Optimization of spatiotemporal gene inactivation in mouse heart by oral application of tamoxifen citrate

Genesis. 2007 Jan;45(1):11-6. doi: 10.1002/dvg.20244.


Inducible and tissue-specific gene inactivation in mice has become a powerful tool to bypass embryonic and postnatal lethality of knockout mice. The most frequently used inducible system is based on Cre recombinase fused to either one or two mutated estrogen receptor ligand binding domains, thus rendering Cre function tamoxifen-dependent. To achieve Cre-mediated inactivation of a given gene, 4-OH tamoxifen (4-OHT) dissolved either in alcohol and/or oil is usually administered by repeated intraperitoneal (i.p.) injections. Since this procedure imposes considerable stress on mice, we compared the effect of tamoxifen citrate, mixed into a standard mouse diet at different concentrations, with that of i.p. administration of 4-OHT on Cre-mediated, heart-specific inactivation of thioredoxin reductase 2. Here we show that tamoxifen citrate in the chow was equally effective as 4-OHT given i.p. Oral tamoxifen administration is thus a convenient and cost-saving way for gene induction, and, most importantly, it reduces stress and avoids adverse effects in mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Integrases / genetics
  • Mice
  • Mice, Transgenic
  • Myocardium / enzymology*
  • Tamoxifen / administration & dosage
  • Tamoxifen / adverse effects
  • Tamoxifen / pharmacology*
  • Thioredoxin Reductase 2
  • Thioredoxin-Disulfide Reductase / biosynthesis*
  • Thioredoxin-Disulfide Reductase / genetics


  • Tamoxifen
  • Thioredoxin Reductase 2
  • Thioredoxin-Disulfide Reductase
  • Txnrd2 protein, mouse
  • Cre recombinase
  • Integrases