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Catalytic iron mediated renal stress responses during experimental cardiorenal syndrome 1 ("CRS-1").
- Source :
-
Translational research : the journal of laboratory and clinical medicine [Transl Res] 2021 Nov; Vol. 237, pp. 53-62. Date of Electronic Publication: 2021 Jul 01. - Publication Year :
- 2021
-
Abstract
- Cardiorenal syndrome I (CRS-1) denotes a state in which acute kidney injury occurs in the setting of acute heart failure (AHF). Isoproterenol (Iso) administration is widly used as an AHF model by transiently inducing extreme tachycardia, hypotension, and myocyte apoptosis and/or necrosis. To gain potential insights into renal manifestations of CRS-1, mice were subjected to the Iso-AHF model (50 mg Iso/kg), followed by renal functional and renal cortical assessments over 4 hours Iso induced acute azotemia (doubling of BUN, plasma creatinine) and significantly reduced renal plasma flow (prolonged plasma para-amino-hippurate clearance). Although no morphologic tubular injury was identified, marked increases in renal cortical 'stress markers' (NGAL, HO-1, IL-6, MCP-1 mRNAs) and oxidant stress (decreased glutathione, increased malondialdehyde) were observed. These changes were catalytic Fe dependent, given that the iron chelator desferrioxamine (DFO) significantly blunted, or completely reversed, these renal cortical abnormalities. Despite these acute changes, no lasting renal injury was observed (assessed over 3 days). To determine whether Iso directly impacts tubular cell integrity, cultured proximal tubule (HK-2) cells were exposed to Iso. Substantial Fe dependent cell injury (decreased MTT uptake), and Fe independent increases in HO-1/IL-6 mRNA expression were observed. We conclude that Iso-induced AHF is a useful reversible model of CRS-1. Despite its largely hemodynamic ('pre-renal') nature, Fe-mediated oxidative stress and pro-inflammatory reactions are induced. These arise, at least in part, from direct Iso- induced tubular cell toxicity, rather than simply being secondary to Iso-mediated hemodynamic events. Finally, Iso-triggered renal cytokine production can potentially contribute to 'organ cross talk' and a systemic pro-inflammatory state.<br /> (Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Biomarkers blood
Cardio-Renal Syndrome complications
Cell Line
Deferoxamine pharmacology
Gene Expression Regulation drug effects
Heme Oxygenase-1 genetics
Heme Oxygenase-1 metabolism
Humans
Interleukin-6 genetics
Interleukin-6 metabolism
Kidney Tubules, Proximal drug effects
Mice
Siderophores pharmacology
Cardio-Renal Syndrome chemically induced
Heart Failure chemically induced
Iron metabolism
Isoproterenol toxicity
Kidney Diseases etiology
Subjects
Details
- Language :
- English
- ISSN :
- 1878-1810
- Volume :
- 237
- Database :
- MEDLINE
- Journal :
- Translational research : the journal of laboratory and clinical medicine
- Publication Type :
- Academic Journal
- Accession number :
- 34217897
- Full Text :
- https://doi.org/10.1016/j.trsl.2021.06.005