Chemopreventive effects of β-ionone and geraniol during rat hepatocarcinogenesis promotion: distinct actions on cell proliferation, apoptosis, HMGCoA reductase, and RhoA

J Nutr Biochem. 2011 Feb;22(2):130-5. doi: 10.1016/j.jnutbio.2009.12.007.

Abstract

Chemopreventive activities of the dietary isoprenoids β-ionone (βI) and geraniol (GOH) were evaluated during the promotion phase of hepatocarcinogenesis. Over 5 consecutive weeks, rats received daily 16 mg/100 g body weight (b.w.) of βI (βI group), 25 mg/100 g b.w. of GOH (GOH group), or only corn oil (CO group, controls). Compared to the CO group, the following was observed: only the βI group showed a decrease in the mean number of visible hepatocyte nodules (P<.05); βI and GOH groups had reduced mean number of persistent preneoplastic lesions (pPNLs) (P<.05), but no differences regarding number of remodeling PNL (rPNLs) were observed; only the βI group exhibited smaller rPNL size and percentage of liver sections occupied by pPNLs (P<.05), whereas the GOH group displayed a smaller percentage of liver sections occupied by rPNLs (P<.05); a trend was observed in the βI group, which showed reduced cell proliferation of pPNLs (P<.10), and the GOH group had increased apoptosis in pPNLs and rPNLs (P<.05); only the βI group displayed reduced total plasma cholesterol concentrations (P<.05) and increased hepatic 3-hydroxy-3-methylglutaryl coenzyme A (HMGCoA) reductase mRNA levels (P<.05); only the GOH group had lower hepatic membrane RhoA protein levels (P<.05); both the βI- and GOH-treated groups had higher hepatic concentrations of βI and GOH, respectively (P<.05). Given these data, βI and GOH show promising chemopreventive effects during promotion of hepatocarcinogenesis by acting through distinct mechanism of actions: βI may inhibit cell proliferation and modulate HMGCoA reductase, and GOH can induce apoptosis and inhibit RhoA activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyclic Monoterpenes
  • Animals
  • Apoptosis*
  • Blotting, Western
  • Carcinoma, Hepatocellular / drug therapy
  • Carcinoma, Hepatocellular / metabolism
  • Cell Proliferation*
  • Chemoprevention
  • Cholesterol / blood
  • Hydroxymethylglutaryl CoA Reductases / metabolism*
  • Liver / pathology
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / metabolism
  • Male
  • Norisoprenoids / pharmacology*
  • Precancerous Conditions / drug therapy
  • Precancerous Conditions / metabolism
  • Rats
  • Rats, Wistar
  • Terpenes / pharmacology*
  • rhoA GTP-Binding Protein / metabolism*

Substances

  • Acyclic Monoterpenes
  • Norisoprenoids
  • Terpenes
  • Cholesterol
  • beta-ionone
  • Hydroxymethylglutaryl CoA Reductases
  • rhoA GTP-Binding Protein
  • geraniol