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

Unsaturated fatty acids repress expression of ATP binding cassette transporter A1 and G1 in RAW 264.7 macrophages

Ku, C. S., Park, Y., Coleman, S. L., & Lee, J. (2011) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2011.07.007 · Cited by 31

Whole-Body Biodistribution, Dosimetry, and Metabolite Correction of [ 11 C]Palmitate: A PET Tracer for Imaging of Fatty Acid Metabolism

Christensen, N. L., Jakobsen, S., Schacht, A. C., Munk, O. L., Alstrup, A. K. O., Tolbod, L. P., Harms, H. J., Nielsen, S., & Gormsen, L. C. (2017) · Molecular Imaging · doi:10.1177/1536012117734485 · Cited by 30

Genetic variants of tumor necrosis factor-α and its levels: A correlation with dyslipidemia and type 2 diabetes susceptibility

Patel, R., Palit, S. P., RATHWA, N. N., Ramachandran, A. V., & Begum, R. (2018) · Clinical Nutrition · doi:10.1016/j.clnu.2018.06.962 · Cited by 30

Alterations of Glucose Metabolism in Type 2 Diabetes Mellitus. An Overview

Bonadonna, R. C. (2004) · Reviews in Endocrine and Metabolic Disorders · doi:10.1023/b:remd.0000021429.89218.c6 · Cited by 29

Small-Molecule Compounds that Modulate Lipolysis in Adipose Tissue: Targeting Strategies and Molecular Classes

Wang, M., & Fotsch, C. H. (2006) · Chemistry & Biology · doi:10.1016/j.chembiol.2006.09.010 · Cited by 30

Ang (1–7) Protects Islet Endothelial Cells from Palmitate-Induced Apoptosis by AKT, eNOS, p38 MAPK, and JNK Pathways

Li, Y., Lu, C., Wang, Y., Li, Y., & Li, X. (2014) · Journal of Diabetes Research · doi:10.1155/2014/391476 · Cited by 29

Palmitate induces cisternal ER expansion via the activation of XBP-1/CCTα-mediated phospholipid accumulation in RAW 264.7 cells

Kim, S. K., Oh, E., Yun, M., Lee, S., & Chae, G. T. (2015) · Lipids in Health and Disease · doi:10.1186/s12944-015-0077-3 · Cited by 29

Polyunsaturated fatty acid relatively decreases cholesterol content in THP-1 macrophage-derived foam cell: partly correlates with expression profile of CIDE and PAT members

Song, Y., Zhang, L., Li, H., Gu, Y., Li, F., Jiang, L., Liu, F., Ye, J., & Li, Q. (2013) · Lipids in Health and Disease · doi:10.1186/1476-511x-12-111 · Cited by 29

Characteristics of the Insulin Resistance Syndrome in a Japanese Population

Kario, K., Nago, N., Kayaba, K., Saegusa, T., Matsuo, H., Goto, T., Tsutsumi, A., Ishikawa, S., Kuroda, T., Miyamoto, T., et al. (1996) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.16.2.269 · Cited by 29

Liraglutide ameliorates palmitate-induced oxidative injury in islet microvascular endothelial cells through GLP-1 receptor/PKA and GTPCH1/eNOS signaling pathways

Le, Y., Wei, R., Yang, K., Lang, S., Gu, L., Liu, J., Hong, T., & Yang, J. (2019) · Peptides · doi:10.1016/j.peptides.2019.170212 · Cited by 28

Virtual metabolic human dynamic model for pathological analysis and therapy design for diabetes

Kurata, H. (2021) · iScience · doi:10.1016/j.isci.2021.102101 · Cited by 26

Low density lipoprotein non-esterified fatty acids and lipoprotein lipase in diabetes

Phillips, C. M., Owens, D., Collins, P. B., & TOMKIN, G. H. (2005) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2004.12.033 · Cited by 28

Rosmarinic acid suppresses adipogenesis, lipolysis in 3T3-L1 adipocytes, lipopolysaccharide-stimulated tumor necrosis factor-α secretion in macrophages, and inflammatory mediators in 3T3-L1 adipocytes

Rui, Y., Tong, L., Cheng, J., Wang, G., Qin, L., & Wan, Z. (2017) · Food & Nutrition Research · doi:10.1080/16546628.2017.1330096 · Cited by 28

Lipid Oxidation Assessed by Indirect Calorimetry Predicts Metabolic Syndrome and Type 2 Diabetes

Pujia, A., Mazza, E., Ferro, Y., Gazzaruso, C., Coppola, A., Doldo, P., Grembiale, R. D., Pujia, R., Romeo, S., & Montalcini, T. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00806 · Cited by 28

Fatty acid-induced atherogenic changes in extracellular matrix proteoglycans

Rodrı́guez-Lee, M., Bondjers, G., & Camejo, G. (2007) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e3282ef534f · Cited by 27

Binding of [3H]palmitate to BSA

Elmadhoun, B., Wang, G. Q., Templeton, J. F., & Burczynski, F. J. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.275.4.g638 · Cited by 28

Reduced Incorporation of Fatty Acids Into Triacylglycerol in Myotubes From Obese Individuals With Type 2 Diabetes

Sparks, L. M., Bosma, M., Brouwers, B., van de Weijer, T., Bilet, L., Schaart, G., Moonen‐Kornips, E., Eichmann, T. O., Lass, A., Hesselink, M. K. C., et al. (2014) · Diabetes · doi:10.2337/db13-1123 · Cited by 28

Fatty Acid-Mediated Inhibition of Metal Binding to the Multi-Metal Site on Serum Albumin: Implications for Cardiovascular Disease

Blindauer, C. A., Khazaipoul, S., Yu, R., & Stewart, A. J. (2016) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026616666160216155927 · Cited by 27

AICAR Protects Vascular Endothelial Cells from Oxidative Injury Induced by the Long-Term Palmitate Excess

Samsonov, M. V., Podkuychenko, N. V., Khapchaev, A. Y., Efremov, E. E., Yanushevskaya, E. V., Vlasik, T. N., Lankin, V. Z., Stafeev, I., Skulachev, M. V., Шестакова, М. В., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010211 · Cited by 29

Palmitate-induced skeletal muscle insulin resistance does not require NF-κB activation

Hommelberg, P. P. H., Plat, J., Sparks, L. M., Schols, A. M. W. J., van Essen, A. L. M., KELDERS, M. C. J. M., van Beurden, D., Mensink, R. P., & LANGEN, R. C. J. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0515-3 · Cited by 27

Vanadyl bisacetylacetonate protects β cells from palmitate-induced cell death through the unfolded protein response pathway

Gao, Z., Zhang, C., Yu, S., Yang, X., & Wang, K. (2011) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-011-0780-0 · Cited by 27

Insulin Increases Ceramide Synthesis in Skeletal Muscle

Hansen, M. E., Tippetts, T. S., Anderson, M. C., Holub, Z. E., Moulton, E. R., Swensen, A., Prince, J. T., & Bikman, B. T. (2014) · Journal of Diabetes Research · doi:10.1155/2014/765784 · Cited by 28

Improved dialytic removal of protein-bound uremic toxins by intravenous lipid emulsion in chronic kidney disease rats

Shi, Y., Zhang, Y., Tian, H., Wang, Y., Shen, Y., Zhu, Q., & Ding, F. H. (2019) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfz079 · Cited by 27

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

Girard, J. R. (2003) · médecine/sciences · doi:10.1051/medsci/20031989827 · Cited by 35

Insulin secretory function in Type 2 diabetes: Does it matter how you measure it?

Reaven, G. M. (2009) · Journal of Diabetes · doi:10.1111/j.1753-0407.2009.00016.x · Cited by 26

Training status diverges muscle diacylglycerol accumulation during free fatty acid elevation

Chow, L. S., Mashek, D. G., Austin, E. E., Eberly, L. E., Persson, X.-M. T., Mashek, M. T., Seaquist, E. R., & Jensen, M. D. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00166.2014 · Cited by 27

Assessment of the phenolic profile, antimicrobial activity and oxidative stability of transgenic Perilla frutescens L.overexpressing tocopherol methyltransferase (γ-tmt) gene

Ghimire, B. K., Yu, C. Y., & Chung, I. (2017) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2017.06.006 · Cited by 26

Adherence to Mediterranean Diet Is Associated With Better Glycemic Control in Children With Type 1 Diabetes: A Cross-Sectional Study

Domínguez‐Riscart, J., Buero-Fernandez, N., García-Zarzuela, A., Morales-Perez, C., García-Ojanguren, A., & Lechuga-Sancho, A. M. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.813989 · Cited by 29

Oleic and linoleic acids are active principles in Nigella sativa and stabilize an E2P conformation of the Na,K-ATPase. Fatty acids differentially regulate cardiac glycoside interaction with the pump

Mahmmoud, Y. A., & Christensen, S. B. (2011) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2011.06.025 · Cited by 26

Fatty acids inhibit growth-factor-induced diacylglycerol kinase α activation in vascular smooth-muscle cells

Du, X., JIANG, Y., Weijun, Q. I. A. N., Lu, X., & WALSH, J. P. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3570275 · Cited by 26

Nutrient-sensing growth hormone secretagogue receptor in macrophage programming and meta-inflammation

Kim, D. M., Lee, J. H., Pan, Q., Han, H. W., Shen, Z., Eshghjoo, S., Wu, C., Yang, W., Noh, J. Y., Threadgill, D. W., et al. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101852 · Cited by 28

Exenatide: first-in-class incretin mimetic for the treatment of Type 2 diabetes mellitus

Triplitt, C. L., & DeFronzo, R. A. (2006) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.1.3.329 · Cited by 25

Elevated NEFA levels impair glucose effectiveness by increasing net hepatic glycogenolysis

Kehlenbrink, S., Koppaka, S., Martin, M., Relwani, R., Cui, M., Hwang, J.-H., Li, Y., Basu, R., Hawkins, M. A., & Kishore, P. (2012) · Diabetologia · doi:10.1007/s00125-012-2662-6 · Cited by 24

Suppression of nocturnal fatty acid concentrations by bedtime carbohydrate supplement in type 2 diabetes: effects on insulin sensitivity, lipids, and glycemic control

Axelsen, M., Lönnroth, P., Lenner, R. A., Taskinen, M., & Smith, U. (2000) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/71.5.1108 · Cited by 24

Hepatic glucose production: therapeutic target in type 2 diabetes?

Stæhr, P., Nielsen, O. H., & Beck‐Nielsen, H. (2002) · Diabetes Obesity and Metabolism · doi:10.1046/j.1463-1326.2002.00177.x · Cited by 25

Metformin usage in type 2 diabetes mellitus: are safety guidelines adhered to?

Huang, W., Castelino, R. L., & Peterson, G. M. (2014) · Internal Medicine Journal · doi:10.1111/imj.12369 · Cited by 24

Oleic Acid Induces MiR-7 Processing through Remodeling of Pri-MiR-7/Protein Complex

Kumar, S., Velasco, A. D. R., & Michlewski, G. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2017.05.001 · Cited by 24

Regulation of hepatic metabolism by enteral delivery of nutrients

Dardevet, D. P., Moore, M. C., Rémond, D., Grueter, C. A., & Cherrington, A. D. (2006) · Nutrition Research Reviews · doi:10.1017/s0954422407315175 · Cited by 26

Determination of Free Fatty Acids in Human Serum by HPLC with Fluorescence Detection

Nishikiori, M., Iizuka, H., Ichiba, H., Sadamoto, K., & Fukushima, T. (2014) · Journal of Chromatographic Science · doi:10.1093/chromsci/bmu081 · Cited by 24

Free fatty acids as target for therapy

Boden, G. H. (2004) · Current Opinion in Endocrinology & Diabetes · doi:10.1097/01.med.0000141928.95173.63 · Cited by 24

Neurobiological characteristics underlying metabolic differences between males and females

Chowen, J. A., Freire‐Regatillo, A., & Argente, J. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.09.001 · Cited by 24

Acute exercise increases the contact between lipid droplets and mitochondria independently of obesity and type 2 diabetes

de Almeida, M. E., Ørtenblad, N., Petersen, M. H., Schjerning, A., Wentorf, E. K., Jensen, K., Højlund, K., & Nielsen, J. (2023) · The Journal of Physiology · doi:10.1113/jp284386 · Cited by 24

Levels of inflammatory markers and their correlation with dyslipidemia in diabetics.

Waheed, P., Naveed, A. K., & Farooq, F. (2009) · PubMed · Cited by 22

Plasma lipidomic signatures of spontaneous obese rhesus monkeys

Wang, J., Zhang, L., Xiao, R., Li, Y., Liao, S., Zhang, Z., Yang, W., & Liang, B. (2019) · Lipids in Health and Disease · doi:10.1186/s12944-018-0952-9 · Cited by 23

Fat-induced liver insulin resistance

Shah, P., Basu, A., & Rizza, R. A. (2003) · Current Diabetes Reports · doi:10.1007/s11892-003-0066-1 · Cited by 23

Ginseng Extract Inhibits Lipolysis in Rat Adipocytes In Vitro by Activating Phosphodiesterase 4

Wang, H., Reaves, L. A., & Edens, N. K. (2006) · Journal of Nutrition · doi:10.1093/jn/136.2.337 · Cited by 23

Heterogeneity in limb fatty acid kinetics in type 2 diabetes

Sacchetti, M., Olsen, D. B., Saltin, B., & van Hall, G. (2005) · Diabetologia · doi:10.1007/s00125-005-1727-1 · Cited by 23

Favorable impact of a vegan diet with exercise on hemorheology: implications for control of diabetic neuropathy

McCarty, M. F. (2002) · Medical Hypotheses · doi:10.1054/mehy.2001.1456 · Cited by 24

The role of serum albumin in the metabolism of Boc5: Molecular identification, species differences and contribution to plasma metabolism

Ge, G., Ai, C., Hu, W., Hou, J., Zhu, L., He, G.-Y., Fang, Z., Liang, S., Wang, F., & Yang, L. (2012) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2012.11.011 · Cited by 22

Palmitate induced secretion of IL-6 and MCP-1 in orbital fibroblasts derived from patients with thyroid-associated ophthalmopathy.

Paik, J., Cho, W., Oh, E., Lee, S., & Yang, S.-W. (2012) · Europe PMC (PubMed Central) · Cited by 22

Insulin resistance in the regulation of lipolysis and ketone body metabolism in non-insulin dependent diabetes is apparent at very low insulin concentrations

Singh, B. M., Krentz, A., & Nattrass, M. (1993) · Diabetes Research and Clinical Practice · doi:10.1016/0168-8227(93)90023-x · Cited by 21

Adipose tissue insulin resistance in adolescents with and without type 2 diabetes

Kelsey, M. M., Forster, J. E., Pelt, R. E. V., Reusch, J. E. B., & Nadeau, K. J. (2013) · Pediatric Obesity · doi:10.1111/j.2047-6310.2013.00189.x · Cited by 22

NO-1886 inhibits size of adipocytes, suppresses plasma levels of tumor necrosis factor-α and free fatty acids, improves glucose metabolism in high-fat/high-sucrose-fed miniature pigs

Yin, W., Liao, D., Wang, Z., Xi, S., Tsutsumi, K., Koike, T., Fan, J., Yi, G., Zhang, Q., Yuan, Z., et al. (2003) · Pharmacological Research · doi:10.1016/j.phrs.2003.09.008 · Cited by 22

Response of Insulin, Glucagon, Lactate, and Nonesterified Fatty Acids to Glucose in Visceral Obesity with and without NIDDM: Relationship to Hypertension

Iannello, S., Campione, R., & Belfiore, F. (1998) · Molecular Genetics and Metabolism · doi:10.1006/mgme.1997.2670 · Cited by 22

GSK256073 acutely regulates NEFA levels via HCA2 agonism but does not achieve durable glycaemic control in type 2 diabetes. A randomised trial

Dobbins, R. L., Byerly, R., Gaddy, R., Gao, F., Mahar, K. M., Napolitano, A., Ambery, P., & de Gouville, A. L. M. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.03.005 · Cited by 21

Pioglitazone and alogliptin combination therapy in type 2 diabetes: a pathophysiologically sound treatment

DeFronzo, R. A., Triplitt, & Cersosimo (2010) · Vascular Health and Risk Management · doi:10.2147/vhrm.s4852 · Cited by 23

Effects of an overnight intravenous lipid infusion on intramyocellular lipid content and insulin sensitivity in African–American versus Caucasian adolescents

Lee, S., Boesch, C., Kuk, J. L., & Arslanian, S. A. (2012) · Metabolism · doi:10.1016/j.metabol.2012.09.007 · Cited by 21

Palmitate-induced impairment of autophagy turnover leads to increased apoptosis and inflammation in peripheral blood mononuclear cells

Rostamirad, A., Ebrahimi, S. S. S., Sadeghi, A., Taghikhani, M., & Meshkani, R. (2017) · Immunobiology · doi:10.1016/j.imbio.2017.10.041 · Cited by 21

Exercise—A Panacea of Metabolic Dysregulation in Cancer: Physiological and Molecular Insights

Raun, S. H., Buch‐Larsen, K., Schwarz, P., & Sylow, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073469 · Cited by 20

Lactylation Modification in Cardiometabolic Disorders: Function and Mechanism

Li, X., Cai, P., Tang, X., Wu, Y., Zhang, Y., & Rong, X. (2024) · Metabolites · doi:10.3390/metabo14040217 · Cited by 23

Intracellular lipid accumulation and shift during diabetes progression

Wolf, P. S., Winhofer, Y., Anderwald, C. H., Krššák, M., & Krebs, M. (2014) · Wiener Medizinische Wochenschrift · doi:10.1007/s10354-014-0292-y · Cited by 20

Effect of exercise on lipolysis in adipose tissue

Polak, J., Bajzová, M., & Štich, V. (2008) · Future Lipidology · doi:10.2217/17460875.3.5.557 · Cited by 22

The therapeutic potential of metabolic hormones in the treatment of age-related cognitive decline and Alzheimer's disease

Grizzanti, J., Lee, H., Camins, A., Pallàs, M., & Casadesús, G. (2016) · Nutrition Research · doi:10.1016/j.nutres.2016.11.002 · Cited by 21

Time-Dependent Effects of Free Fatty Acids on Glucose Effectiveness in Type 2 Diabetes

Kishore, P., Tonelli, J., Koppaka, S., Fratila, C., Bose, A., Lee, D.-E., Reddy, K., & Hawkins, M. A. (2006) · Diabetes · doi:10.2337/db05-0988 · Cited by 21

Fatty acids modulate protein kinase C activation in porcine vascular smooth muscle cells independently of their effect on de novo diacylglycerol synthesis

Lu, X., Yang, X.-Y., Howard, R. L., & Walsh, J. P. (2000) · Diabetologia · doi:10.1007/s001250051504 · Cited by 20

Intracellular Long-Chain Acyl CoAs Activate TRPV1 Channels

Yu, Y., Carter, C. R. J., Youssef, N., Dyck, J. R. B., & Light, P. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096597 · Cited by 20

Increased concentrations of soluble vascular cell adhesion molecule-1 and soluble CD40L in subjects with metabolic syndrome

Palomo, I. F. (2009) · Molecular Medicine Reports · doi:10.3892/mmr_00000125 · Cited by 19

Association between duration of obesity and severity of ovarian dysfunction in rat-cafeteria diet approach

Kannan, S., Srinivasan, D., Raghupathy, P. B., & Bhaskaran, R. S. (2019) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2019.05.012 · Cited by 19

Toward a wholly nutritional therapy for type 2 diabetes

McCarty, M. F. (2000) · Medical Hypotheses · doi:10.1054/mehy.1999.0881 · Cited by 19

Hexosamines and Nutrient Excess Induce Leptin Production and Leptin Receptor Activation in Pancreatic Islets and Clonal -Cells

Emilsson, V., O’Dowd, J. F., Nolan, A. L., & Cawthorne, M. A. (2001) · Endocrinology · doi:10.1210/endo.142.10.8414 · Cited by 19

Low urine pH predicts new onset of diabetes mellitus during a 10‐year period in men: BOREAS‐DM1 study

Higashiura, Y., Tanaka, M., Furuhashi, M., Koyama, M., Ohnishi, H., Numata, K., Hisasue, T., Hanawa, N., Moniwa, N., & Miura, T. (2020) · Journal of Diabetes Investigation · doi:10.1111/jdi.13284 · Cited by 18

Obesity, Anion Accumulation, and Anion Gap Metabolic Acidosis: A Cohort Study

Lambert, D. C., & Abramowitz, M. K. (2021) · Kidney360 · doi:10.34067/kid.0003562021 · Cited by 18

Characterizing 3T3-L1 MBX Adipocyte Cell Differentiation Maintained with Fatty Acids as an In Vitro Model to Study the Effects of Obesity

Mubtasim, N., & Gollahon, L. (2023) · Life · doi:10.3390/life13081712 · Cited by 20

Involvement of Glycogen Synthase Kinase-3β in Palmitate-Induced Human Umbilical Vein Endothelial Cell Apoptosis

Choi, S., KANG, Y. Y., Jang, H.-J., Shin, H.-C., Kim, H.-E., Kim, H.-S., Kim, H. J., Kim, D. J., & Lee, K. W. (2007) · Journal of Vascular Research · doi:10.1159/000102321 · Cited by 18

The Role of Calcium, Lipid Membranes and Islet Amyloid Polypeptide in the Onset of Type 2 Diabetes: Innocent Bystanders or Partners in a Crime?

Milardi, D., Sciacca, M. F. M., Randazzo, L., Raudino, A., & Rosa, C. L. (2014) · Frontiers in Endocrinology · doi:10.3389/fendo.2014.00216 · Cited by 19

Intracellular pH Regulation of Skeletal Muscle in the Milieu of Insulin Signaling

Posa, D. K., & Baba, S. P. (2020) · Nutrients · doi:10.3390/nu12102910 · Cited by 19

Prokineticin receptor 1 ameliorates insulin resistance in skeletal muscle

Mok, J., Park, T. S., Kim, S., Kim, D., Choi, C. S., & Park, J. (2020) · The FASEB Journal · doi:10.1096/fj.202001641r · Cited by 18

Dichotomous responses of inter and postprandial hyperglycaemia to short‐term calorie restriction in patients with type 2 diabetes

Colette, C., Ginet, C., Boegner, C., Bénichou, M., Pham, T. C., Cristol, J., & Monnier, L. (2005) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2005.01482.x · Cited by 18

Complementary measures for promoting insulin sensitivity in skeletal muscle

McCarty, M. F. (1998) · Medical Hypotheses · doi:10.1016/s0306-9877(98)90065-2 · Cited by 19

Interactions of glucagon and free fatty acids with insulin in control of glucose metabolism

Chambrier, C., Picard, S., Vidal, H., Cohen, R., Riou, J. P., & Beylot, M. (1990) · Metabolism · doi:10.1016/0026-0495(90)90311-y · Cited by 18

Partners in diabetes epidemic: A global perspective

Wang, H., Akbari‐Alavijeh, S., Parhar, R. S., Gaugler, R. R., & Hashmi, S. (2023) · World Journal of Diabetes · doi:10.4239/wjd.v14.i10.1463 · Cited by 17

Alteration of hypothalamic glucose and lactate sensing in 48 h hyperglycemic rats

Allard, C., Carneiro, L., Collins, S. C., Chrétien, C., Grall, S., Pénicaud, L., & Leloup, C. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.11.033 · Cited by 17

Cyclosporine A and palmitic acid treatment synergistically induce cytotoxicity in HepG2 cells

Luo, Y., Rana, P., & Will, Y. (2012) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2012.03.022 · Cited by 17

Differential Acute Impacts of Sleeve Gastrectomy, Roux-en-Y Gastric Bypass Surgery and Matched Caloric Restriction Diet on Insulin Secretion, Insulin Effectiveness and Non-Esterified Fatty Acid Levels Among Patients with Type 2 Diabetes

Thomas, F., Smith, G. C., Lu, J., Babor, R., Booth, M., Beban, G. R., Chase, J. G., & Murphy, R. (2016) · Obesity Surgery · doi:10.1007/s11695-015-2038-3 · Cited by 17

Relationships between plasma lactate, plasma alanine, genetic variations in lactate transporters and type 2 diabetes in the Japanese population

Higuchi, I., Kimura, Y., Kobayashi, M., Narumi, K., Furugen, A., Miyoshi, H., Nakamura, A., Yamada, T., Atsumi, T., & Iseki, K. (2019) · Drug Metabolism and Pharmacokinetics · doi:10.1016/j.dmpk.2019.10.001 · Cited by 17

A Rat Model of Human Lipid Emulsion Digestion

Steingoetter, A., Arnold, M., Scheuble, N., Fedele, S., Bertsch, P., Liu, D., Parker, H. L., Langhans, W., & Fischer, P. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00170 · Cited by 18

Effects of short‐term metformin treatment on insulin sensitivity of blood glucose and free fatty acids

Iannello, S., Camuto, M., Cavaleri, A., Milazzo, P., Pisano, M. G., Bellomia, D., & Belfiore, F. (2003) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2004.00306.x · Cited by 17

Fatty acids and insulin secretion

Amery, C. M., & Nattrass, M. (2000) · Diabetes Obesity and Metabolism · doi:10.1046/j.1463-1326.2000.00059.x · Cited by 18

Serum fatty acids in postinfarction middle‐aged men

Leskinen, M. H., Solakivi, T., Kunnas, T. A., Alho, H., & Nikkari, S. T. (2005) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.1080/00365510510025836 · Cited by 17

Suppression of uric acid and lactate production by sodium acetate ameliorates hepatic triglyceride accumulation in fructose-insulin resistant pregnant rats

Oyabambi, A. O., Olaniyi, K. S., Soladoye, A. O., & Olatunji, L. A. (2020) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2020.103452 · Cited by 16

A Lupinoside prevented fatty acid induced inhibition of insulin sensitivity in 3T3 L1 adipocytes

Dey, D., Pal, B. C., Biswas, T., Roy, S. S., Bandyopadhyay, A., Mandal, S. K., Giri, B. B., & Bhattacharya, S. (2006) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-006-9378-1 · Cited by 17

Murine intramyocellular lipids quantified by NMR act as metabolic biomarkers in burn trauma

Tzika, A. A., Astrakas, L. G., Cao, H., Mintzopoulos, D., Zhang, Q., Padfield, K. E., Yu, H., Mindrinos, M. N., Rahme, L. G., & Tompkins, R. G. (2008) · International Journal of Molecular Medicine · doi:10.3892/ijmm.21.6.825 · Cited by 15

Adaptive response of rat pancreatic β-cells to insulin resistance induced by monocrotophos: Biochemical evidence

Nagaraju, R., & Rajini, P. S. (2016) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2016.04.009 · Cited by 17

A review of the putative causal mechanisms associated with lower macular pigment in diabetes mellitus

Scanlon, G., Loughman, J., Farrell, D., & McCartney, D. M. A. (2019) · Nutrition Research Reviews · doi:10.1017/s095442241900012x · Cited by 17

Role of the kidney in hyperglycemia in type 2 diabetes

Meyer, C., & Gerich, J. E. (2002) · Current Diabetes Reports · doi:10.1007/s11892-002-0089-z · Cited by 16

Obesity, insulin resistance, Type 2 diabetes and free fatty acids

Boden, G. H. (2006) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.1.4.499 · Cited by 16

Fatty acids modulate the effect of darglitazone on macrophage CD36 expression

Svensson, L., Camejo, G., Cabré, A., Vallvé, J.-C., Pedreño, J., Norén, K., Wiklund, O., & Hultén, L. M. (2003) · European Journal of Clinical Investigation · doi:10.1046/j.1365-2362.2003.01181.x · Cited by 16

Obesity and Depression: Common Link and Possible Targets

Jitte, S., Keluth, S., Bisht, P., Wal, P., Singh, S., Murti, K., & Kumar, N. (2024) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/0118715273291985240430074053 · Cited by 15

Clinical Decision-Making when Treating Diabetic Macular Edema Patients with Dexamethasone Intravitreal Implants

García‐Layana, A., Figueroa, M. S., Arias, L., Adán, A., López, F. A. C., Abraldes, M. J., Fernández‐Vega, Á., Navarro, R., Cervera, E., da Silva, R. M., et al. (2018) · Ophthalmologica · doi:10.1159/000486800 · Cited by 15

The Epidemic of Type 2 Diabetes Mellitus: Its Links to Obesity, Insulin Resistance, and Lipotoxicity

Cusi, K. J. (2009) · Humana Press eBooks · doi:10.1007/978-1-59745-260-1_1 · Cited by 15

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