NAD+ prevents chronic kidney disease by activating renal tubular metabolism
Chronic kidney disease (CKD) is associated with renal metabolic disturbances, including impaired fatty acid oxidation (FAO). Nicotinamide adenine dinucleotide (NAD+) is a small molecule that participates in hundreds of metabolism-related reactions. NAD+ levels are decreased in CKD, and NAD+ supplementation is protective. However, both the mechanism of how NAD+ supplementation protects from CKD, as well as the cell types involved, are poorly understood. Using a mouse model of Alport syndrome, we show that nicotinamide riboside (NR), an NAD+ precursor, stimulated renal PPARα signaling and restored FAO in the proximal tubules, thereby protecting from CKD in both sexes. Bulk RNA-sequencing showed that renal metabolic pathways were impaired in Alport mice and activated by NR in both sexes. These transcriptional changes were confirmed by orthogonal imaging techniques and biochemical assays. Single-nuclei RNA sequencing and spatial transcriptomics, both the first of their kind to our knowledge from Alport mice, showed that NAD+ supplementation restored FAO in proximal tubule cells. Finally, we also report, for the first time to our knowledge, sex differences at the transcriptional level in this Alport model. In summary, the data herein identify a nephroprotective mechanism of NAD+ supplementation in CKD, and they demonstrate that this benefit localizes to the proximal tubule cells.
Authors
- Briana A. Santo (ORCID: https://orcid.org/0000-0001-8850-2985)
- Komuraiah Myakala (ORCID: https://orcid.org/0000-0003-3233-047X)
- Debora L. Gisch (ORCID: https://orcid.org/0000-0001-9087-4585)
- Ricardo Melo Ferreira (ORCID: https://orcid.org/0000-0003-2063-9744)
- Avi Z. Rosenberg (ORCID: https://orcid.org/0000-0003-2356-950X)
- Julia Panov (ORCID: https://orcid.org/0000-0003-2392-4073)
- Xiaoxin X. Wang (ORCID: https://orcid.org/0000-0001-9205-6228)
- Teruhiko Yoshida (ORCID: https://orcid.org/0000-0002-2049-7347)
- Kyle Korolowicz (ORCID: https://orcid.org/0000-0003-1116-6500)
- Ying‐Hua Cheng (ORCID: https://orcid.org/0000-0001-7871-8141)
- Michael T. Eadon (ORCID: https://orcid.org/0000-0003-3066-2876)
- Sanjay R. Jain (ORCID: https://orcid.org/0000-0003-2804-127X)
- Karen Allen (ORCID: https://orcid.org/0009-0007-2131-3574)
- Elizaveta Taranenko (ORCID: https://orcid.org/0009-0009-1680-5202)
- Moshe Levi (ORCID: https://orcid.org/0000-0001-6403-2261)
- Bryce A. Jones (ORCID: https://orcid.org/0000-0002-6950-8414)
- Amber Sadiq
- Xiaoping Yang (ORCID: https://orcid.org/0000-0003-1263-2710)
Institutions
- National Institutes of Health (US)
- Johns Hopkins University (US)
- Georgetown University (US)
- Washington University in St. Louis (US)
- Johns Hopkins Medicine (US)
- National Institute of Diabetes and Digestive and Kidney Diseases (US)
- Indiana University School of Medicine
- Indiana University – Purdue University Indianapolis (US)
- University of La Verne (US)
- University of Haifa (IL)
Publication Details
- Journal
- JCI Insight
- Published
- 2025-03-09
- DOI
- https://doi.org/10.1172/jci.insight.181443
- Citations
- 8
- Primary Topic
- Adenosine and Purinergic Signaling
- Type
- article
- Field-Weighted Citation Impact
- 8.94
Funders
- University of Florida
- Georgetown University
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases
- National Center for Advancing Translational Sciences