• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

体外消化人参皂苷对3T3-L1脂肪细胞脂质积累的影响。

Effects of in vitro-digested ginsenosides on lipid accumulation in 3T3-L1 adipocytes.

作者信息

Kim Su Na, Lee Ju Hyeon, Shin Heungsop, Son Sung Ho, Kim Yeong Shik

机构信息

College of Pharmacy, Seoul National University, Seoul 151-742, Korea.

出版信息

Planta Med. 2009 May;75(6):596-601. doi: 10.1055/s-0029-1185358. Epub 2009 Feb 9.

DOI:10.1055/s-0029-1185358
PMID:19204893
Abstract

Ginseng, the root of Panax ginseng C. A. Meyer, is frequently used in traditional oriental medicines. The major active components of ginseng are the saponins, which are also called ginsenosides and are known for their pharmacological and biological activities. In this study, the effects of ginsenosides on lipid accumulation in 3T3-L1 adipocytes were investigated after the ginsenosides were in vitro-digested with artificial gastric and intestinal fluids. Ginseng extract was incubated with an artificial digestive fluid, and the changes were analyzed by HPLC, after which the effects of the digest on 3T3-L1 adipocytes were observed. Polar ginsenosides were transformed into less-polar ginsenosides at the low pH of the gastric acid, without any influence from the digestive enzymes. Additionally, the artificially digested ginsenosides showed inhibitory effects on lipid accumulation in 3T3-L1 adipocytes. When the 3T3-L1 adipocytes were treated with various ginseng samples that possessed different polarities, the less polar ginsenosides were more effective in reducing lipid accumulation. Furthermore, when the Rg3, Rk1, and Rg5 ginsenosides were used to treat the cells individually, Rg3 ginsenoside was the most effective at inhibiting lipid accumulation. These results suggest that the less polar ginsenosides, particularly ginsenoside Rg3, effectively reduce lipid accumulation in adipocytes. Accordingly, our results suggest that ginsenoside Rg3 should be developed as an antiobesity treatment.

摘要

人参,即五加科人参属植物人参(Panax ginseng C. A. Meyer)的根,常用于传统东方医学。人参的主要活性成分是皂苷,也称为人参皂苷,以其药理和生物学活性而闻名。在本研究中,人参皂苷经人工胃液和肠液体外消化后,研究了其对3T3-L1脂肪细胞脂质积累的影响。将人参提取物与人工消化液孵育,通过高效液相色谱法(HPLC)分析变化情况,之后观察消化产物对3T3-L1脂肪细胞的影响。在胃酸的低pH值条件下,极性人参皂苷转化为极性较小的人参皂苷,且不受消化酶的影响。此外,人工消化后的人参皂苷对3T3-L1脂肪细胞的脂质积累具有抑制作用。当用具有不同极性的各种人参样品处理3T3-L1脂肪细胞时,极性较小的人参皂苷在减少脂质积累方面更有效。此外,当分别用Rg3、Rk1和Rg5人参皂苷处理细胞时,Rg3人参皂苷在抑制脂质积累方面最有效。这些结果表明,极性较小的人参皂苷,特别是人参皂苷Rg3,能有效减少脂肪细胞中的脂质积累。因此,我们的结果表明人参皂苷Rg3应开发为一种抗肥胖治疗药物。

相似文献

1
Effects of in vitro-digested ginsenosides on lipid accumulation in 3T3-L1 adipocytes.体外消化人参皂苷对3T3-L1脂肪细胞脂质积累的影响。
Planta Med. 2009 May;75(6):596-601. doi: 10.1055/s-0029-1185358. Epub 2009 Feb 9.
2
Ginsenoside F2 possesses anti-obesity activity via binding with PPARγ and inhibiting adipocyte differentiation in the 3T3-L1 cell line.人参皂苷F2通过与过氧化物酶体增殖物激活受体γ(PPARγ)结合并抑制3T3-L1细胞系中的脂肪细胞分化而具有抗肥胖活性。
J Enzyme Inhib Med Chem. 2015 Feb;30(1):9-14. doi: 10.3109/14756366.2013.871006. Epub 2014 Mar 25.
3
Beta-conglycinin embeds active peptides that inhibit lipid accumulation in 3T3-L1 adipocytes in vitro.β-伴大豆球蛋白包埋有可在体外抑制3T3-L1脂肪细胞脂质积累的活性肽。
J Agric Food Chem. 2008 Nov 26;56(22):10533-43. doi: 10.1021/jf802216b.
4
Korean red ginseng (Panax ginseng) inhibits obesity and improves lipid metabolism in high fat diet-fed castrated mice.韩国红参(人参)可抑制肥胖,改善高脂饮食喂养去势雄性小鼠的脂代谢。
J Ethnopharmacol. 2018 Jan 10;210:80-87. doi: 10.1016/j.jep.2017.08.032. Epub 2017 Aug 24.
5
The inhibitory effects of garlic and Panax ginseng extract standardized with ginsenoside Rg3 on the genotoxicity, biochemical, and histological changes induced by ethylenediaminetetraacetic acid in male rats.大蒜和以人参皂苷Rg3标准化的人参提取物对乙二胺四乙酸诱导的雄性大鼠遗传毒性、生化及组织学变化的抑制作用。
Arch Toxicol. 2008 Mar;82(3):183-95. doi: 10.1007/s00204-007-0237-y. Epub 2007 Sep 14.
6
Preparative isolation of four ginsenosides from Korean red ginseng (steam-treated Panax ginseng C. A. Meyer), by high-speed counter-current chromatography coupled with evaporative light scattering detection.采用高速逆流色谱结合蒸发光散射检测法从高丽参(经蒸汽处理的人参C. A. 迈耶)中制备分离四种人参皂苷。
J Chromatogr A. 2007 Jun 1;1151(1-2):37-44. doi: 10.1016/j.chroma.2007.01.038. Epub 2007 Jan 13.
7
A quantified ginseng (Panax ginseng C.A. Meyer) extract influences lipid acquisition and increases adiponectin expression in 3T3-L1 cells.定量的人参(Panax ginseng C.A. Meyer)提取物可影响 3T3-L1 细胞的脂质摄取并增加脂联素的表达。
Molecules. 2011 Jan 10;16(1):477-92. doi: 10.3390/molecules16010477.
8
Ginsenoside Rg3 Induces Browning of 3T3-L1 Adipocytes by Activating AMPK Signaling.人参皂苷 Rg3 通过激活 AMPK 信号诱导 3T3-L1 脂肪细胞的棕色化。
Nutrients. 2020 Feb 7;12(2):427. doi: 10.3390/nu12020427.
9
KG-135, enriched with selected ginsenosides, inhibits the proliferation of human prostate cancer cells in culture and inhibits xenograft growth in athymic mice.KG-135,富含精选的人参皂苷,可抑制体外培养的人前列腺癌细胞增殖,并抑制裸鼠异种移植瘤生长。
Cancer Lett. 2010 Mar 1;289(1):99-110. doi: 10.1016/j.canlet.2009.08.008. Epub 2009 Sep 17.
10
Inhibitory effects of caffeine and its metabolites on intracellular lipid accumulation in murine 3T3-L1 adipocytes.咖啡因及其代谢物对小鼠 3T3-L1 脂肪细胞内脂质积累的抑制作用。
Biofactors. 2008;34(4):293-302. doi: 10.3233/BIO-2009-1083.

引用本文的文献

1
Protopanaxadiol-Enriched Rice Exerted Antiadipogenic Activity during 3T3-L1 Differentiation and Anti-Inflammatory Activity in 3T3-L1 Adipocytes.富含原人参二醇的大米在3T3-L1细胞分化过程中发挥抗脂肪生成活性,并在3T3-L1脂肪细胞中具有抗炎活性。
Pharmaceutics. 2023 Aug 11;15(8):2123. doi: 10.3390/pharmaceutics15082123.
2
Regulation of appetite-related neuropeptides by Panax ginseng: A novel approach for obesity treatment.人参对食欲相关神经肽的调节作用:一种治疗肥胖症的新方法。
J Ginseng Res. 2022 Jul;46(4):609-619. doi: 10.1016/j.jgr.2022.03.007. Epub 2022 Apr 4.
3
Ginsenoside Rb1 Induces Beta 3 Adrenergic Receptor-Dependent Lipolysis and Thermogenesis in 3T3-L1 Adipocytes and Mice.
人参皂苷Rb1在3T3-L1脂肪细胞和小鼠中诱导β3肾上腺素能受体依赖性脂肪分解和产热。
Front Pharmacol. 2019 Oct 15;10:1154. doi: 10.3389/fphar.2019.01154. eCollection 2019.
4
Ginseng and obesity.人参与肥胖
J Ginseng Res. 2018 Jan;42(1):1-8. doi: 10.1016/j.jgr.2016.12.005. Epub 2017 Jan 10.
5
Ginsenoside Rk1 bioactivity: a systematic review.人参皂苷Rk1的生物活性:一项系统综述。
PeerJ. 2017 Nov 17;5:e3993. doi: 10.7717/peerj.3993. eCollection 2017.
6
Anti-adipogenic Effects and Mechanisms of Ginsenoside Rg3 in Pre-adipocytes and Obese Mice.人参皂苷Rg3对前脂肪细胞和肥胖小鼠的抗脂肪生成作用及其机制
Front Pharmacol. 2017 Mar 8;8:113. doi: 10.3389/fphar.2017.00113. eCollection 2017.
7
Effects of pectin lyase-modified red ginseng extracts in high-fat diet-fed obese mice.果胶裂解酶修饰的红参提取物对高脂饮食喂养的肥胖小鼠的影响。
Lab Anim Res. 2014 Dec;30(4):151-60. doi: 10.5625/lar.2014.30.4.151. Epub 2014 Dec 24.
8
Free-fatty-acid-regulating effects of fermented red ginseng are mediated by hormones and by the autonomic nervous system.发酵红参通过激素和自主神经系统调节游离脂肪酸。
J Ginseng Res. 2014 Apr;38(2):97-105. doi: 10.1016/j.jgr.2013.12.003. Epub 2014 Jan 9.
9
Ginsenoside Rg3 reduces lipid accumulation with AMP-Activated Protein Kinase (AMPK) activation in HepG2 cells.人参皂苷Rg3通过激活HepG2细胞中的AMP活化蛋白激酶(AMPK)来减少脂质积累。
Int J Mol Sci. 2012;13(5):5729-5739. doi: 10.3390/ijms13055729. Epub 2012 May 11.
10
A quantified ginseng (Panax ginseng C.A. Meyer) extract influences lipid acquisition and increases adiponectin expression in 3T3-L1 cells.定量的人参(Panax ginseng C.A. Meyer)提取物可影响 3T3-L1 细胞的脂质摄取并增加脂联素的表达。
Molecules. 2011 Jan 10;16(1):477-92. doi: 10.3390/molecules16010477.