Inhibition of the hepatic glucose output is responsible for the hypoglycemic effect of Crataegus aronia against type 2 diabetes mellitus in rats

被引:9
|
作者
Mostafa, Dalia G. [1 ,4 ]
Khaleel, Eman E. [2 ,4 ]
Abdel-Aleem, Ghada A. [3 ,5 ]
机构
[1] Assiut Univ, Fac Med, Dept Med Physiol, Assiut, Egypt
[2] Cairo Univ, Fac Med, Dept Med Physiol, Cairo, Egypt
[3] Tanta Univ, Fac Med, Dept Med Biochem, Tanta, Egypt
[4] King Khalid Univ, Coll Med, Dept Med Physiol, POB 3340, Abha 61421, Saudi Arabia
[5] King Khalid Univ, Coll Med, Dept Med Biochem, Abha, Saudi Arabia
关键词
C; aronia; insulin receptor; liver; GLUT-2; type 2 diabetes mellitus; FATTY LIVER-DISEASE; NF-KAPPA-B; INSULIN-RESISTANCE; NONALCOHOLIC STEATOHEPATITIS; OXIDATIVE STRESS; QUERCETIN; HYPERGLYCEMIA; CELLS; NIDDM; BETA;
D O I
10.2298/ABS170510044M
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study aimed to analyze the ameliorative effect of Crataegus aronia against type 2 diabetes mellitus (type 2-DM). Type 2-DM rats were treated with the extract and the changes in serum parameters (glucose, insulin, HbA(1c) and lipids) and hepatic parameters (oxidative stress, inflammation and mRNA levels of GLUT-2 and gluconeogenesis enzymes) were compared to those of control and untreated type 2-DM rats. Also, levels of hepatic insulin receptors 1A (IR-1A) were measured immunohistochemically and compared between groups. In type 2-DM rats, C. aronia significantly improved the oral glucose tolerance test (OGTT), lowered plasma glucose, serum lipid levels and the hepatic glycogen content. Also, it significantly lowered the levels of hepatic lipid peroxidation, tumor necrosis factor alpha (TNF alpha) and interleukin-6 (IL-6) and enhanced the level of reduced glutathione (GSII) and increased superoxide dismutase (SOD) activity. C. aronia enhanced hepatic mRNA expression of the insulin receptor A isoform (IR-A) and glucose 6-phosphatase (G6Pase), and lowered glucose transporter-2 (GLUT-2) and glycerol kinase (GK) mRNA expression. In conclusion, C. aronia ameliorates T2DM by inhibiting hepatic glucose output.
引用
收藏
页码:277 / 287
页数:11
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