The c-myc Expression on the Opioid Tolerance in Human Neuroblastoma SH-SY5Y Cells

사람 Neuroblastoma SH-SY5Y 세포주에서 Opiate 내성에 의한 c-myc 유전자 표현

  • Park, Chang-Kyo (Department of Pharmacology, Keimyung University School of Medicine, and Institute for Medical Science) ;
  • Kwon, Gee-Youn (Department of Pharmacology, Keimyung University School of Medicine, and Institute for Medical Science) ;
  • Suh, Sung-Il (Department of Microbiology, Keimyung University School of Medicine, and Institute for Medical Science) ;
  • Kim, Soo-Kyung (Department of Pharmacology, Keimyung University School of Medicine, and Institute for Medical Science)
  • 박창교 (계명대학교 의과대학 약리학교실 및 의과학연구소) ;
  • 권지윤 (계명대학교 의과대학 약리학교실 및 의과학연구소) ;
  • 서성일 (계명대학교 의과대학 미생물학교실 및 의과학연구소) ;
  • 김수경 (계명대학교 의과대학 약리학교실 및 의과학연구소)
  • Published : 1997.12.21

Abstract

The mechanisms underlying opiate tolerance and dependence are not fully understood. We used human neuroblastoma SH-SY5Y cells as a model system for studying effects of morphine tolerance and withdrawal on c-myc induction and cAMP levels. It has been reported that regulation of c-fos by acute and chronic morphine withdrawal is mediated through alterations in CREB transcription factor. In this study, we examined the effects of morphine tolerance on c-myc expression and cAMP concentrations. The activation of opiate receptors by an acute morphine administration resulted in an increase in c-myc mRNA and a decrease in cAMP concentrations in a dose-dependent manner $(5,\;10,\;15,\;and\;20\;{\mu}M)$. On the other hand, the chronic treatment of morphine $(10\;{\mu}M\;for\;six\;days)$ did not induce the elevated expression of c-myc mRNA. The c-myc expression was slightly inhibited in comparison with that of the acute morphine response. However, cAMP concentrations were increased with regard to morphine withdrawal response. These results suggest that the alterations in c-myc expression might imply a significant opiate regulation relating to morphine tolerance. This observation differs from increased expression of c-fos via regulation of cAMP pathway.

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