Arctium lappa L. polysaccharide can regulate lipid metabolism in type 2 diabetic rats through the SREBP-1/SCD-1 axis

被引:32
作者
Chen, Min [1 ]
Xu, Jingge [1 ]
Wang, Yan [1 ]
Wang, Zhen [1 ,2 ]
Guo, Lanping [2 ]
Li, Xinpeng [1 ]
Huang, Luqi [2 ]
机构
[1] Linyi Univ, Coll Pharm, Linyi, Shandong, Peoples R China
[2] China Acad Chinese Med Sci, Natl Resources Ctr Chinese Mat Med, Beijing, Peoples R China
关键词
Arctium lappa L. polysaccharide; Type 2 diabetes mellitus; Lipid metabolism; SREBP-1/SCD-1; CHOLESTEROL; RISK; ACCUMULATION; DISEASE; SREBPS; LIVER;
D O I
10.1016/j.carres.2020.108055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the analysis of risk factors of diabetes mellitus with coronary heart disease, dyslipidemia is the most im-portant. Previous studies have found that Arctium lappa L. polysaccharide (ALP) can regulate lipid metabolism in type 1 diabetic rats, but it has not been studied in type 2 diabetes. In this study, the regulatory effect of ALP on lipid metabolism in type 2 diabetic rats was investigated by constructing a model of type 2 diabetes. The results of blood biochemical analysis showed that ALP effectively reduced the synthesis of triglycerides and cholesterol, and reduced the risk of atherosclerosis in diabetic rats. Histopathological observation (hematoxylin and eosin, Masson, Periodic Acid-Schiff and oil red O staining) showed that it also effectively regulated lipid metabolism in the liver of diabetic rats and inhibited the process of liver fibrosis. Immunohistochemistry and Western blot analysis showed that ALP regulated the expression of sterol regulatory element-binding protein-1 (SREBP-1) and stearoyl-CoA desaturase 1 (SCD-1) in the liver of diabetic rats. In conclusion, the results of this study demon-strate that ALP can effectively regulate lipid metabolism and reduce the risk of atherosclerosis in type 2 diabetic rats through the SREBP-1/SCD-1 axis.
引用
收藏
页数:8
相关论文
共 38 条
[1]   Pharmacodynamic-pharmacokinetic profiles of metformin hydrochloride from a mucoadhesive formulation of a polysaccharide with antidiabetic property in streptozotocin-induced diabetic rat models [J].
Adikwu, MU ;
Yoshikawa, Y ;
Takada, K .
BIOMATERIALS, 2004, 25 (15) :3041-3048
[2]   Evaluation and Management of Youth-Onset Type 2 Diabetes: A Position Statement by the American Diabetes Association [J].
Arslanian, Silva ;
Bacha, Fida ;
Grey, Margaret ;
Marcus, Marsha D. ;
White, Neil H. ;
Zeitler, Philip .
DIABETES CARE, 2018, 41 (12) :2648-2668
[3]   Characterizing the Role of HMG-CoA Reductase in Aryl Hydrocarbon Receptor-Mediated Liver Injury in C57BL/6 Mice [J].
Dornbos, Peter ;
Jurgelewicz, Amanda ;
Fader, Kelly A. ;
Williams, Kurt ;
Zacharewski, Timothy R. ;
LaPres, John J. .
SCIENTIFIC REPORTS, 2019, 9 (1)
[4]   SREBP transcription factors:: master regulators of lipid homeostasis [J].
Eberlé, D ;
Hegarty, B ;
Bossard, P ;
Ferré, P ;
Foufelle, F .
BIOCHIMIE, 2004, 86 (11) :839-848
[5]   Low-density lipoprotein receptor structure and folding [J].
Gent, J ;
Braakman, I .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (19-20) :2461-2470
[6]  
Gilbert R.G., 2005, CURR DRUG TARGETS, V16, P1
[7]  
Guerra C, 2001, J CLIN INVEST, V108, P1205, DOI 10.1172/JCI200113103
[8]   Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction [J].
Haffner, SM ;
Lehto, S ;
Rönnemaa, T ;
Pyörälä, K ;
Laakso, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (04) :229-234
[9]  
Helen M.C., 2019, DIABETES, V68, P175
[10]   Cathelicidin suppresses lipid accumulation and hepatic steatosis by inhibition of the CD36 receptor [J].
Hoang-Yen Tran, D. ;
Hoang-Ngoc Tran, D. ;
Mattai, S. A. ;
Sallam, T. ;
Ortiz, C. ;
Lee, E. C. ;
Robbins, L. ;
Ho, S. ;
Lee, J. E. ;
Fisseha, E. ;
Shieh, C. ;
Sideri, A. ;
Shih, D. Q. ;
Fleshner, P. ;
McGovern, D. P. D. ;
Vu, M. ;
Hing, T. C. ;
Bakirtzi, K. ;
Cheng, M. ;
Su, B. ;
Law, I. ;
Karagiannides, I. ;
Targan, S. R. ;
Gallo, R. L. ;
Li, Z. ;
Koon, H. W. .
INTERNATIONAL JOURNAL OF OBESITY, 2016, 40 (09) :1424-1434