Guangdong Engineering Research Center of Natural Products and New Drugs, Guangdong Provincial University Engineering Technology Research Center of Natural Products and Drugs, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Guangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Key Laboratory of Glucolipid Metabolic Disorder, Ministry of Education of China, Institute of Chinese Medicine, Guangdong TCM Key Laboratory for Metabolic Diseases, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Molecules. 2023 Jul 23;28(14):5595. doi: 10.3390/molecules28145595.
Chitooligosaccharide (COS) is a natural product from the ocean, and while many studies have reported its important role in metabolic diseases, no study has systematically elaborated the anti-obesity effect and mechanism of COS. Herein, COSM (MW ≤ 3000 Da) was administered to diet-induced obese mice by oral gavage once daily for eight weeks. The results show that COSM administration reduced body weight; slowed weight gain; reduced serum Glu, insulin, NEFA, TC, TG, and LDL-C levels; increased serum HSL and HDL-C levels; improved inflammation; and reduced lipid droplet size in adipose tissue. Further lipidomic analysis of adipose tissue revealed that 31 lipid species are considered to be underlying lipid biomarkers in COS therapy. These lipids are mainly enriched in pathways involving insulin resistance, thermogenesis, cholesterol metabolism, glyceride metabolism and cyclic adenosine monophosphate (cAMP), which sheds light on the weight loss mechanism of COS. The Western blot assay demonstrated that COSM intervention can improve insulin resistance, inhibit de novo synthesis, and promote thermogenesis and β-oxidation in mitochondria by the AMPK pathway, thereby alleviating high-fat diet-induced obesity. In short, our study can provide a more comprehensive direction for the application of COS in obesity based on molecular markers.
壳寡糖(COS)是一种海洋天然产物,虽然许多研究报道了其在代谢性疾病中的重要作用,但尚无研究系统阐述 COS 的抗肥胖作用及其机制。在此,通过每日口服灌胃给予饮食诱导肥胖的小鼠 COSM(MW≤3000Da),连续 8 周。结果表明,COS 可降低体重、减缓体重增加、降低血清 Glu、胰岛素、NEFA、TC、TG 和 LDL-C 水平、升高血清 HSL 和 HDL-C 水平、改善炎症、减少脂肪组织中脂质滴的大小。进一步对脂肪组织的脂质组学分析表明,有 31 种脂质被认为是 COS 治疗的潜在脂质生物标志物。这些脂质主要富集在涉及胰岛素抵抗、产热、胆固醇代谢、甘油酯代谢和环腺苷酸(cAMP)的途径中,这为 COS 的减肥机制提供了新的见解。Western blot 检测表明,COS 通过 AMPK 通路可改善胰岛素抵抗、抑制从头合成、促进线粒体产热和β-氧化,从而缓解高脂肪饮食诱导的肥胖。总之,我们的研究可以为 COS 在肥胖症中的应用提供更全面的分子标志物方向。