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  1. Article ; Online: Heme Proteins and Kidney Injury: Beyond Rhabdomyolysis.

    Nath, Karl A / Singh, Raman Deep / Croatt, Anthony J / Adams, Christopher M

    Kidney360

    2022  Volume 3, Issue 11, Page(s) 1969–1979

    Abstract: Heme proteins, the stuff of life, represent an ingenious biologic strategy that capitalizes on the biochemical versatility of heme, and yet is one that avoids the inherent risks to cellular vitality posed by unfettered and promiscuously reactive heme. ... ...

    Abstract Heme proteins, the stuff of life, represent an ingenious biologic strategy that capitalizes on the biochemical versatility of heme, and yet is one that avoids the inherent risks to cellular vitality posed by unfettered and promiscuously reactive heme. Heme proteins, however, may be a double-edged sword because they can damage the kidney in certain settings. Although such injury is often viewed mainly within the context of rhabdomyolysis and the nephrotoxicity of myoglobin, an increasing literature now attests to the fact that involvement of heme proteins in renal injury ranges well beyond the confines of this single disease (and its analog, hemolysis); indeed, through the release of the defining heme motif, destabilization of intracellular heme proteins may be a common pathway for acute kidney injury, in general, and irrespective of the underlying insult. This brief review outlines current understanding regarding processes underlying such heme protein-induced acute kidney injury (AKI) and chronic kidney disease (CKD). Topics covered include, among others, the basis for renal injury after the exposure of the kidney to and its incorporation of myoglobin and hemoglobin; auto-oxidation of myoglobin and hemoglobin; destabilization of heme proteins and the release of heme; heme/iron/oxidant pathways of renal injury; generation of reactive oxygen species and reactive nitrogen species by NOX, iNOS, and myeloperoxidase; and the role of circulating cell-free hemoglobin in AKI and CKD. Also covered are the characteristics of the kidney that render this organ uniquely vulnerable to injury after myolysis and hemolysis, and pathobiologic effects emanating from free, labile heme. Mechanisms that defend against the toxicity of heme proteins are discussed, and the review concludes by outlining the therapeutic strategies that have arisen from current understanding of mechanisms of renal injury caused by heme proteins and how such mechanisms may be interrupted.
    MeSH term(s) Humans ; Myoglobin/adverse effects ; Hemolysis ; Rhabdomyolysis/chemically induced ; Kidney/metabolism ; Acute Kidney Injury/etiology ; Heme/adverse effects ; Hemoglobins/adverse effects ; Renal Insufficiency, Chronic/complications
    Chemical Substances Myoglobin ; Heme (42VZT0U6YR) ; Hemoglobins
    Language English
    Publishing date 2022-10-05
    Publishing country United States
    Document type Review ; Journal Article ; Research Support, N.I.H., Extramural
    ISSN 2641-7650
    ISSN (online) 2641-7650
    DOI 10.34067/KID.0005442022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Induction of p16Ink4a Gene Expression in Heme Protein-Induced AKI and by Heme: Pathophysiologic Implications.

    Nath, Karl A / Singh, Raman Deep / Croatt, Anthony J / Ackerman, Allan W / Grande, Joseph P / O'Brien, Daniel R / Garovic, Vesna D / Adams, Christopher M / Tchkonia, Tamara / Kirkland, James L

    Kidney360

    2024  Volume 5, Issue 4, Page(s) 501–514

    MeSH term(s) Acute Kidney Injury/genetics ; Acute Kidney Injury/metabolism ; Humans ; Heme/metabolism ; Cyclin-Dependent Kinase Inhibitor p16/genetics ; Cyclin-Dependent Kinase Inhibitor p16/metabolism ; Animals ; Hemeproteins/genetics ; Hemeproteins/metabolism ; Gene Expression Regulation
    Chemical Substances Heme (42VZT0U6YR) ; Cyclin-Dependent Kinase Inhibitor p16 ; Hemeproteins
    Language English
    Publishing date 2024-02-21
    Publishing country United States
    Document type Journal Article
    ISSN 2641-7650
    ISSN (online) 2641-7650
    DOI 10.34067/KID.0000000000000395
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: KLF11 Is a Novel Endogenous Protectant against Renal Ischemia-Reperfusion Injury.

    Nath, Karl A / Singh, Raman Deep / Croatt, Anthony J / Ackerman, Allan W / Grande, Joseph P / Khazaie, Khasayarsha / Chen, Y Eugene / Zhang, Jifeng

    Kidney360

    2022  Volume 3, Issue 8, Page(s) 1417–1422

    Abstract: Discovering new nephroprotectants may provide therapeutic strategies in AKI.This study provides the first evidence that KLF11, a member of the Krüppel-like factor (KLF) family of proteins, protects against AKI.In the absence of KLF11, exaggerated ... ...

    Abstract Discovering new nephroprotectants may provide therapeutic strategies in AKI.This study provides the first evidence that KLF11, a member of the Krüppel-like factor (KLF) family of proteins, protects against AKI.In the absence of KLF11, exaggerated induction of endothelin-1 and IL-6 occurs after ischemic renal injury and may contribute to worse AKI.
    MeSH term(s) Acute Kidney Injury/prevention & control ; Apoptosis Regulatory Proteins/metabolism ; Endothelin-1/metabolism ; Humans ; Interleukin-6/metabolism ; Kidney/metabolism ; Kruppel-Like Transcription Factors/genetics ; Protective Agents/metabolism ; Reperfusion Injury/prevention & control ; Repressor Proteins/metabolism
    Chemical Substances Apoptosis Regulatory Proteins ; Endothelin-1 ; Interleukin-6 ; KLF11 protein, human ; Kruppel-Like Transcription Factors ; Protective Agents ; Repressor Proteins
    Language English
    Publishing date 2022-05-06
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ISSN 2641-7650
    ISSN (online) 2641-7650
    DOI 10.34067/KID.0002272022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Expression of ACE2 in the Intact and Acutely Injured Kidney.

    Nath, Karl A / Singh, Raman Deep / Grande, Joseph P / Garovic, Vesna D / Croatt, Anthony J / Ackerman, Allan W / Barry, Michael A / Agarwal, Anupam

    Kidney360

    2021  Volume 2, Issue 7, Page(s) 1095–1106

    Abstract: Background: The actions of angiotensin-converting enzyme 2 (ACE2) oppose those of the renin-angiotensin-aldosterone system. ACE2 may be a cytoprotectant in some tissues. This study examined ACE2 expression in models of AKI.: Methods: ACE2 mRNA and ... ...

    Abstract Background: The actions of angiotensin-converting enzyme 2 (ACE2) oppose those of the renin-angiotensin-aldosterone system. ACE2 may be a cytoprotectant in some tissues. This study examined ACE2 expression in models of AKI.
    Methods: ACE2 mRNA and protein expression and ACE2 activity were assessed in murine ischemic AKI. Renal ACE2 mRNA expression was evaluated in LPS-induced AKI in wild-type (C57BL/6J) mice, in heme oxygenase-1
    Results: In ischemic AKI, ACE2 mRNA and protein expression and ACE2 activity were reduced as compared with such indices in the intact kidney. In ischemic AKI, ACE2, which, in health, is prominently expressed in the tubular epithelium, especially proximal tubules, is decreased in expression in these segments. Decreased ACE2 expression in AKI did not reflect reduced GFR, because ACE2 mRNA expression was unaltered after UUO. LPS induced renal ACE2 mRNA expression in wild-type mice, but this effect did not occur in heme oxygenase-1-deficient mice. In ischemic and LPS-induced AKI, renal expression of the Mas receptor was increased. In the intact kidney, renal ACE2 protein expression decreased in female mice as compared with male mice, but was unaltered with age.
    Conclusion: We conclude that renal ACE2 expression is decreased in ischemic AKI, characterized by decreased GFR and abundant cell death, but is upregulated in LPS-induced AKI, an effect requiring heme oxygenase-1. Determining the significance of ACE2 expression in experimental AKI merits further study. We suggest that understanding the mechanism underlying ACE2 downregulation in AKI may offer insights relevant to COVID-19: ACE2 expression is downregulated after ACE2 mediates SARS-CoV-2 cellular entry; such downregulation is proinflammatory; and AKI commonly occurs and determines outcomes in COVID-19.
    MeSH term(s) Acute Kidney Injury/genetics ; Angiotensin-Converting Enzyme 2/genetics ; Animals ; Female ; Kidney ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout
    Chemical Substances Ace2 protein, mouse (EC 3.4.17.23) ; Angiotensin-Converting Enzyme 2 (EC 3.4.17.23)
    Language English
    Publishing date 2021-05-18
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ISSN 2641-7650
    ISSN (online) 2641-7650
    DOI 10.34067/KID.0001562021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Prominent Mitochondrial Injury as an Early Event in Heme Protein-Induced Acute Kidney Injury.

    Singh, Raman Deep / Croatt, Anthony J / Ackerman, Allan W / Grande, Joseph P / Trushina, Eugenia / Salisbury, Jeffrey L / Christensen, Trace A / Adams, Christopher M / Tchkonia, Tamara / Kirkland, James L / Nath, Karl A

    Kidney360

    2022  Volume 3, Issue 10, Page(s) 1672–1682

    Abstract: Background: Mitochondrial injury occurs in and underlies acute kidney injury (AKI) caused by ischemia-reperfusion and other forms of renal injury. However, to date, a comprehensive analysis of this issue has not been undertaken in heme protein-induced ... ...

    Abstract Background: Mitochondrial injury occurs in and underlies acute kidney injury (AKI) caused by ischemia-reperfusion and other forms of renal injury. However, to date, a comprehensive analysis of this issue has not been undertaken in heme protein-induced AKI (HP-AKI). We examined key aspects of mitochondrial function, expression of proteins relevant to mitochondrial quality control, and mitochondrial ultrastructure in HP-AKI, along with responses to heme in renal proximal tubule epithelial cells.
    Methods: The long-established murine glycerol model of HP-AKI was examined at 8 and 24 hours after HP-AKI. Indices of mitochondrial function (ATP and NAD
    Results: ATP and NAD
    Conclusions: Modern concepts pertaining to AKI apply to HP-AKI. This study validates the investigation of novel, clinically relevant therapies such as NAD
    MeSH term(s) Mice ; Animals ; Hemeproteins/metabolism ; NAD/metabolism ; Acute Kidney Injury/etiology ; Mitochondria/metabolism ; Heme/metabolism ; Adenosine Triphosphate/metabolism
    Chemical Substances Hemeproteins ; NAD (0U46U6E8UK) ; Heme (42VZT0U6YR) ; Adenosine Triphosphate (8L70Q75FXE)
    Language English
    Publishing date 2022-08-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ISSN 2641-7650
    ISSN (online) 2641-7650
    DOI 10.34067/KID.0004832022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The spike protein of SARS-CoV-2 induces heme oxygenase-1: Pathophysiologic implications.

    Singh, Raman Deep / Barry, Michael A / Croatt, Anthony J / Ackerman, Allan W / Grande, Joseph P / Diaz, Rosa M / Vile, Richard G / Agarwal, Anupam / Nath, Karl A

    Biochimica et biophysica acta. Molecular basis of disease

    2021  Volume 1868, Issue 3, Page(s) 166322

    Abstract: Background: Acute kidney injury (AKI) is both a consequence and determinant of outcomes in COVID-19. The kidney is one of the major organs infected by the causative virus, SARS-CoV-2. Viral entry into cells requires the viral spike protein, and both the ...

    Abstract Background: Acute kidney injury (AKI) is both a consequence and determinant of outcomes in COVID-19. The kidney is one of the major organs infected by the causative virus, SARS-CoV-2. Viral entry into cells requires the viral spike protein, and both the virus and its spike protein appear in the urine of COVID-19 patients with AKI. We examined the effects of transfecting the viral spike protein of SARS-CoV-2 in kidney cell lines.
    Methods: HEK293, HEK293-ACE2
    Findings: Spike transfection in HEK293-ACE2
    Interpretation: The major conclusions of the study are: 1) Spike protein expression in kidney cells provides a relevant model for the study of maladaptive and adaptive responses germane to AKI in COVID-19; 2) such spike protein expression upregulates HO-1; and 3) quercetin, an HO-1 inducer, may provide a clinically relevant/feasible protective strategy in AKI occurring in the setting of COVID-19.
    Funding: R01-DK119167 (KAN), R01-AI100911 (JPG), P30-DK079337; R01-DK059600 (AA).
    MeSH term(s) Animals ; COVID-19/metabolism ; COVID-19/virology ; Cell Line ; Chlorocebus aethiops ; HEK293 Cells ; Heme Oxygenase-1/metabolism ; Host-Pathogen Interactions/drug effects ; Host-Pathogen Interactions/physiology ; Humans ; Protein Binding/drug effects ; Protein Binding/physiology ; Quercetin/pharmacology ; SARS-CoV-2/pathogenicity ; Signal Transduction/drug effects ; Signal Transduction/physiology ; Spike Glycoprotein, Coronavirus/metabolism ; Up-Regulation/drug effects ; Up-Regulation/physiology ; Vero Cells ; Virus Internalization/drug effects
    Chemical Substances Spike Glycoprotein, Coronavirus ; Quercetin (9IKM0I5T1E) ; HMOX1 protein, human (EC 1.14.14.18) ; Heme Oxygenase-1 (EC 1.14.14.18)
    Language English
    Publishing date 2021-12-14
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 60-7
    ISSN 1879-260X ; 1879-2596 ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1879-260X ; 1879-2596 ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/j.bbadis.2021.166322
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Cyclophilins A and B oppositely regulate renal tubular epithelial cell phenotype.

    Sarró, Eduard / Durán, Mónica / Rico, Ana / Bou-Teen, Diana / Fernández-Majada, Vanesa / Croatt, Anthony J / Nath, Karl A / Salcedo, Maria Teresa / Gundelach, Justin H / Batlle, Daniel / Bram, Richard J / Meseguer, Anna

    Journal of molecular cell biology

    2020  Volume 12, Issue 7, Page(s) 499–514

    Abstract: Restoration of kidney tubular epithelium following sublethal injury sequentially involves partial epithelial-mesenchymal transition (pEMT), proliferation, and further redifferentiation into specialized tubule epithelial cells (TECs). Because the ... ...

    Abstract Restoration of kidney tubular epithelium following sublethal injury sequentially involves partial epithelial-mesenchymal transition (pEMT), proliferation, and further redifferentiation into specialized tubule epithelial cells (TECs). Because the immunosuppressant cyclosporine-A produces pEMT in TECs and inhibits the peptidyl-prolyl isomerase (PPIase) activity of cyclophilin (Cyp) proteins, we hypothesized that cyclophilins could regulate TEC phenotype. Here we demonstrate that in cultured TECs, CypA silencing triggers loss of epithelial features and enhances transforming growth factor β (TGFβ)-induced EMT in association with upregulation of epithelial repressors Slug and Snail. This pro-epithelial action of CypA relies on its PPIase activity. By contrast, CypB emerges as an epithelial repressor, because CypB silencing promotes epithelial differentiation, prevents TGFβ-induced EMT, and induces tubular structures in 3D cultures. In addition, in the kidneys of CypB knockout mice subjected to unilateral ureteral obstruction, inflammatory and pro-fibrotic events were attenuated. CypB silencing/knockout leads to Slug, but not Snail, downregulation. CypB support of Slug expression depends on its endoplasmic reticulum location, where it interacts with calreticulin, a calcium-buffering chaperone related to Slug expression. As CypB silencing reduces ionomycin-induced calcium release and Slug upregulation, we suggest that Slug expression may rely on CypB modulation of calreticulin-dependent calcium signaling. In conclusion, this work uncovers new roles for CypA and CypB in modulating TEC plasticity and identifies CypB as a druggable target potentially relevant in promoting kidney repair.
    MeSH term(s) Animals ; Basigin/metabolism ; Calcium/metabolism ; Cell Line ; Cyclophilins/metabolism ; Endoplasmic Reticulum/drug effects ; Endoplasmic Reticulum/metabolism ; Epithelial Cells/cytology ; Epithelial Cells/drug effects ; Epithelial Cells/metabolism ; Fibrosis ; Gene Silencing/drug effects ; Humans ; Inflammation/pathology ; Ionomycin/pharmacology ; Kidney Tubules/cytology ; Mice ; Phenotype ; Protein Transport/drug effects ; Smad Proteins/metabolism ; Snail Family Transcription Factors/metabolism ; Thapsigargin/pharmacology ; Transforming Growth Factor beta/pharmacology ; Ureteral Obstruction/pathology
    Chemical Substances Smad Proteins ; Snail Family Transcription Factors ; Transforming Growth Factor beta ; Basigin (136894-56-9) ; Ionomycin (56092-81-0) ; Thapsigargin (67526-95-8) ; Cyclophilins (EC 5.2.1.-) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2020-03-11
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2500949-7
    ISSN 1759-4685 ; 1674-2788
    ISSN (online) 1759-4685
    ISSN 1674-2788
    DOI 10.1093/jmcb/mjaa005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Antithrombotic effects of heme-degrading and heme-binding proteins.

    Nath, Karl A / Grande, Joseph P / Belcher, John D / Garovic, Vesna D / Croatt, Anthony J / Hillestad, Matthew L / Barry, Michael A / Nath, Meryl C / Regan, Raymond F / Vercellotti, Gregory M

    American journal of physiology. Heart and circulatory physiology

    2020  Volume 318, Issue 3, Page(s) H671–H681

    Abstract: In the murine venous thrombosis model induced by ligation of the inferior vena cava (IVCL), genetic deficiency of heme oxygenase-1 (HO-1) increases clot size. This study examined whether induction of HO-1 or administration of its products reduces ... ...

    Abstract In the murine venous thrombosis model induced by ligation of the inferior vena cava (IVCL), genetic deficiency of heme oxygenase-1 (HO-1) increases clot size. This study examined whether induction of HO-1 or administration of its products reduces thrombosis. Venous HO-1 upregulation by gene delivery reduced clot size, as did products of HO activity, biliverdin, and carbon monoxide. Induction of HO-1 by hemin reduced clot formation, clot size, and upregulation of plasminogen activator inhibitor-1 (PAI-1) that occurs in the IVCL model, while leaving urokinase plasminogen activator (uPA) and tissue plasminogen activator (tPA) expression unaltered. The reductive effect of hemin on clot size required HO activity. The IVCL model exhibited relatively high concentrations of heme that peaked just before maximum clot size, then declined as clot size decreased. Administration of hemin decreased heme concentration in the IVCL model. HO-2 mRNA was induced twofold in the IVCL model (vs. 40-fold HO-1 induction), but clot size was not increased in HO-2
    MeSH term(s) Animals ; Disease Models, Animal ; Heme Oxygenase-1/genetics ; Heme Oxygenase-1/metabolism ; Heme-Binding Proteins/genetics ; Heme-Binding Proteins/metabolism ; Hemin/pharmacology ; Mice ; Mice, Knockout ; Up-Regulation ; Venous Thrombosis/genetics ; Venous Thrombosis/metabolism
    Chemical Substances Heme-Binding Proteins ; Hemin (743LRP9S7N) ; Heme Oxygenase-1 (EC 1.14.14.18)
    Language English
    Publishing date 2020-01-31
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 603838-4
    ISSN 1522-1539 ; 0363-6135
    ISSN (online) 1522-1539
    ISSN 0363-6135
    DOI 10.1152/ajpheart.00280.2019
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Role of TLR4 signaling in the nephrotoxicity of heme and heme proteins.

    Nath, Karl A / Belcher, John D / Nath, Meryl C / Grande, Joseph P / Croatt, Anthony J / Ackerman, Allan W / Katusic, Zvonimir S / Vercellotti, Gregory M

    American journal of physiology. Renal physiology

    2017  Volume 314, Issue 5, Page(s) F906–F914

    Abstract: Destabilized heme proteins release heme, and free heme is toxic. Heme is now recognized as an agonist for the Toll-like receptor-4 (TLR4) receptor. This study examined whether the TLR4 receptor mediates the nephrotoxicity of heme, specifically, the ... ...

    Abstract Destabilized heme proteins release heme, and free heme is toxic. Heme is now recognized as an agonist for the Toll-like receptor-4 (TLR4) receptor. This study examined whether the TLR4 receptor mediates the nephrotoxicity of heme, specifically, the effects of heme on renal blood flow and inflammatory responses. We blocked TLR4 signaling by the specific antagonist TAK-242. Intravenous administration of heme to mice promptly reduced renal blood flow, an effect attenuated by TAK-242. In vitro, TAK-242 reduced heme-elicited activation of NF-κB and its downstream gene monocyte chemoattractant protein-1(MCP-1); in contrast, TAK-242 failed to reduce heme-induced activation of the anti-inflammatory transcription factor Nrf2 and its downstream gene heme oxygenase-1 (HO-1). TAK-242 did not reduce heme-induced renal MCP-1 upregulation in vivo. TAK-242 did not reduce dysfunction and histological injury in the glycerol model of heme protein-induced acute kidney injury (AKI), findings corroborated by studies in TLR4
    MeSH term(s) Acute Kidney Injury/chemically induced ; Acute Kidney Injury/metabolism ; Acute Kidney Injury/pathology ; Acute Kidney Injury/prevention & control ; Animals ; Cell Line ; Chemokine CCL2/metabolism ; Disease Models, Animal ; Epithelial Cells/drug effects ; Epithelial Cells/metabolism ; Epithelial Cells/pathology ; Glycerol ; Hemin ; Kidney/blood supply ; Kidney/drug effects ; Kidney/metabolism ; Kidney/pathology ; Male ; Mice, Inbred C57BL ; Mice, Knockout ; NF-kappa B/metabolism ; Rats ; Renal Circulation/drug effects ; Signal Transduction/drug effects ; Sulfonamides/pharmacology ; Toll-Like Receptor 4/antagonists & inhibitors ; Toll-Like Receptor 4/deficiency ; Toll-Like Receptor 4/genetics ; Toll-Like Receptor 4/metabolism ; Vasoconstriction/drug effects
    Chemical Substances Ccl2 protein, mouse ; Ccl2 protein, rat ; Chemokine CCL2 ; NF-kappa B ; Sulfonamides ; Tlr4 protein, mouse ; Tlr4 protein, rat ; Toll-Like Receptor 4 ; ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate ; Hemin (743LRP9S7N) ; Glycerol (PDC6A3C0OX)
    Language English
    Publishing date 2017-10-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 603837-2
    ISSN 1522-1466 ; 0363-6127
    ISSN (online) 1522-1466
    ISSN 0363-6127
    DOI 10.1152/ajprenal.00432.2017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Heme oxygenase-2 protects against ischemic acute kidney injury: influence of age and sex.

    Nath, Karl A / Garovic, Vesna D / Grande, Joseph P / Croatt, Anthony J / Ackerman, Allan W / Farrugia, Gianrico / Katusic, Zvonimir S / Belcher, John D / Vercellotti, Gregory M

    American journal of physiology. Renal physiology

    2019  Volume 317, Issue 3, Page(s) F695–F704

    Abstract: Heme oxygenase (HO) activity is exhibited by inducible (HO-1) and constitutive (HO-2) proteins. HO-1 protects against ischemic and nephrotoxic acute kidney injury (AKI). We have previously demonstrated that HO-2 protects against heme protein-induced AKI. ...

    Abstract Heme oxygenase (HO) activity is exhibited by inducible (HO-1) and constitutive (HO-2) proteins. HO-1 protects against ischemic and nephrotoxic acute kidney injury (AKI). We have previously demonstrated that HO-2 protects against heme protein-induced AKI. The present study examined whether HO-2 is protective in ischemic AKI. Renal ischemia was imposed on young and aged HO-2
    MeSH term(s) Acute Kidney Injury/enzymology ; Acute Kidney Injury/pathology ; Acute Kidney Injury/physiopathology ; Acute Kidney Injury/prevention & control ; Age Factors ; Animals ; Disease Models, Animal ; Female ; Heme Oxygenase (Decyclizing)/deficiency ; Heme Oxygenase (Decyclizing)/genetics ; Heme Oxygenase (Decyclizing)/metabolism ; Kidney/enzymology ; Kidney/pathology ; Kidney/physiopathology ; Male ; Mice, Knockout ; Phosphorylation ; Reperfusion Injury/enzymology ; Reperfusion Injury/pathology ; Reperfusion Injury/physiopathology ; Reperfusion Injury/prevention & control ; STAT3 Transcription Factor/metabolism ; Sex Factors ; Signal Transduction
    Chemical Substances STAT3 Transcription Factor ; Stat3 protein, mouse ; Heme Oxygenase (Decyclizing) (EC 1.14.14.18) ; heme oxygenase-2 (EC 1.14.14.18)
    Language English
    Publishing date 2019-06-19
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 603837-2
    ISSN 1522-1466 ; 0363-6127
    ISSN (online) 1522-1466
    ISSN 0363-6127
    DOI 10.1152/ajprenal.00085.2019
    Database MEDical Literature Analysis and Retrieval System OnLINE

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