Department of Food and Biopharmaceuticals, College of Pharmacy, Anhui University of Chinese Medicine, Hefei, China.
Department of Pharmacy, Institute of Pharmaceutics, Anhui Academy of Chinese Medicine, Hefei, China.
J Med Food. 2024 Jun;27(6):477-487. doi: 10.1089/jmf.2023.K.0265. Epub 2024 Mar 18.
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- and IL-1), 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, 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-CPT1 path (associated to -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.
肥胖是威胁公众健康的一个因素,因此需要有效的新型药物。桔梗(PR)是一种具有抗肥胖活性的传统药用/食用植物。本研究采用高脂肪饮食喂养的小鼠,鉴定了 PR 的抗肥胖成分,并进一步阐明了其分子机制。首先,评估了 PR 馏分对肝组织学和生化标志物的影响。随后,测定了脂肪生成和脂肪分解基因和蛋白表达的程度。PR 多糖(PG)(0.80g/kg 体重)口服给药可改善肝功能(丙氨酸氨基转移酶和天冬氨酸氨基转移酶)及其抗氧化活性(总超氧化物歧化酶、谷胱甘肽过氧化物酶和丙二醛),并减轻血脂(总胆固醇、总甘油三酯、高密度脂蛋白胆固醇和低密度脂蛋白胆固醇)值、全身性炎症(TNF-α 和 IL-1)以及肝脏的组织学异常。此外,PG 给药下调了脂肪生成基因(ACC 和 FAS)的表达,上调了脂肪分解基因(PPAR、LPL、CPT1 和 HSL)的表达。重要的是,PG 增加了 AMPK 磷酸化并减少了 SREBP-1c 蛋白合成。因此,PG 可能通过刺激 AMPK-LPL/HSL 途径(脂肪分解途径)和 AMPK-ACC/PPAR-CPT1 途径(与脂肪酸的β-氧化相关),同时抑制 AMPK/(SREBP-1c)-ACC/FAS 途径(脂肪生成途径)来刺激脂质代谢。总之,PG 具有调节脂质代谢的能力,用 PG 药理学激活 AMPK 可能有助于预防和治疗肥胖症。