論文

査読有り
2016年10月

Loss of dopaminergic neurons occurs in the ventral tegmental area and hypothalamus of rats following chronic stress: Possible pathogenetic loci for depression involved in Parkinson's disease

NEUROSCIENCE RESEARCH
  • Shuei Sugama
  • ,
  • Yoshihiko Kakinuma

111
開始ページ
48
終了ページ
55
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.neures.2016.04.008
出版者・発行元
ELSEVIER IRELAND LTD

Parkinson's disease (PD) is a neurodegenerative disease characterized by loss of dopaminergic (DA) neurons in the nigrostriatal and mesolimbic pathways including ventral tegmental area (VTA). Although several factors for the neuronal loss have been suggested, most of the PD cases are sporadic and idiopathic. In our previous study, we demonstrated the first evidence that solely chronic restraint stress (RS) induced the DA neuronal loss in the substantia nigra (SN). In this study, we further investigated whether chronic stress could affect other major DA systems, VTA and tuberoinfundibular system (TIDA), by using immunohistochemical and in situ hybridization techniques. The present study showed that, in the VTA, tyrosine hydroxylase (TH) immunoreactive neurons decreased by 9.8% at 2nd week, 19.2% at 4th week, 39.5% at 8th week, and 40.6% at 16th week during chronic RS as compared to control. Similarly, in the TIDA, the TH neurons decreased by 10.9% at 2nd week, 38.2% at 4th week, 56.3% at 8th week, and 57.1% at 16th week. The in situ hybridization results consistently demonstrated decreases in Th mRNA expressing cells in the VTA and TIDA in a comparable time dependent manner. Thus, exposure to chronic stress may simultaneously induce multiple neuronal loss of DA systems. (C) 2016 Elsevier Ireland Ltd and Japan Neuroscience Society. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.neures.2016.04.008
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000385323200006&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.neures.2016.04.008
  • ISSN : 0168-0102
  • eISSN : 1872-8111
  • Web of Science ID : WOS:000385323200006

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