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Insulin receptor sensitizer, dicholine succinate, prevents both Toll-like receptor 4 (TLR4) upregulation and affective changes induced by a high-cholesterol diet in mice

Strekalova, T. V., Costa-Nunes, J. P., Veniaminova, E. A., Kubatiev, A. A., Lesch, K., Chekhonin, V. P., Evans, M. C., & Steinbusch, H. W. M. (2016) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.02.045 · Cited by 31 · see citing works

Downregulation of lipin-1 induces insulin resistance by increasing intracellular ceramide accumulation in C2C12 myotubes

Huang, S., Huang, S., Wang, X., Zhang, Q., Liu, J., & Leng, Y. (2016) · International Journal of Biological Sciences · doi:10.7150/ijbs.17149 · Cited by 27 · see citing works

Endurance exercise training and high-fat diet differentially affect composition of diacylglycerol molecular species in rat skeletal muscle

Kawanishi, N., Takagi, K., Lee, H., Nakano, D., Okuno, T., Yokomizo, T., & Machida, S. (2018) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00371.2017 · Cited by 26 · see citing works

Chronic muscle stimulation improves insulin sensitivity while increasing subcellular lipid droplets and reducing selected diacylglycerol and ceramide species in obese Zucker rats

Holloway, G. P., Han, X., Jain, S. S., Bonen, A., & Chabowski, A. (2014) · Diabetologia · doi:10.1007/s00125-014-3169-0 · Cited by 26 · see citing works

SIRT1 overexpression in skeletal muscle in vivo induces increased insulin sensitivity and enhanced complex I but not complex II–V functions in individual subsarcolemmal and intermyofibrillar mitochondria

Zhang, H., Qin, G.-J., Li, X., Zhang, Y., Du, P., Zhang, P.-Y., Zhao, Y., & Wu, J. (2015) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-015-0396-x · Cited by 25 · see citing works

LA and ALA prevent glucose intolerance in obese male rats without reducing reactive lipid content, but cause tissue-specific changes in fatty acid composition

Matravadia, S., Zabielski, P., Chabowski, A., Mutch, D. M., & Holloway, G. P. (2016) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00297.2015 · Cited by 24 · see citing works

α-Linolenic acid supplementation and exercise training reveal independent and additive responses on hepatic lipid accumulation in obese rats

Miotto, P. M., Horbatuk, M., Proudfoot, R., Matravadia, S., Bakovic, M., Chabowski, A., & Holloway, G. P. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00438.2016 · Cited by 21 · see citing works

Roles of Fatty Acid Oversupply and Impaired Oxidation in Lipid Accumulation in Tissues of Obese Rats

Oakes, N. D., Kjellstedt, A., Thalén, P., Ljung, B., & Turner, N. A. (2013) · Journal of Lipids · doi:10.1155/2013/420754 · Cited by 20 · see citing works

Similar changes in muscle lipid metabolism are induced by chronic high‐fructose feeding and high‐fat feeding in C57 BL /J6 mice

Song, G., Ren, L., Chen, S., Wang, C., Liu, N., Wei, L., Li, F., Sun, W., Peng, L., & Tang, Y. P. (2012) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12017 · Cited by 20 · see citing works

The complex interplay between oxinflammation, mitochondrial dysfunction and lipotoxicity: Focus on their role in the pathogenesis of skeletal muscle insulin resistance and modulation by dietary fatty acids

Passaro, A., Sanz, J. M., Naumovski, N., & Sergi, D. (2024) · Advances in Redox Research · doi:10.1016/j.arres.2024.100100 · Cited by 17 · see citing works

Insulin and diet-induced changes in the ubiquitin-modified proteome of rat liver

Nagarajan, S. R., Brandon, A. E., McKenna, J. A., Shtein, H. C., Nguyen, T., Suryana, E., Poronnik, P., Cooney, G. J., Saunders, D. N., & Hoy, A. J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174431 · Cited by 14 · see citing works

Integrated lipidomic and transcriptomic analyses reveal the mechanism of large yellow croaker roe phospholipids on lipid metabolism in normal-diet mice

Zhong, R., Zhu, Y., Zhang, H., Huo, Y., Huang, Y., Cheng, W., & Liang, P. (2022) · Food & Function · doi:10.1039/d2fo02736d · Cited by 13 · see citing works

Increasing Acyl CoA thioesterase activity alters phospholipid profile without effect on insulin action in skeletal muscle of rats

Bakshi, I., Brown, S. H. J., Brandon, A. E., Suryana, E., Mitchell, T. W., Turner, N. A., & Cooney, G. J. (2018) · Scientific Reports · doi:10.1038/s41598-018-32354-w · Cited by 14 · see citing works

Optimizing hyaluronidase dose and plasmid DNA delivery greatly improves gene electrotransfer efficiency in rat skeletal muscle

Akerstrom, T. C. A., Vedel, K., Needham, J., Højman, P., Kontou, E. E., Hellsten, Y., & Wojtaszewski, J. F. P. (2015) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2015.10.007 · Cited by 12 · see citing works

Acetyl-CoA carboxylase 2 inhibition reduces skeletal muscle bioactive lipid content and attenuates progression of type 2 diabetes in Zucker diabetic fatty rats

Takagi, H., Ikehara, T., Hashimoto, K., Tanimoto, K., Shimazaki, A., Kashiwagi, Y., Sakamoto, S. X., & Yukioka, H. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174451 · Cited by 11 · see citing works

Prenatal Low-Protein Diet Affects Mitochondrial Structure and Function in the Skeletal Muscle of Adult Female Offspring

Vidyadharan, V. A., Betancourt, A., Smith, C., Yallampalli, C., & Blesson, C. S. (2022) · Nutrients · doi:10.3390/nu14061158 · Cited by 10 · see citing works

New Insights Into Mitochondrial Dysfunction at Disease Susceptibility Loci in the Development of Type 2 Diabetes

Maude, H., Lau, W., Maniatis, N., & Andrew, T. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.694893 · Cited by 7 · see citing works

Mitochondrial Metabolism and Insulin Action

Turner, N. A. (2013) · InTech eBooks · doi:10.5772/56449 · Cited by 6 · see citing works

Effect of Ethyl Pyruvate on Skeletal Muscle Metabolism in Rats Fed on a High Fat Diet

Olek, R. A., Ziółkowski, W., Wierzba, T. H., & Kaczor, J. J. (2013) · Nutrients · doi:10.3390/nu5072372 · Cited by 7 · see citing works

GPAT1 Activity and Abundant Palmitic Acid Impair Insulin Suppression of Hepatic Glucose Production in Primary Mouse Hepatocytes

Zhang, C., Steadman, M., Junior, H. P. D. O. S., Shaikh, S. R., & Xavier, R. M. (2024) · Journal of Nutrition · doi:10.1016/j.tjnut.2024.02.004 · Cited by 4 · see citing works

Peroxisome proliferator-activated receptor γ coactivator 1β (PGC-1β) improves skeletal muscle mitochondrial function and insulin sensitivity

Handschin, C. (2011) · Diabetologia · doi:10.1007/s00125-011-2135-3 · Cited by 4 · see citing works

Insights into the promising prospect of pharmacological approaches targeting mitochondrial dysfunction in major human diseases: At a glance

Rahman, M. M., Sarker, M. T., Ahmed, S., Uddin, M. N., Islam, M. R., Islam, M. R., Das, S., Mukherjee, N., Hemeg, H. A., Rauf, A., et al. (2023) · Process Biochemistry · doi:10.1016/j.procbio.2023.07.007 · Cited by 4 · see citing works

SIRT3 overexpression in rat muscle does not ameliorate peripheral insulin resistance

Osborne, B., Wright, L. E., Brandon, A. E., Stuart, E., Small, L., Joris Hoeks, J., Schrauwen, P., Sinclair, D. A., Montgomery, M. K., Cooney, G. J., et al. (2023) · Journal of Endocrinology · doi:10.1530/joe-22-0101 · Cited by 1 · see citing works

Da-Cheng-Qi decoction attenuates inflammatory edema and endoplasmic reticulum stress in acute pancreatitis via suppressing NF-κB pathway

Shang, J., Ma, L., Su, R., Jiang, X., Jiang, Y., Fan, Y., Wang, Y., Li, X., You, M., Tian, Z., et al. (2026) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2026.121523 · Cited by 1 · see citing works

Effect of regular exercise-induced apelin on dyslipidemia of type 2 diabetic rats

Kazemi, F., Khosroo, E., & Asl, S. Z. (2016) · Research in Medicine · Cited by 1 · see citing works

The effect of viscous and fermentable dietary fiber consumption on adiposity, insulin resistance and fuel utilization in rats

Brockman, D. A. (2013) · University of Minnesota Digital Conservancy (University of Minnesota) · Cited by 1 · see citing works

Master Switch of Mitochondrial Biogenesis: A Clinical Target for Health Span Enhancement?

Mendelsohn, A. R., & Larrick, J. W. (2011) · Rejuvenation Research · doi:10.1089/rej.2011.1194 · Cited by 1 · see citing works

The impact of lifestyle factors on whole-body lipid handling and skeletal muscle mitochondrial content and function

Matravadia, S. (2016) · The Atrium (University of Guelph)

Current World Literature

(2012) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e3283543033

Role of PGC-1β and TIF2 co-regulators in mouse skeletal muscle function

Ramamoorthy, T. G. (2013) · doi:10.70675/e05002c4z4806z4363z90b1z0e406b6c0e4c

Peroxisome proliferator-activated receptor γ coactivator 1β (PGC-1β) improves skeletal muscle mitochondrial function and insulin sensitivity

Handschin, C. (2011) · Diabetologia · doi:10.1007/s00125-011-2135-3 · Cited by 4 · see citing works

Increased levels of peroxisome proliferator-activated receptor gamma, coactivator 1 alpha (PGC-1α) improve lipid utilisation, insulin signalling and glucose transport in skeletal muscle of lean and insulin-resistant obese Zucker rats

Benton, C. R., Holloway, G. P., Han, X.-X., Yoshida, Y., Snook, L. A., Lally, J., Glatz, J. F. C., Luiken, J. J. F. P., Chabowski, A., & Bonen, A. (2010) · Diabetologia · doi:10.1007/s00125-010-1773-1 · Cited by 143 · see citing works

The relationship between mitochondrial metabolism and insulin action in skeletal muscle

Wright, L. E. (2022) · UNSWorks (University of New South Wales, Sydney, Australia) · doi:10.26190/unsworks/15180

PGC-1α-induced improvements in skeletal muscle metabolism and insulin sensitivityThis paper is one of a selection of papers published in this Special Issue, entitled 14th International Biochemistry of Exercise Conference – Muscles as Molecular and Metabolic Machines, and has undergone the Journal’s usual peer review process.

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Mechanisms of peroxisome proliferator-activated receptor gamma coactivator 1α in high-fat diet-induced skeletal muscle mitochondrial dysfunction in rats

Ma, H., Zhang, D., Wang, X., Wang, Z., Song, G., & Ma, H. (2019) · Zhonghua laonian yixue zazhi · doi:10.3760/cma.j.issn.0254-9026.2019.04.022