Immersing lungs in hydrogen-rich saline attenuates lung ischaemia-reperfusion injury

Eur J Cardiothorac Surg. 2017 Mar 1;51(3):442-448. doi: 10.1093/ejcts/ezw342.

Abstract

Objectives: Anti-oxidant effects of hydrogen have been reported in studies examining ischaemia-reperfusion injury (IRI). In this study, we evaluated the therapeutic efficacy of immersing lungs in hydrogen-rich saline on lung IRI.

Methods: Lewis rats were divided into three groups: (i) sham, (ii) normal saline and (iii) hydrogen-rich saline. In the first experiment, the left thoracic cavity was filled with either normal saline or hydrogen-rich saline for 1 h. Then, we measured the hydrogen concentration in the left lung using a sensor gas chromatograph ( N = 3 per group). In the second experiment, lung IRI was induced by occlusion of the left pulmonary hilum for 1 h, followed by reperfusion for 3 h. During the ischaemic period, the left thoracic cavity was filled with either normal saline or hydrogen-rich saline. After reperfusion, we assessed lung function, histological changes and cytokine production ( N = 5-7 per group).

Results: Immersing lungs in hydrogen-rich saline resulted in an elevated hydrogen concentration in the lung (6.9 ± 2.9 μmol/1 g lung). After IRI, pulmonary function (pulmonary compliance and oxygenation levels) was significantly higher in the hydrogen-rich saline group than in the normal saline group ( P < 0.05). Similarly, pro-inflammatory cytokine levels (interleukin-1β and interleukin-6) in the left lung were significantly lower in the hydrogen-rich saline group than in the normal saline group ( P < 0.05).

Conclusions: Immersing lungs in hydrogen-rich saline delivered hydrogen into the lung and consequently attenuated lung IRI. Hydrogen-rich solution appears to be a promising approach to managing lung IRI.

Keywords: Hydrogen-rich solution; Lung ischaemia–reperfusion injury; Lung preservation.

Publication types

  • Evaluation Study

MeSH terms

  • Animals
  • Antioxidants / pharmacokinetics*
  • Antioxidants / pharmacology
  • Cytokines / biosynthesis
  • Hydrogen / pharmacokinetics*
  • Hydrogen / pharmacology
  • Inflammation Mediators / metabolism
  • Lung / blood supply*
  • Lung / metabolism
  • Lung Compliance / drug effects
  • Organ Preservation
  • Organ Preservation Solutions / chemistry
  • Organ Preservation Solutions / pharmacology
  • Oxygen Consumption / drug effects
  • Rats, Inbred Lew
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / physiopathology
  • Reperfusion Injury / prevention & control*
  • Sodium Chloride
  • Solubility

Substances

  • Antioxidants
  • Cytokines
  • Inflammation Mediators
  • Organ Preservation Solutions
  • Sodium Chloride
  • Hydrogen