Literature DB >> 30354231

Intravenous Heme Arginate Induces HO-1 (Heme Oxygenase-1) in the Human Heart.

Martin Andreas1, Claudia Oeser1, Frieda-Maria Kainz1, Shiva Shabanian1, Tandis Aref1, Martin Bilban2,3, Barbara Messner1, Julian Heidtmann1, Guenther Laufer1, Alfred Kocher1, Michael Wolzt3.   

Abstract

Objective- HO-1 (heme oxygenase-1) induction may prevent or reduce ischemia-reperfusion injury. We previously evaluated its in vivo induction after a single systemic administration of heme arginate in peripheral blood mononuclear cells. The current trial was designed to assess the pharmacological tissue induction of HO-1 in the human heart with heme arginate in vivo. Approach and Results- Patients planned for conventional aortic valve replacement received placebo (n=8), 1 mg/kg (n=7) or 3 mg/kg (n=9) heme arginate infused intravenously 24 hours before surgery. A biopsy of the right ventricle was performed directly before aortic cross-clamping and after cross-clamp release. In addition, the right atrial appendage was partially removed for analysis. HO-1 protein and mRNA concentrations were measured in tissue samples and in peripheral blood mononuclear cells before to and up to 72 hours after surgery. No study medication-related adverse events occurred. A strong, dose-dependent effect on myocardial HO-1 mRNA levels was observed (right ventricle: 7.9±5.0 versus 88.6±49.1 versus 203.6±148.7; P=0.002 and right atrium: 10.8±8.8 versus 229.8±173.1 versus 392.7±195.7; P=0.001). This was paralleled by a profound increase of HO-1 protein concentration in atrial tissue (8401±3889 versus 28 585±10 692 versus 29 022±8583; P<0.001). Surgery and heme arginate infusion significantly increased HO-1 mRNA concentration in peripheral blood mononuclear cells ( P<0.001). HO-1 induction led to a significant increase of postoperative carboxyhemoglobin (1.7% versus 1.4%; P=0.041). No effect on plasma HO-1 protein levels could be detected. Conclusions- Myocardial HO-1 mRNA and protein can be dose-dependently induced by heme arginate. Protective effects of this therapeutic strategy should be evaluated in upcoming clinical trials. Clinical Trial Registration- URL: http://www.clinicaltrials.gov . Unique identifier: NCT02314780.

Entities:  

Keywords:  carboxyhemoglobin; myocardial ischemia; neutrophil; reactive oxygen species; reperfusion injury

Mesh:

Substances:

Year:  2018        PMID: 30354231     DOI: 10.1161/ATVBAHA.118.311832

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  6 in total

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Authors:  John A McClung; Lior Levy; Victor Garcia; David E Stec; Stephen J Peterson; Nader G Abraham
Journal:  Pharmacol Ther       Date:  2021-09-06       Impact factor: 12.310

2.  Heme cytotoxicity is the consequence of endoplasmic reticulum stress in atherosclerotic plaque progression.

Authors:  Dávid Pethő; Zoltán Hendrik; Annamária Nagy; Lívia Beke; Andreas Patsalos; László Nagy; Szilárd Póliska; Gábor Méhes; Csaba Tóth; László Potor; John W Eaton; Harry S Jacob; György Balla; József Balla; Tamás Gáll
Journal:  Sci Rep       Date:  2021-05-17       Impact factor: 4.379

3.  Heme-Mediated Activation of the Nrf2/HO-1 Axis Attenuates Calcification of Valve Interstitial Cells.

Authors:  Enikő Balogh; Arpan Chowdhury; Haneen Ababneh; Dávid Máté Csiki; Andrea Tóth; Viktória Jeney
Journal:  Biomedicines       Date:  2021-04-15

4.  Icariin inhibits hypoxia/reoxygenation-induced ferroptosis of cardiomyocytes via regulation of the Nrf2/HO-1 signaling pathway.

Authors:  Xiu-Juan Liu; Yan-Fei Lv; Wen-Zhu Cui; Yan Li; Yang Liu; Yi-Tao Xue; Feng Dong
Journal:  FEBS Open Bio       Date:  2021-09-27       Impact factor: 2.693

5.  Dexmedetomidine alleviated sepsis‑induced myocardial ferroptosis and septic heart injury.

Authors:  Chunyan Wang; Wenlin Yuan; Anmin Hu; Juan Lin; Zhengyuan Xia; Catherine F Yang; Yalan Li; Zhongjun Zhang
Journal:  Mol Med Rep       Date:  2020-05-04       Impact factor: 2.952

6.  Multiple roles of haem in cystathionine β-synthase activity: implications for hemin and other therapies of acute hepatic porphyria.

Authors:  Abdulla A-B Badawy
Journal:  Biosci Rep       Date:  2021-07-30       Impact factor: 3.840

  6 in total

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