Abstract
Bilirubin is the end product of the catabolism of heme via the heme oxygenase pathway. Heme oxygenase generates carbon monoxide (CO) and biliverdin from the breakdown of heme, and biliverdin is rapidly reduced to bilirubin by the enzyme biliverdin reductase (BVR). Bilirubin has long been thought of as a toxic product that is only relevant to health when blood levels are severely elevated, such as in clinical jaundice. The physiologic functions of bilirubin correlate with the growing body of evidence demonstrating the protective effects of serum bilirubin against cardiovascular and metabolic diseases. Although the correlative evidence suggests a protective effect of serum bilirubin against many diseases, the mechanism by which bilirubin offers protection against cardiovascular and metabolic diseases remains unanswered. We recently discovered a novel function for bilirubin as a signaling molecule capable of activating the peroxisome proliferator-activated receptor α (PPARα) transcription factor. This review summarizes the new finding of bilirubin as a signaling molecule and proposes several mechanisms by which this novel action of bilirubin may protect against cardiovascular and kidney diseases.
| Original language | English |
|---|---|
| Pages (from-to) | 945-953 |
| Number of pages | 9 |
| Journal | Kidney360 |
| Volume | 3 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 26 2022 |
Bibliographical note
Publisher Copyright:Copyright © 2022 by the American Society of Nephrology.
Funding
This work was supported by the National Institutes of Health (1R01DK121797-01A1 to T.D. Hinds and 1R01DK126884-01A1 to D.E. Stec), the National Heart, Lung, and Blood Institute (K01HL-125445 to T.D. Hinds and P01 HL05197-11 to D.E. Stec), and the National Institute of General Medical Sciences (P20GM104357-02 to D.E. Stec). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Acknowledgments
| Funders | Funder number |
|---|---|
| National Institutes of Health (NIH) | 1R01DK126884-01A1, 1R01DK121797-01A1 |
| National Institutes of Health (NIH) | |
| National Heart, Lung, and Blood Institute Family Blood Pressure Program | P01 HL05197-11, K01HL-125445 |
| National Heart, Lung, and Blood Institute Family Blood Pressure Program | |
| National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical Sciences | P20GM104357-02 |
| National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical Sciences |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- PPARα
- acute kidney injury
- basic science
- bilirubin
- biliverdin reductase-A
- cardiovascular disease
- heme oxygenase
- hormone
- hypertension
- kidney disease
- peroxisome proliferator-activated receptor
- renal physiology
ASJC Scopus subject areas
- Nephrology
- Medicine (miscellaneous)
- General Medicine
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