The Effect of Chrysin-Loaded Phytosomes on Insulin Resistance and Blood Sugar Control in Type 2 Diabetic db/db Mice

被引:25
作者
Kim, Seong-min [1 ]
Imm, Jee-Young [1 ]
机构
[1] Kookmin Univ, Dept Foods & Nutr, Seoul 02707, South Korea
关键词
chrysin; phytosome; blood sugar control; C57BLKS; J-db; db mice; insulin resistance; VASCULAR COMPLICATIONS; GLUCOSE-PRODUCTION; LIVER; DIET; PHOSPHATIDYLCHOLINE; CHOLESTEROL; IMPROVEMENT; GLUCOKINASE; HOMEOSTASIS; METABOLISM;
D O I
10.3390/molecules25235503
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although a variety of beneficial health effects of natural flavonoids, including chrysin, has been suggested, poor solubility and bioavailability limit their practical use. As a promising delivery system, chrysin-loaded phytosomes (CPs) were prepared using egg phospholipid (EPL) at a 1:3 molar ratio and its antidiabetic effects were assessed in db/db diabetic mice. Male C57BLKS/J-db/db mice were fed a normal diet (control), chrysin diet (100 mg chrysin/kg), CP diet (100 mg chrysin equivalent/kg), metformin diet (200 mg/kg) or EPL diet (vehicle, the same amount of EPL used for CP preparation) for 9 weeks. Administration of CP significantly decreased fasting blood glucose and insulin levels in db/db mice compared with the control. An oral glucose tolerance test and homeostatic model assessment for insulin resistance were significantly improved in the CP group (p < 0.05). CP treatment suppressed gluconeogenesis via downregulation of phosphoenolpyruvate carboxykinase while it promoted glucose uptake in the skeletal muscle and liver of db/db mice (p < 0.05). The CP-mediated improved glucose utilization in the muscle was confirmed by upregulation of glucose transporter type 4, hexokinase2 and peroxisome proliferator-activated receptor gamma during treatment (p < 0.05). The CP-induced promotion of GLUT4 plasma translocation was confirmed in the skeletal muscle of db/db mice (p < 0.05). Based on the results, CP showed greater antidiabetic performance compared to the control by ameliorating insulin resistance in db/db mice and phytosome can be used as an effective antidiabetic agent.
引用
收藏
页数:12
相关论文
共 56 条
[1]   Chrysin, an anti-inflammatory molecule, abrogates renal dysfunction in type 2 diabetic rats [J].
Ahad, Amjid ;
Ganai, Ajaz Ahmad ;
Mujeeb, Mohd ;
Siddiqui, Waseem Ahmad .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2014, 279 (01) :1-7
[2]  
Andrade N, 2019, FOOD FUNCT, V10, P4566, DOI [10.1039/c9fo01142k, 10.1039/C9FO01142K]
[3]   Chronic consumption of the dietary polyphenol chrysin attenuates metabolic disease in fructose-fed rats [J].
Andrade, Nelson ;
Andrade, Sara ;
Silva, Claudia ;
Rodrigues, Ilda ;
Guardao, Luisa ;
Guimaraes, Joao T. ;
Keating, Elisa ;
Martel, Fatima .
EUROPEAN JOURNAL OF NUTRITION, 2020, 59 (01) :151-165
[4]   Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension [J].
Barroso, I ;
Gurnell, M ;
Crowley, VEF ;
Agostini, M ;
Schwabe, JW ;
Soos, MA ;
Maslen, GL ;
Williams, TDM ;
Lewis, H ;
Schafer, AJ ;
Chatterjee, VKK ;
O'Rahilly, S .
NATURE, 1999, 402 (6764) :880-883
[5]   Novel concepts in insulin regulation of hepatic gluconeogenesis [J].
Barthel, A ;
Schmoll, D .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 285 (04) :E685-E692
[6]   Type 2 diabetes impairs splanchnic uptake of glucose but does not alter intestinal glucose absorption during enteral glucose feeding - Additional evidence for a defect in hepatic glucokinase activity [J].
Basu, A ;
Basu, R ;
Shah, P ;
Vella, A ;
Johnson, CM ;
Jensen, M ;
Nair, KS ;
Schwenk, WF ;
Rizza, RA .
DIABETES, 2001, 50 (06) :1351-1362
[7]   Insulin sensitivity of suppression of endogenous glucose production is the single most important determinant of glucose tolerance [J].
Båvenholm, PN ;
Pigon, J ;
Östenson, CG ;
Efendic, S .
DIABETES, 2001, 50 (06) :1449-1454
[8]   HbA1c as a screening tool for detection of Type 2 diabetes:: a systematic review [J].
Bennett, C. M. ;
Guo, M. ;
Dharmage, S. C. .
DIABETIC MEDICINE, 2007, 24 (04) :333-343
[9]   GLUT4, AMP kinase, but not the insulin receptor, are required for hepatoportal glucose sensor-stimulated muscle glucose utilization [J].
Burcelin, R ;
Crivelli, V ;
Perrin, C ;
Da Costa, A ;
Mu, J ;
Kahn, BB ;
Birnbaum, MJ ;
Kahn, CR ;
Vollenweider, P ;
Thorens, B .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (10) :1555-1562
[10]   Evolution and regulatory role of the hexokinase [J].
Cárdenas, ML ;
Cornish-Bowden, A ;
Ureta, T .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1998, 1401 (03) :242-264