Anacardic acid mitigates liver fat accumulation and impaired glucose tolerance in mice fed a high-fat and high-sucrose diet

被引:12
作者
Chung, Sangwon [1 ]
Shin, Eun Ju [1 ]
Choi, Hyo-Kyoung [1 ]
Park, Jae Ho [1 ]
Hwang, Jin-Taek [1 ,2 ]
机构
[1] Korea Food Res Inst, Wanju Gun, Jeollabuk Do, South Korea
[2] Univ Sci & Technol, Dept Food Biotechnol, Daejeon 34113, South Korea
来源
FOOD SCIENCE & NUTRITION | 2020年 / 8卷 / 02期
关键词
anacardic acid; antidiabetes; high-fat and high-sucrose diet; homeostasis model assessment of insulin resistance; mice; INHIBITS ADIPOGENESIS; INSULIN-RESISTANCE; PPAR-GAMMA; DISEASE; OBESITY; APOPTOSIS; ROLES; MECHANISMS; CURCUMIN; EXTRACT;
D O I
10.1002/fsn3.1322
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In this study, we evaluated the effects of anacardic acid (AA), a phenolic lipid found in cashew nuts (Anacardium occidentale), on metabolic disorders related to obesity, fatty liver disease, and diabetes using both in vitro and in vivo models. The application of AA led to a reduction in lipid accumulation in 3T3-L1 cells without observable cytotoxicity. Results from Western blot analysis revealed that AA treatment also led to decreased expression of fatty acid synthase and peroxisome proliferator-activated receptor gamma. In vivo studies were performed to evaluate the effects of AA treatment on fatty liver disease and diabetes. Mice fed a high-fat and high-sucrose diet had significantly higher body and liver weights, and higher levels of liver fat, cholesterol, fasting glucose, and homeostasis model assessment of insulin resistance (HOMA-IR). However, 12 weeks of oral treatment with 500 mu g/kg BW AA slowed down lipid accumulation rates in the liver and mitigated insulin resistance in these mice. Thus, AA may reduce lipid levels and have an antidiabetic effect.
引用
收藏
页码:796 / 804
页数:9
相关论文
共 32 条
  • [1] [Anonymous], 2013, EVID-BASED COMPL ALT, DOI DOI 10.1155/2013/921012
  • [2] Progression of NAFLD to diabetes mellitus, cardiovascular disease or cirrhosis
    Anstee, Quentin M.
    Targher, Giovanni
    Day, Christopher P.
    [J]. NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2013, 10 (06) : 330 - 344
  • [3] Dietary Anthocyanins and Insulin Resistance: When Food Becomes a Medicine
    Belwal, Tarun
    Nabavi, Seyed Fazel
    Nabavi, Seyed Mohammad
    Habtemariam, Solomon
    [J]. NUTRIENTS, 2017, 9 (10):
  • [4] Integration of metabolism and inflammation by lipid-activated nuclear receptors
    Bensinger, Steven J.
    Tontonoz, Peter
    [J]. NATURE, 2008, 454 (7203) : 470 - 477
  • [5] PPAR Agonists and Metabolic Syndrome: An Established Role?
    Botta, Margherita
    Audano, Matteo
    Sahebkar, Amirhossein
    Sirtori, Cesare R.
    Mitro, Nico
    Ruscica, Massimiliano
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (04)
  • [6] Epigallocatechin-3-Gallate, a Histone Acetyltransferase Inhibitor, Inhibits EBV-Induced B Lymphocyte Transformation via Suppression of ReIA Acetylation
    Choi, Kyung-Chul
    Jung, Myung Gu
    Lee, Yoo-Hyun
    Yoon, Joo Chun
    Kwon, Seung Hyun
    Kang, Hee-Bum
    Kim, Mi Jeong
    Cha, Jeong-Heon
    Kim, Young Jun
    Jun, Woo Jin
    Lee, Jae Myun
    Yoon, Ho-Geun
    [J]. CANCER RESEARCH, 2009, 69 (02) : 583 - 592
  • [7] PPARs and the complex journey to obesity
    Evans, RM
    Barish, GD
    Wang, YX
    [J]. NATURE MEDICINE, 2004, 10 (04) : 355 - 361
  • [8] Insulin regulation of fatty acid synthase gene transcription: Roles of USF and SREBP-1c
    Griffin, MJ
    Sul, HS
    [J]. IUBMB LIFE, 2004, 56 (10) : 595 - 600
  • [9] PPARs in obesity-induced T2DM, dyslipidaemia and NAFLD
    Gross, Barbara
    Pawlak, Michal
    Lefebvre, Philippe
    Staels, Bart
    [J]. NATURE REVIEWS ENDOCRINOLOGY, 2017, 13 (01) : 36 - 49
  • [10] Emerging Roles of Anacardic Acid and Its Derivatives: A Pharmacological Overview
    Hemshekhar, Mahadevappa
    Santhosh, Martin Sebastin
    Kemparaju, Kempaiah
    Girish, Kesturu S.
    [J]. BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2012, 110 (02) : 122 - 132