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大豆胚芽提取物和酶法改性异槲皮苷的抗肥胖作用。

Anti-Obesity Effects of Soybean Embryo Extract and Enzymatically-Modified Isoquercitrin.

机构信息

College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea.

College of Pharmacy, Pusan National University, Busan 46241, Korea.

出版信息

Biomolecules. 2020 Sep 30;10(10):1394. doi: 10.3390/biom10101394.

Abstract

Soy isoflavones are bioactive phytoestrogens with known health benefits. Soybean embryo extract (SEE) has been consumed as a source of isoflavones, mainly daidzein, glycitein, and genistein. While previous studies have reported the anti-obesity effects of SEE, this study investigates their molecular mechanisms and the synergistic effects of co-treatment with SEE and enzymatically modified isoquercitrin (EMIQ). SEE upregulated genes involved in lipolysis and brown adipocyte markers and increased mitochondrial content in differentiated C3H10T1/2 adipocytes in vitro. Next, we use a high-fat diet-induced obesity mouse model to determine the anti-obesity effect of SEE. Two weeks of single or combined treatment with SEE and EMIQ significantly reduced body weight gain and improved glucose tolerance. Mechanistically, SEE treatment increased mitochondrial content and upregulated genes involved in lipolysis in adipose tissue through the cAMP/PKA-dependent signaling pathway. These effects required a cytosolic lipase adipose triglyceride lipase (ATGL) expression, confirmed by an adipocyte-specific ATGL knockout mouse study. Collectively, this study demonstrates that SEE exerts anti-obesity effects through the activation of adipose tissue metabolism and exhibits a synergistic effect of co-treatment with EMIQ. These results improve our understanding of the mechanisms underlying the anti-obesity effects of SEE related to adipose tissue metabolism.

摘要

大豆异黄酮是具有已知健康益处的生物活性植物雌激素。大豆胚芽提取物(SEE)一直被作为异黄酮的来源被食用,主要是大豆甙元、黄豆黄素和染料木黄酮。虽然先前的研究已经报道了 SEE 的抗肥胖作用,但本研究调查了其分子机制以及与酶改性异槲皮苷(EMIQ)联合治疗的协同作用。体外实验中,SEE 上调了脂肪分解和棕色脂肪细胞标志物相关的基因,并增加了分化的 C3H10T1/2 脂肪细胞中的线粒体含量。接下来,我们使用高脂肪饮食诱导的肥胖小鼠模型来确定 SEE 的抗肥胖作用。单剂量或联合使用 SEE 和 EMIQ 治疗两周,显著降低了体重增加,并改善了葡萄糖耐量。从机制上讲,通过 cAMP/PKA 依赖性信号通路,SEE 处理增加了脂肪组织中线粒体含量和参与脂肪分解的基因表达。这些作用需要细胞质脂肪酶脂肪甘油三酯脂肪酶(ATGL)的表达,这一作用在脂肪细胞特异性 ATGL 敲除小鼠研究中得到了证实。总之,本研究表明,SEE 通过激活脂肪组织代谢发挥抗肥胖作用,并与 EMIQ 联合治疗具有协同作用。这些结果提高了我们对与脂肪组织代谢相关的 SEE 抗肥胖作用的机制的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90b2/7601939/27b0bbff6b4d/biomolecules-10-01394-g001.jpg

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