Excerpt:

There was a relationship between the amount of [male rats’] sexual activity executed and the degree of internalization for MOR [opioid receptors in the ventral tegmental area], but not for DOR [opioid receptors in the ventral tegmental area]. … It is suggested that copulation to satiety might be useful as a model system to study the biological significance of receptor internalization.

Brain Res.

2013 Dec 6;1541:22-32. doi: 10.1016/j.brainres.2013.10.015.

Garduño-Gutiérrez R1León-Olea MRodríguez-Manzo G.

Abstract

Opioid receptors internalize upon specific agonist stimulation. The in vivo significance of receptor internalization is not well established, partly due to the limited in vivo models used to study this phenomenon. Ejaculation promotes endogenous opioid release which activates opioid receptors at the brain, including the mesolimbic system and medial preoptic area. The objective of the present work was to analyze if there was a correlation between the degree of in vivo mu (MOR) and delta opioid receptor (DOR) internalization in the ventral tegmental area and the execution of different amounts of ejaculatory behavior of male rats. To this aim, we analyzed the brains of rats that ejaculated once or six successive times and of sexually exhausted rats with an established sexual inhibition, using immunofluorescence and confocal microscopy.

Results showed that MOR and DOR internalization increased as a consequence of ejaculation.

There was a relationship between the amount of sexual activity executed and the degree of internalization for MOR, but not for DOR. MOR internalization was larger in rats that ejaculated repeatedly than in animals ejaculating only once. Significant DOR internalization was found only in animals ejaculating once. Changes in MOR, DOR and beta arrestin2 detection, associated to sexual activity, were also found. It is suggested that copulation to satiety might be useful as a model system to study the biological significance of receptor internalization.