Department of Public Health and Applied and Nutrition, Institute of Health Bioscience, University of Tokushima, 3-18-15 Kuramoto, Tokushima 770-8503, Japan.
Tokushima Prefectural Industrial Technology Center, Tokushima, Japan.
Nutr Metab (Lond). 2014 Jul 4;11:32. doi: 10.1186/1743-7075-11-32. eCollection 2014.
Obesity is a major risk factor for insulin resistance, type 2 diabetes, and stroke. Flavonoids are effective antioxidants that protect against these chronic diseases. In this study, we evaluated the effects of sudachitin, a polymethoxylated flavonoid found in the skin of the Citrus sudachi fruit, on glucose, lipid, and energy metabolism in mice with high-fat diet-induced obesity and db/db diabetic mice. In our current study, we show that sudachitin improves metabolism and stimulates mitochondrial biogenesis, thereby increasing energy expenditure and reducing weight gain.
C57BL/6 J mice fed a high-fat diet (40% fat) and db/db mice fed a normal diet were treated orally with 5 mg/kg sudachitin or vehicle for 12 weeks. Following treatment, oxygen expenditure was assessed using indirect calorimetry, while glucose tolerance, insulin sensitivity, and indices of dyslipidemia were assessed by serum biochemistry. Quantitative polymerase chain reaction was used to determine the effect of sudachitin on the transcription of key metabolism-regulating genes in the skeletal muscle, liver, and white and brown adipose tissues. Primary myocytes were also prepared to examine the signaling mechanisms targeted by sudachitin in vitro.
Sudachitin improved dyslipidemia, as evidenced by reduction in triglyceride and free fatty acid levels, and improved glucose tolerance and insulin resistance. It also enhanced energy expenditure and fatty acid β-oxidation by increasing mitochondrial biogenesis and function. The in vitro assay results suggest that sudachitin increased Sirt1 and PGC-1α expression in the skeletal muscle.
Sudachitin may improve dyslipidemia and metabolic syndrome by improving energy metabolism. Furthermore, it also induces mitochondrial biogenesis to protect against metabolic disorders.
肥胖是胰岛素抵抗、2 型糖尿病和中风的主要危险因素。类黄酮是有效的抗氧化剂,可以预防这些慢性疾病。在这项研究中,我们评估了在高脂肪饮食诱导肥胖的小鼠和 db/db 糖尿病小鼠中,一种存在于日本蜜柑果皮中的多甲氧基类黄酮——川陈皮素对葡萄糖、脂质和能量代谢的影响。在我们目前的研究中,我们表明川陈皮素可以改善代谢并刺激线粒体生物发生,从而增加能量消耗并减轻体重增加。
用高脂肪饮食(40%脂肪)喂养 C57BL/6J 小鼠和用普通饮食喂养 db/db 小鼠,并用 5mg/kg 的川陈皮素或载体口服处理 12 周。治疗后,通过间接测热法评估耗氧量,同时通过血清生化评估葡萄糖耐量、胰岛素敏感性和血脂异常指数。用定量聚合酶链反应来确定川陈皮素对骨骼肌、肝脏和白色和棕色脂肪组织中关键代谢调节基因转录的影响。还制备了原代肌细胞来体外研究川陈皮素作用的信号机制。
川陈皮素改善了血脂异常,表现为甘油三酯和游离脂肪酸水平降低,葡萄糖耐量和胰岛素抵抗改善。它还通过增加线粒体生物发生和功能来增强能量消耗和脂肪酸β氧化。体外试验结果表明,川陈皮素增加了骨骼肌中的 Sirt1 和 PGC-1α 的表达。
川陈皮素通过改善能量代谢可能改善血脂异常和代谢综合征。此外,它还诱导线粒体生物发生以预防代谢紊乱。