IDEAS home Printed from https://ideas.repec.org/a/gam/jijerp/v16y2019i24p4987-d295468.html
   My bibliography  Save this article

The Beneficial Effects of Stingless Bee Honey from Heterotrigona itama against Metabolic Changes in Rats Fed with High-Carbohydrate and High-Fat Diet

Author

Listed:
  • Nur Zuliani Ramli

    (Department of Anatomy, Faculty of Medicine, UKM Medical Centre, Universiti Kebangsaan Malaysia, Cheras 56000, Kuala Lumpur, Malaysia
    Department of Biomedical Sciences and Therapeutics, Faculty of Medicine and Health Sciences, Universiti Malaysia Sabah, Jalan UMS, Kota Kinabalu 88400, Sabah, Malaysia)

  • Kok-Yong Chin

    (Department of Pharmacology, Faculty of Medicine, UKM Medical Centre, Universiti Kebangsaan Malaysia, Cheras 56000, Kuala Lumpur, Malaysia)

  • Khairul Anwar Zarkasi

    (Department of Biomedical Sciences and Therapeutics, Faculty of Medicine and Health Sciences, Universiti Malaysia Sabah, Jalan UMS, Kota Kinabalu 88400, Sabah, Malaysia
    Department of Biochemistry, Faculty of Medicine, UKM Medical Centre, Universiti Kebangsaan Malaysia, Cheras 56000, Kuala Lumpur, Malaysia)

  • Fairus Ahmad

    (Department of Anatomy, Faculty of Medicine, UKM Medical Centre, Universiti Kebangsaan Malaysia, Cheras 56000, Kuala Lumpur, Malaysia)

Abstract

Metabolic syndrome (MetS) is a group of conditions including central obesity, hyperglycemia, dyslipidemia, and hypertension that increases the risk for cardiometabolic diseases. Kelulut honey (KH) produced by stingless honey bees has stronger antioxidant properties compared to other honey types and may be a functional food against MetS. This study aimed to determine the efficacy of KH in preventing metabolic changes in rats with MetS induced by high-carbohydrate and high-fat (HCHF) diet. Male Wistar rats were randomly assigned to the control (C), HCHF diet-induced MetS (S), and MetS supplemented with KH (K) groups. The K group was given KH (1 g/kg/day) for eight weeks. Compared to the control, the S group had significant higher omental fat mass, serum triglyceride, systolic blood pressure, diastolic blood pressures, adipocyte area, and adipocyte perimeter ( p < 0.05). KH supplementation significantly prevented these MetS-induced changes at week 16 ( p < 0.05). Several compounds, including 4-hydroxyphenyl acetic acid, coumaric and caffeic acids, had been detected via liquid chromatography-mass spectrometry analysis that might contribute to the reversal of these changes. The beneficial effects of KH against MetS-induced rats provide the basis for future KH research to investigate its potential use in humans and its molecular mechanisms in alleviating the disease.

Suggested Citation

  • Nur Zuliani Ramli & Kok-Yong Chin & Khairul Anwar Zarkasi & Fairus Ahmad, 2019. "The Beneficial Effects of Stingless Bee Honey from Heterotrigona itama against Metabolic Changes in Rats Fed with High-Carbohydrate and High-Fat Diet," IJERPH, MDPI, vol. 16(24), pages 1-17, December.
  • Handle: RePEc:gam:jijerp:v:16:y:2019:i:24:p:4987-:d:295468
    as

    Download full text from publisher

    File URL: https://www.mdpi.com/1660-4601/16/24/4987/pdf
    Download Restriction: no

    File URL: https://www.mdpi.com/1660-4601/16/24/4987/
    Download Restriction: no
    ---><---

    References listed on IDEAS

    as
    1. Kirsty L. Spalding & Erik Arner & Pål O. Westermark & Samuel Bernard & Bruce A. Buchholz & Olaf Bergmann & Lennart Blomqvist & Johan Hoffstedt & Erik Näslund & Tom Britton & Hernan Concha & Moustapha , 2008. "Dynamics of fat cell turnover in humans," Nature, Nature, vol. 453(7196), pages 783-787, June.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Clark, Andrew E. & Etilé, Fabrice, 2011. "Happy house: Spousal weight and individual well-being," Journal of Health Economics, Elsevier, vol. 30(5), pages 1124-1136.
    2. Belot, Michèle & James, Jonathan, 2022. "Incentivizing dietary choices among children: Review of experimental evidence," Food Policy, Elsevier, vol. 111(C).
    3. Shao-Chin Wu & Yuan-Ming Lo & Jui-Hao Lee & Chin-Yau Chen & Tung-Wei Chen & Hong-Wen Liu & Wei-Nan Lian & Kate Hua & Chen-Chung Liao & Wei-Ju Lin & Chih-Yung Yang & Chien-Yi Tung & Chi-Hung Lin, 2022. "Stomatin modulates adipogenesis through the ERK pathway and regulates fatty acid uptake and lipid droplet growth," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    4. Sang Mun Han & Eun Seo Park & Jeu Park & Hahn Nahmgoong & Yoon Ha Choi & Jiyoung Oh & Kyung Min Yim & Won Taek Lee & Yun Kyung Lee & Yong Geun Jeon & Kyung Cheul Shin & Jin Young Huh & Sung Hee Choi &, 2023. "Unique adipose tissue invariant natural killer T cell subpopulations control adipocyte turnover in mice," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    5. Wei Perng & Mercedes Mora-Plazas & Constanza Marín & Laura S Rozek & Ana Baylin & Eduardo Villamor, 2013. "A Prospective Study of LINE-1DNA Methylation and Development of Adiposity in School-Age Children," PLOS ONE, Public Library of Science, vol. 8(4), pages 1-7, April.
    6. Liam McAllan & Damir Baranasic & Sergio Villicaña & Scarlett Brown & Weihua Zhang & Benjamin Lehne & Marco Adamo & Andrew Jenkinson & Mohamed Elkalaawy & Borzoueh Mohammadi & Majid Hashemi & Nadia Fer, 2023. "Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
    7. Jennifer MacKellar & Samuel W Cushman & Vipul Periwal, 2010. "Waves of Adipose Tissue Growth in the Genetically Obese Zucker Fatty Rat," PLOS ONE, Public Library of Science, vol. 5(1), pages 1-9, January.

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jijerp:v:16:y:2019:i:24:p:4987-:d:295468. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.