Screening of Platycodonis Radix Fractions for Antiobesity Activities and Elucidation of Its Molecular Mechanisms in High-Fat Diet-Fed C57BL/6 Mice

被引:0
|
作者
Zhi, Nannan [1 ]
Chang, Xiangwei [1 ,2 ,3 ,4 ,5 ,7 ]
Wang, Xinrui [1 ]
Zhang, Xiaobo [6 ]
Wang, Jutao [1 ]
Zha, Liangping [1 ,5 ]
Gui, Shuangying [1 ,2 ,3 ,4 ,5 ,7 ]
机构
[1] Anhui Univ Chinese Med, Coll Pharm, Dept Food & Biopharmaceut, Hefei, Peoples R China
[2] Anhui Acad Chinese Med, Inst Pharmaceut, Dept Pharm, Hefei, Peoples R China
[3] Anhui Prov Key Lab Pharmaceut Preparat Technol & A, Dept Pharm, Hefei, Peoples R China
[4] Anhui Educ Dept AUCM, Engn Technol Res Ctr Modernized Pharmaceut, Dept Pharm, Hefei, Peoples R China
[5] MOE Anhui Joint Collaborat Innovat Ctr Qual Improv, Dept Tradit Chinese Med Resource, Hefei, Peoples R China
[6] State Key Lab Dao di Herbs, Dept Tradit Chinese Med Resource, Beijing, Peoples R China
[7] Anhui Univ Chinese Med, Coll Pharm, Dept Food & Biopharmaceut, Hefei 230012, Peoples R China
基金
中国国家自然科学基金;
关键词
antiobesity; mechanism; Platycodonis Radix fractions; polysaccharides; POLYSACCHARIDE; ACCUMULATION; GRANDIFLORUM; EXTRACT; OBESITY; CELLS;
D O I
10.1089/jmf.2023.K.0265
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Obesity is a threat to public health and effective new medications are required. Platycodonis Radix (PR) is a traditional medicinal/dietary plant with activities against obesity. Using mice given a diet rich in fat, the antiobesity components of PR were identified and their molecular mechanisms were clarified further in this investigation. Initially, the impacts of PR fractions on liver histology and biochemical markers were assessed. Subsequently, the degrees of lipogenic and lipolytic gene and protein expressions were determined. Oral administration of PR polysaccharides (PG) (0.80 g/kg body weight) improved liver function (alanine aminotransferase and aspartate aminotransferase) and its antioxidant activities (total superoxide dismutase, glutathione peroxidase, and malondialdehyde), as well as alleviated blood lipid (total cholesterol, total triglyceride, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol) values, inflammatory systemic (TNF-alpha and IL-1 beta), and histological abnormalities within the liver. Furthermore, PG administration downregulated the expression for lipogenic genes (ACC and FAS) and upregulated the expression for the lipolytic gene (PPAR alpha, LPL, CPT1, and HSL). Importantly, PG raised AMPK phosphorylation and decreased SREBP-1c protein synthesis. Thus, it is possible that PG stimulates the AMPK-LPL/HSL path (lipolytic route) plus the AMPK-ACC/PPAR alpha-CPT1 path (associated to beta-oxidation of fatty acids), while inhibiting the AMPK/(SREBP-1c)-ACC/FAS path (lipogenic route). In summary, PG has the ability to regulate lipid metabolism, and it may be useful to pharmacologically activate AMPK with PG to prevent and cure obesity.
引用
收藏
页码:477 / 487
页数:11
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