Glp-1 Mimetics and Autophagy in Diabetic Milieu: State-of-the-Art

  • Authors: Yaribeygi H.1, Maleki M.2, Santos R.3, Jamialahmadi T.4,5, Sahebkar A.4,6,7
  • Affiliations:
    1. Research Center of Physiology, Semnan University of Medical Sciences, Semnan, Iran
    2. Urology and Nephrology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    3. Lipid Clinic Heart Institute (Incor), University of São Paulo, Medical School Hospital, São Paulo, Brazil
    4. Medical Toxicolgy Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
    5. Surgical Oncology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
    6. Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran
    7. Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Issue: Vol 20, No 10 (2024)
  • Section: Medicine
  • URL: https://snv63.ru/1573-3998/article/view/642957
  • DOI: https://doi.org/10.2174/0115733998276570231222105959
  • ID: 642957

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Abstract

The diabetic milieu is associated with cascades of pathophysiological pathways that culminate in diabetic complications and tissue injuries. Autophagy is an essential process mandatory for cell survival and tissue homeostasis by degrading damaged organelles and removing injured cells. However, it may turn into a pathological process in an aberrant mode in the diabetic and/or malignant milieu. Moreover, autophagy could serve as a promising therapeutic target for many complications related to tissue injury. Glp-1 mimetics are a class of newer antidiabetic agents that reduce blood glucose through several pathways. However, some evidence suggests that they can provide extra glycemic benefits by modulating autophagy, although there is no complete understanding of this mechanism and its underlying molecular pathways. Hence, in the current review, we aimed to provide new insights on the possible impact of Glp-1 mimetics on autophagy and consequent benefits as well as mediating pathways.

About the authors

Habib Yaribeygi

Research Center of Physiology, Semnan University of Medical Sciences, Semnan, Iran

Author for correspondence.
Email: info@benthamscience.net

Mina Maleki

Urology and Nephrology Research
Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Email: info@benthamscience.net

Raul Santos

Lipid Clinic Heart Institute (Incor), University
of São Paulo, Medical School Hospital, São Paulo, Brazil

Email: info@benthamscience.net

Tannaz Jamialahmadi

Medical Toxicolgy Research Center, Mashhad University
of Medical Sciences, Mashhad, Iran; Surgical Oncology Research Center, Mashhad University of Medical Sciences,
Mashhad, Iran

Email: info@benthamscience.net

Amirhossein Sahebkar

Medical Toxicolgy Research Center, Mashhad University
of Medical Sciences, Mashhad, Iran; Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of
Medical Sciences, Mashhad, Iran; Applied Biomedical Research Center, Mashhad University of Medical Sciences,
Mashhad, Iran

Author for correspondence.
Email: info@benthamscience.net

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