The regulation of δ‐opiate receptor density on 108CC15 neuroblastoma × glioma hybrid cells

Article date: January 1984

By: Margaret A. Moses, Christopher R. Snell in Volume 81, Issue 1, pages 169-174

The effect of exogenous substances on the expression of opiate receptors on 108CC15 neuroblastoma × glioma hybrid cells has been studied.

Cell differentiation by culture in the presence of N6‐O2‐dibutyryl adenosine 3′,5′‐cyclic monophosphate induced a three fold increase in opiate receptor density.

When the cells were grown in the presence of 10−5m morphine hydrochloride for up to 23 days, opiate receptor densities were reduced by only 30% when compared with matched controls.

Culture in the presence of 10−7md‐Ala2d‐Leu5‐enkephalin produced opiate receptor down regulation of 73% compared to controls after only 4 h of treatment.

The down regulation process could be inhibited by continued exposure to d‐Ala2d‐Leu5‐enkephalin at concentrations greater than 4 nm; below this concentration down regulation was rapid and irreversible.

A model to explain these observations is described.

The effect of exogenous substances on the expression of opiate receptors on 108CC15 neuroblastoma × glioma hybrid cells has been studied.

Cell differentiation by culture in the presence of N6‐O2‐dibutyryl adenosine 3′,5′‐cyclic monophosphate induced a three fold increase in opiate receptor density.

When the cells were grown in the presence of 10−5m morphine hydrochloride for up to 23 days, opiate receptor densities were reduced by only 30% when compared with matched controls.

Culture in the presence of 10−7md‐Ala2d‐Leu5‐enkephalin produced opiate receptor down regulation of 73% compared to controls after only 4 h of treatment.

The down regulation process could be inhibited by continued exposure to d‐Ala2d‐Leu5‐enkephalin at concentrations greater than 4 nm; below this concentration down regulation was rapid and irreversible.

A model to explain these observations is described.

DOI: 10.1111/j.1476-5381.1984.tb10757.x

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