IDEAS home Printed from https://ideas.repec.org/a/tec/bioche/ojs13309.html

GLP-1 Agonists Reimagined: The Tripartite Applications of the Semaglutide Hormone

Author

Listed:
  • Joon Daniel Park

    (Northern Valley Regional High School at Old Tappan, 100 Central Ave, Old Tappan, NJ 07675, United States)

  • Merajur Rahman

    (The Bronx High School of Science, 75 W 205th St, Bronx, NY 10468, United States)

  • Jeffrey Ye

    (Francis Lewis High School, 58-20 Utopia Pkwy, Fresh Meadows, NY 11365, United States)

Abstract

Semaglutide, a GLP-1 receptor agonist has been initially adopted as a treatment and regulator for the Type 2 Diabetes disease. In this essay, we will be focusing on the three primary roles that the semaglutide fulfills throughout day to day life or in potential real world applications. We examined different hormones related to the endocrine system, and identified differences in weaknesses and strengths between GLP-1 and semaglutide. We also assessed the different roles that semaglutide may be used for. The original intended use being Type 2 Diabetes regulation, where we established the utilization of the potent insulin releasing trait of semaglutide being the key factor for Type 2 Diabetes regulation. A repurposed use for weight reduction, where we identified the secondary symptoms of insulin release such as lower appetite. Finally, a speculative application where the diabetes regulation capabilities may have a positive correlation in affecting neurological diseases such as dementia. Through the compilation and review of historic and recent sources, this paper highlights the broader usage of the semaglutide compound. The findings suggest that semaglutide’s mechanisms and variety makes it a promising candidate for future metabolic and potentially groundbreaking neurological medicine.

Suggested Citation

  • Joon Daniel Park & Merajur Rahman & Jeffrey Ye, 2025. "GLP-1 Agonists Reimagined: The Tripartite Applications of the Semaglutide Hormone," Technium BioChemMed: Journal of Multidisciplinary Research, Biology, Chemistry and Medicine ISSN 2734 - 7990, Technium Science, vol. 13, pages 212-226, November.
  • Handle: RePEc:tec:bioche:ojs:13309
    DOI: 10.47577/biochemmed.v13i.13309
    as

    Download full text from publisher

    File URL: https://techniumscience.com/index.php/biochemmed/article/view/13309
    Download Restriction: no

    File URL: https://libkey.io/10.47577/biochemmed.v13i.13309?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    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:tec:bioche:ojs:13309. 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.

    We have no bibliographic references for this item. You can help adding them by using 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: Anna Maria Golita (email available below). General contact details of provider: .

    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.