Metabolic stress and altered glucose transport: activation of AMP-activated protein kinase as a unifying coupling mechanism.

Transient activation of fission yeast AMPK is required for cell proliferation during osmotic stress

Schutt, K. L., & Moseley, J. B. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-04-0235 · Cited by 23

Enhanced antioxidant effect of prenylated polyphenols as Fyn inhibitor

Kim, A., Lee, D. Y., Lee, D. Y., Li, H., Jeon, R., Ryu, J., & Kim, S. G. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.06.039 · Cited by 21

Caffeine and contraction synergistically stimulate 5′-AMP-activated protein kinase and insulin-independent glucose transport in rat skeletal muscle

Tsuda, S., Egawa, T., Kitani, K., Oshima, R., Ma, X., & Hayashi, T. (2015) · Physiological Reports · doi:10.14814/phy2.12592 · Cited by 22

Macrophage migration inhibitory factor diminishes muscle glucose transport induced by insulin and AICAR in a muscle type-dependent manner

Miyatake, S., Manabe, Y., Inagaki, A., Furuichi, Y., Takagi, M., Taoka, M., Isobe, T., Hirota, K., & FUJII, N. L. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.01.089 · Cited by 22

Administration of biotin prevents the development of insulin resistance in the skeletal muscles of Otsuka Long-Evans Tokushima fatty rats

Sasaki, Y., Sone, H., Kamiyama, S., Shimizu, M., Shirakawa, H., Kagawa, Y., Komai, M., & Furukawa, Y. (2012) · Food & Function · doi:10.1039/c2fo10175k · Cited by 21

Differential attenuation of AMPK activation during acute exercise following exercise training or AICAR treatment

McConell, G. K., Manimmanakorn, A., Lee, R. S., Kemp, B. E., Linden, K. C., & Wadley, G. D. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01371.2007 · Cited by 22

A monoclonal antibody activating AdipoR for type 2 diabetes and nonalcoholic steatohepatitis

Asahara, N., Okada‐Iwabu, M., Iwabu, M., Wada, K., Oka, K., Yamauchi, T., & Kadowaki, T. (2023) · Science Advances · doi:10.1126/sciadv.adg4216 · Cited by 21

Progesterone impairs cell respiration and suppresses a compensatory increase in glucose transport in isolated rat skeletal muscle: a non-genomic mechanism contributing to metabolic adaptation to late pregnancy?

Gras, F., Brunmair, B., Quarré, L., Szöcs, Z., Waldhäusl, W. K., & Fürnsinn, C. (2007) · Diabetologia · doi:10.1007/s00125-007-0836-4 · Cited by 20

Induction of mitochondrial uncoupling enhances VEGF₁₂₀ but reduces MCP-1 release in mature 3T3-L1 adipocytes: Possible regulatory mechanism through endogenous ER stress and AMPK-related pathways

Miyokawa-Gorin, K., Takahashi, K., Handa, K., Kitahara, A., Sumitani, Y., Katsuta, H., Tanaka, T., Nishida, S., Yoshimoto, K., Ohno, H., et al. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.01.145 · Cited by 18

Exercise Improves Heart Function after Myocardial Infarction: The Merits of AMPK

Zhang, X., Zhao, Y., Guo, D., Luo, M., Zhang, Q., Zhang, L., & Zhang, D. (2024) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-024-07564-2 · Cited by 20

Ascofuranone prevents ER stress-induced insulin resistance via activation of AMP-activated protein kinase in L6 myotube cells

Hwang, S., Chang, H., Lee, I., Yang, B.-K., Magae, J., & Chang, Y. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.05.034 · Cited by 18

Mild Mitochondrial Uncoupling Decreases Experimental Atherosclerosis, A Proof of Concept

Dorighello, G. G., Rovani, J. C., Paim, B. A., Rentz, T., Assis, L. H. P., Vercesi, A. E., & Oliveira, H. C. F. (2021) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.62796 · Cited by 17

Effects of tributyrin and alanyl-glutamine dipeptide on intestinal health of largemouth bass (Micropterus salmoides) fed with high soybean meal diet

Zhao, J., Yang, X. X., Qiu, Z., Zhang, R., Xu, H., & Wang, T. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1140678 · Cited by 17

Efeitos moleculares do exercício físico sobre as vias de sinalização insulínica

Ropelle, E. R., Pauli, J. R., & Carvalheira, J. B. C. (2005) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · doi:10.5016/297 · Cited by 16

Evidence for organic cation transporter-mediated metformin transport and 5′-adenosine monophosphate-activated protein kinase activation in rat skeletal muscles

Oshima, R., Yamada, M., Kurogi, E., Ogino, Y., Serizawa, Y., Tsuda, S., Ma, X., Egawa, T., & Hayashi, T. (2014) · Metabolism · doi:10.1016/j.metabol.2014.10.037 · Cited by 17

AICAR stimulation metabolome widely mimics electrical contraction in isolated rat epitrochlearis muscle

Miyamoto, L., Egawa, T., Oshima, R., Kurogi, E., Tomida, Y., Tsuchiya, K., & Hayashi, T. (2013) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00162.2013 · Cited by 18

Diverse Signals Regulate Glucose Uptake into Skeletal Muscle

Wijesekara, N., Thong, F. S. L., Antonescu, C. N., & Klip, A. (2006) · Canadian Journal of Diabetes · doi:10.1016/s1499-2671(06)01006-9 · Cited by 16

Short-term metformin and exercise training effects on strength, aerobic capacity, glycemic control, and mitochondrial function in children with burn injury

Rivas, E., Herndon, D. N., Porter, C. C., Meyer, W. J., & Suman-Vejas, O. E. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00194.2017 · Cited by 17

Role of adipose tissue in the development of vascular complications in type 2 diabetes mellitus

Kowalska, I. (2007) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2007.10.007 · Cited by 17

Altered energy state reversibly controls smooth muscle contractile function in human saphenous vein during acute hypoxia–reoxygenation: Role of glycogen, AMP-activated protein kinase, and insulin-independent glucose uptake

Pyla, R., Pichavaram, P., Fairaq, A., Park, M. A., Kozak, M., Kamath, V. M., Patel, V. S., & Segar, L. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.06.036 · Cited by 16

Molecular Effects of Diphenyl Diselenide on Cholesterol and Glucose Cell Metabolism

da Rocha, J. T., Trapani, L., Segatto, M., Rosa, P. L., Nogueira, C. W., Zeni, G. R., & Pallottini, V. (2013) · Current Medicinal Chemistry · doi:10.2174/0929867311320350007 · Cited by 16

Insulin-mediated capillary recruitment in skeletal muscle: Is this a mediator of insulin action on glucose metabolism?

Rattigan, S., Barrett, E. J., & Clark, M. G. (2003) · Current Diabetes Reports · doi:10.1007/s11892-003-0063-4 · Cited by 15

Skeletal muscle glucose uptake during treadmill exercise in neuronal nitric oxide synthase-μ knockout mice

Hong, Y. H., Yang, C., Betik, A. C., Lee, R. S., & McConell, G. K. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00513.2015 · Cited by 15

Isoform-specific AMPK association with TBC1D1 is reduced by a mutation associated with severe obesity

Thomas, E. C., Hook, S. C., Gray, A., Chadt, A., Carling, D., Al‐Hasani, H., Heesom, K. J., Hardie, D. G., & Tavaré, J. M. (2018) · Biochemical Journal · doi:10.1042/bcj20180475 · Cited by 15

Adipose tissue-specific knockout of AMPKα1/α2 results in normal AICAR tolerance and glucose metabolism

Choi, R. H., McConahay, A., Johnson, M. B., Jeong, H., & Koh, H. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.09.049 · Cited by 16

Augmented Carbohydrate Oxidation under Moderate Hypobaric Hypoxia Equivalent to Simulated Altitude of 2500 m.

Goto, K., Morishima, T., Kurobe, K., Huang, Z., & Ogita, F. (2015) · Tohoku journal of experimental medicine · doi:10.1620/tjem.236.163 · Cited by 12

cDNA cloning and functional characterization of a novel splice variant of c-Cbl-associated protein from mouse skeletal muscle

Alcazar, O., Ho, R. C., FUJII, N. L., & Goodyear, L. J. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.03.038 · Cited by 15

Inhibition of calpain results in impaired contraction-stimulated GLUT4 translocation in skeletal muscle

Otani, K., Polonsky, K. S., Holloszy, J. O., & Han, D.-H. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00510.2005 · Cited by 14

Associations among adenosine monophosphate-activated protein kinase, glycolysis, muscle characteristics, and apoptosis in postmortem bovines longissimus muscle

Gao, Y., Zhang, J., He, L., Shi, X., Han, L., Yu, Q., Yang, Y., Song, R., Han, M., & Zhao, S. (2020) · European Food Research and Technology · doi:10.1007/s00217-020-03458-3 · Cited by 12

Skeletal muscle basal AMP-activated protein kinase activity is chronically elevated in alloxan-diabetic dogs: impact of exercise

Christopher, M., Chen, Z.-P., Rantzau, C., Kemp, B. E., & ALFORD, F. P. (2003) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00199.2003 · Cited by 14

AMP-activated protein kinase and familial Wolff–Parkinson–White syndrome: new perspectives on heart development and arrhythmogenesis

Gollob, M. H. (2002) · European Heart Journal · doi:10.1053/euhj.2001.2954 · Cited by 14

Contrasting effects of exercise, AICAR, and increased fatty acid supply on in vivo and skeletal muscle glucose metabolism

Rantzau, C., Christopher, M., & ALFORD, F. P. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00500.2007 · Cited by 14

The effects of exercise training under mild hypoxic conditions on body composition and circulating adiponectin in postmenopausal women

Nishiwaki, M., Kawakami, R., Saito, K., Tamaki, H., & Ogita, F. (2015) · Clinical Physiology and Functional Imaging · doi:10.1111/cpf.12252 · Cited by 13

Multiple AMPK activators inhibit l -carnitine uptake in C2C12 skeletal muscle myotubes

Shaw, A., Jeromson, S., Watterson, K. R., Pediani, J. D., Gallagher, I. J., Whalley, T., Dreczkowski, G., Brooks, N. E., Galloway, S. D. R., & Hamilton, D. L. (2017) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00026.2016 · Cited by 13

Hypoxic exposure can improve blood glycemic control in high-fat diet-induced obese mice

Park, Y., Jang, I., Park, H., Kim, J., & Lim, K. (2020) · Physical Activity and Nutrition · doi:10.20463/pan.2020.0004 · Cited by 13

Mitochondrial uncoupling protein 3 (UCP3) in skeletal muscle

Tsuboyama-Kasaoka, N. (2001) · Frontiers in bioscience · doi:10.2741/kasaoka · Cited by 14

Polyphenols in Regulation of Redox Signaling and Inflammation During Cardiovascular Diseases

Niu, L., He, X., Wang, Q., Fu, M., Xu, F., Xue, Y., Wang, Z., & An, X.-J. (2015) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-014-0492-5 · Cited by 13

Phytochemical regulation of Fyn and AMPK signaling circuitry

Lee, C. G., Koo, J. H., & Kim, S. G. (2015) · Archives of Pharmacal Research · doi:10.1007/s12272-015-0611-x · Cited by 12

Synthesis of TMPA Derivatives through Sequential Ir(III)-Catalyzed C–H Alkylation and Their Antidiabetic Evaluation

Lee, S. H., Kundu, A. B., Han, S. H., Mishra, N. K., Kim, K. S., Choi, M. H., Pandey, A. K., Park, J. S., Kim, H. S., & Kim, I. S. (2018) · ACS Omega · doi:10.1021/acsomega.8b00179 · Cited by 12

Decreased Insulin Secretion and Accumulation of Triglyceride in .BETA. Cells Overexpressing a Dominant-negative Form of AMP-activated Protein Kinase

Okazaki, Y., Kazuhiro, E. T. O., Yamashita, T., Okamoto, M., Ohsugi, M., Noda, M., Terauchi, Y., Ueki, K., & Kadowaki, T. (2010) · Endocrine Journal · doi:10.1507/endocrj.k09e-284 · Cited by 12

Acute systemic insulin intolerance does not alter the response of the Akt/GSK-3 pathway to environmental hypoxia in human skeletal muscle

D’Hulst, G., Sylow, L., Hespel, P., & Deldicque, L. (2015) · European Journal of Applied Physiology · doi:10.1007/s00421-015-3103-2 · Cited by 11

Peroxynitrite activates glucose uptake in 3T3-L1 adipocytes through a pi3-k-dependent mechanism

Alberto, M. G.-G. (2005) · Frontiers in bioscience · doi:10.2741/1505 · Cited by 11

Cytoplasmic signaling in the control of mitochondrial uproar?

Hermann, M., Kuznetsov, A. V., Maglione, M., Smigelskaite, J., Margreiter, R., & Troppmair, J. (2008) · Cell Communication and Signaling · doi:10.1186/1478-811x-6-4 · Cited by 11

Regulation of the exercise-induced expression of the monocarboxylate transporters MCT1 and MCT4 in skeletal muscle

Hamada, T., & Takimoto, M. (2013) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.2.85 · Cited by 10

AMPK'nin Biyokimyası: Etki Mekanizmaları ve Diyabetin Tedavisindeki Önemi

KİSMİROĞLU, C., CENGİZ, S., & Yaman, M. (2020) · European Journal of Science and Technology · doi:10.31590/ejosat.676335 · Cited by 11

Nitrite Activates 5′AMP-Activated Protein Kinase-Endothelial Nitric Oxide Synthase Pathway in Human Glomerular Endothelial Cells

Miyamoto, L., Yamane, M., Tomida, Y., Kono, M., Yamaoka, T., Kawasaki, A., Hatano, A., Tsuda, K., Xu, W., Ikeda, Y., et al. (2017) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b17-00316 · Cited by 10

Salicylate acutely stimulates 5′-AMP-activated protein kinase and insulin-independent glucose transport in rat skeletal muscles

Serizawa, Y., Oshima, R., Yoshida, M., Sakon, I., Kitani, K., Goto, A., Tsuda, S., & Hayashi, T. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.09.066 · Cited by 9

Kinase Activity Determination of Specific AMPK Complexes/Heterotrimers in the Skeletal Muscle

Birk, J. B., & Wojtaszewski, J. F. P. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7598-3_14 · Cited by 9

The long-term effects of anti-retroviral protease inhibitors on sugar transport in L6 cells

Germinario, R. J., Colby-Germinario, S. P., Cammalleri, C., & Wainberg, M. A. (2003) · Journal of Endocrinology · doi:10.1677/joe.0.1780449 · Cited by 9

Glicocorticóides e síndrome metabólica: aspectos favoráveis do exercício físico nesta patofisiologia

Pauli, J. R., Souza, L. S., Rogatto, G. P., Gomes, R., & Luciano, E. (2006) · Revista Portuguesa de Ciências do Desporto · doi:10.5628/rpcd.06.02.217 · Cited by 10

Does impaired mitochondrial function affect insulin signaling and action in cultured human skeletal muscle cells?

Brown, A. E., Elstner, M., Yeaman, S. J., Turnbull, D. M., & Walker, M. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00267.2007 · Cited by 8

Effects of Simulated High Altitude on Blood Glucose Levels During Exercise in Individuals With Type 1 Diabetes

Dugan, C., Maloney, S. K., Abramoff, K. J., Panag, S. S., Davis, E. A., Jones, T. W., & Fournier, P. A. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgab881 · Cited by 8

CREG1 stimulates AMPK phosphorylation and glucose uptake in skeletal muscle cells

Goto, A., Endo, Y., & Yamashita, H. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.12.028 · Cited by 8

Antihyperglycaemic activity of 2,4:3,5‐dibenzylidene‐D‐xylose‐diethyl dithioacetal in diabetic mice

Gruzman, A., Elgart, A., Viskind, O., Billauer, H., Dotan, S., Cohen, G., Mishani, E., Hoffman, A., Cerasi, E., & Sasson, S. (2011) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2011.01340.x · Cited by 8

Simple thermodynamic model of unassisted proton shuttle uncoupling and prediction of activity from calculated speciation, lipophilicity, and molecular geometry

Martineau, L. C. (2012) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2012.02.032 · Cited by 8

Progressive Resistance Training as Complementary Therapy for Polycystic Ovarian Syndrome

Kogure, G. S., & dos Reis, R. M. (2017) · Revista Brasileira Ginecologia e Obstetrícia · doi:10.1055/s-0037-1602705 · Cited by 12

Role of PKC and AMPK in hypertonicity-stimulated water reabsorption in rat inner medullary collecting ducts

Liwang, J. K., Ruiz, J. A., LaRocque, L. M., Rianto, F., Ma, F., & Wang, Y. (2018) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00491.2017 · Cited by 8

Differentiation-Inducing Factor 1 Activates Cofilin Through Pyridoxal Phosphatase and AMP-Activated Protein Kinase, Resulting in Mitochondrial Fission

Inoue, T., Miura, K., Han, R., Tetsuo, F., Arioka, M., Igawa, K., Tomooka, K., & Sasaguri, T. (2022) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2023.02.009 · Cited by 8

AICAR reverses ketone body mediated insulin resistance in isolated oxidative muscle

Ivarsson, N., Zhang, S., & Katz, A. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.09.122 · Cited by 8

Regulatory Mechanism of Skeletal Muscle Glucose Transport by Phenolic Acids

Egawa, T., Tsuda, S., Oshima, R., Goto, A., Ma, X., Goto, K., & Hayashi, T. (2017) · InTech eBooks · doi:10.5772/65968 · Cited by 10

Up-regulation of lipolysis genes and increased production of AMP-activated protein kinase protein in the skeletal muscle of rats after resistance training

An, J.-H., Yoon, J.-H., Suk, M., & Shin, Y. (2016) · Journal of Exercise Rehabilitation · doi:10.12965/jer.1632578.289 · Cited by 7

AMPK as a Metabolic Intersection between Diet and Physical Exercise

Miyamoto, L. (2018) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.18-00091-6 · Cited by 7

Ectopic Fat Accumulation and Glucose Homeostasis: Role of Leptin in Glucose and Lipid Metabolism and Mass Maintenance in Skeletal Muscle

Morioka, T., Mori, K., Motoyama, K., & Emoto, M. (2016) · Springer eBooks · doi:10.1007/978-4-431-55720-3_14 · Cited by 9

An improved glucose transport assay system for isolated mouse skeletal muscle tissues

Inagaki, A., Maruo, K., Furuichi, Y., Miyatake, S., Tamura, K., FUJII, N. L., & Manabe, Y. (2016) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2016.1210503 · Cited by 6

Lipophilicity as a determinant of thiazolidinedione action in vitro: findings from BLX-1002, a novel compound without affinity to PPARs

Brunmair, B., Staniek, K., Lehner, Z., Dey, D., Bolten, C. W., Stadlbauer, K., Luger, A., & Fürnsinn, C. (2011) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00401.2010 · Cited by 6

Experimental research models for skeletal muscle contraction

Manabe, Y., & FUJII, N. L. (2016) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.5.373 · Cited by 6

Exercise Regulation of Insulin Action in Skeletal Muscle

Ho, R. C., Alcazar, O., & Goodyear, L. J. (2005) · Wiley eBooks · doi:10.1002/9780470757826.ch27 · Cited by 6

Alpha-ketoglutaric acid mitigates the detrimental effects of soy antigenic protein on the intestinal health and growth performance of Mirror carp Cyprinus carpio

Zhou, Z., Zhao, J., de Cruz, C. R., Xu, H. T., Wang, L., & Xu, Q. (2023) · Fish Physiology and Biochemistry · doi:10.1007/s10695-023-01234-0 · Cited by 5

Novel Strategies for Treating Lifestyle-related Diseases Using Various Approaches

Miyamoto, L. (2016) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.15-00251 · Cited by 5

Potential Benefits of Glitazones for Cancer and Vascular Disease

Pérez-Ortiz, J., Llorens, S., Llopis, J., Tranque, P., & Nava, E. (2008) · Current Drug Therapy · doi:10.2174/157488508784221271 · Cited by 4

Coptidis Rhizoma Water Extract Stimulates 5′-AMP-Activated Protein Kinase in Rat Skeletal Muscle

Tatsuro, Egawa, T., Oshima, R., Oshima, Eriko, Kurogi, Hiroko, Tanabe, Satoshi, S., Tsuda, et al. (2011) · Chinese Journal of Natural Medicines · doi:10.3724/sp.j.1009.2011.00215 · Cited by 4

The Effects of Normobaric Hypoxia on the Acute Physiological Responses to Resistance Training: A Narrative Review

Allsopp, G. L., Britto, F. A., Wright, C. R., & Deldicque, L. (2024) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0000000000004909 · Cited by 4

Significance of 5’AMP-activated protein kinase in metabolomic regulation by skeletal muscle contraction

Miyamoto, L. (2015) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.4.93 · Cited by 5

Forelimb Resistance Exercise Protects Against Neuromuscular Junction Denervation in the SOD1-G93A Rat Model of ALS

Nishimune, H., Stanford, K. G., Chen, J., Odum, J. D., Rorie, A. D., Rogers, R. S., Wheatley, J. L., Geiger, P. C., & Stanford, J. A. (2022) · Degenerative Neurological and Neuromuscular Disease · doi:10.2147/dnnd.s388455 · Cited by 4

Roles of adenosine monophosphate–activated protein kinase in skeletal muscle: fatty acid oxidation, glucose transport, and gene regulation

Winder, W. W. (2001) · Current Opinion in Endocrinology & Diabetes · doi:10.1097/00060793-200108000-00003 · Cited by 4

Nutritional interventions to promote post-exercise muscle protein synthesis

Koopman, R. (2006) · Research Publications (Maastricht University) · doi:10.26481/dis.20060622rk · Cited by 4

Activation of 5′AMP-activated protein kinase in skeletal muscle by exercise and phytochemicals

Egawa, T., Tsuda, S., Oshima, R., Goto, K., & Hayashi, T. (2014) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.3.55 · Cited by 3

Maternal Diet and Exercise: Influences on Obesity and Insulin Resistance

Carter, L. G., Tamashiro, K. L., & Pearson, K. J. (2014) · Oxidative stress and disease · doi:10.1201/b17530-4 · Cited by 3

Ethylacetate extracts of the muscles of Anguilla japonica suppress glucose levels in db/db mice via activation of AMP-activated protein kinase

Jeong, Y., Yang, J., Li, X., Kim, G. J., Kim, D. S., Kim, C., Na, M. K., & Chang, H. W. (2014) · Food Science and Biotechnology · doi:10.1007/s10068-014-0231-0 · Cited by 2

Mechanism of Skeletal Muscle Contraction: Intracellular Signaling in Skeletal Muscle Contraction

Manabe, Y. (2016) · Springer eBooks · doi:10.1007/978-4-431-55720-3_10 · Cited by 2

Protective and multi-organ effects of MOTS-c and other mitochondrial-derived peptides in the endocrine system

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Effects of dietary α-ketoglutarate supplementation on growth performance, digestive enzyme activity, immune gene expression, and intestinal morphology of largemouth bass (Micropterus salmoides) fed high soybean diet

Zheng, D., Yang, X. X., Liang, J. F., Zhao, J., & Xu, Q. (2025) · Aquaculture Reports · doi:10.1016/j.aqrep.2025.102706 · Cited by 2

Short bouts of hypoxia improve insulin sensitivity in adults with type 2 diabetes

Zhao, J., Massoudian, S. D., Stray-Gundersen, S. O., Wojan, F., & Lalande, S. (2025) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00932.2024 · Cited by 2

Synthesis of a Methylene Analog of 5-Amino-1-β- D -ribofuranosylimidazole-4-carboxamide Monophosphate (ZMP)

Kohyama, N., Hayashi, T., & Yamamoto, Y. (2005) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.69.836 · Cited by 2

Regulation of glucose transport in skeletal muscle during and after exercise

Kawanaka, K. (2012) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.1.563 · Cited by 2

Possible Role of Cellular Polyamine Metabolism in Neuronal Apoptosis

Ji, X., Yu, W., Jin, M.-J., Lu, L., Yin, H., & Wang, H. (2024) · Current Medical Science · doi:10.1007/s11596-024-2843-9 · Cited by 2

Effects of Heat Stress on Energetic Metabolism in Rats

Sanders, S. R. (2010) · UA Campus Repository (The University of Arizona) · Cited by 2

Ischaemia and insulin, but not ischaemia and contraction, act synergistically in stimulating muscle glucose uptake in vivo in humans

Bosselaar, M., Smits, P., & Tack, C. J. (2008) · Clinical Science · doi:10.1042/cs20080087 · Cited by 2

Offspring and Maternal Health Benefits of Exercise during Pregnancy

Carter, L. G. (2013) · UKnowledge (University of Kentucky) · Cited by 1

Extracellular hyperosmotic stress stimulates glucose uptake in incubated fast-twitch rat skeletal muscle

Farlinger, C. M., Lui, A. J., Harrison, R. C., LeBlanc, P. J., Peters, S. J., & Roy, B. D. (2013) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2012-0236 · Cited by 1

Metabolic and endocrine responses to hypoxic exposure

Goto, K. (2013) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.2.215 · Cited by 1

Constitutive activation of AMP-activated protein kinase (AMPK) propel mitochondrial biogenesis

Paul, B. B., Afsar, U. A., & Paul, R. F. (2014) · Journal of Cell Biology and Genetics · doi:10.5897/jcbg2013.0037 · Cited by 1

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Evidence for 5' AMP-activated protein kinase mediation of the effect of muscle contraction on glucose transport

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Effect of AMPK activation on muscle glucose metabolism in conscious rats

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Possible involvement of the α1 isoform of 5′AMP-activated protein kinase in oxidative stress-stimulated glucose transport in skeletal muscle

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