Induction of gap junctional communication by 4-oxoretinoic acid generated from its precursor canthaxanthin

Arch Biochem Biophys. 1995 Mar 10;317(2):423-8. doi: 10.1006/abbi.1995.1184.

Abstract

The activity of 4-oxoretinoic acid as an inducer of gap junctional communication was investigated in C3H/10T1/2 murine fibroblasts. Two isomers of this retinoid, all-trans- and 13-cis-4-oxoretinoic acid, enhance gap junctional communication. This is accompanied by increased expression of connexin43 mRNA. Decomposition fractions of canthaxanthin were isolated by preparative high-performance liquid chromatography and shown to be active in the cell-cell communication assay. Two of the decomposition compounds were identified as all-trans- and 13-cis-4-oxoretinoic acid. Therefore, it is concluded that the biological activity of canthaxanthin regarding cell-cell communication is at least in part due to the formation of active decomposition products such as 4-oxoretinoic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Canthaxanthin / isolation & purification
  • Canthaxanthin / metabolism*
  • Cell Communication / drug effects*
  • Cell Line
  • Chromatography, High Pressure Liquid
  • Connexin 43 / genetics
  • Fibroblasts / ultrastructure
  • Gap Junctions / drug effects*
  • Gene Expression
  • Mice
  • Mice, Inbred C3H
  • RNA, Messenger / metabolism
  • Tretinoin / analogs & derivatives*
  • Tretinoin / isolation & purification
  • Tretinoin / pharmacology

Substances

  • Connexin 43
  • RNA, Messenger
  • 4-oxoretinoic acid
  • Canthaxanthin
  • Tretinoin