Abstract | AIMS: MAIN METHODS: We established a diabetic nephropathy model in C57BL/6J mice with diabetes induced by streptozotocin and fed with diets containing high level of AGEs. Diabetic symptoms, renal functions, and pathohistology of pancreas and kidney were evaluated. AGE-RAGE pathway and oxidative stress parameters were determined. KEY FINDINGS: The model mice exhibited characteristic symptoms of diabetes including weight loss, polydipsia, polyphagia, polyuria, elevated blood glucose levels and low serum insulin levels during the experiments. However, loganin at doses of 0.02 and 0.1g/kg effectively improved these diabetic symptoms. Loganin reduced kidney/ body weight ratio, 24h urine protein levels, and serum levels of urea nitrogen and creatinine in diabetic mice to different degrees compared to positive controls. Moreover, loganin improved the histology of pancreas and kidney, and alleviated the structural alterations in endothelial cells, mesangial cells and podocytes in renal cortex. Finally, we found that loganin reduced AGE levels in serum and kidney and downregulated mRNA and protein expression of receptors for AGEs in kidney in diabetic mice. Loganin also reduced the levels of malondialdehyde and increased the levels of superoxide dismutase in serum and kidney. SIGNIFICANCE:
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Authors | Kai Liu, Huiqin Xu, Gaohong Lv, Bin Liu, Maxwell Kim Kit Lee, Chunhong Lu, Xing Lv, Yunhao Wu |
Journal | Life sciences
(Life Sci)
Vol. 123
Pg. 78-85
(Feb 15 2015)
ISSN: 1879-0631 [Electronic] Netherlands |
PMID | 25623853
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015 Elsevier Inc. All rights reserved. |
Chemical References |
- DNA Primers
- Glycation End Products, Advanced
- Iridoids
- Receptor for Advanced Glycation End Products
- Receptors, Immunologic
- Malondialdehyde
- Superoxide Dismutase
- loganin
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Topics |
- Analysis of Variance
- Animals
- Blood Urea Nitrogen
- Blotting, Western
- DNA Primers
(genetics)
- Diabetes Mellitus, Experimental
(complications)
- Diabetic Nephropathies
(drug therapy, etiology)
- Disease Models, Animal
- Dose-Response Relationship, Drug
- Gene Expression Regulation
(drug effects)
- Glycation End Products, Advanced
(adverse effects, blood)
- Iridoids
(chemistry, pharmacology, therapeutic use)
- Kidney
(physiopathology, ultrastructure)
- Malondialdehyde
(blood)
- Mice
- Mice, Inbred C57BL
- Microscopy, Electron, Transmission
- Molecular Structure
- Oxidative Stress
(physiology)
- Pancreas
(physiopathology)
- Proteinuria
(drug therapy)
- Receptor for Advanced Glycation End Products
- Receptors, Immunologic
(metabolism)
- Reverse Transcriptase Polymerase Chain Reaction
- Superoxide Dismutase
(blood)
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