In vitro free radical production in rat esophageal mucosa induced by nicotine

Dig Dis Sci. 1995 Apr;40(4):853-8. doi: 10.1007/BF02064991.

Abstract

Oxidative stress induced by nicotine was investigated in the esophageal mucosa of rats. The homogenized mucosa was incubated for 30 min with 50, 100, 200, 400, and 800 ng/mg protein/ml nicotine or with 200 ng/mg protein/ml nicotine for 15, 30, 45, and 60 min. Esophageal mucosa was also incubated for 30 min with 200 ng/mg protein/ml nicotine with or without the scavengers superoxide dismutase (SOD), catalase, SOD+catalase, inactivated SOD, inactivated catalase, or albumin. Incubation with 0.9% NaCl served as control. There was a strong correlation between chemiluminescence and the nicotine dose (r = 0.75) or the nicotine incubation time (r = 0.77). Thirty-minute incubation of the esophageal mucosa with 200 ng/mg protein/ml nicotine increased chemiluminescence 5.5-fold and lipid peroxidation 3.3-fold. This response was dampened by SOD or catalase and abolished by SOD+catalase. Inactivated enzymes or albumin had no scavenging effect. These results demonstrate that nicotine causes oxidative stress to the esophageal mucosa.

MeSH terms

  • Animals
  • Catalase / pharmacology
  • Dose-Response Relationship, Drug
  • Esophagus / metabolism*
  • Free Radicals / metabolism*
  • In Vitro Techniques
  • Lipid Peroxidation
  • Luminescent Measurements
  • Mucous Membrane / metabolism
  • Nicotine / pharmacology*
  • Oxidative Stress*
  • Rats
  • Rats, Sprague-Dawley
  • Serum Albumin, Bovine / pharmacology
  • Superoxide Dismutase / pharmacology
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • Free Radicals
  • Thiobarbituric Acid Reactive Substances
  • Serum Albumin, Bovine
  • Nicotine
  • Catalase
  • Superoxide Dismutase