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Transforming obesity: The advancement of multi-receptor drugs

  • Christine M. Kusminski
  • , Diego Perez-Tilve
  • , Timo D. Müller
  • , Richard D. DiMarchi
  • , Matthias H. Tschöp
  • , Philipp E. Scherer
  • UT Southwestern Medical Center
  • University of Cincinnati College of Medicine
  • Helmholtz Munich
  • Ludwig-Maximilians-Universität München
  • Indiana University Bloomington
  • Helmholtz Munich

Research output: Contribution to journalReview articlepeer-review

91 Scopus citations

Abstract

For more than a century, physicians have searched for ways to pharmacologically reduce excess body fat. The tide has finally turned with recent advances in biochemically engineered agonists for the receptor of glucagon-like peptide-1 (GLP-1) and their use in GLP-1-based polyagonists. These polyagonists reduce body weight through complementary pharmacology by incorporating the receptors for glucagon and/or the glucose-dependent insulinotropic polypeptide (GIP). In their most advanced forms, gut-hormone polyagonists achieve an unprecedented weight reduction of up to ∼20%–30%, offering a pharmacological alternative to bariatric surgery. Along with favorable effects on glycemia, fatty liver, and kidney disease, they also offer beneficial effects on the cardiovascular system and adipose tissue. These new interventions, therefore, hold great promise for the future of anti-obesity medications.

Original languageEnglish
Pages (from-to)3829-3853
Number of pages25
JournalCell
Volume187
Issue number15
DOIs
StatePublished - 25 Jul 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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