期刊文献+

3-Nitropropionic acid modifies neurotrophin mRNA expression in the mouse striatum: 18S-rRNA is a reliable control gene for studies of the striatum 被引量:1

3-Nitropropionic acid modifies neurotrophin mRNA expression in the mouse striatum: 18S-rRNA is a reliable control gene for studies of the striatum
原文传递
导出
摘要 Objective The aim of the present study was to determine the changes in the mRNA levels of neurotrophins and their receptors in the striatal tissue of mice treated with 3-nitropropionic acid (3-NP). Methods At 1 and 48 h after the last drug administration, the mRNA expression of nerve growth factor, brain-derived neurotrophic factor, neurotrophin-3 and neurotrophin-4/5 as well as their receptors p75, TrkA, TrkB and TrkC, was evaluated using semi-quantitative (semi- Q) and real-time RT-PCR. β-actin mRNA and ribosomal 18S (18S rRNA) were tested as internal controls. Results 3-NP treatment did not affect mRNA expression of all neurotrophins and their respective receptors equally. Also, differences in neurotrophin and receptor mRNA expression were observed between semi-Q and real-time RT-PCR. Real-time RT-PCR was more accurate in evaluating the mRNA expression of the neurotrophins than semi-Q, and 18S rRNA was more reliable than β-actin as an internal control. Conclusion Neurotrophins and their receptors expression is differentially affected by neuronal damage produced by inhibition of mitochondrial respiration with 3-NP treatment in low, sub-chronic doses in vivo. Objective The aim of the present study was to determine the changes in the mRNA levels of neurotrophins and their receptors in the striatal tissue of mice treated with 3-nitropropionic acid (3-NP). Methods At 1 and 48 h after the last drug administration, the mRNA expression of nerve growth factor, brain-derived neurotrophic factor, neurotrophin-3 and neurotrophin-4/5 as well as their receptors p75, TrkA, TrkB and TrkC, was evaluated using semi-quantitative (semi- Q) and real-time RT-PCR. β-actin mRNA and ribosomal 18S (18S rRNA) were tested as internal controls. Results 3-NP treatment did not affect mRNA expression of all neurotrophins and their respective receptors equally. Also, differences in neurotrophin and receptor mRNA expression were observed between semi-Q and real-time RT-PCR. Real-time RT-PCR was more accurate in evaluating the mRNA expression of the neurotrophins than semi-Q, and 18S rRNA was more reliable than β-actin as an internal control. Conclusion Neurotrophins and their receptors expression is differentially affected by neuronal damage produced by inhibition of mitochondrial respiration with 3-NP treatment in low, sub-chronic doses in vivo.
机构地区 Unidad de Biomedicina
出处 《Neuroscience Bulletin》 SCIE CAS CSCD 2012年第5期517-531,共15页 神经科学通报(英文版)
基金 supported by the Consejo Nacional de Ciencia y Tecnología (Grant No. 42598)
关键词 NEUROTROPHINS STRIATUM neurodegenerative disease PCR 18S 3-nitropropionic acid neurotrophins; striatum; neurodegenerative disease; PCR; 18S; 3-nitropropionic acid
  • 相关文献

参考文献51

  • 1Huang E J, Reichardt LF. Neurotrophins: Roles in neuronal devel- opment and function. Annu Rev Neurosei 2001, 24: 677-736.
  • 2Connor B, Dragunow M. The role of neuronal growth factors in neurodegenerative disorders of the human brain. Brain Res Rev 1998, 27:1-39.
  • 3Hofer M, Pagliusi SR, Hohn A, Leibrock J, Barde YA. Regional distribution of brain-derived neurotrophic factor mRNA in the adult mouse brain. EMBO J 1990, 9: 2459-2464.
  • 4Canals JM, Marco S, Checa N, Michels A, P6rez-Navarro E, Arenas E. Differential regulation of the expression of nerve growth factor, brain-derived neurotrophic factor, and neurotrophin-3 after exci- totoxicity in a rat model of Huntington's disease. Neurobiol Dis 1998, 5: 357-364.
  • 5Timmusk T, Belluardo N, Metsis M, Persson H. Widespread and developmentally regulated expression of neurotrophin-4 mRNA in rat brain and peripheral tissues. Eur J Neurosci 1993, 5: 605-613.
  • 6Lee PD, Sladek R, Greenwood CM, Hudson TJ. Control genes and variability: absence of ubiquitous reference transcripts in diverse mammalian expression studies. Genome Res 2002, 12: 292-297.
  • 7Boda E, Pini A, Hoxha E, Parolisi R, Tempia F. Selection of refer- ence genes for quantitative real-time RT-PCR studies in mouse brain. J Mol Neurosci 2009, 37: 238-253.
  • 8Canals JM, Checa N, Marco S, Michels A, P6rez-Navarro E, Alberch J. The neurotrophin receptors trkA, trkB and trkC are differentially regulated after excitotoxic lesion in rat striatum. Mol Brain Res 1999, 69:242-248.
  • 9Hanbury R, Charles V, Chen EY, Leventhal L, Rosenstein JM, Mufson E J, et al. Excitotoxic and metabolie damage to the rodent striatum: role of the P75 neurotrophin receptor and glial progeni- tors. J Comp Neurol 2002, 444:291-305.
  • 10Pickrell AM, Fukui H, Wang X, Pinto M, Moraes CT. The striatum is highly susceptible to mitochondrial oxidative phosphorylation dysfunctions. J Neurosci 2011, 31: 9895-9904.

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部