共 66 条
Vitamin D as a modulating agent of metformin and insulin in patients with type 2 diabetes
被引:2
作者:
Abdi, Fatemeh
[1
]
Movahedi, Monireh
[1
]
Alavi Nikje, Mir Mohammad
[2
]
Ghanei, Laleh
[3
]
Mirzaie, Sako
[4
]
机构:
[1] Islamic Azad Univ, Dept Cellular & Mol Biol, Tehran North Branch, Tehran, Iran
[2] Imam Khomeini Int Univ, Fac Sci, Dept Chem, POB 288, Qazvin, Iran
[3] Islamic Azad Univ, Tehran Med Sci Branch, Dept Endocrinol, Tehran, Iran
[4] Islamic Azad Univ, Sanandaj Branch, Dept Biochem, Sanandaj, Iran
来源:
JOURNAL OF RESEARCH IN PHARMACY
|
2019年
/
23卷
/
03期
关键词:
Diabetes mellitus type 2;
metformin;
vitamin D;
molecular dynamics;
vitamin D receptor;
QM/MM;
D-RECEPTOR;
OVEREXPRESSING GLUT4;
GLUCOSE-PRODUCTION;
MOLECULAR DOCKING;
LIGAND;
DYNAMICS;
ACTIVATION;
MUSCLE;
DOMAIN;
GENE;
D O I:
10.12991/jrp.2019.144
中图分类号:
R9 [药学];
学科分类号:
100702 [药剂学];
摘要:
Diabetes, which is one of the most important health challenges for humankind, is associated with impaired glucose metabolism. Diabetes mellitus (DM) includes two major types of diabetes, type 1 (T1DM) and type 2 (T2DM). In this study, in the beginning, interventional and experimental studies were performed on 45 patients with T2DM, and the modulating effects of vitamin D were evaluated on the biochemical parameters of patients with the restricted diet, consuming metformin or insulin. With regard to our experimental results, the combination treatment of metformin/ vitamin D or insulin/ vitamin D can reduce the fasting blood sugar (FBS). A combination of vitamin D with insulin decreases the insulin resistance and raises the insulin sensitivity in patients with T2DM. The combination treatment of vitamin D and metformin led to a decrease in the level of mRNA of GLUT4, and also it's trafficking from the cytosol to the plasma membrane. At the second phase of the present study, molecular dynamics (MD), molecular docking, IATM/PBSA, and QM/MM were occupied to examine the structural behavior of VDR, in the free or ligand bound state, during 50 ns. The MD results exhibited that in the presence of metformin, the flexibility of residues comprising helix 12 from vitamin D-bound VDR was decreased. In addition, metformin decreased the radius of gyration of agonist-bound VDR. In addition, QM/MM results showed that metformin diminished the binding free energy between VDR and vitamin D. Our computational data demonstrated that metformin, in the presence of vitamin D, reinforces the interaction between VDR and its co-activator protein.
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页码:360 / 378
页数:19
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