Abstract
Morphine, given acutely, inhibits oxytocin secretion in adult female rats, but chronic intracerebroventricular infusion for five to six days induces tolerance and dependence in the mechanisms regulating oxytocin secretion. One explanation for tolerance could be that there is a loss of opioid receptors. To test this hypothesis cryostat sections of selected brain regions and the pituitary, from six control and six intracerebroventricular morphine-infused rats, were processed for quantitative in vitro receptor autoradiography. [ 3H]Etorphine or [ 3H](−)-bremazocine were used as ligands, and DAGO, DPDPE and U50,488H as selective displacers from μ-, δ-, and κ-receptors, respectively. Control incubations had naloxone determined specificity. The supraoptic nucleus (site of oxytocin-secreting magnocellular perikarya) contained both μ- and κ-receptors in control rats (mean ± S.E.M. binding of μ-selective [ 3H]etorphine was 91.8 ± 25.4 fmol/mg of tissue, and of κ-selective [ 3H](−)-bremazocine was 130.4 ± 25.6 fmol/mg). Chronic morphine treatment caused a 83.9% decrease in binding in μ-selective conditions ( P < 0.05), but no significant change in κ-selective binding. In the median preoptic nucleus (which projects to the supraoptic nucleus) mean ± S.E.M. binding of [ 3H]etorphine decreased by 77.0% ( P < 0.01) in chronic morphine-treated rats, from the control value of 76.2 ± 9.8 fmol/mg of tissue. In the posterior pituitary gland (site of the terminals of the oxytocin-secreting magnocellular perikarya) binding with [ 3H](−)-bremazocine in controls was over 90% lower than in the supraoptic nucleus. No changes followed chronic morphine treatment. Thus chronic morphine exposure reduces the numbers of available μ-receptors in the supraoptic nucleus, and of opioid receptors in the median preoptic nucleus, perhaps accounting for morphine-tolerance in relation to oxytocin secretion.
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