Literature DB >> 36128497

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

David E Stec1, Claudio Tiribelli2, Olufunto O Badmus1, Terry D Hinds3,4,5.   

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.
Copyright © 2022 by the American Society of Nephrology.

Entities:  

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

Mesh:

Substances:

Year:  2022        PMID: 36128497      PMCID: PMC9438427          DOI: 10.34067/KID.0000062022

Source DB:  PubMed          Journal:  Kidney360        ISSN: 2641-7650


  100 in total

1.  A bilirubin-inducible fluorescent protein from eel muscle.

Authors:  Akiko Kumagai; Ryoko Ando; Hideyuki Miyatake; Peter Greimel; Toshihide Kobayashi; Yoshio Hirabayashi; Tomomi Shimogori; Atsushi Miyawaki
Journal:  Cell       Date:  2013-06-13       Impact factor: 41.582

2.  Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease.

Authors:  P N Hopkins; L L Wu; S C Hunt; B C James; G M Vincent; R R Williams
Journal:  Arterioscler Thromb Vasc Biol       Date:  1996-02       Impact factor: 8.311

3.  Bilirubin is an antioxidant of possible physiological importance.

Authors:  R Stocker; Y Yamamoto; A F McDonagh; A N Glazer; B N Ames
Journal:  Science       Date:  1987-02-27       Impact factor: 47.728

4.  Protective effects of exogenous bilirubin on ischemia-reperfusion injury in the isolated, perfused rat kidney.

Authors:  Christopher A Adin; Byron P Croker; Anupam Agarwal
Journal:  Am J Physiol Renal Physiol       Date:  2004-11-23

5.  Role of renal medullary heme oxygenase in the regulation of pressure natriuresis and arterial blood pressure.

Authors:  Ningjun Li; Fan Yi; Elisabete A dos Santos; Dustin K Donley; Pin-Lan Li
Journal:  Hypertension       Date:  2006-10-30       Impact factor: 10.190

Review 6.  Bilirubin, a Cardiometabolic Signaling Molecule.

Authors:  Terry D Hinds; David E Stec
Journal:  Hypertension       Date:  2018-10       Impact factor: 10.190

7.  Kidney-specific induction of heme oxygenase-1 prevents angiotensin II hypertension.

Authors:  Trinity Vera; Silvia Kelsen; David E Stec
Journal:  Hypertension       Date:  2008-08-11       Impact factor: 10.190

8.  Clofibrate prevents the development of hypertension in Dahl salt-sensitive rats.

Authors:  R J Roman; Y H Ma; B Frohlich; B Markham
Journal:  Hypertension       Date:  1993-06       Impact factor: 10.190

9.  Fenofibrate attenuates ischemia reperfusion-induced acute kidney injury and associated liver dysfunction in rats.

Authors:  Jashanpreet Kaur; Tajpreet Kaur; Ashwani Kumar Sharma; Japneet Kaur; Harlokesh Narayan Yadav; Devendra Pathak; Amrit Pal Singh
Journal:  Drug Dev Res       Date:  2020-11-23       Impact factor: 4.360

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.