see citing works

Human skeletal muscle mitochondrial metabolism in youth and senescence: no signs of functional changes in ATP formation and mitochondrial oxidative capacity

Rasmussen, U. F., Krustrup, P., Kjær, M., & Rasmussen, H. (2003) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-003-1022-2 · Cited by 82 · see citing works

Long-term caloric restriction abrogates the age-related decline in skeletal muscle aerobic function

Hepple, R. T., Baker, D. J., Kaczor, J. J., & Krause, D. J. (2005) · The FASEB Journal · doi:10.1096/fj.04-3535fje · Cited by 80 · see citing works

Greater capillary-fiber interface per fiber mitochondrial volume in skeletal muscles of old rats

Mathieu-Costello, O. A., Ju, Y., Trejo, M., & Cui, L. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00750.2004 · Cited by 67 · see citing works

Mitochondrial turnover and aging of long-lived postmitotic cells: the mitochondrial-lysosomal axis theory of aging

Terman, A., Kurz, T., Navratil, M., Arriaga, E. A., & Brunk, U. T. (2010) · Antioxidants &amp; Redox Signaling · doi:10.1089/ars.2009.2598 · Cited by 490 · see citing works

Brown versus White Adipose Tissue: A Mini-Review

Saely, C. H., Geiger, K. D., & Drexel, H. (2010) · Gerontology · doi:10.1159/000321319 · Cited by 461 · see citing works

Mitochondria and Neuroplasticity

Cheng, A., Hou, Y., & Mattson, M. P. (2010) · ASN NEURO · doi:10.1042/an20100019 · Cited by 433 · see citing works

Sirtuins — novel therapeutic targets to treat age-associated diseases

Lavu, S., Boss, O., Elliott, P. J., & Lambert, P. (2008) · Nature Reviews Drug Discovery · doi:10.1038/nrd2665 · Cited by 425 · see citing works

Cellular and molecular mechanisms underlying age-related skeletal muscle wasting and weakness

Ryall, J. G., Schertzer, J. D., & Lynch, G. S. (2008) · Biogerontology · doi:10.1007/s10522-008-9131-0 · Cited by 423 · see citing works

The Mitochondrial Basis of Aging and Age-Related Disorders

Srivastava, S. (2017) · Genes · doi:10.3390/genes8120398 · Cited by 428 · see citing works

Mitochondria and ageing: Role in heart, skeletal muscle and adipose tissue

Boengler, K., Kosiol, M., Mayr, M., Schulz, R., & Rohrbach, S. (2017) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12178 · Cited by 421 · see citing works

Mitochondrial biogenesis and healthy aging

López-Lluch, G., Irusta, P. M., Navas, P., & de Cabo, R. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.06.014 · Cited by 364 · see citing works

Cardiac Aging: From Molecular Mechanisms to Significance in Human Health and Disease

Dai, D.-F., Chen, T., Johnson, S. C., Szeto, H., & Rabinovitch, P. S. (2012) · Antioxidants &amp; Redox Signaling · doi:10.1089/ars.2011.4179 · Cited by 334 · see citing works

Skeletal Muscle Mitochondria and Aging: A Review

Peterson, C. M., Johannsen, D. L., & Ravussin, É. (2012) · Journal of Aging Research · doi:10.1155/2012/194821 · Cited by 318 · see citing works

Mitochondrial morphology is altered in atrophied skeletal muscle of aged mice

Leduc-Gaudet, J.-P., Picard, M., Pelletier, F. S.-J., Sgarioto, N., Auger, M.-J., Vallée, J., Robitaille, R., St-Pierre, D. H., & Gouspillou, G. (2015) · Oncotarget · doi:10.18632/oncotarget.4235 · Cited by 273 · see citing works

Mitochondrial Dynamics and Mitophagy in Skeletal Muscle Health and Aging

Leduc-Gaudet, J.-P., Hussain, S. N. A., Barreiro, E., & Gouspillou, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158179 · Cited by 268 · see citing works

Mitochondrial Energy Metabolism and Redox Signaling in Brain Aging and Neurodegeneration

Yin, F., Boveris, A., & Cadenas, E. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4774 · Cited by 246 · see citing works

Reconsidering the Role of Mitochondria in Aging

Gonzalez-Freire, M., de Cabo, R., Bernier, M., Sollott, S. J., Fabbri, E., Navas, P., & Ferrucci, L. (2015) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glv070 · Cited by 244 · see citing works

Chronic Caloric Restriction Preserves Mitochondrial Function in Senescence without Increasing Mitochondrial Biogenesis

Lanza, I. R., Zabielski, P., Klaus, K. A., Morse, D. M., Heppelmann, C. J., Bergen, H. R., Dasari, S., Walrand, S., Short, K. R., Johnson, M. L., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.11.003 · Cited by 227 · see citing works

Hormonal and Metabolic Changes of Aging and the Influence of Lifestyle Modifications

Pataky, M. W., Young, W. F., & Nair, K. S. (2021) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2020.07.033 · Cited by 207 · see citing works

The coordination of nuclear and mitochondrial communication during aging and calorie restriction

Finley, L. W. S., & Haigis, M. C. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.03.003 · Cited by 207 · see citing works

Potential Therapeutic Benefits of Strategies Directed to Mitochondria

Camara, A. K. S., Lesnefsky, E. J., & Stowe, D. F. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2788 · Cited by 195 · see citing works

Mitophagy and Oxidative Stress: The Role of Aging

Gaetano, A. D., Gibellini, L., Zanini, G., Nasi, M., Cossarizza, A., & Pinti, M. (2021) · Antioxidants · doi:10.3390/antiox10050794 · Cited by 188 · see citing works

Determinants ofVO2 maxdecline with aging: an integrated perspective

Betik, A. C., & Hepple, R. T. (2008) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h07-174 · Cited by 176 · see citing works

Caloric restriction: From soup to nuts

Spindler, S. R. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.10.003 · Cited by 168 · see citing works

The Role of Oxidative Stress in Cardiovascular Aging and Cardiovascular Diseases

Izzo, C., Vitillo, P., Pietro, P. D., Visco, V., Strianese, A., Virtuoso, N., Ciccarelli, M., Galasso, G., Carrizzo, A., & Vecchione, C. (2021) · Life · doi:10.3390/life11010060 · Cited by 167 · see citing works

Calorie Restriction and Dietary Restriction Mimetics: A Strategy for Improving Healthy Aging and Longevity

Testa, G., Biasi, F., Poli, G., & Chiarpotto, E. (2014) · Current Pharmaceutical Design · doi:10.2174/13816128113196660699 · Cited by 148 · see citing works

Crosstalk between mitochondrial (dys)function and mitochondrial abundance

Michel, S., Wanet, A., Pauw, A. D., Rommelaere, G., Arnould, T., & Renard, P. (2011) · Journal of Cellular Physiology · doi:10.1002/jcp.23021 · Cited by 132 · see citing works

Highly resistant macromolecular components and low rate of generation of endogenous damage: Two key traits of longevity

Pamplona, R., & Barja, G. (2007) · Ageing Research Reviews · doi:10.1016/j.arr.2007.06.002 · Cited by 126 · see citing works

The many roles of PGC-1α in muscle — recent developments

Chan, M. C., & Arany, Z. P. (2014) · Metabolism · doi:10.1016/j.metabol.2014.01.006 · Cited by 125 · see citing works

Parkin overexpression protects from ageing‐related loss of muscle mass and strength

Leduc‐Gaudet, J., Reynaud, O., Hussain, S. N., & Gouspillou, G. (2019) · The Journal of Physiology · doi:10.1113/jp277157 · Cited by 119 · see citing works

Oxidative stress, aging, antioxidant supplementation and their impact on human health: An overview

Martemucci, G., Portincasa, P., Ciaula, A. D., Mariano, M., Centonze, V., & D‘Alessandro, A. G. (2022) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2022.111707 · Cited by 110 · see citing works

α-Lipoic acid increases energy expenditure by enhancing adenosine monophosphate–activated protein kinase–peroxisome proliferator-activated receptor-γ coactivator-1α signaling in the skeletal muscle of aged mice

Wang, Y., Li, X., Guo, Y., Chan, L., & Guan, X. (2009) · Metabolism · doi:10.1016/j.metabol.2009.10.018 · Cited by 105 · see citing works

Transcriptional response to aging and caloric restriction in heart and adipose tissue

Linford, N. J., Beyer, R. P., Gollahon, K. A., Krajcik, R. A., Malloy, V. L., Demas, V., Burmer, G. C., & Rabinovitch, P. S. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00319.x · Cited by 100 · see citing works

Molecular Bases of Caloric Restriction Regulation of Neuronal Synaptic Plasticity

Fontán‐Lozano, Á., López‐Lluch, G., Delgado-Garcia, J. M., Navas, P., & Carrión, Á. M. (2008) · Molecular Neurobiology · doi:10.1007/s12035-008-8040-1 · Cited by 98 · see citing works

The impact of diet upon mitochondrial physiology (Review)

Kyriazis, I. D., Vassi, E., Alvanou, M. V., Angelakis, C., Skaperda, Z., Tekos, F., Garikipati, V. N. S., Spandidos, D. A., & Kouretas, D. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5191 · Cited by 91 · see citing works

Mitochondrial longevity pathways

Raffaello, A., & Rizzuto, R. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.10.007 · Cited by 87 · see citing works

Peroxisome Proliferator-Activated Receptors and Caloric Restriction—Common Pathways Affecting Metabolism, Health, and Longevity

Duszka, K., Gregor, A., Guillou, H., König, J. S., & Wahli, W. (2020) · Cells · doi:10.3390/cells9071708 · Cited by 82 · see citing works

Lowered methionine ingestion as responsible for the decrease in rodent mitochondrial oxidative stress in protein and dietary restriction

Lopez‐Torres, M., & Barja, G. (2008) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2008.01.007 · Cited by 78 · see citing works

Commonly adopted caloric restriction protocols often involve malnutrition

Cerqueira, F. M., & Kowaltowski, A. J. (2010) · Ageing Research Reviews · doi:10.1016/j.arr.2010.05.002 · Cited by 76 · see citing works

Age-Related Deficit in Load-Induced Skeletal Muscle Growth

Hwee, D. T., & Bodine, S. C. (2009) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glp026 · Cited by 74 · see citing works

Effects of Aging and Caloric Restriction on Fiber Type Composition, Mitochondrial Morphology and Dynamics in Rat Oxidative and Glycolytic Muscles

Faitg, J., Leduc-Gaudet, J.-P., Reynaud, O., Ferland, G., Gaudreau, P., & Gouspillou, G. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00420 · Cited by 72 · see citing works

Invertebrate models of age-related muscle degeneration

Augustin, H., & Partridge, L. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.06.011 · Cited by 66 · see citing works

Cellular Senescence: Ageing and Androgenetic Alopecia

Deng, Y., Wang, M., He, Y., Liu, F., Chen, L., & Xia, X. (2023) · Dermatology · doi:10.1159/000530681 · Cited by 68 · see citing works

Myricetin improves endurance capacity and mitochondrial density by activating SIRT1 and PGC-1α

Jung, H., Lee, D.-Y., Ryu, H. G., Choi, B.-H., Go, Y., Lee, N., Lee, D., Son, H. G., Jeon, J., Kim, S., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-05303-2 · Cited by 65 · see citing works

Caloric Restriction Promotes Structural and Metabolic Changes in the Skin

Forni, M. F., Peloggia, J., Braga, T. T., Chinchilla, J. E. O., Shinohara, J. S., Navas, C. A., Câmara, N. O. S., & Kowaltowski, A. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.052 · Cited by 63 · see citing works

Effects of two years of calorie restriction on aerobic capacity and muscle strength

RACETTE, S. B., ROCHON, J., UHRICH, M. L., VILLAREAL, D. T., DAS, S. K., FONTANA, L., BHAPKAR, M., MARTIN, C. K., REDMAN, L. M., FUSS, P. J., et al. (2017) · Medicine &amp; Science in Sports &amp; Exercise · doi:10.1249/mss.0000000000001353 · Cited by 58 · see citing works

Mitochondrial function and dynamics in neural stem cells and neurogenesis: Implications for neurodegenerative diseases

Coelho, P., Fão, L., Mota, S. I., & Rego, A. C. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101667 · Cited by 57 · see citing works

Energetic interventions for healthspan and resiliency with aging

Huffman, D. M., Schafer, M. J., & LeBrasseur, N. K. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.05.012 · Cited by 53 · see citing works

Mitochondria and mitochondria-induced signalling molecules as longevity determinants

Rose, G., Santoro, A., & Salvioli, S. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.12.002 · Cited by 56 · see citing works

Caloric Restriction Retards the Age-Related Decline in Mitochondrial Function of Brown Adipose Tissue

Valle, A., Guevara, R., García-Palmer, F., Roca, P., & Oliver, J. (2008) · Rejuvenation Research · doi:10.1089/rej.2007.0626 · Cited by 52 · see citing works

The role of exercise capacity in the health and longevity of centenarians

Venturelli, M., Schena, F. F., & Richardson, R. S. (2012) · Maturitas · doi:10.1016/j.maturitas.2012.07.009 · Cited by 50 · see citing works

Slow twitch soleus muscle is not protected from sarcopenia in senescent rats

Carter, E. E., Thomas, M. M., Murynka, T., Rowan, S. L., Wright, K. J., Huba, E., & Hepple, R. T. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.04.001 · Cited by 49 · see citing works

Effects of lithium on age-related decline in mitochondrial turnover and function in Caenorhabditis elegans.

Tam, Z.-Y., Gruber, J., Ng, L., Halliwell, B., & Gunawan, R. (2014) · The journals of gerontology. Series A, Biological sciences and medical sciences · doi:10.1093/gerona/glt210 · Cited by 50 · see citing works

Dietary restriction increases skeletal muscle mitochondrial respiration but not mitochondrial content in C57BL/6 mice

Hempenstall, S., Page, M. M., Wallen, K. R., & Selman, C. (2012) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.12.002 · Cited by 47 · see citing works

Mechanisms driving the ageing heart

Anderson, R., Richardson, G. D., & Passos, J. F. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.10.015 · Cited by 46 · see citing works

Energy restriction and potential energy restriction mimetics

Nikolai, S., Pallauf, K., Huebbe, P., & Rimbach, G. H. (2015) · Nutrition Research Reviews · doi:10.1017/s0954422415000062 · Cited by 43 · see citing works

Mitochondrial form, function and signalling in aging

Amigo, I., da Cunha, F. M., Forni, M. F., Garcia-Neto, W., Kakimoto, P. A., Luévano‐Martínez, L. A., Macedo, F. P., Menezes‐Filho, S. L., Peloggia, J., & Kowaltowski, A. J. (2016) · Biochemical Journal · doi:10.1042/bcj20160451 · Cited by 42 · see citing works

Facts and controversies in our understanding of how caloric restriction impacts the mitochondrion

Gouspillou, G., & Hepple, R. T. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.03.004 · Cited by 42 · see citing works

Update on emerging drugs for sarcopenia – age-related muscle wasting

Lynch, G. S. (2008) · Expert Opinion on Emerging Drugs · doi:10.1517/14728210802544476 · Cited by 36 · see citing works

Low mitochondrial DNA content associates with familial longevity: the Leiden Longevity Study

van Leeuwen, N., Beekman, M., Deelen, J., van den Akker, E. B., de Craen, A. J. M., Slagboom, P. E., & Hart, L. M. ‘. (2014) · AGE · doi:10.1007/s11357-014-9629-0 · Cited by 33 · see citing works

Mitophagy Activation by Urolithin A to Target Muscle Aging

Faitg, J., D’Amico, D., Rinsch, C., & Singh, A. (2023) · Calcified Tissue International · doi:10.1007/s00223-023-01145-5 · Cited by 31 · see citing works

Calorie Restriction Hysteretically Primes Aging Saccharomyces cerevisiae toward More Effective Oxidative Metabolism

Tahara, E. B., da Cunha, F. M., Basso, T. O., Della-Bianca, B. E., Gombert, A. K., & Kowaltowski, A. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056388 · Cited by 31 · see citing works

The influence of dietary lipid composition on liver mitochondria from mice following 1 month of calorie restriction

Chen, Y., Hagopian, K., Bibus, D. M., Villalba, J. M., López‐Lluch, G., Navas, P., Kim, K., McDonald, R. B., & Ramsey, J. J. (2012) · Bioscience Reports · doi:10.1042/bsr20120060 · Cited by 29 · see citing works

Muscle Physiology Changes Induced by Every Other Day Feeding and Endurance Exercise in Mice: Effects on Physical Performance

Rodríguez-Bies, E., Calvo, S. S.-C., Fontán‐Lozano, Á., Peña, J., de la Rosa, F. J. B., Carrión, Á. M., Navas, P., & López‐Lluch, G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013900 · Cited by 28 · see citing works

The Case for Prioritizing Research on Late-Onset Life-Extension Interventions in Mammals

de Grey, A. D. N. J. (2007) · Rejuvenation Research · doi:10.1089/rej.2007.0547 · Cited by 26 · see citing works

Endopolyploidy Changes with Age-Related Polyethism in the Honey Bee, Apis mellifera

Rangel, J., Strauss, K., Seedorf, K., Hjelmen, C. E., & Johnston, J. S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0122208 · Cited by 24 · see citing works

Mitochondrial Theory of Aging in Human Age-Related Sarcopenia

Parise, G., & Lisio, M. D. (2010) · Interdisciplinary topics in gerontology and geriatrics · doi:10.1159/000319999 · Cited by 22 · see citing works

Serum from Calorie-Restricted Rats Activates Vascular Cell eNOS through Enhanced Insulin Signaling Mediated by Adiponectin

Cerqueira, F. M., Brandizzi, L. I., da Cunha, F. M., Laurindo, F. R. M., & Kowaltowski, A. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031155 · Cited by 22 · see citing works

Biological Effects of Calorie Restriction: Implications for Modification of Human Aging

Spindler, S. R. (2010) · Springer eBooks · doi:10.1007/978-90-481-3999-6_12 · Cited by 19 · see citing works

Energy restriction in obese subjects impact differently two mitochondrial function markers

Crujeiras, A. B., Parra, D., Goyenechea, E., Abete, I., González‐Muniesa, P., & Martínez, J. A. (2008) · Journal of Physiology and Biochemistry · doi:10.1007/bf03178844 · Cited by 20 · see citing works

The influence of dietary fat source on liver and skeletal muscle mitochondrial modifications and lifespan changes in calorie-restricted mice

Villalba, J. M., Lopez-Dominguez, J. A., Chen, Y., Khraiwesh, H. M., González-Reyes, J. A., Fernández-del-Río, L., Gutiérrez-Casado, E., del Río-Moreno, M., Calvo‐Rubio, M., Ariza, J., et al. (2015) · Biogerontology · doi:10.1007/s10522-015-9572-1 · Cited by 19 · see citing works

Effects of Calorie Restriction and Fiber Type on Glucose Uptake and Abundance of Electron Transport Chain and Oxidative Phosphorylation Proteins in Single Fibers from Old Rats

Wang, H., Arias, E. B., Yu, C. S., Verkerke, A. R. P., & Cartee, G. D. (2017) · The Journals of Gerontology Series A · doi:10.1093/gerona/glx099 · Cited by 18 · see citing works

Calorie restriction does not restore brain mitochondrial function in P301L tau mice, but it does decrease mitochondrial F0F1-ATPase activity

Delic, V., Brownlow, M. L., Joly‐Amado, A., Zivkovic, S., Noble, K. V., Phan, T.-A., Ta, Y., Zhang, Y., Bell, S. D., Kurien, C., et al. (2015) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2015.06.001 · Cited by 17 · see citing works

Inverse Lansing Effect: Maternal Age and Provisioning Affecting Daughters’ Longevity and Male Offspring Production

Anderson, C. E., Malek, M. C., Jonas-Closs, R. A., Cho, Y., Peshkin, L., Kirschner, M. W., & Yampolsky, L. Y. (2022) · The American Naturalist · doi:10.1086/721148 · Cited by 16 · see citing works

Restricción calórica, estrés oxidativo y longevidad

Lopez‐Torres, M., & Barja, G. (2008) · Revista Española de Geriatría y Gerontología · doi:10.1016/s0211-139x(08)71190-9 · Cited by 16 · see citing works

A Survey of Selected Recent Theses Relevant to Combating Aging

(2007) · Rejuvenation Research · doi:10.1089/rej.2007.7992 · Cited by 12 · see citing works

Calorie Restriction Rescues Mitochondrial Dysfunction in Adck2-Deficient Skeletal Muscle

Hernández‐Camacho, J. D., Fernández‐Ayala, D. J. M., Vicente‐García, C., Navas‐Enamorado, I., López‐Lluch, G., Oliva, C., Artuch, R., García‐Villoria, J., Ribes, A., de Cabo, R., et al. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.898792 · Cited by 9 · see citing works

Genetics of aging and longevity

Moskalev, A., Proshkina, E., Belyi, A. A., & Solovev, I. A. (2017) · Russian Journal of Genetics Applied Research · doi:10.1134/s2079059717040074 · Cited by 10 · see citing works

Effect of caloric restriction and subsequent re-alimentation on oxidative stress in the liver of Hu sheep ram lambs

Zhang, G., Zhang, T., Jin, Y., Liu, J., Guo, Y., Fan, Y., El-Samahy, M. A., Meng, F., Wang, F., & Lei, Z. (2018) · Animal Feed Science and Technology · doi:10.1016/j.anifeedsci.2018.01.009 · Cited by 8 · see citing works

Retrospective: Rejuvenation Research in 2006

de Grey, A. D. N. J. (2007) · Rejuvenation Research · doi:10.1089/rej.2007.0589 · Cited by 8 · see citing works

Physical enhancement of older adults using hyperbaric oxygen: a randomized controlled trial

Hadanny, A., Sasson, E., Copel, L., Daniel-Kotovsky, M., Yaakobi, E., Lang, E., Fishlev, G., Polak, N., Friedman, M., Doenyas‐Barak, K., et al. (2024) · BMC Geriatrics · doi:10.1186/s12877-024-05146-3 · Cited by 7 · see citing works

Mitochondrial Dysfunction in Aging, HIV, and Long COVID: Mechanisms and Therapeutic Opportunities

Delpino, M. V., & Quarleri, J. F. (2025) · Pathogens · doi:10.3390/pathogens14101045 · Cited by 6 · see citing works

Genetics of aging and longevity

Moskalev, A., Proshkina, E., Belyi, A. A., & Solovev, I. A. (2016) · Vavilov Journal of Genetics and Breeding · doi:10.18699/vj16.171 · Cited by 5 · see citing works

Nutrient restriction preserves calcium cycling and mitochondrial function in cardiac myocytes during ischemia and reperfusion

Wang, S., Chen, J., & Valderrábano, M. (2012) · Cell Calcium · doi:10.1016/j.ceca.2012.02.009 · Cited by 5 · see citing works

Edmonton: A Future Center for Pioneering Biomedical Gerontology?

de Grey, A. D. N. J. (2007) · Rejuvenation Research · doi:10.1089/rej.2007.0590 · Cited by 5 · see citing works

Alterations in Mitochondria and Their Impact in Aging Skeletal Muscle

Hepple, R. T. (2010) · Springer eBooks · doi:10.1007/978-90-481-9713-2_7 · Cited by 4 · see citing works

Mitochondrial Free Radical Production and Caloric Restriction: Implications in Vertebrate Longevity and Aging

Lopez‐Torres, M., & Barja, G. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-420-9_9 · Cited by 4 · see citing works

Nutrition and Exercise in Cardiovascular Aging: Metabolic and Pharmacological Interventions

Marı́n-Garcı́a, J., Goldenthal, M. J., & Moe, G. W. P. L. (2007) · Springer eBooks · doi:10.1007/978-0-387-74072-0_15 · Cited by 3 · see citing works

Prevention of Skeletal Muscle Wasting: Disuse Atrophy and Sarcopenia

Naomi, E., & Kathryn, H. (2012) · InTech eBooks · doi:10.5772/47856 · Cited by 2 · see citing works

Dietary Restriction as a Potential Intervention to Retard Age-associated Impairment of Brain Functions

Kaur, G., & Lakhman, S. S. (2012) · Springer eBooks · doi:10.1007/978-94-007-5237-5_10 · Cited by 1 · see citing works

Molecular Mechanisms of Cardiovascular Aging

Meiliana, A., & Wijaya, A. (2013) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v5i3.64 · Cited by 1 · see citing works

Mitochondrial Inheritance and Function in the Lifespan Control of Budding Yeast

McFaline-Figueroa, J. R. (2012) · doi:10.7916/d8zw1t00

Estudo dos efeitos metabólicos e redox de dietas intermitentes

de Freitas, B. C. (2015) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.46.2015.tde-22092015-081157

Mitochondrial dynamics and quality control in ageing

Tam, Z.-Y. (2013) · Repository for Publications and Research Data (ETH Zurich) · doi:10.3929/ethz-a-009756828

Molecular Bases of Caloric Restriction Regulation of Neuronal

Fontán‐Lozano, Á., López‐Lluch, G., María, J., Navas, P., & Carrión, Á. M. (2008)

The Effects of Gene Therapy in an Ovine Osteoarthritis Model

Collier, C. (2020) · Digital Commons - USU (Utah State University) · doi:10.26076/95ec-6796

Étude sur les mécanismes moléculaires impliqués dans l’auto-renouvellement, la différenciation et la conversion thermogénique des cellules adipocytaires dans différentes situations pathologiques

Paré, M. (2019) · doi:10.70675/feb9ef60z24d4z46adz9408zf77248e4a74d

Caloric restriction prevents the age‐related decline in cardiac complex IV activity with aging in male F344BN rats

McConkey, M. J., Norris, R., Krause, D. J., & Hepple, R. T. (2006) · The FASEB Journal · doi:10.1096/fasebj.20.4.a384-a

No Decline in Skeletal Muscle Oxidative Capacity With Aging in Long-Term Calorically Restricted Rats: Effects Are Independent of

Integrity, M. D., Baker, D. J., Betik, A. C., & Krause, D. J. (2013)

Long-term caloric restriction abrogates the age-related decline in skeletal muscle aerobic function

Hepple, R. T., Baker, D. J., Kaczor, J. J., & Krause, D. J. (2005) · The FASEB Journal · doi:10.1096/fj.04-3535fje · Cited by 80 · see citing works

No decline in skeletal muscle oxidative capacity with aging in long-term calorically restricted rats: Effects are independent of mitochondrial DNA integrity

Baker, D. J., Betik, A. C., Krause, D. J., & Hepple, R. T. (2006) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/61.7.675 · Cited by 89 · see citing works

Caloric Restriction Attenuates Many Age‐Related Changes in Skeletal Muscle Mitochondrial Physiology

Lanza, I. R., Li, E., Jakaitis, D. R., Ali, B., & Nair, K. S. (2010) · The FASEB Journal · doi:10.1096/fasebj.24.1_supplement.621.1