DOI QR코드

DOI QR Code

Anti-diabetic effect of purple corn extract on C57BL/KsJ db/db mice

  • Huang, Bo (College of Food Science and Engineering, Liaoning Medical University) ;
  • Wang, Zhiqiang (Department of Food Science and Nutrition and Center for Aging and HealthCare, Hallym University) ;
  • Park, Jong Hyuk (Institute of Natural Medicine, Hallym University Medical School) ;
  • Ryu, Ok Hyun (Division of Endocrinology and Metabolism, Department of Internal Medicine, Hallym University) ;
  • Choi, Moon Ki (Division of Endocrinology and Metabolism, Department of Internal Medicine, Hallym University) ;
  • Lee, Jae-Yong (Institute of Natural Medicine, Hallym University Medical School) ;
  • Kang, Young-Hee (Department of Food Science and Nutrition and Center for Aging and HealthCare, Hallym University) ;
  • Lim, Soon Sung (Institute of Natural Medicine, Hallym University Medical School)
  • Received : 2013.12.27
  • Accepted : 2014.10.08
  • Published : 2015.02.01

Abstract

BACKGROUND/OBJECTIVES: Recently, anthocyanins have been reported to have various biological activities. Furthermore, anthocyanin-rich purple corn extract (PCE) ameliorated insulin resistance and reduced diabetes-associated mesanginal fibrosis and inflammation, suggesting that it may have benefits for the prevention of diabetes and diabetes complications. In this study, we determined the anthocyanins and non-anthocyanin component of PCE by HPLC-ESI-MS and investigated its anti-diabetic activity and mechanisms using C57BL/KsJ db/db mice. MATERIALS/METHODS: The db/db mice were divided into four groups: diabetic control group (DC), 10 or 50 mg/kg PCE (PCE 10 or PCE 50), or 10 mg/kg pinitol (pinitol 10) and treated with drugs once per day for 8 weeks. During the experiment, body weight and blood glucose levels were measured every week. At the end of treatment, we measured several diabetic parameters. RESULTS: Compared to the DC group, Fasting blood glucose levels were 68% lower in PCE 50 group and 51% lower in the pinitol 10 group. Furthermore, the PCE 50 group showed 2-fold increased C-peptide and adiponectin levels and 20% decreased HbA1c levels, than in the DC group. In pancreatic islets morphology, the PCE- or pinitol-treated mice showed significant prevention of pancreatic ${\beta}$-cell damage and higher insulin content. Microarray analyses results indicating that gene and protein expressions associated with glycolysis and fatty acid metabolism in liver and fat tissues. In addition, purple corn extract increased the phosphorylation of AMP-activated protein kinase (AMPK) and decreased phosphoenolpyruvate carboxykinase (PEPCK), glucose 6-phosphatase (G6pase) genes in liver, and also increased glucose transporter 4 (GLUT4) expressions in skeletal muscle. CONCLUSIONS: Our results suggested that PCE exerted anti-diabetic effects through protection of pancreatic ${\beta}$-cells, increase of insulin secretion and AMPK activation in the liver of C57BL/KsJ db/db mice.

Keywords

References

  1. Vinik AI, Vinik E. Prevention of the complications of diabetes. Am J Manag Care 2003;3:S63-80.
  2. Goldfrank L, Lewin N, Flomenbaum N, Howland MA. The pernicious panacea: herbal medicine. Hosp Physician 1982;10:64-9.
  3. Bailey CJ, Day C. Traditional plant medicines as treatments for diabetes. Diabetes Care 1989;8:553-64.
  4. Jing P, Giusti MM. Characterization of anthocyanin-rich waste from purple corncobs (Zea mays L.) and its application to color milk. J Agric Food Chem 2005;22:8775-81.
  5. Fossen T, Slimestad R, Andersen OM. Anthocyanins from maize (Zea mays) and reed canarygrass (Phalaris arundinacea). J Agric Food Chem 2001;5:2318-21.
  6. Hagiwara A, Miyashita K, Nakanishi T, Sano M, Tamano S, Kadota T, Koda T, Nakamura M, Imaida K, Ito N, Shirai T. Pronounced inhibition by a natural anthocyanin, purple corn color, of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-associated colorectal carcinogenesis in male F344 rats pretreated with 1,2-dimethylhydrazine. Cancer Lett 2001;1:17-25.
  7. Tsuda T, Horio F, Osawa T. Dietary cyanidin 3-O-beta-D-glucoside increases ex vivo oxidation resistance of serum in rats. Lipids 1998; 6:583-8.
  8. Tsuda T, Shiga K, Ohshima K, Kawakishi S, Osawa T. Inhibition of lipid peroxidation and the active oxygen radical scavenging effect of anthocyanin pigments isolated from Phaseolus vulgaris L. Biochem Pharmacol 1996;7:1033-9.
  9. Yoshimoto M, Okuno S, Yoshinaga M, Yamakawa O, Yamaguchi M, Yamada J. Antimutagenicity of sweetpotato (Ipomoea batatas) roots. Biosci Biotechnol Biochem 1999;3:537-41.
  10. Li J, Lim SS, Lee JY, Kim JK, Kang SW, Kim JL, Kang YH. Purple corn anthocyanins dampened high-glucose-induced mesangial fibrosis and inflammation: possible renoprotective role in diabetic nephropathy. J Nutr Biochem 2012;4:320-31.
  11. Tsuda T, Horio F, Uchida K, Aoki H, Osawa T. Dietary cyanidin 3-O-beta-D-glucoside-rich purple corn color prevents obesity and ameliorates hyperglycemia in mice. J Nutr 2003;7:2125-30.
  12. Trinder P. Determination of blood glucose using an oxidaseperoxidase system with a non-carcinogenic chromogen. J Clin Pathol 1969;2:158-61.
  13. Goldstein BJ. Insulin resistance as the core defect in type 2 diabetes mellitus. Am J Cardiol 2002;90:3G-10G.
  14. Liu F, Kim J, Li Y, Liu X, Li J, Chen X. An extract of Lagerstroemia speciosa L. has insulin-like glucose uptake-stimulatory and adipocyte differentiation-inhibitory activities in 3T3-L1 cells. J Nutr 2001;9: 2242-7.
  15. Guo H, Guo J, Jiang X, Li Z, Ling W. Cyanidin-3-O-b-glucoside, a typical anthocyanin, exhibits antilipolytic effects in 3T3-L1 adipocytes during hyperglycemia: Involvement of FoxO1-mediated transcription of adipose triglyceride lipase. Food chem Toxicol 2012;9: 3040-7.
  16. Zhao X, Corrales M, Zhang C, Hu X, Ma Y, Tauscher B. Composition and thermal stability of anthocyanins from chinese purple corn (Zea mays L.). J Agric Food Chem 2008;22:10761-6.
  17. Libby P, Plutzky J. Diabetic macrovascular disease: the glucose paradox? Circulation 2002;22:2760-3.
  18. Nishina PM, Naggert JK, Verstuyft J, Paigen B. Atherosclerosis in genetically obese mice: the mutants obese, diabetes, fat, tubby, and lethal yellow. Metabolism 1994;5:554-8.
  19. Narayanan CR, Joshi DD, Mudjumdar AM, Dhekne VV. Pinitol, a new anti-diabetic compound from the leaves of Bougainvillea spectabilis. Curr Sci 1987;56:139-41.
  20. Hong S, Heo J, Kim J, Kwon S, Yeo K, Bakowska-Barczak A, Kolodziejczyk, P, Ryu O, Choi M, Kang Y, Lim S, Suh H, Huh S, Lee J. Antidiabetic and Beta Cell-Protection Activities of Purple Corn Anthocyanins. Biomol Ther 2013;21:284-9. https://doi.org/10.4062/biomolther.2013.016
  21. Alberti KG, Zimmet PZ. New diagnostic criteria and classification of diabetes--again? Diabet Med 1998;7:535-6.
  22. Scott DK, O'Doherty RM, Stafford JM, Newgard CB, Granner DK. The repression of hormone-activated PEPCK gene expression by glucose is insulin-independent but requires glucose metabolism. J Biol Chem 1998;37:24145-51.
  23. Bressler R, Brendel K. The role of carnitine and carnitine acyltransferase in biological acetylations and fatty acid synthesis. J Biol Chem 1966;17:4092-7.
  24. Kelly DP, Gordon JI, Alpers R, Strauss AW. The tissue-specific expression and developmental regulation of two nuclear genes encoding rat mitochondrial proteins. Medium chain acyl-CoA dehydrogenase and mitochondrial malate dehydrogenase. J Biol Chem 1989;32:18921-5.
  25. Ling B, Aziz C, Alcorn J. Systematic Evaluation of Key L-Carnitine Homeostasis Mechanisms during Postnatal Development in Rat. Nutr Metab (Lond) 2012;1:66.
  26. Nemali MR, Usuda N, Reddy MK, Oyasu K, Hashimoto T, Osumi T, Rao MS, Reddy JK. Comparison of constitutive and inducible levels of expression of peroxisomal beta-oxidation and catalase genes in liver and extrahepatic tissues of rat. Cancer Res 1988;18:5316-24.
  27. Tsuchida T, Fukuda S, Aoyama H, Taniuchi N, Ishihara T, Ohashi N, Sato H, Wakimoto K, Shiotani M, Oku A. MGAT2 deficiency ameliorates high-fat diet-induced obesity and insulin resistance by inhibiting intestinal fat absorption in mice. Lipids Health Dis 2012; 11:75. https://doi.org/10.1186/1476-511X-11-75
  28. Jiang Z, Michal JJ, Chen J, Daniels TF, Kunej T, Garcia MD, Gaskins CT, Busboom JR, Alexander LJ, Wright RW Jr, Macneil MD. Discovery of novel genetic networks associated with 19 economically important traits in beef cattle. Int J Biol Sci 2009;6:528-42.
  29. Wu XL, Macneil MD, De S, Xiao QJ, Michal JJ, Gaskins CT, Reeves JJ, Busboom JR, Wright RW Jr, Jiang Z. Evaluation of candidate gene effects for beef backfat via Bayesian model selection. Genetica 2005; 1:103-13.
  30. Hardie DG. The AMP-activated protein kinase pathway--new players upstream and downstream. J Cell Sci 2004;23:5479-87.
  31. Towler MC, Hardie DG. AMP-activated protein kinase in metabolic control and insulin signaling. Circ Res 2007;3:328-41.
  32. Kemp BE, Mitchelhill KI, Stapleton D, Michell BJ, Chen ZP, Witters LA. Dealing with energy demand: the AMP-activated protein kinase. Trends Biochem Sci 1999;1:22-5.
  33. Rutter GA, Da Silva Xavier G, Leclerc I. Roles of 5'-AMP-activated protein kinase (AMPK) in mammalian glucose homoeostasis. Biochem J 2003;1:1-16.
  34. Velasco G, Geelen MJ, Guzman M. Control of hepatic fatty acid oxidation by 5'-AMP-activated protein kinase involves a malonyl-CoA-dependent and a malonyl-CoA-independent mechanism. Arch Biochem Biophys 1997;2:169-75.
  35. Merrill GF, Kurth EJ, Hardie DG, Winder WW. AICA riboside increases AMP-activated protein kinase, fatty acid oxidation, and glucose uptake in rat muscle. Am J Physiol 1997;1:E1107-12.

Cited by

  1. Effect of African Mango (Irvingia gabonesis, IGOB 131TM) Extract on Glucose Regulation in STZ-Induced Diabetes vol.44, pp.11, 2015, https://doi.org/10.3746/jkfn.2015.44.11.1607
  2. Optimization of extraction parameters of PTP1β (protein tyrosine phosphatase 1β), inhibitory polyphenols, and anthocyanins from Zea mays L. using response surface methodology (RSM) vol.16, pp.1, 2016, https://doi.org/10.1186/s12906-016-1296-5
  3. Anti-diabetic effect of Alpinia oxyphylla extract on 57BL/KsJ db-/db- mice vol.13, pp.4, 2017, https://doi.org/10.3892/etm.2017.4152
  4. Blue Maize Extract Improves Blood Pressure, Lipid Profiles, and Adipose Tissue in High-Sucrose Diet-Induced Metabolic Syndrome in Rats vol.20, pp.2, 2017, https://doi.org/10.1089/jmf.2016.0087
  5. Dietary Anthocyanins and Insulin Resistance: When Food Becomes a Medicine vol.9, pp.10, 2017, https://doi.org/10.3390/nu9101111
  6. Antidiabetic Potential of Monoterpenes: A Case of Small Molecules Punching above Their Weight vol.19, pp.1, 2017, https://doi.org/10.3390/ijms19010004
  7. Rebelling against the (Insulin) Resistance: A Review of the Proposed Insulin-Sensitizing Actions of Soybeans, Chickpeas, and Their Bioactive Compounds vol.10, pp.4, 2018, https://doi.org/10.3390/nu10040434
  8. Studies on the Antidiabetic and Antinephritic Activities of Paecilomyces hepiali Water Extract in Diet-Streptozotocin-Induced Diabetic Sprague Dawley Rats vol.2016, pp.None, 2015, https://doi.org/10.1155/2016/4368380
  9. Antidiabetic and Antinephritic Activities of Aqueous Extract of Cordyceps militaris Fruit Body in Diet-Streptozotocin-Induced Diabetic Sprague Dawley Rats vol.2016, pp.None, 2016, https://doi.org/10.1155/2016/9685257
  10. A Yellow Waxy Corn Single Cross Hybrid 'Goldchal' with High Carotenoid Content vol.50, pp.3, 2018, https://doi.org/10.9787/kjbs.2018.50.3.268
  11. The target cells of anthocyanins in metabolic syndrome vol.59, pp.6, 2019, https://doi.org/10.1080/10408398.2018.1491022
  12. Effect of sulfur dioxide and lactic acid in steeping water on the extraction of anthocyanins and bioactives from purple corn pericarp vol.96, pp.3, 2019, https://doi.org/10.1002/cche.10157
  13. Polyphenols targeting diabetes via the AMP-activated protein kinase pathway; future approach to drug discovery vol.56, pp.7, 2015, https://doi.org/10.1080/10408363.2019.1648376
  14. Foods from Mayan Communities of Yucatán as Nutritional Alternative for Diabetes Prevention vol.23, pp.4, 2015, https://doi.org/10.1089/jmf.2019.0125
  15. Sweet Cherry Extract Targets the Hallmarks of Cancer in Prostate Cells: Diminished Viability, Increased Apoptosis and Suppressed Glycolytic Metabolism vol.72, pp.6, 2015, https://doi.org/10.1080/01635581.2019.1661502
  16. Anthocyanins, Vibrant Color Pigments, and Their Role in Skin Cancer Prevention vol.8, pp.9, 2015, https://doi.org/10.3390/biomedicines8090336
  17. Purple corn extract (PCE) alleviates cigarette smoke (CS)-induced DNA damage in rodent blood cells by activation of AMPK/Foxo3a/MnSOD pathway vol.25, pp.1, 2015, https://doi.org/10.1080/19768354.2021.1883734
  18. The role of anthocyanins as antidiabetic agents: from molecular mechanisms to in vivo and human studies vol.77, pp.1, 2015, https://doi.org/10.1007/s13105-020-00739-z
  19. Purple corn extract alleviates 2,4-dinitrochlorobenzene-induced atopic dermatitis-like phenotypes in BALB/c mice vol.25, pp.5, 2015, https://doi.org/10.1080/19768354.2021.1974938
  20. Acylated anthocyanins: A review on their bioavailability and effects on postprandial carbohydrate metabolism and inflammation vol.20, pp.6, 2015, https://doi.org/10.1111/1541-4337.12836
  21. Dietary Antioxidant Anthocyanins Mitigate Type II Diabetes through Improving the Disorder of Glycometabolism and Insulin Resistance vol.69, pp.45, 2021, https://doi.org/10.1021/acs.jafc.1c05630