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Combined effects of both bacteria and gastric juice on pneumonia in mice

K Iwasaki1, T Ohrui, Q Wang

  • 1Department of Geriatric Medicine, Tohoku University School of Medicine, Sendai, Japan.

Respiration Physiology
|September 16, 1999
PubMed

Insights

Combined gastric juice and Streptococcus pneumoniae significantly increased pneumonia mortality in mice. A free radical scavenger, pyran-superoxide dismutase (pyran-SOD), reduced mortality and xanthine oxidase activity, suggesting a role in pneumonia pathogenesis.

Area of Science:

  • Microbiology
  • Pathophysiology
  • Toxicology

Background:

  • Pneumonia is a significant global health concern.
  • The role of gastric juice in bacterial lung infections is not fully understood.
  • Streptococcus pneumoniae is a common cause of bacterial pneumonia.

Purpose of the Study:

  • To investigate the synergistic effects of gastric juice and Streptococcus pneumoniae on mouse lung infections.
  • To evaluate the impact of combined agents on mortality rates and lung tissue xanthine oxidase (XO) activity.
  • To assess the efficacy of a free radical scavenger, pyran-superoxide dismutase (pyran-SOD), in mitigating these effects.

Main Methods:

  • Mice were inoculated with Streptococcus pneumoniae, gastric juice, or both.
  • Survival rates were monitored over 18 days.
  • Xanthine oxidase (XO) activity in lung tissue was measured.
  • Mice received pyran-superoxide dismutase (pyran-SOD) to assess its protective effects.

Main Results:

  • Combined inoculation resulted in an 81% mortality rate, compared to 10% for individual inoculations.
  • XO activity was significantly elevated in mice exposed to both agents.
  • Administration of pyran-SOD reduced mortality to 25% and decreased XO activity.
  • Pyran-SOD effectively counteracted the increase in XO activity induced by the combined agents.

Conclusions:

  • Gastric juice potentiates the pathogenicity of Streptococcus pneumoniae, leading to increased pneumonia mortality.
  • Xanthine oxidase (XO) activity plays a crucial role in the observed synergistic toxicity.
  • Free radical scavenging with pyran-SOD demonstrates a potential therapeutic strategy against this combined insult.

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