Measurement of Plasma Glucose, Free Fatty Acid, Lactate, and Insulin for 24 h in Patients With NIDDM

Decrease in malate dehydrogenase activities in peripheral leucocytes of type 1 diabetic dogs

Arai, T., Nakamura, M., Magori, E., Fukuda, H., & Sako, T. (2003) · Research in Veterinary Science · doi:10.1016/s0034-5288(02)00177-7 · Cited by 15

Chronic exposure to high fatty acids impedes receptor agonist-induced nitric oxide production and increments of cytosolic Ca2+ levels in endothelial cells

Tang, Y., & Li, G. (2011) · Journal of Molecular Endocrinology · doi:10.1530/jme-11-0082 · Cited by 15

Metabolic and Molecular Pathogenesis of Type 2 Diabetes Mellitus

DeFronzo, R. A., Mandarino, L. J., & Ferrannini, E. (2003) · Wiley eBooks · doi:10.1002/0470862092.d0310 · Cited by 15

Lipidomics Analysis of Free Fatty Acids in Human Plasma of Healthy and Diabetic Subjects by Liquid Chromatography-High Resolution Mass Spectrometry (LC-HRMS)

Kokotou, M. G., Mantzourani, C., Batsika, C. S., Mountanea, O. G., Eleftheriadou, I., Kosta, O. A., Tentolouris, N., & Kokotos, G. (2022) · Biomedicines · doi:10.3390/biomedicines10051189 · Cited by 18

Stearic acid‐induced cardiac lipotoxicity is independent of cellular lipid and is mitigated by the fatty acids oleic and capric acid but not by the PPAR agonist troglitazone

Rabkin, S. W., & Lodha, P. (2009) · Experimental Physiology · doi:10.1113/expphysiol.2009.048082 · Cited by 14

Obese type 2 diabetics and obese patients have comparable plasma phospholipid fatty acid compositions deviating from that of healthy individuals

Rodríguez, Y., Giri, M., Rottiers, R., & Christophe, A. (2004) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2004.04.004 · Cited by 14

Elevation in Intracellular Long-Chain Acyl-Coenzyme A Esters Lead to Reduced β-Cell Excitability via Activation of Adenosine 5′-Triphosphate-Sensitive Potassium Channels

Webster, N. J., Searle, G. J., Lam, P. P. L., Huang, Y., Riedel, M. J., Harb, G., Gaisano, H. Y., Holt, A., & Light, P. E. (2008) · Endocrinology · doi:10.1210/en.2007-1138 · Cited by 14

Palmitate induces RIP1-dependent necrosis in RAW 264.7 cells

Kim, S. K., Seo, G., Oh, E., Jin, S.-H., Chae, G. T., & Lee, S. (2012) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2012.09.021 · Cited by 14

Proinsulin maturation disorder is a contributor to the defect of subsequent conversion to insulin in β-cells

Wang, J., & Osei, K. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.06.119 · Cited by 15

Effect of dietary vegetable oil consumption on blood glucose levels, lipid profile and weight in diabetic mice: an experimental case—control study

Ngala, R. A., Ampong, I., Sakyi, S. A., & Anto, E. O. (2016) · BMC Nutrition · doi:10.1186/s40795-016-0053-y · Cited by 16

Genetic variants and clinical relevance associated with gestational diabetes mellitus in Chinese women: a case-control study

Yan, J., Su, R., Ao, D., Wang, Y., Wang, H., & Yang, H. (2017) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767058.2017.1336225 · Cited by 13

Histone deacetylase inhibition of cardiac autophagy in rats on a high‑fat diet with low‑dose streptozotocin-induced type 2 diabetes mellitus

Lee, T., Bai, K., Chen, Y., Lee, T., Chung, C., Tsai, W., Tsao, S., & Kao, Y. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7905 · Cited by 14

Insulin Sensitivity is Related to Fat Oxidation and Protein Kinase C Activity in Children With Acute Burn Injury

Cree‐Green, M., Zwetsloot, J. J., Herndon, D. N., Newcomer, B. R., Fram, R. Y., Angel, C. A., Green, J. M., Dohm, G. L., Sun, D., Aarsland, A. A., et al. (2008) · Journal of Burn Care & Research · doi:10.1097/bcr.0b013e31817db88f · Cited by 14

Fatty Acids Differentially Modulate Insulin-Stimulated Endothelial Nitric Oxide Production by an Akt-Independent Pathway

Lynn, M. A., Rupnow, H. L., Kleinhenz, D. J., Kanner, W. A., Dudley, S. C., & Hart, C. M. (2004) · Journal of Investigative Medicine · doi:10.1136/jim-52-02-22 · Cited by 14

New insights into lactate in exercise adaptations: does protein lactylation play a role?

Wang, Z., & Zhu, L. (2025) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00225.2025 · Cited by 17

Distinct Shift in Beta-Cell Glutaredoxin 5 Expression Is Mediated by Hypoxia and Lipotoxicity Both In Vivo and In Vitro

Petry, S. F., Sun, L. M., Knapp, A., Reinl, S., & Linn, T. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00084 · Cited by 13

Macrophage-derived secretome is sufficient to confer olanzapine-mediated insulin resistance in human adipocytes

Dipta, P., Sarsenbayeva, A., Shmuel, M., Forno, F., Eriksson, J. W., Pereira, M. J., Abalo, X. M., Wabitsch, M., Thaysen‐Andersen, M., & Tirosh, B. (2021) · Comprehensive Psychoneuroendocrinology · doi:10.1016/j.cpnec.2021.100073 · Cited by 13

Unsaturated fatty acids repress the expression of ATP-binding cassette transporter A1 in HepG2 and FHs 74 Int cells

Ku, C. S., Rasmussen, H. E., Park, Y., Jesch, E. D., & Lee, J. (2011) · Nutrition Research · doi:10.1016/j.nutres.2011.03.007 · Cited by 13

The effect of an acute elevation of NEFA concentrations on glucagon-stimulated hepatic glucose output

Grueter, C. A., Edgerton, D. S., Donahue, E. P., Vaughan, S., Chu, C. A., Sindelar, D. K., & Cherrington, A. D. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00043.2006 · Cited by 13

Dosage plan of a flurbiprofen injection product using inhibition of protein binding by lipid emulsion in rats

Ogata, K., Takamura, N., Tokunaga, J., Kawai, K., Arimori, K., & Higuchi, S. (2007) · Journal of Pharmacy and Pharmacology · doi:10.1211/jpp.60.1.0002 · Cited by 13

Addition of basal insulin to oral antidiabetic agents: a goal-directed approach to type 2 diabetes therapy.

Kuritzky, L. (2006) · PubMed Central · Cited by 13

Fatty Acid Metabolism in the Heart Following Diabetes

Lopaschuk, G. D. (1996) · Developments in cardiovascular medicine · doi:10.1007/978-1-4613-1269-7_10 · Cited by 13

Dehydroepiandrosterone Alters Zucker Rat Soleus and Cardiac Muscle Lipid Profiles

Abadie, J. M., Malcom, G. T., Porter, J. R., & Svec, F. (2001) · Experimental Biology and Medicine · doi:10.1177/153537020222600811 · Cited by 12

Low-grade metabolic acidosis as a driver of insulin resistance

DiNicolantonio, J. J., & O’Keefe, J. H. (2021) · Open Heart · doi:10.1136/openhrt-2021-001788 · Cited by 12

Fatty acids induce increased granulocyte macrophage‐colony stimulating factor secretion through protein kinase C‐activation in THP‐1 macrophages

Bahramian, N., Östergren‐Lundén, G., Bondjers, G., & Olsson, U. (2004) · Lipids · doi:10.1007/s11745-004-1226-2 · Cited by 12

High Plasma Free Fatty Acids Decrease Splanchnic Glucose Uptake in Patients with Non-Insulin-Dependent Diabetes Mellitus.

Tomita, T., Yamasaki, Y., Kubota, M., Tohdo, R., Katsura, M., IKEDA, M., Nakahara, I., Shiba, Y., Matsuhisa, M., & HORI, M. (1998) · Endocrine Journal · doi:10.1507/endocrj.45.165 · Cited by 13

Mechanisms of the glucose lowering effect of a carnitine palmitoyl transferase inhibitor in normal and diabetic rats

Martin, C., Odeon, M., Cohen, R., & Beylot, M. (1991) · Metabolism · doi:10.1016/0026-0495(91)90154-o · Cited by 12

Malonyl Coa Control of Fatty Acid Oxidation in the Diabetic Rat Heart

Lopaschuk, G. D. (2001) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-1321-6_21 · Cited by 12

Effects of insulin and free fatty acids on matrix metalloproteinases

Boden, G. H., & Song, W. (2008) · Current Diabetes Reports · doi:10.1007/s11892-008-0041-y · Cited by 12

Lactate promotes fatty acid oxidation by the tricarboxylic acid cycle and mitochondrial respiration in muscles of obese mice

Park, S.-Y., Jung, S., Kim, J.-Y., Kim, Y.-W., Sung, H., Park, S., Doh, K., & Koh, J. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00060.2024 · Cited by 12

Saturated fatty acids bound to albumin enhance osteopontin expression and cleavage in renal proximal tubular cells.

Cobbs, A., Ballou, K., Chen, X., George, J., & Zhao, X. (2018) · PubMed Central · Cited by 11

Marine Bromophenol Derivative 3,4-Dibromo-5-(2-bromo-3,4-dihydroxy-6-isopropoxymethyl benzyl)benzene-1,2-diol Protects Hepatocytes from Lipid-Induced Cell Damage and Insulin Resistance via PTP1B Inhibition

Luo, J., Wu, N., Jiang, B., Wang, L., Wang, S., Li, X., Wang, B., Wang, C., & Shi, D. (2015) · Marine Drugs · doi:10.3390/md13074452 · Cited by 11

Comparison of the effects of glimepiride and glibenclamide on adipose tissue tumour necrosis factor‐α mRNA expression and cellularity

Mori, Y., Komiya, H., Kurokawa, N., & Tajima, N. (2003) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2004.00305.x · Cited by 11

Plasma free fatty acids do not provide the link between obesity and insulin resistance or β‐cell dysfunction: results of the Reading, Imperial, Surrey, Cambridge, Kings ( RISCK ) study

Johns, I., Goff, L. M., Bluck, L. J. C., Griffin, B. A., Jebb, S. A., Lovegrove, J. A., Sanders, T. A. B., Frost, G. S., & Dornhorst, A. (2014) · Diabetic Medicine · doi:10.1111/dme.12550 · Cited by 11

Diabetic Risk Factors Promote Islet Amyloid Polypeptide Misfolding by a Common, Membrane-mediated Mechanism

Okada, A. K., Teranishi, K., Isas, J. M., Bedrood, S., Chow, R. H.-P., & Langen, R. (2016) · Scientific Reports · doi:10.1038/srep31094 · Cited by 11

Palmitate induces RIP1/RIP3-dependent necrosis via MLKL-mediated pore formation in the plasma membrane of RAW 264.7 cells

Kim, S. K., Yun, M., Seo, G., Lee, J., & Lee, S. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.11.068 · Cited by 11

Association between the membrane transporter proteins and type 2 diabetes mellitus

Saha, S. (2020) · Expert Review of Clinical Pharmacology · doi:10.1080/17512433.2020.1729125 · Cited by 12

Obesity and the Risk of Low Bicarbonate: A Cohort Study

Lambert, D. C., & Abramowitz, M. K. (2021) · Kidney Medicine · doi:10.1016/j.xkme.2021.02.006 · Cited by 11

Nonesterified fatty acid exposure activates protective and mitogenic pathways in vascular smooth muscle cells by alternate signaling pathways

Schauer, I. E., & Reusch, J. E. B. (2009) · Metabolism · doi:10.1016/j.metabol.2008.10.003 · Cited by 12

Magnetic resonance spectroscopy shows an inverse correlation between intramyocellular lipid content in human calf muscle and local glycogen synthesis rate

van der Graaf, M., Tack, C. J., de Haan, J. H., Klomp, D. W. J., & Heerschap, A. (2009) · NMR in Biomedicine · doi:10.1002/nbm.1433 · Cited by 11

Islet transplantation improves glucose oxidation and mechanical function in diabetic rat hearts

Lopaschuk, G. D., Lakey, J. R. T., Barr, R. L., Wambolt, R. B., Thomson, A. B. R., Clandinin, M. T., & Rajotte, R. V. (1993) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y93-136 · Cited by 11

Rôle des acides gras libres dans la sécrétion et l’action de l’insuline: mécanismes de la lipotoxicité

Girard, J. R. (2003) · Érudit (Université de Montréal) · doi:10.7202/007112ar · Cited by 11

The Pathophysiological Consequences of Adipose Tissue Insulin Resistance

Reaven, G. M. (1999) · Humana Press eBooks · doi:10.1007/978-1-59259-716-1_12 · Cited by 11

Comparison of the efficacy and safety of insulin degludec/aspart (twice-daily injections), insulin glargine 300 u/ml, and insulin glulisine (basal-bolus therapy)

Kawaguchi, Y., Sawa, J., Hamai, C., Nishimura, Y., & Kumeda, Y. (2019) · Journal of Diabetes Investigation · doi:10.1111/jdi.13038 · Cited by 10

A battery-free smart mask for long-term exhaled breath biochemical sensing

Heng, W., Putz, C., Tang, W., Min, J., Lehner, L. E., Demchyshyn, S., Kim, G., Wang, C., Hailegnaw, B., Rippatha, E., et al. (2026) · Nature Sensors · doi:10.1038/s44460-026-00041-3 · Cited by 10

Palmitate induces COX-2 expression via the sphingolipid pathway-mediated activation of NF-κB, p38, and ERK in human dermal fibroblasts

Oh, E., Yun, M., Kim, S. K., Seo, G., Bae, J. S., Joo, K. W., Chae, G. T., & Lee, S. (2013) · Archives of Dermatological Research · doi:10.1007/s00403-013-1434-6 · Cited by 10

Prevention of Elevation in Plasma Triacylglycerol with High-Dose Bezafibrate Treatment Abolishes Insulin Resistance and Attenuates Glucose Intolerance Induced by Short-Term Treatment with Dexamethasone in Rats

Inácio, M. D., Rafacho, A., Camaforte, N. A. D. P., Teixeira, P., Vareda, P. M. P., Violato, N. M., & Bosqueiro, J. R. (2018) · International Journal of Endocrinology · doi:10.1155/2018/3257812 · Cited by 10

A computational model of the effects of macronutrients absorption and physical exercise on hormonal regulation and metabolic homeostasis

Palumbo, M. C., de Graaf, A. D., Morettini, M., Tieri, P., Krishnan, S., & Castiglione, F. (2023) · Comput. Biol. Medicine · doi:10.1016/j.compbiomed.2023.107158 · Cited by 9

Nuclear factor-κB is a common upstream signal for growth differentiation factor-5 expression in brown adipocytes exposed to pro-inflammatory cytokines and palmitate

Hinoi, E., Iezaki, T., Ozaki, K., & Yoneda, Y. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.09.022 · Cited by 10

Effects of acute exercise on lipid content and dietary lipid uptake in liver and skeletal muscle of lean and diabetic rats

Janssens, S., Jonkers, R. A. M., Groen, A. K., Nicolay, K., van Loon, L. J. C., & Prompers, J. J. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00292.2015 · Cited by 11

Clove and Its Active Compound Attenuate Free Fatty Acid-Mediated Insulin Resistance in Skeletal Muscle Cells and in Mice

Ghaffar, S., Afridi, S. K., Aftab, M. F., Murtaza, M., Hafizur, R. M., Sara, S., Begum, S., & Waraich, R. S. (2017) · Journal of Medicinal Food · doi:10.1089/jmf.2016.3835 · Cited by 10

Association of Proteins Modulating Immune Response and Insulin Clearance during Gestation with Antenatal Complications in Patients with Gestational or Type 2 Diabetes Mellitus

Kopylov, A. T., Kaysheva, A. L., Папышева, О. В., Gribova, I., Kotaysch, G., Харитонова, Л. А., Mayatskaya, T., Krasheninnikova, A., & Morozov, S. (2020) · Cells · doi:10.3390/cells9041032 · Cited by 10

The assessment of potentially interfering metabolites and dietary components in blood using an osmotic glucose sensor based on the concanavalin A–dextran affinity assay

Krushinitskaya, O., Tønnessen, T. I., Jakobsen, H., & Johannessen, E. A. (2011) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2011.07.019 · Cited by 10

Effects on blood glucose, insulin, lipid and proatherosclerotic parameters in stable type 2 diabetic subjects during an oral fat challenge.

Wu, C.-J., & Yu, Z. (2004) · Lipids in Health and Disease · doi:10.1186/1476-511x-3-17 · Cited by 10

Lactic acid and lactates

Schreurs, V. V. A. M., & Schaafsma, G. (2010) · Nutrafoods · doi:10.1007/bf03223326 · Cited by 10

The role of nonesterified fatty acids in pathogenesis of cardiovascular diseases

Tsvetkova, M. V., Хирманов, В. Н., & Zybina, N. N. (2010) · Arterial’naya Gipertenziya (Arterial Hypertension) · doi:10.18705/1607-419x-2010-16-1-93-103 · Cited by 10

Effects of different lipid substrates on glucose metabolism in normal postabsorptive humans

Broussolle, C., Beylot, M., CHASSARD, D., & Beaufrère, B. (1992) · Metabolism · doi:10.1016/0026-0495(92)90096-s · Cited by 10

Serum levels of unbound free fatty acids. I: Normative data in term newborn infants.

Patel, M. N., Kleinfeld, A. M., Richeiri, G. V., Ruben, S., Hiatt, M., & Hegyi, T. (1997) · Journal of the American College of Nutrition · doi:10.1080/07315724.1997.10718653 · Cited by 10

The effect of free fatty acids on spectrin organization in lymphocytes

Fd, S., Yokota, S. J., & Repasky, E. A. (1990) · Cell Biophysics · doi:10.1007/bf02990722 · Cited by 10

Gender differences of disturbed hemostasis related to fasting insulin level in healthy very elderly Japanese aged ≥75 years

Kario, K. (1995) · Atherosclerosis · doi:10.1016/0021-9150(95)05544-7 · Cited by 9

Oleic Acid Activates Mitochondrial Energy Metabolism and Reduces Oxidative Stress Resistance in the Pancreatic β-Cell Line INS-1

Suzuki, M., Endo, K., Nagata, R., & Iida‐Tanaka, N. (2023) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b23-00559 · Cited by 9

Increased molar ratio of free fatty acids to albumin in blood as cause and early biomarker for the development of cataracts and Alzheimer's disease

Glaesser, D., & Iwig, M. (2024) · Experimental Eye Research · doi:10.1016/j.exer.2024.109888 · Cited by 9

A novel therapeutic target, GPR43; Where it stands in drug discovery

Kim, S., Kim, Y., & Kwak, Y. (2012) · Archives of Pharmacal Research · doi:10.1007/s12272-012-0900-6 · Cited by 9

Exendin-4 Promotes Survival of Mouse Pancreaticβ-Cell Line in Lipotoxic Conditions, through the Extracellular Signal-Related Kinase 1/2 Pathway

Gu, J., Wei, Q., Zheng, H., Meng, X., Zhang, J., & Wang, D. (2016) · Journal of Diabetes Research · doi:10.1155/2016/5294025 · Cited by 9

Effect of Crocetin on Basal Lipolysis in 3T3-L1 Adipocytes

Cimas, F. J., de la Cruz-Morcillo, M. Á., Cifuentes, C., Moratalla‐López, N., Alonso, G. L., Nava, E., & Llorens, S. (2023) · Antioxidants · doi:10.3390/antiox12061254 · Cited by 9

Associations between common polymorphisms of adenosine triphosphate-binding cassette transporter A1 and coronary artery disease in a Tunisian population

Rejeb, J., Omezzine, A., Rebhi, L., Boumaiza, I., Kchock, K., Belkahla, R., Rejeb, N. B., Nabli, N., Abdelaziz, A. B., Boughzala, E., et al. (2010) · Archives of cardiovascular diseases · doi:10.1016/j.acvd.2010.10.003 · Cited by 9

An assessment of the in vivo efficacy of the glycogen phosphorylase inhibitor GPi688 in rat models of hyperglycaemia

Poucher, S. M., Freeman, S., Loxham, S. J. G., Convey, G., Bartlett, J. B., de Schoolmeester, J., Teague, J., Walker, M., Turnbull, A. V., Charles, A., et al. (2007) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707502 · Cited by 9

Differential Telomere Shortening in Blood versus Arteries in an Animal Model of Type 2 Diabetes

Tajbakhsh, S., Aliakbari, K., Hussey, D. J., Lower, K. M., Donato, A. J., & Sokoya, E. M. (2015) · Journal of Diabetes Research · doi:10.1155/2015/153829 · Cited by 9

Heat Shock Protein 90β1 Is Essential for Polyunsaturated Fatty Acid-induced Mitochondrial Ca2+ Efflux

Zhang, H., Li, Z.-H., Zhang, M. Q., Katz, M. S., & Zhang, B.-X. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m707192200 · Cited by 9

Acipimox Acutely Increases GLP-1 Concentrations in Overweight Subjects and Hypopituitary Patients

Vestergaard, E. T., Hjelholt, A. J., Kuhre, R. E., Møller, N., Larraufie, P., Gribble, F. M., Reimann, F. M., Jessen, N., Holst, J. J., & Jørgensen, J. O. L. (2019) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-02503 · Cited by 9

Dehydroepiandrosterone alters lipid profiles in Zucker rats

Abadie, J. M., Malcom, G. T., Porter, J. R., & Svec, F. (2000) · Lipids · doi:10.1007/s11745-000-0564-4 · Cited by 9

Free Fatty Acids, A Major Link Between Obesity, Insulin Resistance, Inflammation, and Atherosclerotic Vascular Disease

Boden, G. H. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-141-3_4 · Cited by 8

Linoleic Acid Attenuates Endothelium-Derived Relaxing Factor Production by Suppressing cAMP-Hydrolyzing Phosphodiesterase Activity

Wei, J., Takeuchi, K., & Watanabe, H. (2013) · Circulation Journal · doi:10.1253/circj.cj-13-0248 · Cited by 8

Glycemic control after metabolic surgery: a Granger causality and graph analysis

Previti, E., Salinari, S., BERTUZZI, A., Capristo, E., Bornstein, S. R., & Mingrone, G. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00042.2017 · Cited by 8

Palmitate exacerbates bisphenol A toxicity via induction of ER stress and mitochondrial dysfunction

Mondal, A., Burchat, N., & Sampath, H. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2020.158816 · Cited by 8

The Gut Microbiome and Type 2 Diabetes Mellitus

Panwar, S., Arora, S., Sharma, S., & Tripathi, P. (2020) · Springer eBooks · doi:10.1007/978-3-030-53370-0_21 · Cited by 8

The metabolic syndrome: evolving evidence that thiazolidinediones provide rational therapy

Wyne, K. L. (2006) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2005.00522.x · Cited by 8

Elevated Adipose Triglyceride Lipase in Newly Diagnosed Type 2 Diabetes Mellitus With Hypertension

Xu, S., Li, L., Yang, G., Yang, M., Li, S., & Liu, H. (2011) · The American Journal of the Medical Sciences · doi:10.1097/maj.0b013e318218482f · Cited by 8

Integrated analysis of chronic lipotoxicity on muscle metabolism and stress and its reversal by antioxidants

Verma, M. K., Yateesh, A. N., Smitha, R., Neelima, K., Pallavi, P. M., Reddy, M., Poornima, J., Oommen, A. M., Jagannath, M. R., & Somesh, B. P. (2014) · SpringerPlus · doi:10.1186/2193-1801-3-251 · Cited by 8

Metabolic responses, performance, and reticuloruminal pH of early-lactating cows fed concentrates treated with lactic acid, with or without inorganic phosphorus supplementation

Khol‐Parisini, A., Humer, E. C., Harder, H., Mickdam, E., & Zebeli, Q. (2016) · Journal of Dairy Science · doi:10.3168/jds.2016-11208 · Cited by 8

Arachidonic acid inhibits the production of angiotensin-converting enzyme in human primary adipocytes via a NF-κB-dependent pathway

Li, X., Schüler, R., Xu, C., Seebeck, N., Markova, M., Murahovschi, V., & Pfeiffer, A. F. H. (2020) · Annals of Translational Medicine · doi:10.21037/atm-20-7514 · Cited by 7

Peroxisome proliferator‐activated receptor gamma agonism modifies the effects of growth hormone on lipolysis and insulin sensitivity

Krag, M. B., Nielsen, S., Guo, Z., Pedersen, S. B., Schmitz, O., Christiansen, J. S., & Jørgensen, J. O. L. (2008) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2008.03231.x · Cited by 8

Utility of metformin as an adjunct to hydroxycitrate/carnitine for reducing body fat in diabetics

McCarty, M. F. (1998) · Medical Hypotheses · doi:10.1016/s0306-9877(98)90035-4 · Cited by 8

Role of ectopic fat in the pathogenesis of insulin resistance

Kantartzis, K., Totsikas, C., Häring, H., & Stefan, N. (2009) · Clinical Lipidology · doi:10.2217/clp.09.35 · Cited by 7

Palmitate Stimulates the Epithelial Sodium Channel by Elevating Intracellular Calcium, Reactive Oxygen Species, and Phosphoinositide 3‐Kinase Activity

Wang, Q., Chen, L., Niu, N., Yang, X., Chen, X., Song, B., Yu, C., Wu, M., Zhang, Z., & Ma, H. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/7560610 · Cited by 7

Ventricular Dysfunction in Obese and Nonobese Rats with Metabolic Syndrome

Torres-Jácome, J., Ortiz-Fuentes, B. S., Sánchez, D. A. B., López-Silva, B., Velasco, M., Ita-Amador, M. L., & Albarado-Ibáñez, A. (2022) · Journal of Diabetes Research · doi:10.1155/2022/9321445 · Cited by 7

The role of the lipotoxicity in the pathogenesis of type 2 diabetes mellitus and obesity

Абдулкадирова, Ф. Р., As, A., Doskina, E. V., & Покровская, Р. А. (2014) · Obesity and metabolism · doi:10.14341/omet201428-12 · Cited by 7

Determination of sex-based differences in serum γ-linoleic acid and dihomo-γ-linoleic acid using gas chromatography–mass spectrometry

Onozato, M., Nishikiori, M., Iizuka, H., Ichiba, H., Sadamoto, K., & Fukushima, T. (2015) · Journal of Chromatography B · doi:10.1016/j.jchromb.2015.05.011 · Cited by 7

Hypoglycaemia is uncommon with a combination of antidiabetic drugs and bedtime NPH insulin for type 2 diabetes

Allen, K. A., McAulay, V., Sommerfield, A., & Frier, B. M. (2004) · Practical Diabetes · doi:10.1002/pdi.637 · Cited by 7

Incorporation of beta cell redifferentiation therapy into a lipoprivic strategy for reversing type 2 diabetes

McCarty, M. F. (2002) · Medical Hypotheses · doi:10.1054/mehy.2001.1454 · Cited by 7

Zukünftige Angriffspunkte für die Therapie des Typ-2-Diabetes

Stingl, H., & Roden, M. (2004) · Wiener klinische Wochenschrift · doi:10.1007/bf03041051 · Cited by 7

The Glucose–Insulin Control System

Hallgreen, C. E., Korsgaard, T. V., Hansen, R. N., & Colding‐Jørgensen, M. (2007) · Wiley eBooks · doi:10.1002/9783527622672.ch6 · Cited by 7

Free Radicals and Metabolic Disorders

Cohen, G., Riahi, Y., & Sasson, S. (2012) · Wiley eBooks · doi:10.1002/9781119953678.rad057 · Cited by 7

Non‐alcoholic Fatty Liver Disease and Insulin Resistance

Petersen, M. C., Samuel, V. T., Petersen, K. F., & Shulman, G. I. (2020) · Wiley eBooks · doi:10.1002/9781119436812.ch37 · Cited by 10

Lactate Metabolism in Health and Disease

Kane, D. A., Goodwin, M. L., & Gladden, L. B. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-88361-3_24 · Cited by 8

Short‐term acipimox treatment is associated with decreased cardiac parasympathetic modulation

Vestergaard, E. T., Cichosz, S. L., Møller, N., Jørgensen, J. O. L., & Fleischer, J. (2017) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.13384 · Cited by 6

Blood lactate concentration in diabetic dogs.

Silva, P. C., Gimenes, A. M., de Castro, J. R., Mantovani, M. M., Kanayama, K. K., Simões, D. M. N., & Schwartz, D. S. (2017) · PubMed Central · Cited by 6

In Vivo and In Vitro Quantification of Glucose Kinetics: From Bedside to Bench

Kim, I., Park, S., Kim, Y., Chang, Y., Choi, C. S., Suh, S., & Wolfe, R. R. (2020) · Endocrinology and Metabolism · doi:10.3803/enm.2020.406 · Cited by 6

Which predictors could effect on remission of type 2 diabetes mellitus after the metabolic surgery: A general perspective of current studies?

Akkuş, G., & Tetıker, T. (2021) · World Journal of Diabetes · doi:10.4239/wjd.v12.i8.1312 · Cited by 6

Adipose Tissue and Insulin Resistance

Borst, S. E. (2007) · Humana Press eBooks · doi:10.1007/978-1-59745-370-7_21 · Cited by 6

Ambient Plasma Free Fatty Acid Concentrations in Noninsulin-Dependent Diabetes Mellitus: Evidence for Insulin Resistance*

Fraze, E., Donner, C. C., Swislocki, A., Chiou, Y.-A. M., Chen, Y. I., & Reaven, G. M. (1985) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-61-5-807 · Cited by 214

Documentation of Hyperglucagonemia Throughout the Day in Nonobese and Obese Patients with Noninsulin-Dependent Diabetes Mellitus*

REAVEN, G. M., CHEN, Y.-D. I., GOLAY, A., SWISLOCKI, A. L. M., & JASPAN, J. B. (1987) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-64-1-106 · Cited by 326

Comparative Study on the Relationship Between Serum Free Fatty Acid, Plasma Glucose and Insulin Resistance in Patients With NIDDM

Chen, J.-Z. (2004)

Relationship between plasma glucose and insulin concentration, glucose production, and glucose disposal in normal subjects and patients with non-insulin-dependent diabetes.

Chen, Y. I., Jeng, C. Y., Hollenbeck, C. B., Wu, M. ‐., & Reaven, G. M. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113572 · Cited by 51

Relationship Between Hepatic Glucose Production and Fasting Plasma Glucose Concentration in Patients With NIDDM

Jeng, C.-Y., Sheu, W. H., Fuh, M. M.-T., Chen, Y. I., & Reaven, G. M. (1994) · Diabetes · doi:10.2337/diab.43.12.1440 · Cited by 118