Synergistic effects of metformin, resveratrol, and hydroxymethylbutyrate on insulin sensitivity

被引:59
作者
Bruckbauer, Antje [1 ]
Zemel, Michael B. [1 ,2 ]
机构
[1] NuSirt Sci Inc, Nashville, TN USA
[2] Univ Tennessee, Dept Nutr, Knoxville, TN 37931 USA
关键词
diabetes; AMP-activated protein kinase; Sirt1; fat oxidation;
D O I
10.2147/DMSO.S40840
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: The purpose of this study was to determine whether a mixture of the polyphenol, resveratrol, and the leucine metabolite, hydroxymethylbutyrate (HMB), acts synergistically with low doses of metformin to impact insulin sensitivity and AMP-activated protein kinasedependent outcomes in cell culture and in diabetic mice. Methods: C2C12 skeletal myotubes and 3T3-L1 adipocytes were treated with resveratrol 0.2 mu M, HMB 5 mu M, and metformin 0.1 mM alone or in combination. db/db mice were treated for 2 weeks with high (1.5 g/kg diet), low (0.75 g/kg diet), or very low (0.25 g/kg diet) doses of metformin alone or in combination with a diet containing resveratrol 12.5 mg and CaHMB 2 g/kg. Results: The combination of metformin-resveratrol-HMB significantly increased fat oxidation, AMP-activated protein kinase, and Sirt1 activity in muscle cells compared with metformin or resveratrol-HMB alone. A similar trend was found in 3T3L1 adipocytes. In mice, the two lower doses of metformin exerted no independent effect but, when combined with resveratrol-HMB, both low-dose and very low-dose metformin improved insulin sensitivity (HOMAIR), plasma insulin levels, and insulin tolerance test response to a level comparable with that found for high-dose metformin. In addition, the metformin-resveratrol-HMB combination decreased visceral fat and liver weight in mice. Conclusion: Resveratrol-HMB combined with metformin may act synergistically on AMP-activated protein kinase-dependent pathways, leading to increased insulin sensitivity, which may reduce the therapeutic doses of metformin necessary in the treatment of diabetes.
引用
收藏
页码:93 / 101
页数:9
相关论文
共 40 条
[1]
Effect of 5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside infusion on in vivo glucose and lipid metabolism in lean and obese Zucker rats [J].
Bergeron, R ;
Previs, SF ;
Cline, GW ;
Perret, P ;
Russell, RR ;
Young, LH ;
Shulman, GI .
DIABETES, 2001, 50 (05) :1076-1082
[2]
Synergistic effects of leucine and resveratrol on insulin sensitivity and fat metabolism in adipocytes and mice [J].
Bruckbauer, Antje ;
Zemel, Michael B. ;
Thorpe, Teresa ;
Akula, Murthy R. ;
Stuckey, Alan C. ;
Osborne, Dustin ;
Martin, Emily B. ;
Kennel, Stephen ;
Wall, Jonathan S. .
NUTRITION & METABOLISM, 2012, 9
[3]
Effects of dairy consumption on SIRT1 and mitochondrial biogenesis in adipocytes and muscle cells [J].
Bruckbauer, Antje ;
Zemel, Michael B. .
NUTRITION & METABOLISM, 2011, 8
[4]
PGC-1α, SIRT1 and AMPK, an energy sensing network that controls energy expenditure [J].
Canto, Carles ;
Auwerx, Johan .
CURRENT OPINION IN LIPIDOLOGY, 2009, 20 (02) :98-105
[5]
Metformin opposes impaired AMPK and SIRT1 function and deleterious changes in core clock protein expression in white adipose tissue of genetically-obese db/db mice [J].
Caton, P. W. ;
Kieswich, J. ;
Yaqoob, M. M. ;
Holness, M. J. ;
Sugden, M. C. .
DIABETES OBESITY & METABOLISM, 2011, 13 (12) :1097-1104
[6]
Metformin suppresses hepatic gluconeogenesis through induction of SIRT1 and GCN5 [J].
Caton, Paul W. ;
Nayuni, Nanda K. ;
Kieswich, Julius ;
Khan, Noorafza Q. ;
Yaqoob, Muhammed M. ;
Corder, Roger .
JOURNAL OF ENDOCRINOLOGY, 2010, 205 (01) :97-106
[7]
Identification and characterization of a small molecule AMPK activator that treats key components of type 2 diabetes and the metabolic syndrome [J].
Cool, Barbara ;
Zinker, Bradley ;
Chiou, William ;
Kifle, Lemma ;
Cao, Ning ;
Perham, Matthew ;
Dickinson, Robert ;
Adler, Andrew ;
Gagne, Gerard ;
Iyengar, Rajesh ;
Zhao, Gang ;
Marsh, Kennan ;
Kym, Philip ;
Jung, Paul ;
Camp, Heidi S. ;
Frevert, Ernst .
CELL METABOLISM, 2006, 3 (06) :403-416
[8]
Specific SIRT1 Activation Mimics Low Energy Levels and Protects against Diet-induced Metabolic Disorders by Enhancing Fat Oxidation [J].
Feige, Jerome N. ;
Lagouge, Marie ;
Canto, Carles ;
Strehle, Axelle ;
Houten, Sander M. ;
Milne, Jill C. ;
Lambert, Philip D. ;
Mataki, Chikage ;
Elliott, Peter J. ;
Auwerx, Johan .
CELL METABOLISM, 2008, 8 (05) :347-358
[9]
The anti-diabetic drugs rosiglitazone and metformin stimulate AMP-activated protein kinase through distinct signaling pathways [J].
Fryer, LGD ;
Parbu-Patel, A ;
Carling, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (28) :25226-25232
[10]
Ablation of AMP-Activated Protein Kinase α2 Activity Exacerbates Insulin Resistance Induced by High-Fat Feeding of Mice [J].
Fujii, Nobuharu ;
Ho, Richard C. ;
Manabe, Yasuko ;
Jessen, Niels ;
Toyoda, Taro ;
Holland, William L. ;
Summers, Scott A. ;
Hirshman, Michael F. ;
Goodyear, Laurie J. .
DIABETES, 2008, 57 (11) :2958-2966