Low Level of Autophagy-Related Gene 10 (ATG10) Expression in the 6-Hydroxydopamine Rat Model of Parkinson\'s Disease

نویسندگان

  • Ali Noori-Zadeh Department of Clinical Biochemistry, Faculty of Medicine, Ilam University of Medical Sciences, Ilam,Iran
  • Farzad Rajaei Cellular and Molecular Research Center, Qazvin University of Medical Science, Qazvin, Iran
  • Hojjat Allah Abbaszadeh Hearing Disorder Research center, Shahid Beheshti University of Medical Science,Tehran, Iran
  • Marzieh Shams Nooraei Cellular and Molecular Research Center, Qazvin University of Medical Science, Qazvin, Iran
  • Shahram Darabi Cellular and Molecular Research Center, Qazvin University of Medical Science, Qazvin, Iran
  • Zohreh Golmohammadi Cellular and Molecular Research Center, Qazvin University of Medical Science, Qazvin, Iran
چکیده مقاله:

Background: Autophagy is a mechanism disassembling the damaged organelles from the cell. This study attempted to examine the expression of several autophagy-related genes in Parkinson’s disease (PD) rat model. Methods: The male Wistar rats were divided into three groups as control, sham, and lesion. In the latter group, the PD rat model was induced by the injection of 6-hydroxydopamine in the striatum. The behavioral test was conducted one (baseline) and four weeks after the surgery through apomorphine hydrochloride. Then the RT-PCR technique was employed to evaluate the expressions of p62/SQSTM, autophagy-related genes (ATG)5, ATG12, ATG16L1, ATG10, as well as GAPDH and LC3. Results: By injecting apomorphine, the striatal lesion group showed a significant contralateral rotation at fourth week as compared to the baseline. The examination of p62, ATG5, ATG12, ATG16L1, and LC3 expressions using RT-PCR revealed that p62, ATG5, ATG12, LC3, and ATG16L1 were expressed in the substantia nigra of PD rat model, while ATG10 was not expressed. Conclusion: ATG10 expression is necessary for the initiation of autophagy. Thus, these results show that autophagy deregulation occurs in the initiation stages of the process in the rat model of PD.

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عنوان ژورنال

دوره 22  شماره 1

صفحات  15- 21

تاریخ انتشار 2018-01

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