4.5 Article

6-hydroxydopamine increases the level of TNFα and bax mRNA in the striatum and induces apoptosis of doparninergic neurons in hemiparkinsonian rats

Journal

BRAIN RESEARCH
Volume 996, Issue 2, Pages 237-245

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ELSEVIER
DOI: 10.1016/j.brainres.2003.10.035

Keywords

6-OHDA; DA-ergic neurons; apoptosis; TNF alpha; TNF alpha R1; bax

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This study was focused on the apoptosis (programmed cell death) induction involved in the loss of dopaminmergic (DA-ergic) neurons in 6-hydroxydopamine (6-OHDA) hemiparkinsonian rats. The apoptosis in the striatum and substantia nigra pars compacta (SNpc), was examined 6, 24 h and 7 days after the 6-OHDA lesions employing the TUNEL method. The changes in mRNA levels of pro-apoptotic protein tumor necrosis factor alpha (TNFalpha) and its death receptor TNFalphaRI and then bax mRNA, as an important regulator of apoptotic neurodegeneration were followed by RT-PCR procedure. In situ analysis revealed an increased number of TUNEL-positive neurons in 6-OHDA-treated animals in all examined time points. The highest number of apoptotic neurons was detected 24 h after the lesion, both in the ipsilateral striatum (3.41 +/- 0.18) and SNpc (5.8 +/- 0.79). A significant increase in the level of TNFalpha mRNA was observed in 6-OHDA-lesioned striatum, with maximal value after 24 h (46%) comparing to the control. In contrast, 6-OHDA did not significantly change the level of TNFalphaRI mRNA in any time point. Six and 24 h post-operatively, we observed a significant increase of bax mRNA expression (40% and 45%, respectively) in the ipsilateral striatum of treated animals in comparison with the right striatum of the controls. However, the highest level of the bax mRNA expression was reached 7 days after the surgery (94%) in the ipsilateral striatum of 6-OHDA-treated animals. These results suggest that striatal injection of 6-OHDA can induce early changes that would be an important regulator of apoptotic neurodegeneration of dopamine-producing neurons, during the first post-operative week. (C) 2003 Elsevier B.V. All rights reserved.

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