A systematic review on anti-diabetic action of 7-O-galloyl-D- sedoheptulose, a polyphenol from Corni Fructus, in type 2 diabetic mice with hepatic and pancreatic damage

被引:1
作者
Park, Chan Hum [1 ]
Noh, Jeong Sook [2 ]
Jeon, Jin Pyeong [3 ,6 ]
Yokozawa, Takako [4 ,5 ]
机构
[1] Hallym Univ, Inst New Frontier Res Team, Res Inst Med Bio Convergence, Chunchon, South Korea
[2] Tongmyong Univ, Dept Food Sci & Nutr, Busan, South Korea
[3] Hallym Univ, Coll Med, Dept Neurosurg, Chunchon, South Korea
[4] Univ Toyama, Grad Sch Sci & Engn Res, Toyama, Japan
[5] Univ Toyama, Grad Sch Sci & Engn Res, 3190 Gofuku, Toyama 9308555, Japan
[6] Hallym Univ, Coll Med, Dept Neurosurg, Chunchon 24252, South Korea
关键词
7-O-galloyl-D-sedoheptulose; type; 2; diabetes; liver; pancreas; oxidative stress; inflammation; fibrosis; HACHIMI-JIO-GAN; OXIDATIVE STRESS; INSULIN-RESISTANCE; GLUCOSE TOXICITY; NAD(P)H OXIDASE; INCREASED EXPRESSION; NITRIC-OXIDE; CELL-LINE; BETA; 7-O-GALLOYL-D-SEDOHEPTULOSE;
D O I
10.5582/ddt.2022.01097
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Traditional medicines are recently being focused on to treat diabetes and its complications because of their lack of toxic and/or side effects. This report describes the effects of 7-O-galloyl-D-sedoheptulose (GS), a polyphenolic compound isolated from Corni Fructus, on type 2 diabetic db/db mice with hepatic and pancreatic damage. We examined several biochemical factors and oxidative stress-and inflammation-related markers. In the serum, levels of glucose, leptin, insulin, C-peptide, resistin, tumor necrosis factor-alpha, and interleukin-6 were down-regulated, while adiponectin was augmented by GS treatment. In addition, GS suppressed the reactive oxygen species and lipid peroxidation in the serum, liver, and pancreas, but increased the pancreatic insulin and pancreatic C-peptide contents. These results were derived from attenuating the expression of nicotinamide adenine dinucleotide phosphate oxidase subunit proteins, Nox-4 and p22phox. Augmented nuclear factor (NF)-E2-related factor 2 and heme oxygenase-1 were reduced with a decrease in oxidative stress during GS treatment. NF-kappa B-related pro-inflammatory factors were also alleviated in hepatic tissue. Moreover, GS modulated the protein expressions of pro-inflammatory NF-kappa B, cyclooxygenase-2, inducible nitric oxide synthase, c-Jun N-terminal kinase (JNK), phosphor-JNK, activator protein-1, transforming growth factor-131, and fibronectin. Based on these results, we demonstrated that the anti-diabetic action of GS may be due to its anti-oxidative stress property and anti-inflammatory action.
引用
收藏
页码:151 / 156
页数:6
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