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丝素和家蚕蛹肽可抑制高脂肪饮食喂养大鼠前体脂肪细胞的脂肪生成和脂肪积累。

Silk and silkworm pupa peptides suppress adipogenesis in preadipocytes and fat accumulation in rats fed a high-fat diet.

机构信息

College of Veterinary Medicine and Research Institute of Veterinary Medicine, Chungbuk National University, 52 Naesudongro, Gaesin-dong, Cheongju, Chungbuk 361-763, Korea.

出版信息

Eur J Nutr. 2012 Dec;51(8):1011-9. doi: 10.1007/s00394-011-0280-6. Epub 2011 Dec 13.

Abstract

PURPOSE

The objective was to confirm the anti-obesity activity of a silk peptide (SP) and a silkworm pupa peptide (SPP) in rats fed a high-fat diet (HFD) and to elucidate their action mechanism(s) in a preadipocyte culture system.

METHODS

In an in vitro mechanistic study, the differentiation and maturation of 3T3-L1 preadipocytes were stimulated with insulin (5 μg/mL), and effects of SP and SPP on the adipogenesis of mature adipocytes were assessed. In an in vivo anti-obesity study, male C57BL/6 mice were fed an HFD containing SP or SPP (0.3, 1.0, or 3.0%) for 8 weeks, and blood and tissue parameters of obesity were analyzed.

RESULTS

Hormonal stimulation of preadipocytes led to a 50-70% increase in adipogenesis. Polymerase chain reaction and Western blot analyses revealed increases in adipogenesis-specific genes (leptin and Acrp30) and proteins (peroxisome proliferator-activated receptor-γ and Acrp30). The hormone-induced adipogenesis and activated gene expression was substantially inhibited by treatment with SP and SPP (1-50 μg/mL). The HFD markedly increased body weight gain by increasing the weight of epididymal and mesenteric fat. Body and fat weights were significantly reduced by SP and SPP, in which decreases in the area of abdominal adipose tissue and the size of epididymal adipocytes were confirmed by magnetic resonance imaging and microscopic examination, respectively. Long-term HFD caused hepatic lipid accumulation and increased blood triglycerides and cholesterol, in addition to their regulatory factors Acrp30 and leptin. However, SP and SPP recovered the concentrations of Acrp30 and leptin, and attenuated steatosis.

CONCLUSIONS

SP and SPP inhibit the differentiation of preadipocytes and adipogenesis by modulating signal transduction pathways and improve HFD-induced obesity by reducing lipid accumulation and the size of adipocytes.

摘要

目的

确认丝肽(SP)和蚕蛹肽(SPP)在高脂肪饮食(HFD)喂养大鼠中的抗肥胖活性,并阐明它们在脂肪前体细胞培养系统中的作用机制。

方法

在体外机制研究中,用胰岛素(5μg/mL)刺激 3T3-L1 脂肪前体细胞的分化和成熟,并评估 SP 和 SPP 对成熟脂肪细胞的脂肪生成作用。在体内抗肥胖研究中,雄性 C57BL/6 小鼠用含 SP 或 SPP(0.3、1.0 或 3.0%)的 HFD 喂养 8 周,分析肥胖的血液和组织参数。

结果

激素刺激脂肪前体细胞导致脂肪生成增加 50-70%。聚合酶链反应和 Western blot 分析显示,脂肪生成特异性基因(瘦素和 Acrp30)和蛋白(过氧化物酶体增殖物激活受体-γ 和 Acrp30)增加。SP 和 SPP(1-50μg/mL)处理显著抑制激素诱导的脂肪生成和激活基因表达。HFD 通过增加附睾和肠系膜脂肪的重量显著增加体重增加。SP 和 SPP 显著降低体重和脂肪重量,磁共振成像和显微镜检查分别证实了腹部脂肪组织面积和附睾脂肪细胞大小的减少。长期 HFD 导致肝脂质积累,增加血液甘油三酯和胆固醇,以及它们的调节因子 Acrp30 和瘦素。然而,SP 和 SPP 恢复了 Acrp30 和瘦素的浓度,并减轻了脂肪变性。

结论

SP 和 SPP 通过调节信号转导通路抑制脂肪前体细胞的分化和脂肪生成,并通过减少脂质积累和脂肪细胞大小改善 HFD 诱导的肥胖。

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