Long-term resveratrol administration reduces metabolic disturbances and lowers blood pressure in obese Zucker rats

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

Bligh, E. G., & Dyer, W. J. (1959) · Canadian Journal of Biochemistry and Physiology · doi:10.1139/o59-099 · Cited by 54,751 · see citing works

Homeostasis model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin concentrations in man

Matthews, D. R., Hosker, J. P., Rudenski, A. S., Naylor, B. A., Treacher, D. F., & Turner, R. C. (1985) · Diabetologia · doi:10.1007/bf00280883 · Cited by 31,502 · see citing works

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

Bligh, E. G., & Dyer, W. J. (1959) · Canadian Journal of Biochemistry and Physiology · doi:10.1139/y59-099 · Cited by 23,189 · see citing works

Role of Insulin Resistance in Human Disease

Reaven, G. M. (1988) · Diabetes · doi:10.2337/diab.37.12.1595 · Cited by 12,154 · see citing works

Resveratrol improves health and survival of mice on a high-calorie diet

Baur, J. A., Pearson, K. J., Price, N. L., Jamieson, H. A., Lerin, C., Kalra, A., Prabhu, V. V., Allard, J. S., Lopez-Lluch, G., Lewis, K., et al. (2006) · Nature · doi:10.1038/nature05354 · Cited by 4,290 · see citing works

Adiponectin stimulates glucose utilization and fatty-acid oxidation by activating AMP-activated protein kinase

Yamauchi, T., Kamon, J., Minokoshi, Y., Ito, Y., Waki, H., Uchida, S., Yamashita, S., Noda, M., Kita, S., Ueki, K., et al. (2002) · Nature Medicine · doi:10.1038/nm788 · Cited by 4,238 · see citing works

Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α

Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057 · see citing works

Increased adipose tissue expression of tumor necrosis factor-alpha in human obesity and insulin resistance.

Hotamisligil, G. S., Arner, P., Caro, J. F., Atkinson, R. L., & Spiegelman, B. M. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117936 · Cited by 3,543 · see citing works

Leptin stimulates fatty-acid oxidation by activating AMP-activated protein kinase

Minokoshi, Y., Kim, Y.-B., Peroni, O. D., Fryer, L. G. D., Müller, C., Carling, D., & Kahn, B. B. (2002) · Nature · doi:10.1038/415339a · Cited by 2,053 · see citing works

Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes

Milne, J. C., Lambert, P. D., Schenk, S., Carney, D. P., Smith, J. J., Gagne, D. J., Jin, L., Boss, O., Perni, R. B., Vu, C. B., et al. (2007) · Nature · doi:10.1038/nature06261 · Cited by 1,707 · see citing works

Metabolic syndrome: A comprehensive perspective based on interactions between obesity, diabetes, and inflammation

Dandona, P., Aljada, A., Chaudhuri, A., Mohanty, P., & Garg, R. (2005) · Circulation · doi:10.1161/01.cir.0000158483.13093.9d · Cited by 1,263 · see citing works

AMP-Activated Protein Kinase in Metabolic Control and Insulin Signaling

Towler, M. C., & Hardie, D. G. (2007) · Circulation Research · doi:10.1161/01.res.0000256090.42690.05 · Cited by 1,247 · see citing works

Pathophysiology of insulin resistance in human disease

Reaven, G. M. (1995) · Physiological Reviews · doi:10.1152/physrev.1995.75.3.473 · Cited by 1,235 · see citing works

Minireview: The AMP-Activated Protein Kinase Cascade: The Key Sensor of Cellular Energy Status

Hardie, D. G. (2003) · Endocrinology · doi:10.1210/en.2003-0982 · Cited by 994 · see citing works

Leptin receptor missense mutation in the fatty Zucker rat

Phillips, M. S., Liu, Q., Hammond, H. A., Dugan, V., Hey, P. J., Caskey, C. T., & Hess, J. F. (1996) · Nature Genetics · doi:10.1038/ng0596-18 · Cited by 822 · see citing works

SIRT1 Regulates Hepatocyte Lipid Metabolism through Activating AMP-activated Protein Kinase

Hou, X., Xu, S., Maitland-Toolan, K. A., Sato, K., Jiang, B., Ido, Y., Lan, F., Walsh, K., Wierzbicki, M., Verbeuren, T. J., et al. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m802187200 · Cited by 778 · see citing works

Elevated circulating free fatty acid levels impair endothelium-dependent vasodilation

Steinberg, H. O., Tarshoby, M., Monestel, R., Hook, G., Cronin, J., Johnson, A., Bayazeed, B., & Baron, A. D. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119636 · Cited by 761 · see citing works

Resveratrol stimulates AMP kinase activity in neurons

Dasgupta, B., & Milbrandt, J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610068104 · Cited by 723 · see citing works

Activation of AMP-activated protein kinase increases mitochondrial enzymes in skeletal muscle

Winder, W. W., Holmes, B. F., Rubink, D. S., Jensen, E. B., Chen, M., & Holloszy, J. O. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.88.6.2219 · Cited by 709 · see citing works

Resveratrol, a Polyphenolic Phytoalexin Present in Red Wine, Enhances Expression and Activity of Endothelial Nitric Oxide Synthase

Wallerath, T., Deckert, G., Ternes, T. A., Anderson, H., Li, H., Witte, K. K., & Förstermann, U. (2002) · Circulation · doi:10.1161/01.cir.0000029925.18593.5c · Cited by 665 · see citing works

Insulin resistance: definition and consequences

Lebovitz, H. (2001) · Experimental and Clinical Endocrinology & Diabetes · doi:10.1055/s-2001-18576 · Cited by 664 · see citing works

Polyphenols Stimulate AMP-Activated Protein Kinase, Lower Lipids, and Inhibit Accelerated Atherosclerosis in Diabetic LDL Receptor–Deficient Mice

Zang, M., Xu, S., Maitland, K. A., Zuccollo, A., Hou, X., Jiang, B., Wierzbicki, M., Verbeuren, T. J., & Cohen, R. A. (2006) · Diabetes · doi:10.2337/db05-1188 · Cited by 663 · see citing works

Regulation of fatty acid synthesis and oxidation by the AMP-activated protein kinase

Hardie, D. G., & Pan, D. A. (2002) · Biochemical Society Transactions · doi:10.1042/bst0301064 · Cited by 561 · see citing works

Aging-associated reductions in AMP-activated protein kinase activity and mitochondrial biogenesis

Reznick, R. M., Zong, H., Li, J., Morino, K., Moore, I. K., Yu, H. J., Liu, Z.-X., Dong, J., Mustard, K. J., Hawley, S. A., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.01.008 · Cited by 555 · see citing works

Targeted disruption of inducible nitric oxide synthase protects against obesity-linked insulin resistance in muscle

Perreault, M., & Marette, A. (2001) · Nature Medicine · doi:10.1038/nm1001-1138 · Cited by 540 · see citing works

Insulin resistance, hyperlipidemia, and hypertension in mice lacking endothelial nitric oxide synthase

Duplain, H., Burcelin, R., Sartori, C., Cook, S., Egli, M., Lepori, M., Vollenweider, P., Pedrazzini, T., Nicod, P., Thorens, B., et al. (2001) · Circulation · doi:10.1161/01.cir.104.3.342 · Cited by 533 · see citing works

Cardiovascular Protective Effects of Resveratrol

Bradamante, S., Barenghi, L., & Villa, A. M. (2004) · Cardiovascular Drug Reviews · doi:10.1111/j.1527-3466.2004.tb00139.x · Cited by 528 · see citing works

Biological Effects of Resveratrol

Bhat, K., Kosmeder, J. W., & Pezzuto, J. M. (2001) · Antioxidants and Redox Signaling · doi:10.1089/152308601317203567 · Cited by 510 · see citing works

Quercetin ameliorates metabolic syndrome and improves the inflammatory status in obese Zucker rats

Rivera, L., Morón, R., Sánchez, M., Zarzuelo, A., & Galisteo, M. (2008) · Obesity · doi:10.1038/oby.2008.315 · Cited by 473 · see citing works

AMP kinase and malonyl-CoA: targets for therapy of the metabolic syndrome

Ruderman, N., & Prentki, M. (2004) · Nature Reviews Drug Discovery · doi:10.1038/nrd1344 · Cited by 451 · see citing works

5′-AMP Activates the AMP-activated Protein Kinase Cascade, and Ca2+/Calmodulin Activates the Calmodulin-dependent Protein Kinase I Cascade, via Three Independent Mechanisms

Hawley, S. A., Selbert, M. A., Goldstein, E. G., Edelman, A. M., Carling, D., & Hardie, D. G. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.45.27186 · Cited by 441 · see citing works

Insulin and Obesity in the Zucker Genetically Obese Rat “Fatty”

Zucker, L. M., & Antoniades, H. N. (1972) · Endocrinology · doi:10.1210/endo-90-5-1320 · Cited by 420 · see citing works

Insulin resistance reduces arterial prostacyclin synthase and eNOS activities by increasing endothelial fatty acid oxidation

Du, X., Edelstein, D., Obici, S., Higham, N., Zou, M., & Brownlee, M. (2006) · Journal of Clinical Investigation · doi:10.1172/jci23354 · Cited by 344 · see citing works

Epigallocatechin-3-gallate (EGCG), A Green Tea Polyphenol, Suppresses Hepatic Gluconeogenesis through 5′-AMP-activated Protein Kinase

Collins, Q. F., Liu, H.-Y., Pi, J., Liu, Z., Quon, M. J., & Cao, W. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702390200 · Cited by 333 · see citing works

TNF- downregulates eNOS expression and mitochondrial biogenesis in fat and muscle of obese rodents

Valerio, A. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28570 · Cited by 327 · see citing works

The Zucker fatty rat as a genetic model of obesity and hypertension.

Kurtz, T. W., Morris, R. C., & Pershadsingh, H. A. (1989) · Hypertension · doi:10.1161/01.hyp.13.6.896 · Cited by 261 · see citing works

The Possible Implication of trans-Resveratrol in the Cardioprotective Effects of Long-Term Moderate Wine Consumption

Orallo, F., Álvarez, E., Camiña, M., Leiro, J. M., Gómez, E., & Fernández, P. (2002) · Molecular Pharmacology · doi:10.1124/mol.61.2.294 · Cited by 247 · see citing works

Long-Term AICAR Administration Reduces Metabolic Disturbances and Lowers Blood Pressure in Rats Displaying Features of the Insulin Resistance Syndrome

Buhl, E. S., Jessen, N., Pold, R., Ledet, T., Flyvbjerg, A., Pedersen, S. B., Pedersen, O. B., Schmitz, O., & Lund, S. A. (2002) · Diabetes · doi:10.2337/diabetes.51.7.2199 · Cited by 241 · see citing works

Resveratrol stimulates glucose transport in C2C12 myotubes by activating AMP-activated protein kinase

Park, C.-E., Kim, M., Lee, J. H., Min, B.-I., Bae, H., Choe, W., Kim, S. S., & Ha, J. (2007) · Experimental & Molecular Medicine · doi:10.1038/emm.2007.25 · Cited by 239 · see citing works

Meal modulation of circulating interleukin 18 and adiponectin concentrations in healthy subjects and in patients with type 2 diabetes mellitus

Esposito, K., Nappo, F., Giugliano, F., Palo, C. D., Ciotola, M., Barbieri, M., Paolisso, G., & Giugliano, D. (2003) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/78.6.1135 · Cited by 225 · see citing works

Agonist-modulated Regulation of AMP-activated Protein Kinase (AMPK) in Endothelial Cells

Levine, Y. C., Li, G. K., & Michel, T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702182200 · Cited by 207 · see citing works

Diabetes: insulin resistance and derangements in lipid metabolism. Cure through intervention in fat transport and storage

Raz, I., Eldor, R., Cernea, S., & Shafrir, E. (2004) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.493 · Cited by 194 · see citing works

Effects ofcis-resveratrol on inflammatory murine macrophages: antioxidant activity and down-regulation of inflammatory genes

Leiro, J. M., Álvarez, E., Arranz, J. A., Laguna, R., Uriarte, E., & Orallo, F. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.1103561 · Cited by 184 · see citing works

Protective effects of the flavonoid quercetin in chronic nitric oxide deficient rats

Duarte, J., Jiménez, R., O’Valle, F., Galisteo, M., Pérez‐Palencia, R., Vargas, F., Pérez‐Vizcaíno, F., Zarzuelo, A., & Tamargo, J. L. (2002) · Journal of Hypertension · doi:10.1097/00004872-200209000-00031 · Cited by 150 · see citing works

Leptinomimetic effects of the AMP kinase activator AICAR in leptin-resistant rats: prevention of diabetes and ectopic lipid deposition

Yu, X., McCorkle, S. K., Wang, M., Lee, Y., Li, J., Saha, A. K., Unger, R. H., & Ruderman, N. B. (2004) · Diabetologia · doi:10.1007/s00125-004-1570-9 · Cited by 149 · see citing works

Phenotype-Linked Amino Acid Alteration in Leptin Receptor cDNA from Zucker Fatty(fa/fa)Rat

Iida, M., Murakami, T., Ishida, K., Mizuno, A., Kuwajima, M., & Shima, K. (1996) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1996.0691 · Cited by 139 · see citing works

Influence of Plasma Free Fatty Acids on Lipoprotein Synthesis and Diabetic Dyslipidemia

Julius, U. (2003) · Experimental and Clinical Endocrinology & Diabetes · doi:10.1055/s-2003-41284 · Cited by 131 · see citing works

Antidiabetes and Antiobesity Effect of Cryptotanshinone via Activation of AMP-Activated Protein Kinase

Kim, E. J., Jung, S., Son, K. H., Kim, S. R., Ha, T. Y., Park, M. G., Jo, I. G., Park, J. G., Choe, W., Kim, S. S., et al. (2007) · Molecular Pharmacology · doi:10.1124/mol.107.034447 · Cited by 122 · see citing works

A Diet Supplemented with Husks of Plantago ovata Reduces the Development of Endothelial Dysfunction, Hypertension, and Obesity by Affecting Adiponectin and TNF-α in Obese Zucker Rats

Galisteo, M., Sánchez, M., Vera, R., González, M., Anguera, A., Duarte, J., & Zarzuelo, A. (2005) · Journal of Nutrition · doi:10.1093/jn/135.10.2399 · Cited by 97 · see citing works

Effects of trans-resveratrol on hypertension-induced cardiac hypertrophy using the partially nephrectomized rat model

Liu, Z., Yan, S., Zhang, X., Liu, Z., Zhang, W., Mao, W., Wang, W., Cui, W., Zhang, X., Jia, X., et al. (2005) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2005.04303.x · Cited by 88 · see citing works

Molecular Mechanisms of the Chemopreventive Effects of Resveratrol and Its Analogs in Colorectal Cancer: Key Role of Polyamines?

Wolter, F., Ulrich, S., & Stein, J. M. (2004) · Journal of Nutrition · doi:10.1093/jn/134.12.3219 · Cited by 82 · see citing works

Effects of trans‐resveratrol on hypertension‐induced cardiac hypertrophy using the partially nephrectomized rat model

Liu, Z., Song, Y., Zhang, X., Liu, Z., Zhang, W., Mao, W., Wang, W., Cui, W., Zhang, X., Jia, X., et al. (2005) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2005.04299.x · Cited by 55 · see citing works

Triglyceride-Rich Lipoprotein-Associated Apolipoprotein C-III Production Is Stimulated by Plasma Free Fatty Acids in Humans

Pavlic, M., Valéro, R., Duez, H., Xiao, C., Szeto, L., Patterson, B. W., & Lewis, G. F. (2008) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.108.169383 · Cited by 52 · see citing works

Calorie Restriction-like Effects of 30 Days of Resveratrol Supplementation on Energy Metabolism and Metabolic Profile in Obese Humans

Timmers, S., Konings, E., Bilet, L., Houtkooper, R. H., van de Weijer, T., Goossens, G. H., Hoeks, J., van der Krieken, S., Ryu, D., Kersten, S., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.10.002 · Cited by 1,320 · see citing works

Novel insights of dietary polyphenols and obesity

Wang, S. F., Moustaïd‐Moussa, N., Chen, L., Mo, H., Shastri, A. A., Su, R., Bapat, P., Kwun, I., & Shen, C. (2013) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2013.09.001 · Cited by 903 · see citing works

Resveratrol improves insulin sensitivity, reduces oxidative stress and activates the Akt pathway in type 2 diabetic patients

Brasnyó, P., Molnár, G. A., Mohás, M., Markó, L., Laczy, B., Cseh, J., Mikolás, E., Szijártó, I. A., Mérei, Á., Halmai, R., et al. (2011) · British Journal Of Nutrition · doi:10.1017/s0007114511000316 · Cited by 680 · see citing works

Effects of Flavonoids and other Polyphenols on Inflammation

González, R., Ballester, I., López-Posadas, R., Suárez, M. D., Zarzuelo, A., Martínez‐Augustin, O., & de Medina, F. S. (2011) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408390903584094 · Cited by 572 · see citing works

High-Dose Resveratrol Supplementation in Obese Men

Poulsen, M. M., Vestergaard, P. F., Clasen, B. F., Radko, Y., Christensen, L. P., Stødkilde-Jørgensen, H., Møller, N., Jessen, N., Pedersen, S. B., & Jørgensen, J. O. L. (2013) · Diabetes · doi:10.2337/db12-0975 · Cited by 455 · see citing works

Natural products for the treatment of type 2 diabetes mellitus: Pharmacology and mechanisms

Xu, L., Li, Y., Dai, Y., & Peng, J. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.01.015 · Cited by 452 · see citing works

Resveratrol and Clinical Trials: The Crossroad from In Vitro Studies to Human Evidence

Tomé‐Carneiro, J., Larrosa, M., González‐Sarrías, A., Tomás-Barberán, F. A., García‐Conesa, M., & Espı́n, J. C. (2013) · Current Pharmaceutical Design · doi:10.2174/13816128113199990407 · Cited by 451 · see citing works

Resveratrol and Cardiovascular Diseases

Bonnefont‐Rousselot, D. (2016) · Nutrients · doi:10.3390/nu8050250 · Cited by 447 · see citing works

What Is New for an Old Molecule? Systematic Review and Recommendations on the Use of Resveratrol

Vang, O., Ahmad, N., Baile, C. A., Baur, J. A., Brown, K., Csiszár, A., Das, D. K., Delmas, D., Gottfried, C., Lin, H., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019881 · Cited by 433 · see citing works

Dietary Polyphenols and Obesity

Meydani, M., & Hasan, S. T. (2010) · Nutrients · doi:10.3390/nu2070737 · Cited by 389 · see citing works

Effects of resveratrol on cerebral blood flow variables and cognitive performance in humans: a double-blind, placebo-controlled, crossover investigation

Kennedy, D. O., Wightman, E. L., Reay, J. L., Lietz, G., Okello, E. J., Wilde, A., & Haskell, C. F. (2010) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.28641 · Cited by 415 · see citing works

Resveratrol and diabetes: from animal to human studies.

Szkudelski, T., & Szkudelska, K. (2015) · Biochimica et Biophysica Acta · doi:10.1016/j.bbadis.2014.10.013 · Cited by 322 · see citing works

Resveratrol, obesity and diabetes

Szkudelska, K., & Szkudelski, T. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.02.054 · Cited by 342 · see citing works

Preclinical and clinical evidence for the role of resveratrol in the treatment of cardiovascular diseases

Zordoky, B. N. M., Robertson, I. M., & Dyck, J. R. B. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.10.016 · Cited by 340 · see citing works

Resveratrol exerts anti-obesity effects via mechanisms involving down-regulation of adipogenic and inflammatory processes in mice

Kim, S., Jin, Y., Choi, Y., & Park, T. (2011) · Biochemical Pharmacology · doi:10.1016/j.bcp.2011.03.012 · Cited by 332 · see citing works

Resveratrol: A miraculous natural compound for diseases treatment

Koushki, M., Dashatan, N. A., Ahmadi, N., Abbaszadeh, H., & Rezaei–Tavirani, M. (2018) · Food Science & Nutrition · doi:10.1002/fsn3.855 · Cited by 319 · see citing works

Oxidative stress and metabolic pathologies: from an adipocentric point of view

Le Lay, S., Simard, G., Martinez, M. C., & Andriantsitohaina, R. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/908539 · Cited by 291 · see citing works

An overview of the crosstalk between inflammatory processes and metabolic dysregulation during diabetic cardiomyopathy

Palomer, X., Salvadó, L., Barroso, E., & Vázquez‐Carrera, M. (2013) · International Journal of Cardiology · doi:10.1016/j.ijcard.2013.07.150 · Cited by 289 · see citing works

Antioxidants and Atherosclerosis: Mechanistic Aspects

Malekmohammad, K., Sewell, R. D. E., & Rafieian‐Kopaei, M. (2019) · Biomolecules · doi:10.3390/biom9080301 · Cited by 282 · see citing works

Resveratrol supplementation: Where are we now and where should we go?

Novelle, M. G., Wahl, D., Diéguez, C., Bernier, M., & de Cabo, R. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.01.002 · Cited by 247 · see citing works

Anti‐diabetic effects of resveratrol

Szkudelski, T., & Szkudelska, K. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05844.x · Cited by 241 · see citing works

Grape Resveratrol Increases Serum Adiponectin and Downregulates Inflammatory Genes in Peripheral Blood Mononuclear Cells: A Triple-Blind, Placebo-Controlled, One-Year Clinical Trial in Patients with Stable Coronary Artery Disease

Tomé‐Carneiro, J., Gonzálvez, M., Larrosa, M., Yáñez-Gascón, M. J., García‐Almagro, F. J., Ruiz‐Ros, J. A., Tomás-Barberán, F. A., García‐Conesa, M., & Espı́n, J. C. (2012) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-012-6427-8 · Cited by 241 · see citing works

Resveratrol Improves Adipose Insulin Signaling and Reduces the Inflammatory Response in Adipose Tissue of Rhesus Monkeys on High-Fat, High-Sugar Diet

Jiménez, Y., Mattison, J. A., Pearson, K. J., Martín‐Montalvo, A., Palacios, H. H., Sossong, A. M., Ward, T. M., Younts, C. M., Lewis, K. N., Allard, J. S., et al. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.09.004 · Cited by 240 · see citing works

The Fluid Aspect of the Mediterranean Diet in the Prevention and Management of Cardiovascular Disease and Diabetes: The Role of Polyphenol Content in Moderate Consumption of Wine and Olive Oil

Ditano-Vázquez, P., Torres-Peña, J. D., Valle, F. G., Pérez-Caballero, A. I., Rodríguez, P. D., López‐Miranda, J., Katsiki, N., Delgado‐Lista, J., & Alvarez-Sala-Walther, L. A. (2019) · Nutrients · doi:10.3390/nu11112833 · Cited by 242 · see citing works

Transcriptional and post-translational regulation of adiponectin

Liu, M., & Liu, F. (2009) · Biochemical Journal · doi:10.1042/bj20091045 · Cited by 235 · see citing works

Obesity and metabolic syndrome: Potential benefit from specific nutritional components

Abete, I., Goyenechea, E., Zulet, M. Á., & Martínez, J. A. (2011) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2011.05.001 · Cited by 215 · see citing works

Molecular mechanisms of the cardiovascular protective effects of polyphenols

Andriantsitohaina, R., Auger, C., Chataigneau, T., Étienne-Selloum, N., Li, H., Martínez, M. C., Schini‐Kerth, V. B., & Laher, I. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512003406 · Cited by 215 · see citing works

Resveratrol: Anti-Obesity Mechanisms of Action

Aguirre, L., Fernández-Quintela, A., Arias, N., & Portillo, M. (2014) · Molecules · doi:10.3390/molecules191118632 · Cited by 205 · see citing works

Resveratrol and Vascular Function

Li, H., Xia, N., Hasselwander, S., & Daiber, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092155 · Cited by 204 · see citing works

Mitochondrial Biogenesis as a Pharmacological Target: A New Approach to Acute and Chronic Diseases

Whitaker, R. M., Corum, D. G., Beeson, C., & Schnellmann, R. G. (2015) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010715-103155 · Cited by 200 · see citing works

The effects of resveratrol supplementation on cardiovascular risk factors in patients with non-alcoholic fatty liver disease: A randomised, double-blind, placebo-controlled study

Faghihzadeh, F., Adibi, P., & Hekmatdoost, A. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515002433 · Cited by 188 · see citing works

Oxidative Stress as Pathogenesis of Cardiovascular Risk Associated with Metabolic Syndrome

Otani, H. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3739 · Cited by 181 · see citing works

Effects of resveratrol and other wine polyphenols on vascular function: an update

Gresele, P., Cerletti, C., Guglielmini, G., Pignatelli, P., de Gaetano, G., & Violi, F. (2010) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2010.07.004 · Cited by 178 · see citing works

Phytochemicals in regulating fatty acid β-oxidation: Potential underlying mechanisms and their involvement in obesity and weight loss

Rupasinghe, H. P. V., Sekhon-Loodu, S., Mantso, T., & Panayiotidis, M. I. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.06.005 · Cited by 175 · see citing works

Resveratrol improves hepatic steatosis by inducing autophagy through the cAMP signaling pathway

Zhang, Y., Chen, M., Zhou, Y., Yi, L., Gao, Y., Ran, L., Chen, S., Zhang, T., Zhou, X., Zou, D., et al. (2015) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500016 · Cited by 170 · see citing works

Effects of resveratrol alone or in combination with piperine on cerebral blood flow parameters and cognitive performance in human subjects: a randomised, double-blind, placebo-controlled, cross-over investigation

Wightman, E. L., Reay, J. L., Haskell‐Ramsay, C. F., Williamson, G., Dew, T. P., & Kennedy, D. O. (2014) · British Journal Of Nutrition · doi:10.1017/s0007114514000737 · Cited by 172 · see citing works

Role of cAMP and phosphodiesterase signaling in liver health and disease

Wahlang, B., McClain, C., Barve, S., & Gobejishvili, L. (2018) · Cellular Signalling · doi:10.1016/j.cellsig.2018.06.005 · Cited by 168 · see citing works

Resveratrol prevents endothelial nitric oxide synthase uncoupling and attenuates development of hypertension in spontaneously hypertensive rats

Bhatt, S., Lokhandwala, M. F., & Banday, A. A. (2011) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2011.05.026 · Cited by 169 · see citing works

Modulation of endothelial nitric oxide by plant-derived products

Schmitt, C. A., & Dirsch, V. M. (2009) · Nitric Oxide · doi:10.1016/j.niox.2009.05.006 · Cited by 169 · see citing works

Phytochemicals and their impact on adipose tissue inflammation and diabetes

Leiherer, A., Muendlein, A., & Drexel, H. (2012) · Vascular Pharmacology · doi:10.1016/j.vph.2012.09.002 · Cited by 169 · see citing works

Calorie restriction and resveratrol in cardiovascular health and disease

Dolinsky, V. W., & Dyck, J. R. B. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.06.010 · Cited by 168 · see citing works

Resveratrol attenuates steatosis in obese Zucker rats by decreasing fatty acid availability and reducing oxidative stress

Gómez‐Zorita, S., Fernández‐Quintela, A., Macarulla, M. T., Aguirre, L., Hijona, E., Bujanda, L., Milagro, F. I., Martínez, J. A., & Portillo, M. P. (2011) · British Journal Of Nutrition · doi:10.1017/s0007114511002753 · Cited by 164 · see citing works

Resveratrol: Cellular actions of a potent natural chemical that confers a diversity of health benefits

Marques, F. Z., Markus, M. A., & Morris, B. J. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.06.003 · Cited by 162 · see citing works

Effect of resveratrol on blood pressure: A meta-analysis of randomized controlled trials

Liu, Y., Ma, W., Zhang, P., Shun-chuan, H., & Huang, D. (2014) · Clinical Nutrition · doi:10.1016/j.clnu.2014.03.009 · Cited by 161 · see citing works

Antioxidant effects of resveratrol and other stilbene derivatives on oxidative stress and NO bioavailability: Potential benefits to cardiovascular diseases

Frombaum, M., Clanche, S. L., Bonnefont‐Rousselot, D., & Borderie, D. (2011) · Biochimie · doi:10.1016/j.biochi.2011.11.001 · Cited by 156 · see citing works

Resveratrol activates duodenal Sirt1 to reverse insulin resistance in rats through a neuronal network

Côté, C. D., Rasmussen, B. A., Duca, F. A., Zadeh‐Tahmasebi, M., Baur, J. A., Daljeet, M., Breen, D. M., Filippi, B., & Lam, T. K. T. (2015) · Nature Medicine · doi:10.1038/nm.3821 · Cited by 148 · see citing works

Resveratrol attenuates hyperglycemia-mediated oxidative stress, proinflammatory cytokines and protects hepatocytes ultrastructure in streptozotocin–nicotinamide-induced experimental diabetic rats

Periyasamy, P., Sivakumar, S., & Subramanian, S. (2010) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2010.03.028 · Cited by 145 · see citing works

Biochemical effects of SIRT1 activators

Baur, J. A. (2009) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2009.10.025 · Cited by 144 · see citing works

Resveratrol Improves Vascular Function in Patients With Hypertension and Dyslipidemia by Modulating NO Metabolism

Carrizzo, A., Puca, A. A., Damato, A., Marino, M., Franco, E., Pompeo, F., Traficante, A., Civitillo, F., Santini, L., Trimarco, V., et al. (2013) · Hypertension · doi:10.1161/hypertensionaha.111.01009 · Cited by 144 · see citing works

Resveratrol Increases Bone Mineral Density and Bone Alkaline Phosphatase in Obese Men: A Randomized Placebo-Controlled Trial

Ørnstrup, M. J., Harsløf, T., Kjær, T. N., Langdahl, B. L., & Pedersen, S. B. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-2799 · Cited by 143 · see citing works

Effects of resveratrol and other polyphenols in hepatic steatosis

Aguirre, L. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i23.7366 · Cited by 143 · see citing works

Resveratrol ameliorates diabetes‐related metabolic changes via activation of AMP‐activated protein kinase and its downstream targets in db/db mice

Do, G., Jung, U. J., Park, H., Kwon, E., Jeon, S.-M., McGregor, R. A., & Choi, M. (2012) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201200067 · Cited by 141 · see citing works

Resveratrol protects against hyperglycemia-induced oxidative damage to mitochondria by activating SIRT1 in rat mesangial cells

Xu, Y. X., Nie, L., Yin, Y., Tang, J.-L., Zhou, J., Li, D., & Zhou, S.-W. (2011) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2011.09.028 · Cited by 137 · see citing works

Self-emulsifying drug delivery systems as a tool to improve solubility and bioavailability of resveratrol

Balata, G. F., Eassa, E., Shamrool, H., Zidan, S., & Abourehab, M. A. S. (2016) · Drug Design Development and Therapy · doi:10.2147/dddt.s95905 · Cited by 137 · see citing works

Resveratrol Prevents β-Cell Dedifferentiation in Nonhuman Primates Given a High-Fat/High-Sugar Diet

Fiori, J. L., Shin, Y., Kim, W., Krzysik-Walker, S. M., González‐Mariscal, I., Carlson, O. D., Sanghvi, M., Moaddel, R., Farhang, K., Gadkaree, S. K., et al. (2013) · Diabetes · doi:10.2337/db13-0266 · Cited by 136 · see citing works

Resveratrol and obesity: can resveratrol relieve metabolic disturbances?

de Ligt, M., Timmers, S., & Schrauwen, P. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.11.012 · Cited by 135 · see citing works

Resveratrol and inflammation: Challenges in translating pre-clinical findings to improved patient outcomes

Poulsen, M. M., Fjeldborg, K., Ørnstrup, M. J., Kjær, T. N., Nøhr, M. K., & Pedersen, S. B. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.12.024 · Cited by 133 · see citing works

Hypertension, Nitric Oxide, Oxidants, and Dietary Plant Polyphenols

Galleano, M., Pecháňová, O., & Fraga, C. G. (2010) · Current Pharmaceutical Biotechnology · doi:10.2174/138920110793262114 · Cited by 133 · see citing works

Resveratrol regulates lipolysis via adipose triglyceride lipase

Lasa, A., Schweiger, M., Kotzbeck, P., Churruca, I., Simón, E., Zechner, R., & Portillo, M. P. (2011) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2010.12.014 · Cited by 132 · see citing works

Differential effects of low-dose resveratrol on adiposity and hepatic steatosis in diet-induced obese mice

Cho, S.-J., Jung, U. J., & Choi, M. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512000347 · Cited by 130 · see citing works

Dietary quercetin attenuates oxidant-induced endothelial dysfunction and atherosclerosis in apolipoprotein E knockout mice fed a high-fat diet: A critical role for heme oxygenase-1

Shen, Y., Ward, N. C., Hodgson, J. M., Puddey, I. B., Wang, Y., Zhang, D., Maghzal, G. J., Stocker, R., & Croft, K. D. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.08.185 · Cited by 128 · see citing works

Polyphenols: Planting the seeds of treatment for the metabolic syndrome

Cherniack, E. P. (2011) · Nutrition · doi:10.1016/j.nut.2010.10.013 · Cited by 127 · see citing works

Actions of “antioxidants” in the protection against atherosclerosis

Lönn, M. E., Dennis, J. M., & Stocker, R. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.05.027 · Cited by 124 · see citing works

Thermogenesis is involved in the body-fat lowering effects of resveratrol in rats

Alberdi, G., Rodríguez, V. M., Miranda, J., Macarulla, M. T., Churruca, I., & Portillo, M. P. (2013) · Food Chemistry · doi:10.1016/j.foodchem.2013.03.085 · Cited by 125 · see citing works

Potential mechanisms underlying cardiovascular protection by polyphenols: Role of the endothelium

Oak, M., Auger, C., Belcastro, E., Park, S., Lee, H.-H., & Schini‐Kerth, V. B. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.03.018 · Cited by 125 · see citing works

Vascular Oxidative Stress: The Common Link in Hypertensive and Diabetic Vascular Disease

Cohen, R. A., & Tong, X. (2010) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e3181d89670 · Cited by 124 · see citing works

Modified resveratrol Longevinex improves endothelial function in adults with metabolic syndrome receiving standard treatment

Fujitaka, K., Otani, H., Jo, F., Jo, H., Nomura, E., Iwasaki, M., Nishikawa, M., Iwasaka, T., & Das, D. K. (2011) · Nutrition Research · doi:10.1016/j.nutres.2011.09.028 · Cited by 123 · see citing works

Resveratrol – pills to replace a healthy diet?

Chachay, V., Kirkpatrick, C. M. J., Hickman, I. J., Ferguson, M. L., Prins, J. B., & Martin, J. H. (2011) · British Journal of Clinical Pharmacology · doi:10.1111/j.1365-2125.2011.03966.x · Cited by 119 · see citing works

Changes in white adipose tissue metabolism induced by resveratrol in rats

Alberdi, G., Rodríguez, V. M., Miranda, J., Macarulla, M. T., Arias, N., Andrés‐Lacueva, C., & Portillo, M. P. (2011) · Nutrition & Metabolism · doi:10.1186/1743-7075-8-29 · Cited by 118 · see citing works

Resveratrol mediates anti-atherogenic effects on cholesterol flux in human macrophages and endothelium via PPARγ and adenosine

Voloshyna, I., Hai, O. Y., Littlefield, M. J., Carsons, S. E., & Reiss, A. B. (2012) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2012.08.024 · Cited by 117 · see citing works

Resveratrol suppresses body mass gain in a seasonal non-human primate model of obesity

Dal‐Pan, A., Blanc, S., & Aujard, F. (2010) · BMC Physiology · doi:10.1186/1472-6793-10-11 · Cited by 114 · see citing works

Epigallocatechin gallate, cerebral blood flow parameters, cognitive performance and mood in healthy humans: a double‐blind, placebo‐controlled, crossover investigation

Wightman, E. L., Haskell‐Ramsay, C. F., Forster, J. S., Veasey, R. C., & Kennedy, D. O. (2012) · Human Psychopharmacology Clinical and Experimental · doi:10.1002/hup.1263 · Cited by 116 · see citing works

Anti-inflammatory and antiobesity effects of mulberry leaf and fruit extract on high fat diet-induced obesity

Lim, H. H., Lee, S. O., Kim, S. Y., Yang, S. J., & Lim, Y. (2013) · Experimental Biology and Medicine · doi:10.1177/1535370213498982 · Cited by 115 · see citing works

Therapeutic Roles of Heme Oxygenase-1 in Metabolic Diseases: Curcumin and Resveratrol Analogues as Possible Inducers of Heme Oxygenase-1

Son, Y. H., Lee, J. H., Chung, H., & Pae, H. (2013) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2013/639541 · Cited by 115 · see citing works

Effects of different doses of resveratrol on body fat and serum parameters in rats fed a hypercaloric diet

Macarulla, M. T., Alberdi, G., Gómez‐Zorita, S., Tueros, I., Bald, C., Rodríguez, V. M., Martínez, J. A., & Portillo, M. P. (2009) · Journal of Physiology and Biochemistry · doi:10.1007/bf03185932 · Cited by 114 · see citing works

Red Wine Polyphenols Prevent Metabolic and Cardiovascular Alterations Associated with Obesity in Zucker Fatty Rats (Fa/Fa)

Agouni, A., Lagrue-Lak-Hal, A.-H., Mostefai, H. A., Tesse, A., Mulder, P. G. H., Rouet, P., Desmoulin, F., Heymes, C., Martínez, M. C., & Andriantsitohaina, R. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005557 · Cited by 111 · see citing works

Upregulation of Nox4 by TGFβ1 Oxidizes SERCA and Inhibits NO in Arterial Smooth Muscle of the Prediabetic Zucker Rat

Tong, X., Hou, X., Jourd’heuil, D., Weisbrod, R. M., & Cohen, R. A. (2010) · Circulation Research · doi:10.1161/circresaha.110.221242 · Cited by 110 · see citing works

The Protective Effect of Antioxidants Consumption on Diabetes and Vascular Complications

Dal-Ros, S., & Sigrist, S. (2016) · Diseases · doi:10.3390/diseases4030024 · Cited by 112 · see citing works

Metabolic effects of resveratrol: Addressing the controversies

Bitterman, J. L., & Chung, J. H. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1808-8 · Cited by 109 · see citing works

Resveratrol in Cancer Patients: From Bench to Bedside

Berretta, M., Bignucolo, A., Francia, R. D., Comello, F., Facchini, G., Ceccarelli, M., Iaffaioli, R. V., Quagliariello, V., & Maurea, N. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21082945 · Cited by 107 · see citing works

Hepatic lipid metabolic pathways modified by resveratrol in rats fed an obesogenic diet

Alberdi, G., Rodríguez, V. M., Macarulla, M. T., Miranda, J., Churruca, I., & Portillo, M. P. (2012) · Nutrition · doi:10.1016/j.nut.2012.09.011 · Cited by 106 · see citing works

The role of nutrition and nutraceutical supplements in the treatment of hypertension

Houston, M. C. (2014) · World Journal of Cardiology · doi:10.4330/wjc.v6.i2.38 · Cited by 108 · see citing works

Delipidating effect of resveratrol metabolites in 3<scp>T</scp>3‐<scp>L</scp>1 adipocytes

Lasa, A., Churruca, I., Eseberri, I., Andrés‐Lacueva, C., & Portillo, M. P. (2012) · Molecular Nutrition &amp; Food Research · doi:10.1002/mnfr.201100772 · Cited by 103 · see citing works

Resveratrol improves insulin signaling in a tissue-specific manner under insulin-resistant conditions only: in vitro and in vivo experiments in rodents

Kang, W., Hong, H. J., Guan, J., Kim, D. G., Yang, E.-J., Koh, G., Park, D.-B., Han, C. H., Lee, Y. J., & Lee, D.-H. (2011) · Metabolism · doi:10.1016/j.metabol.2011.08.003 · Cited by 103 · see citing works

The effects of chronictrans-resveratrol supplementation on aspects of cognitive function, mood, sleep, health and cerebral blood flow in healthy, young humans

Wightman, E. L., Haskell‐Ramsay, C. F., Reay, J. L., Williamson, G., Dew, T. P., Zhang, W., & Kennedy, D. O. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515003037 · Cited by 103 · see citing works

Resveratrol Improves Vascular Function and Mitochondrial Number but Not Glucose Metabolism in Older Adults

Pollack, R. M., Barzilai, N., Anghel, V., Kulkarni, A. S., Golden, A., Broin, P. Ó., Sinclair, D. A., Bonkowski, M. S., Coleville, A. J., Powell, D. S., et al. (2017) · The Journals of Gerontology Series A · doi:10.1093/gerona/glx041 · Cited by 102 · see citing works

Resveratrol restored Nrf2 function, reduced renal inflammation, and mitigated hypertension in spontaneously hypertensive rats

Javkhedkar, A. A., Quiroz, Y., Rodríguez‐Iturbe, B., Vaziri, N. D., Lokhandwala, M. F., & Banday, A. A. (2015) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00308.2014 · Cited by 100 · see citing works

Anti-atherogenic effects of resveratrol

Ramprasath, V. R., & Jones, P. J. H. (2010) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2010.77 · Cited by 100 · see citing works

Low doses of grape seed procyanidins reduce adiposity and improve the plasma lipid profile in hamsters

Caimari, A., Bas-Prior, J. M. D., Crescenti, A., & Arola, L. (2012) · International Journal of Obesity · doi:10.1038/ijo.2012.75 · Cited by 99 · see citing works

Resveratrol induces Sirt1-dependent apoptosis in 3T3-L1 preadipocytes by activating AMPK and suppressing AKT activity and survivin expression

Chen, S., Xiao, X., Feng, X., Li, W., Zhou, N., Zheng, L., Sun, Y., Zhang, Z., & Zhu, W. (2011) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2011.06.003 · Cited by 97 · see citing works

Targeting Nitric Oxide with Natural Derived Compounds as a Therapeutic Strategy in Vascular Diseases

Forte, M., Conti, V., Damato, A., Ambrosio, M., Puca, A. A., Sciarretta, S., Frati, G., Vecchione, C., & Carrizzo, A. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/7364138 · Cited by 96 · see citing works

Resveratrol enhances fatty acid oxidation capacity and reduces resistin and Retinol-Binding Protein 4 expression in white adipocytes

Mercader, J., Palou, A., & Bonet, M. L. (2010) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2010.07.007 · Cited by 95 · see citing works

Distribution of Resveratrol Metabolites in Liver, Adipose Tissue, and Skeletal Muscle in Rats Fed Different Doses of This Polyphenol

Andrés‐Lacueva, C., Macarulla, M. T., Rotchés-Ribalta, M., Boto‐Ordóñez, M., Urpí-Sardà, M., Rodríguez, V. M., & Portillo, M. P. (2012) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf3001108 · Cited by 96 · see citing works

Resveratrol in metabolic health: an overview of the current evidence and perspectives

Poulsen, M. M., Jørgensen, J. O. L., Jessen, N., Richelsen, B., & Pedersen, S. B. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12141 · Cited by 95 · see citing works

Resveratrol prevents embryonic oxidative stress and apoptosis associated with diabetic embryopathy and improves glucose and lipid profile of diabetic dam

Singh, C. K., Kumar, A., Hitchcock, D. B., Fan, D., Goodwin, R. L., LaVoie, H. A., Nagarkatti, P. S., DiPette, D. J., & Singh, U. S. (2011) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201000457 · Cited by 95 · see citing works

Up-regulation of Adiponectin by Resveratrol

Wang, A., Liu, M., Liu, X., Dong, L., Glickman, R. D., Slaga, T. J., Zhou, Z., & Liu, F. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.188144 · Cited by 92 · see citing works

Comparison of Calorie-Restricted Diet and Resveratrol Supplementation on Anthropometric Indices, Metabolic Parameters, and Serum Sirtuin-1 Levels in Patients With Nonalcoholic Fatty Liver Disease: A Randomized Controlled Clinical Trial

Asghari, S., Jafarabadi, M. A., Somi, M. H., Ghavami, S.-M., & Rafraf, M. (2018) · Journal of the American College of Nutrition · doi:10.1080/07315724.2017.1392264 · Cited by 92 · see citing works

Can metabolically healthy obesity be explained by diet, genetics, and inflammation?

Navarro, E., Funtikova, A. N., Fitó, M., & Schröder, H. (2014) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201400521 · Cited by 91 · see citing works

Resveratrol inhibits proliferation, angiogenesis and induces apoptosis in colon cancer cells

Fouad, M. A., Agha, A., Merzabani, M. A., & Shouman, S. A. (2013) · Human & Experimental Toxicology · doi:10.1177/0960327113475679 · Cited by 90 · see citing works

Resveratrol Upregulated SIRT1, FOXO1, and Adiponectin and Downregulated PPARγ1–3 mRNA Expression in Human Visceral Adipocytes

Costa, C. D. S., Rohden, F., Hammes, T. O., Margis, R., Bortolotto, J. W., Padoin, A. V., Mottin, C. C., & Guaragna, R. M. V. D. C. (2010) · Obesity Surgery · doi:10.1007/s11695-010-0251-7 · Cited by 90 · see citing works

Resveratrol Reduce Metabolic Disorders in Obese Rats

Abbas, N., AL-Awwadi, N. A. J., & Alyassin, F. F. (2011) · Cited by 1 · see citing works

Effect of resveratrol in gestational diabetes mellitus and its complications

Ma, H.-Z., Chen, Y., Guo, H.-H., Wang, J., Xin, X., Li, Y.-C., & Liu, Y. (2023) · World Journal of Diabetes · doi:10.4239/wjd.v14.i6.808 · Cited by 14 · see citing works

Hepatic lipid metabolic pathways modified by resveratrol in rats fed an obesogenic diet

Alberdi, G., Rodríguez, V. M., Macarulla, M. T., Miranda, J., Churruca, I., & Portillo, M. P. (2012) · Nutrition · doi:10.1016/j.nut.2012.09.011 · Cited by 106 · see citing works

Resveratrol ameliorates diabetes‐related metabolic changes via activation of AMP‐activated protein kinase and its downstream targets in db/db mice

Do, G., Jung, U. J., Park, H., Kwon, E., Jeon, S.-M., McGregor, R. A., & Choi, M. (2012) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201200067 · Cited by 141 · see citing works

Effects of Resveratrol Against Induced Metabolic Syndrome in Rats: Role of Oxidative Stress, Inflammation, and Insulin Resistance

Reda, D., Elshopakey, G. E., Mahgoub, H. A., Risha, E., Khan, A. A., Rajab, B. S., El‐Boshy, M., & Abdelhamid, F. (2022) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2022/3362005 · Cited by 16 · see citing works