Effects of physiological versus pharmacological beta-carotene supplementation on cell proliferation and histopathological changes in the lungs of cigarette smoke-exposed ferrets

Carcinogenesis. 2000 Dec;21(12):2245-53. doi: 10.1093/carcin/21.12.2245.

Abstract

There remains a remarkable discordance between the results of observational epidemiological studies and intervention trials using beta-carotene as a potential chemopreventive agent. One question that needs to be examined is whether the adverse outcomes of human beta-carotene trials are related to the large doses of beta-carotene that were administered. In the present study, ferrets were given a physiological (low) dose or a pharmacological (high) dose of beta-carotene supplementation (0.43 mg versus 2.4 mg/kg body wt/day, which is equivalent to 6 mg versus 30 mg/day in humans) and exposed to cigarette smoke for 6 months. We investigated the effects of these doses of beta-carotene on retinoid concentrations, expression of retinoic acid receptors (RARs), activator protein 1 (AP-1; c-Jun and c-Fos), cyclin D1, proliferating cellular nuclear antigen (PCNA), and histopathological changes in the lungs of both normal and cigarette smoke-exposed ferrets. Thirty-six male ferrets were treated in six groups-control, smoke-exposed (SM), low-dose beta-carotene (LBC), high-dose beta-carotene (HBC), low-dose beta-carotene plus smoke exposure (LBC+SM) or high-dose beta-carotene plus smoke exposure (HBC+SM)-for 6 months. Retinoic acid concentration and RAR beta gene expression, but not expression of RAR alpha and RAR gamma, was reduced in the lung tissue of HBC+SM, HBC, SM and LBC+SM ferrets, but not in that of LBC ferrets, as compared with the control group. Expression of AP-1 and PCNA was greater in HBC+SM, HBC, SM and LBC+SM ferrets, but not in the LBC ferrets, as compared with the control group. Increased amounts of cyclin D1 and keratinized squamous metaplasia were observed in the lung tissue of HBC+SM, HBC and SM groups but not in that of the LBC+SM, LBC or control groups. These data suggest that, in contrast with a pharmacological dose of beta-carotene, a physiological dose of beta-carotene in smoke-exposed ferrets has no potentially detrimental effects and may afford weak protection against lung damage induced by cigarette smoke.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Division
  • Cyclin D1 / analysis
  • Dietary Supplements
  • Diterpenes
  • Dose-Response Relationship, Drug
  • Ferrets
  • Humans
  • Lung / drug effects
  • Lung / metabolism
  • Lung / pathology*
  • Male
  • Proliferating Cell Nuclear Antigen / analysis
  • Proto-Oncogene Proteins c-fos / analysis
  • Proto-Oncogene Proteins c-jun / analysis
  • Retinyl Esters
  • Tobacco Smoke Pollution / adverse effects*
  • Tretinoin / blood
  • Tretinoin / metabolism
  • Vitamin A / analogs & derivatives
  • Vitamin A / blood
  • Vitamin A / metabolism
  • beta Carotene / administration & dosage
  • beta Carotene / metabolism
  • beta Carotene / pharmacology*

Substances

  • Diterpenes
  • Proliferating Cell Nuclear Antigen
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • Retinyl Esters
  • Tobacco Smoke Pollution
  • beta Carotene
  • Vitamin A
  • Cyclin D1
  • retinol palmitate
  • Tretinoin