Anti-Obesity Effect and Mechanism of Chitooligosaccharides Were Revealed Based on Lipidomics in Diet-Induced Obese Mice.
Minchuan ZhouJingqing HuangJingwen ZhouCuiting ZhiYan BaiQishi CheHua CaoJiao GuoZhengquan SuPublished in: Molecules (Basel, Switzerland) (2023)
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.
Keyphrases
- insulin resistance
- adipose tissue
- high fat diet induced
- weight gain
- weight loss
- high fat diet
- skeletal muscle
- polycystic ovary syndrome
- metabolic syndrome
- type diabetes
- body weight
- glycemic control
- body mass index
- single cell
- bariatric surgery
- fatty acid
- randomized controlled trial
- oxidative stress
- protein kinase
- high throughput
- roux en y gastric bypass
- hydrogen peroxide
- nitric oxide
- south africa
- cell death
- gestational age
- birth weight
- stem cells
- single molecule
- reactive oxygen species
- obese patients
- binding protein
- gastric bypass
- chemotherapy induced
- bone marrow
- case control
- replacement therapy