Abstract |
This study aimed to investigate the structure of a new heteropolysaccharide (MC-Pa) from Moutan Cortex (MC), and its protection on diabetic nephropathy (DN). The MC-Pa composed of D-glucose and L-arabinose (3.31:2.25) was characterized with homogeneous molecular weight of 1.64 × 105 Da, and the backbone was 4)-α-D-Glcp-(1 → 5-α-L-Araf-(1 → 3,5-α-L-Araf-(1→, branched partially at O-3 with α-L-Araf-(1 → residue with methylated-GC-MS and NMR. Furthermore, MC-Pa possessed strong antioxidant activity in vitro and inhibited the production of ROS caused by AGEs. In vivo, MC-Pa could alleviate mesangial expansion and tubulointerstitial fibrosis of DN rats in histopathology and MC-Pa could decrease significantly the serum levels of AGEs and RAGE. Western blot and immunohistochemical analysis showed that MC-Pa can reduce the expression of main protein (FN and Col IV) of extracellular-matrix, down-regulate the production of inflammatory factors (ICAM-1 and VCAM-1), and therefore regulate the pathway of TGF-β1. The above indicated that MC-Pa has an improving effect on DN.
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Authors | Yuanpei Lian, Maomao Zhu, Juan Chen, Bing Yang, Qinglin Lv, Long Wang, Shuchen Guo, Xiaobin Tan, Chang Li, Weiquan Bu, Wenbo Ding, Xiaobin Jia, Liang Feng |
Journal | International journal of biological macromolecules
(Int J Biol Macromol)
Vol. 176
Pg. 589-600
(Apr 15 2021)
ISSN: 1879-0003 [Electronic] Netherlands |
PMID | 33581205
(Publication Type: Journal Article)
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Copyright | Copyright © 2021. Published by Elsevier B.V. |
Chemical References |
- Drugs, Chinese Herbal
- Glycation End Products, Advanced
- Polysaccharides
- moutan cortex
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Topics |
- Animals
- Diabetes Mellitus, Experimental
(drug therapy, metabolism, pathology)
- Diabetic Nephropathies
(drug therapy, metabolism, pathology)
- Drugs, Chinese Herbal
(chemistry)
- Glycation End Products, Advanced
(metabolism)
- Human Umbilical Vein Endothelial Cells
- Humans
- Male
- Paeonia
(chemistry)
- Polysaccharides
(chemistry, pharmacology)
- Rats
- Rats, Sprague-Dawley
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