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首页> 外文期刊>Pharmaceutical Biology >Saponin-enriched sea cucumber extracts exhibit an antiobesity effect through inhibition of pancreatic lipase activity and upregulation of LXR-β signaling
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Saponin-enriched sea cucumber extracts exhibit an antiobesity effect through inhibition of pancreatic lipase activity and upregulation of LXR-β signaling

机译:富含皂苷的海参提取物通过抑制胰腺脂肪酶活性和上调LXR-β信号传导表现出抗肥胖作用

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Abstract Context: Sea cucumbers have been consumed as tonic, food, and nutrition supplements for many years. Objective: The objective of this study is to investigate the antiobesity and lipid-lowering effects of sea cucumber extracts in in vitro and in vivo models and elucidate the mechanism of action of the extracts on obesity and dyslipidemia. Materials and methods: The 60% ethanol extracts from the body walls of 10 different sea cucumbers were investigated for the inhibition of pancreatic lipase (PL) activity in vitro. The optimal active extract (SC-3) was further chemically analyzed by LC-MS and UV. And 0.1% and 0.2% of SC-3 was mixed with a high-fat diet to treat C57/BL6 mice for 6 weeks or 2 weeks as preventive and therapeutic study. The body weight, serum, and liver lipid profile in the mice were investigated. Results: The crude extract of Pearsonothuria graeffei Semper (Holothuriidae) inhibited the PL activity by 36.44% of control at 0.5?μg/mL. SC-3 and echinoside A inhibited PL with an IC50 value at 2.86?μg/mL and 0.76?μM. 0.1% of SC-3 reduced the body weight (23.0?±?0.62 versus 26.3?±?0.76 g), the serum TC (2.46?±?0.04 versus 2.83?±?0.12?mmol/L), TG (0.19?±?0.08 versus 0.40?±?0.03?mmo/L), and LDL-c (0.48?±?0.02 versus 0.51?±?0.02?mmol/L), and liver TC (1.19?±?0.17 versus 1.85?±?0.13?mmol/mg) and TG (6.18?±?0.92 versus 10.87?±?0.97?mmol/mg) contents of the obese C57BL/six mice on a high-fat diet. Discussion and conclusion: Sea cucumber may be used for developing antiobesity and antihyperlipidemia drugs.
机译:摘要背景:海参作为滋补品,食物和营养补品已被食用多年。目的:本研究的目的是研究海参提取物在体内和体外模型中的抗肥胖和降脂作用,并阐明该提取物对肥胖和血脂异常的作用机理。材料和方法:研究了从10种不同海参体壁提取的60%乙醇提取物在体外对胰腺脂肪酶(PL)活性的抑制作用。最佳活性提取物(SC-3)通过LC-MS和UV进一步化学分析。将0.1%和0.2%的SC-3与高脂饮食混合,对C57 / BL6小鼠进行6周或2周的预防和治疗研究。研究了小鼠的体重,血清和肝脂质谱。结果:在0.5μg/ mL的条件下,重生斑节肢生毛虫的粗提物对PL活性的抑制率为对照的36.44%。 SC-3和棘球side苷A抑制PL的IC 50 值为2.86?μg/ mL和0.76?μM。 0.1%的SC-3降低了体重(23.0%±0.62比26.3%±0.76 g),血清TC(2.46%±0.04对2.83%±0.12mmol / L),TG(0.19%/ L)降低了体重。 ±?0.08对0.40?±?0.03?mmo / L)和LDL-c(0.48?±?0.02对0.51?±?0.02?mmol / L)和肝TC(1.19?±?0.17对1.85?±高脂饮食的肥胖C57BL /六只小鼠的胆固醇含量分别为(0.13?mmol / mg)和TG(6.18?±?0.92对10.87?±?0.97?mmol / mg)含量。讨论与结论:海参可用于开发抗肥胖和高脂血症药物。

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