Thrombopoietin is ineffective in a mouse model of motor neuron disease

Amyotroph Lateral Scler. 2008 Dec;9(6):354-8. doi: 10.1080/17482960802103040.

Abstract

This study assessed the therapeutic efficacy of thrombopoietin (TPO) in the mouse model of ALS using two treatment paradigms. TPO was administered either daily or in 13-day treatment cycles to SOD1-G93A mice. Quantitative analysis of platelet levels, VEGF and TGF-beta1 trophic factors were assessed. The effect of TPO on disease progression was analyzed by behavioral analysis and clinical examination. TPO treatment increased levels of platelets and TGF-beta1 but not VEGF. This treatment did not affect onset or survival in these mice. Although biologically active, demonstrated by increased platelet and TGF-beta1 levels, rmTPO did not attenuate disease progression in ALS mice.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis / drug therapy
  • Amyotrophic Lateral Sclerosis / genetics
  • Amyotrophic Lateral Sclerosis / pathology
  • Animals
  • Disease Models, Animal*
  • Female
  • Male
  • Mice
  • Mice, Transgenic
  • Motor Neuron Disease / drug therapy*
  • Motor Neuron Disease / genetics
  • Motor Neuron Disease / pathology
  • Thrombopoietin / therapeutic use*

Substances

  • Thrombopoietin