Korean J Physiol Pharmacol.
1997 Dec;1(6):691-697.
The c-myc expression on the opioid tolerance in human neuroblastoma
SH-SY5Y cells
- Affiliations
-
- 1Department of Pharmacology, Keimyung University, School of Medicine, Taegu 700-712, South Korea.
- 2Department of Microbiology, Keimyung University, School of Medicine, Taegu 700-712, South Korea.
- 3Department of Institute for Medical Science, Keimyung University, School of Medicine, Taegu 700-712, South Korea.
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 muM).
On the other hand, the chronic treatment of morphine (10 muM 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.