Tea Polypeptide Ameliorates Diabetic Nephropathy through RAGE and NF-κB Signaling Pathway in Type 2 Diabetes Mice

被引:41
作者
Deng, Xuming [1 ,2 ]
Sun, Lingli [1 ]
Lai, Xingfei [1 ]
Xiang, Limin [1 ]
Li, Qiuhua [1 ]
Zhang, Wenji [1 ]
Zhang, Lingzhi [2 ]
Sun, Shili [1 ]
机构
[1] Guangdong Acad Agr Sci, Guangdong Prov Key Lab Tea Plant Resources Innova, Tea Res Inst, Dafeng Rd 6, Guangzhou 510640, Guangdong, Peoples R China
[2] South China Univ Technol, Coll Hort, Dept Tea Sci, Guangzhou 510641, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
tea polypeptide; type; 2; diabetes; diabetic nephropathy; AGEs; NF-kappa B; GROWTH-FACTOR-BETA; TGF-BETA; BIOACTIVE PEPTIDES; HEART-FAILURE; RENAL-DISEASE; EXPRESSION; GLUCOSE; ACTIVATION; RAT; INVOLVEMENT;
D O I
10.1021/acs.jafc.8b04819
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Diabetic nephropathy (DN) is a major complication of type 2 diabetes (T2D), which is a key determinant of mortality in diabetic patients. Developing new therapeutic drugs which can not only control T2D but also prevent the development of DN is of great significance. We studied the therapeutic potential of Cuiyu tea polypeptides (TP), natural bioactive peptides isolated from a type of green tea, against DN and its underlying molecular mechanisms. TP (1000 mg/kg bw/day, p.o.) administration for 5 weeks significantly reduced the fasting blood glucose by 52.04 +/- 9.23% in the high fat diet/streptozocin (HFD/STZ)-induced (30 mg/kg bw) diabetic mice. Compared to the model group, the serum insulin level of the TP group was decreased by 25.54 +/- 6.06%, while at the same time, the HOMA-IR, HOMA-IS, and lipid levels showed different degrees of recovery (p < 0.05). Moreover, in TP group mice the total urinary protein, creatinine, and urine nitrogen, all which can reflect the damage degree of the glomerular filtration function to a certain extent, dramatically declined by 34.51 +/- 2.65%, 42.24 +/- 15.24%, and 80.30 +/- 6.01% compared to the model group, respectively. Mechanistically, TP stimulated the polyol PKC zeta/JNK/NF-kappa B/THF-alpha/iNOS and AGEs/RAGE/TGF-beta 1 pathways, upregulated the expression of podocin in the glomeruli, and decreased the release of pro -inflammatory cytokines. These results strongly indicate the therapeutic potential of TP against DN.
引用
收藏
页码:11957 / 11967
页数:11
相关论文
共 57 条
[1]   Tryptic amaranth glutelin digests induce endothelial nitric oxide production through inhibition of ACE: Antihypertensive role of amaranth peptides [J].
Barba de la Rosa, A. P. ;
Barba Montoya, A. ;
Martinez-Cuevas, Pedro ;
Hernandez-Ledesma, B. ;
Leon-Galvan, M. F. ;
De Leon-Rodriguez, A. ;
Gonzalez, C. .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2010, 23 (02) :106-111
[2]   Mechanistic insight of diabetic nephropathy and its pharmacotherapeutic targets: An update [J].
Bhattacharjee, Niloy ;
Barma, Sujata ;
Konwar, Nandita ;
Dewanjee, Saikat ;
Manna, Prasenjit .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2016, 791 :8-24
[3]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[4]   Green tea polyphenol extract regulates the expression of genes involved in glucose uptake and insulin signaling in rats fed a high fructose diet [J].
Cao, Heping ;
Hininger-Favier, Isabelle ;
Kelly, Meghan A. ;
Benaraba, Rachida ;
Dawson, Harry D. ;
Coves, Sara ;
Roussel, Anne M. ;
Anderson, Richard A. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (15) :6372-6378
[5]   Inhibition of high glucose-induced inflammation and fibrosis by a novel curcumin derivative prevents renal and heart injury in diabetic mice [J].
Chen, Hongjin ;
Yang, Xi ;
Lu, Kongqin ;
Lu, Chun ;
Zhao, Yunjie ;
Zheng, Suqing ;
Li, Jieli ;
Huang, Zhangjian ;
Huang, Yi ;
Zhang, Yali ;
Liang, Guang .
TOXICOLOGY LETTERS, 2017, 278 :48-58
[6]   Extracellular signals and intracellular pathways in diabetic nephropathy [J].
Chuang, LY ;
Guh, JY .
NEPHROLOGY, 2001, 6 (04) :165-172
[7]   Early events leading to renal injury in obese Zucker (fatty) rats with type II diabetes [J].
Coimbra, TM ;
Janssen, U ;
Gröne, HJ ;
Ostendorf, T ;
Kunter, U ;
Schmidt, H ;
Brabant, G ;
Floege, J .
KIDNEY INTERNATIONAL, 2000, 57 (01) :167-182
[8]   Interaction of metabolic and haemodynamic factors in mediating experimental diabetic nephropathy [J].
Cooper, ME .
DIABETOLOGIA, 2001, 44 (11) :1957-1972
[9]   Optimization of Protein Extraction and Decoloration Conditions for Tea Residues [J].
Cui Qiaoyun ;
Ni Xinghong ;
Zeng Liang ;
Tu Zheng ;
Li Jin ;
Sun Kang ;
Chen Xuan ;
Li Xinghui .
HORTICULTURAL PLANT JOURNAL, 2017, 3 (04) :172-176
[10]   Kidney involvement in a nongenetic rat model of type 2 diabetes [J].
Danda, RS ;
Habiba, NM ;
Rincon-Choles, H ;
Bhandari, BK ;
Barnes, JL ;
Abboud, HE ;
Pergola, PE .
KIDNEY INTERNATIONAL, 2005, 68 (06) :2562-2571