Mesna ameliorates acute lung injury induced by intestinal ischemia-reperfusion in rats

Samia Adel Abd El-Baset1, Manal R Abd El-Haleem2,3, Rehab S Abdul-Maksoud4

  • 1Department of Medical Histology and Cell Biology, Faculty of Medicine, Zagazig University, Zagazig, 44519, Asharquia, Egypt. drsamia2013@yahoo.com.

Scientific Reports
|June 26, 2021
PubMed

Insights

Mesna administration mitigates lung damage from intestinal ischemia-reperfusion (I-R) injury. This thiol compound reduces inflammation, oxidative stress, and apoptosis, offering a promising treatment for remote lung injury.

Area of Science:

  • Physiology
  • Pathology
  • Pharmacology

Background:

  • Intestinal ischemia-reperfusion (I-R) injury significantly impacts lung function.
  • Mesna, a thiol compound, exhibits anti-inflammatory and antioxidant properties.
  • Understanding Mesna's protective effects against lung damage from intestinal I-R is crucial.

Purpose of the Study:

  • To investigate the potential protective effects of Mesna against acute lung damage induced by intestinal I-R in a rat model.
  • To evaluate Mesna's impact on lung histopathology, oxidative stress, and inflammatory markers.
  • To assess Mesna's efficacy when administered before ischemia or after reperfusion.

Main Methods:

  • Intestinal I-R was induced in adult male albino rats, with Mesna administered intraperitoneally at 100 mg/kg before ischemia or after reperfusion.
  • Parameters assessed included arterial blood gases, bronchoalveolar lavage (BAL) fluid protein content, lung tissue biochemical markers (proinflammatory cytokines, oxidative stress markers), and histopathological examination (light and electron microscopy).
  • Neutrophil infiltration (myeloperoxidase levels), ICAM-1 mRNA expression, NF-κB pathway activation, antioxidant enzymes (GPx, SOD), and HSP70 expression were analyzed.

Main Results:

  • Mesna treatment significantly attenuated lung histopathological damage and apoptosis following intestinal I-R.
  • Mesna administration improved systemic oxygenation and reduced neutrophil infiltration and myeloperoxidase (MPO) levels.
  • Mesna suppressed key inflammatory mediators, including ICAM-1 mRNA, NF-κB pathway activation, TNF-α, IL-1β, and IL-6, while preserving antioxidant capacity by increasing GPx and SOD and decreasing HSP70.

Conclusions:

  • Mesna demonstrates significant protective effects against acute lung injury secondary to intestinal I-R.
  • Mesna's therapeutic benefits stem from its anti-inflammatory and antioxidant actions, mitigating cellular damage and improving lung function.
  • Mesna represents a promising therapeutic strategy for preventing or treating remote lung injury associated with intestinal I-R.

Related Concept Videos