Natural Saponins on Cholesterol-Related Diseases: Treatment and Mechanism

被引:3
作者
Xiao, Man-Yu [1 ]
Li, Si [1 ]
Pei, Wen-Jing [1 ]
Gu, Yu-Long [1 ]
Piao, Xiang-Lan [1 ]
机构
[1] Minzu Univ China, Sch Pharm, Beijing, Peoples R China
关键词
atherosclerosis; cancer; cholesterol metabolism; diabetes; hyperlipidemia; saponin; HIGH-FAT DIET; PANAX-NOTOGINSENG SAPONINS; EXCESS BODY-WEIGHT; LIPID-METABOLISM; ASTRAGALOSIDE IV; SEA-CUCUMBER; IN-VITRO; TRITERPENE-SAPONINS; SIGNALING PATHWAYS; FUROSTANOL SAPONIN;
D O I
10.1002/ptr.8432
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Saponins are compounds composed of lipophilic aglycones linked to hydrophilic sugars. Natural saponins are isolated from plants and some Marine organisms. As important cholesterol-lowering drugs, natural saponins have attracted wide attention for their therapeutic potential in a variety of cholesterol-related metabolic diseases. To review the effects of natural saponins on cholesterol-related metabolic diseases, and to deepen the understanding of the cholesterol-lowering mechanism of saponins. The literature related to saponins and cholesterol-lowering diseases was collected using keywords "saponins" and "cholesterol" from PubMed, Web of Science, and Google Scholar from January 2000 to May 2024. The total number of articles related to saponins and cholesterol-lowering diseases was 240 after excluding irrelevant articles. Natural saponins can regulate cholesterol to prevent and treat a variety of diseases, such as atherosclerosis, diabetes, liver disease, hyperlipidemia, cancer, and obesity. Mechanistically, natural saponins regulate cholesterol synthesis and uptake through the AMPK/SREBP2/3-hydroxy-3-methyl-glutaryl coenzyme A reductase pathway and PCSK9/LDLR pathway, and regulate cholesterol efflux and esterification targeting Liver X receptor/ABC pathway and ACAT family. Natural saponins have broad application prospects in regulating cholesterol metabolism, for the development of more cholesterol-lowering drugs provides a new train of thought. However, it is still necessary to further explore the molecular mechanism and expand clinical trials to provide more evidence.
引用
收藏
页码:1292 / 1318
页数:27
相关论文
共 224 条
[1]   Karaya root saponin exerts a hypocholesterolemic response in rats fed a high-cholesterol diet [J].
Afrose, Sadia ;
Hossain, Md. S. ;
Maki, Takaaki ;
Tsujii, Hirotada .
NUTRITION RESEARCH, 2009, 29 (05) :350-354
[2]   Niemann-Pick C1 like 1 protein is critical for intestinal cholesterol absorption [J].
Altmann, SW ;
Davis, HR ;
Zhu, LJ ;
Yao, XR ;
Hoos, LM ;
Tetzloff, G ;
Iyer, SPN ;
Maguire, M ;
Golovko, A ;
Zeng, M ;
Wang, LQ ;
Murgolo, N ;
Graziano, MP .
SCIENCE, 2004, 303 (5661) :1201-1204
[3]  
[Anonymous], 2018, DIABETES CARE, V41, pS1, DOI [10.2337/dc18-SINT01, 10.2337/dc18-Sint01]
[4]   Antidiabetic effects of Panax ginseng berry extract and the identification of an effective component [J].
Attele, AS ;
Zhou, YP ;
Xie, JT ;
Wu, JA ;
Zhang, L ;
Dey, L ;
Pugh, W ;
Rue, PA ;
Polonsky, KS ;
Yuan, CS .
DIABETES, 2002, 51 (06) :1851-1858
[5]  
Azubuike Nkiruka Chinonyelum, 2018, Pak J Pharm Sci, V31, P2143
[6]   Distribution of Saponins in the Sea Cucumber Holothuria lessoni; the Body Wall Versus the Viscera, and Their Biological Activities [J].
Bahrami, Yadollah ;
Zhang, Wei ;
Franco, Christopher M. M. .
MARINE DRUGS, 2018, 16 (11)
[7]   Proposed mechanisms for the extracellular release of PD-L1 by the anticancer saponin platycodin D [J].
Bailly, Christian ;
Vergoten, Gerard .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2020, 85
[8]   Inhibition of HUVEC tubulogenesis by hederacolchiside-A1 is associated with plasma membrane cholesterol sequestration and activation of the Ha-Ras/MEK/ERK cascade [J].
Barthomeuf, C ;
Boivin, D ;
Béliveau, R .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2004, 54 (05) :432-440
[9]  
Benjamin EJ, 2018, CIRCULATION, V137, pE67, DOI [10.1161/CIR.0000000000000558, 10.1161/CIR.0000000000000485, 10.1161/CIR.0000000000000530]
[10]   Retrospective on Cholesterol Homeostasis: The Central Role of Scap [J].
Brown, Michael S. ;
Radhakrishnan, Arun ;
Goldstein, Joseph L. .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 87, 2018, 87 :783-807