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Novel Function for Bilirubin as a Metabolic Signaling Molecule: Implications for Kidney Diseases

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

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 languageEnglish
Pages (from-to)945-953
Number of pages9
JournalKidney360
Volume3
Issue number5
DOIs
StatePublished - 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

FundersFunder number
National Institutes of Health (NIH)1R01DK126884-01A1, 1R01DK121797-01A1
National Institutes of Health (NIH)
National Heart, Lung, and Blood Institute Family Blood Pressure ProgramP01 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 SciencesP20GM104357-02
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)

    1. SDG 3 - Good Health and Well-being
      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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