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根提取物对3T3-L1脂肪细胞和SD大鼠模型中脂肪生成和脂质生成的影响。

Effects of root extract on adipogenesis and lipogenesis in 3T3-L1 adipocytes and SD rat models.

作者信息

Kim Kyoung Kon, Lee Hye Rim, Jang Sun Min, Kim Tae Woo

机构信息

Newgen Healthcare Co., Chuncheon 24232, Korea.

Kangwon National University Well-Being Bioproducts R&D Center, Hoengseong 25209, Korea.

出版信息

Nutr Res Pract. 2024 Apr;18(2):180-193. doi: 10.4162/nrp.2024.18.2.180. Epub 2024 Mar 21.

Abstract

BACKGROUND/OBJECTIVES: Obesity is a major cause of metabolic disorders; to prevent obesity, research is ongoing to develop natural and safe ingredients with few adverse effects. In this study, we determined the anti-obesity effects of root extract (KWFD-H01) in 3T3-L1 adipocytes and Sprague-Dawley (SD) rats.

MATERIALS/METHODS: The anti-obesity effects of KWFD-H01in 3T3-L1 adipocytes and SD rats were examined using various assays, including Oil Red O staining, gene expression analyses, protein expression analyses, and blood biochemical analyses.

RESULTS

KWFD-H01 reduced intracellular lipid accumulation and inhibited the mRNA expression of peroxisome proliferator-activated receptor γ (PPARγ), cytidine-cytidine-adenosine-adenosine-thymidine (CCAAT)/enhancer binding proteins (C/EBPα), sterol regulatory element-binding transcription factor 1 (SREBP-1c), acetyl-CoA carboxylase (ACC), and fatty acid synthase (FAS) in 3T3-L1 cells. KWFD-H01 also reduced body weight, weight gain, and the levels of triglycerides, total and LDL-cholesterol, glucose, and leptin, while increasing high-density lipoprotein-cholesterol and adiponectin in SD rats. PPARγ, C/EBPα, SREBP-1c, ACC, and FAS protein expression was inhibited in the epididymal fat of SD rats.

CONCLUSION

Overall, these results confirm the anti-obesity effects of KWFD-H01 in 3T3-L1 adipocytes and SD rats, indicating their potential as baseline data for developing functional health foods or pharmaceuticals to control obesity.

摘要

背景/目的:肥胖是代谢紊乱的主要原因;为预防肥胖,正在开展研究以开发副作用少的天然安全成分。在本研究中,我们测定了根提取物(KWFD-H01)对3T3-L1脂肪细胞和Sprague-Dawley(SD)大鼠的抗肥胖作用。

材料/方法:使用多种检测方法,包括油红O染色、基因表达分析、蛋白质表达分析和血液生化分析,检测KWFD-H01对3T3-L1脂肪细胞和SD大鼠的抗肥胖作用。

结果

KWFD-H01减少了3T3-L1细胞内的脂质积累,并抑制了过氧化物酶体增殖物激活受体γ(PPARγ)、胞嘧啶-胞嘧啶-腺嘌呤-腺嘌呤-胸腺嘧啶(CCAAT)/增强子结合蛋白(C/EBPα)、固醇调节元件结合转录因子1(SREBP-1c)、乙酰辅酶A羧化酶(ACC)和脂肪酸合酶(FAS)的mRNA表达。KWFD-H01还降低了SD大鼠的体重、体重增加以及甘油三酯、总胆固醇和低密度脂蛋白胆固醇、葡萄糖和瘦素水平,同时提高了高密度脂蛋白胆固醇和脂联素水平。PPARγ、C/EBPα、SREBP-1c、ACC和FAS蛋白表达在SD大鼠附睾脂肪中受到抑制。

结论

总体而言,这些结果证实了KWFD-H01对3T3-L1脂肪细胞和SD大鼠的抗肥胖作用,表明它们作为开发控制肥胖的功能性健康食品或药物的基线数据的潜力。

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