Pathophysiology
Volume 18, Issue 4 , Pages 263-272, September 2011

Alteration of rat hippocampal neurogenesis and neuronal nitric oxide synthase expression upon prenatal exposure to tamoxifen

  • Maliheh Nobakht

      Affiliations

    • Department of Histology and Neuroscience, School of Medicine, Tehran University of Medical Science, Tehran, Iran
    • Cellular and Molecular Research Center, Tehran University of Medical Science, Tehran, Iran
    • Anti-microbial Resistance Research Center, Tehran University of Medical Science, Tehran, Iran
  • ,
  • Mohammad Javad Gharavi

      Affiliations

    • Department of Medical Parasitology, Tehran University of Medical Science, Tehran, Iran
  • ,
  • Kazem Mousavizadeh

      Affiliations

    • Oncopathology Research Center, Tehran University of Medical Science, Tehran, Iran
  • ,
  • Maasoumeh Bakhshayesh

      Affiliations

    • Cellular and Molecular Research Center, Tehran University of Medical Science, Tehran, Iran
  • ,
  • Pedram Ghafourifar

      Affiliations

    • Tri-State Institute of Pharmaceutical Sciences, Huntington, WV, USA
    • Corresponding Author InformationCorresponding author.

Received 3 March 2009; received in revised form 17 July 2009; accepted 21 January 2011.

Abstract 

The present study delineates the effect of tamoxifen on neuronal density and expression of neuronal nitric oxide synthase (nNOS) in hippocampal nerve cells during prenatal and postnatal periods in rats. Pregnant rats were administered with tamoxifen one day prior to labor (E21) and on the childbirth day (E22). Hippocampi of embryos at E22 and newborns at postnatal days of 1, 7, and 21 (P1, P7, and P21) were investigated. Density of the neurons in areas of the developing hippocampus including cornu ammonis (CA1, CA3), dentate gyrus, and subiculum were studied. Our findings show that the number of pyramidal neurons was significantly decreased in CA1 and subiculum of tamoxifen-treated rats in E22, P1, and P7. We found that cellular density was lower in early stages of development, however, cellular density and thickness gradually increased during the development particularly in the third week. We found that nNOS expression was decreased in E22, P1, and P7 in animals treated with tamoxifen. The present study shows that tamoxifen affects development and differentiation of postnatal rat hippocampus, CA1 neurons, and nNOS expression.

Keywords: Hippocampus, Tamoxifen, Developing brain, Rat, Nitric oxide

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PII: S0928-4680(11)00030-7

doi:10.1016/j.pathophys.2011.01.002

Pathophysiology
Volume 18, Issue 4 , Pages 263-272, September 2011