Evidence map›Paper›PMID 26498251›Full record

ReviewAmerican journal of physiology. Lung cellular and molecular physiology2015

Carbon monoxide in the treatment of sepsis.

Kiichi Nakahira, Augustine M K Choi

Abstract readReview
In one paragraph

Review in American journal of physiology. Lung cellular and molecular physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Gas entrapping materials for damage control.Advanced drug delivery reviews · 2026
    Review
  5. Review
  6. Visible Light Triggerable CO Releasing Micelles.Journal of the American Chemical Society · 2024
    Article
  7. Article
  8. Review
  9. Review
  10. Gases in Sepsis: Novel Mediators and Therapeutic Targets.International journal of molecular sciences · 2022
    Review
  11. "CO in a pill": Towards oral delivery of carbon monoxide for therapeutic applications.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Sepsis Therapies: Insights from Population Health to Cellular Therapies and Genomic Medicine.American journal of respiratory and critical care medicine · 2018
    Article
  18. Carbon monoxide releasing molecule-2 protects mice against acute kidney injury through inhibition of ER stress.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2018
    Article
  19. Article
  20. Carbon monoxide in lung cell physiology and disease.American journal of physiology. Cell physiology · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Kiichi NakahiraJoan and Sanford I. Weill Department of Medicine, Weill Cornell Medical College and New York-Presbyterian Hospital, New York, New York; and Division of Pulmonary and Crit Care Medicine, Weill Cornell Medical College, New York, New York.
Augustine M K ChoiJoan and Sanford I. Weill Department of Medicine, Weill Cornell Medical College and New York-Presbyterian Hospital, New York, New York; and Division of Pulmonary and Crit Care Medicine, Weill Cornell Medical College, New York, New York amchoi@med.cornell.edu.

Funding

The Role of HEME Oxygenase in Hyperoxic Lung InjuryR01HL055330 · NHLBI · YALE UNIVERSITY · PI CHOI, AUGUSTINE M, CHOI, MARY E · 1998 to 2021
$6.6M
Heme oxygenase-1: Regulation and Function in CaveolaeR01HL079904 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHOI, MARY E · 2005 to 2014
$2.9M
INTRACELLULAR REDOX STATE AND ENDOTHELIAL DYSFUNCTIONF32HL010088 · NHLBI · BOSTON MEDICAL CENTER · PI BIEGELSEN, ELIZABETH S · 1998 to 2000
$41k
NHLBI NIH HHS P01 HL1008801NHLBI NIH HHS R01 HL055330NHLBI NIH HHS R01 HL079904
6 · The paper itself

Abstract

Carbon monoxide (CO), a low-molecular-weight gas, is endogenously produced in the body as a product of heme degradation catalyzed by heme oxygenase (HO) enzymes. As the beneficial roles of HO system have been elucidated in vitro and in vivo, CO itself has also been reported as a potent cytoprotective molecule. Whereas CO represents a toxic inhalation hazard at high concentration, low-dose exogenous CO treatment (~250-500 parts per million) demonstrates protective functions including but not limited to the anti-inflammatory and antiapoptotic effects in preclinical models of human diseases. Of note, CO exposure confers protection in animal models of sepsis by inhibiting inflammatory responses and also enhancing bacterial phagocytosis in leukocytes. These unique functions of CO including both dampening inflammation and promoting host defense mechanism are mediated by multiple pathways such as autophagy induction or biosynthesis of specialized proresolving lipid mediators. We suggest that CO gas may represent a novel therapy for patients with sepsis.

Indexed as

AnimalsAnti-Inflammatory AgentsCarbon MonoxideHeme Oxygenase (Decyclizing)HumansInflammationSepsisSignal TransductionAnti-Inflammatory AgentsCarbon MonoxideHeme Oxygenase (Decyclizing)carbon monoxideclinical trialsepsis

Identifiers

PMID26498251
PMCPMC4683310

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.