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高脂饮食诱导肥胖小鼠的异黄酮脂肪酸酯的减肥作用及其潜在机制。

Anti-obesity effect of an isoflavone fatty acid ester on obese mice induced by high fat diet and its potential mechanism.

机构信息

Nanjing Brain Hospital affiliated to Nanjing Medical University, Nanjing 210029, PR China.

出版信息

Lipids Health Dis. 2010 May 19;9:49. doi: 10.1186/1476-511X-9-49.

Abstract

BACKGROUND

The novel compound 1a is one of the isoflavone fatty acid esters. In order to investigate the anti-obesity effect of compound 1a and its potential mechanism of influence in adipocyte differentiation, Obese male C57BL/6J mice induced by high-fat diet (HFD) and rat preadipocytes (3T3-L1 cell) were used.

METHODS

After 4-week HFD induction, the obese model was made successfully. After treatment with compound 1a, mice plasma biochemistry parameters were analyzed. In addition, mice hepatic tissue slice was observed. In in vitro research, 3T3-L1 cell differentiation by Oil-Red-O staining and adipocyte apoptosis was detected by flow cytometry.

RESULTS

The in vivo results implied that compound 1a significantly decreased the body weight, white adipose tissue weight of obesity mice (p<0.05), reduced leptin and TG in plasma (p<0.05), elevated HDL-C in serum (p<0.05). The in vitro results suggested that compound 1a could significantly suppress the adipocyte viability and lipid accumulation in the differentiation of preadipocyte, and induce apoptosis in both preadipocytes and mature adipocytes (p<0.05).

CONCLUSION

Compound 1a regulates serum lipid profiles, decreases adipose tissue mass and body weight gain by inducing adipocyte apoptosis in high fat diet induced mice. Thus, it may be used to treat obese patients with hypercholesterolemia and hypertriglyceridemia.

摘要

背景

新型化合物 1a 是异黄酮脂肪酸酯之一。为了研究化合物 1a 的抗肥胖作用及其在脂肪细胞分化中的潜在影响机制,本研究使用了高脂饮食(HFD)诱导的肥胖雄性 C57BL/6J 小鼠和大鼠前脂肪细胞(3T3-L1 细胞)。

方法

经过 4 周的 HFD 诱导,成功建立肥胖模型。用化合物 1a 处理后,分析小鼠血浆生化参数。此外,还观察了小鼠肝组织切片。在体外研究中,通过油红 O 染色检测 3T3-L1 细胞分化,通过流式细胞术检测脂肪细胞凋亡。

结果

体内结果表明,化合物 1a 显著降低肥胖小鼠的体重和白色脂肪组织重量(p<0.05),降低血浆中瘦素和 TG(p<0.05),升高血清中 HDL-C(p<0.05)。体外结果表明,化合物 1a 可显著抑制前脂肪细胞分化过程中的脂肪细胞活力和脂质积累,并诱导前脂肪细胞和成熟脂肪细胞凋亡(p<0.05)。

结论

化合物 1a 通过诱导脂肪细胞凋亡来调节高脂饮食诱导的小鼠血清脂质谱,减少脂肪组织质量和体重增加。因此,它可能用于治疗伴有高胆固醇血症和高三酰甘油血症的肥胖患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cfd/2889992/15a08189c2b5/1476-511X-9-49-1.jpg

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