Free radical production in nicotine treated pancreatic tissue

Free Radic Biol Med. 1995 May;18(5):877-82. doi: 10.1016/0891-5849(94)00221-5.

Abstract

The ability of nicotine to induce oxidative stress in the pancreatic tissue of rats was investigated. Homogenized pancreatic tissue of Sprague-Dawley rats was incubated with nicotine in a dose of 200 ng/mg protein/ml for 15, 30, 45, and 60 min or was incubated for 30 min with nicotine in a dose of 50, 100, 200, 400, and 800 ng/mg protein/ml. Pancreatic tissue was also incubated 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 positive correlation between the duration of nicotine incubation and chemiluminescence (r = 0.6) or lipid peroxidation (r = 0.71) and also between the nicotine dose and chemiluminescence (r = 0.54) or lipid peroxidation (r = 0.66). Thirty minutes incubation of pancreatic tissue with nicotine in a dose of 200 ng/mg protein/ml increased chemiluminescence 5 fold and lipid peroxidation 2.5 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 pancreatic tissue of rats.

MeSH terms

  • Animals
  • Catalase / pharmacology*
  • Dose-Response Relationship, Drug
  • Free Radical Scavengers / pharmacology
  • Free Radicals / metabolism
  • Kinetics
  • Lipid Peroxidation / drug effects*
  • Luminescent Measurements
  • Nicotine / pharmacology*
  • Pancreas / drug effects
  • Pancreas / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase / pharmacology*
  • Time Factors

Substances

  • Free Radical Scavengers
  • Free Radicals
  • Nicotine
  • Catalase
  • Superoxide Dismutase