SGLT2 inhibitors activate pantothenate kinase in the human heart
Abstract Inhibitors of sodium glucose cotransporter-2 (SGLT2i) demonstrate strong symptomatic and mortality benefits in the treatment of heart failure but appear to do so independently of SGLT2. The relevant pharmacologic target of SGLT2i remains unclear. We show here that SGLT2i directly activate pantothenate kinase 1 (PANK1), the rate-limiting enzyme that initiates the conversion of pantothenate (vitamin B5) to coenzyme-A (CoA), an obligate co-factor for all major pathways of fuel use in the heart. Using stable-isotope infusion studies, we show that SGLT2i promote pantothenate consumption, activate CoA synthesis, rescue decreased levels of CoA in human failing hearts, and broadly stimulate fuel use in ex vivo perfused human cardiac blocks from patients with heart failure. Furthermore, we show that SGLT2i bind to PANK1 directly at physiological concentrations and promote PANK1 enzymatic activity in assays with purified components. Novel in silico dynamic modeling identified the site of SGLT2i binding on PANK1 and indicated a mechanism of activation involving prevention of allosteric inhibition of PANK1 by acyl-CoA species. Finally, we show that inhibition of PANK1 prevents SGLT2i-mediated increased contractility of isolated adult human cardiomyocytes. In summary, we demonstrate robust and specific off-target activation of PANK1 by SGLT2i, promoting CoA synthesis and efficient fuel use in human hearts, providing a likely explanation for the remarkable clinical benefits of SGLT2i.
Authors
- Kollin Schultz (ORCID: https://orcid.org/0000-0002-4456-8349)
- Kenneth B. Margulies (ORCID: https://orcid.org/0000-0002-8093-4465)
- Zoltan Pierre Arany (ORCID: https://orcid.org/0000-0003-1368-2453)
- Ivan A. Kuznetsov (ORCID: https://orcid.org/0000-0003-0023-3405)
- Deborah Eaton (ORCID: https://orcid.org/0000-0002-6913-7668)
- Daniel S. Kantner (ORCID: https://orcid.org/0000-0001-7202-1554)
- Kristina Li (ORCID: https://orcid.org/0000-0002-4417-0998)
- Claire Brady
- Jialiu A. Liang (ORCID: https://orcid.org/0000-0003-1475-2353)
- Trace Thome (ORCID: https://orcid.org/0000-0003-4823-8547)
- Louis G. Smith (ORCID: https://orcid.org/0000-0001-9576-0421)
- Nicholas Forelli
- Yijun Yang (ORCID: https://orcid.org/0000-0002-6971-2503)
- Gregory R. Bowman (ORCID: https://orcid.org/0000-0002-2083-4892)
- Jae Woo Jung (ORCID: https://orcid.org/0000-0001-7178-7400)
- Nesrine Bouhrira (ORCID: https://orcid.org/0000-0002-6406-2302)
- Kenneth C Bedi (ORCID: https://orcid.org/0000-0003-3588-9324)
- Ryo Kawakami (ORCID: https://orcid.org/0000-0002-4979-410X)
- Kushol Gupta (ORCID: https://orcid.org/0000-0002-7006-2667)
- Nathaniel W. Snyder (ORCID: https://orcid.org/0000-0001-5643-8747)
- Caitlyn E. Bowman (ORCID: https://orcid.org/0000-0003-2310-581X)
- Jonathan Edwards (ORCID: https://orcid.org/0000-0001-5334-821X)
- Kaustubh Koya
- Emily Megill
- Kirsten Branch
- Jiten Patel (ORCID: https://orcid.org/0009-0007-3072-9205)
- Cristin F. MacIntosh (ORCID: https://orcid.org/0009-0000-8091-0028)
Institutions
- Children's Hospital of Philadelphia (US)
- Cardiovascular Institute of the South (US)
- University of Pennsylvania (US)
- Temple University (US)
Publication Details
- Journal
- Science
- Published
- 2026-08-27
- DOI
- https://doi.org/10.1126/science.aeh4856
- Citations
- 16
- Primary Topic
- Neurological diseases and metabolism
- Type
- article
- Field-Weighted Citation Impact
- 19.80
Funders
- Children's Hospital of Philadelphia
- University of Pennsylvania
- Sarnoff Cardiovascular Research Foundation
- Fondation Leducq
- National Institutes of Health