Ultrastructural evidence for mu and delta opioid receptors at noradrenergic dendrites and glial profiles in the cat locus coeruleus

Brain Res. 2021 Jul 1:1762:147443. doi: 10.1016/j.brainres.2021.147443. Epub 2021 Mar 19.

Abstract

The Locus Coeruleus (LC) is a pontine nucleus involved in many physiological processes, including the control of the sleep/wake cycle (SWC). At cellular level, the LC displays a high density of opioid receptors whose activation decreases the activity of LC noradrenergic neurons. Also, microinjections of morphine administered locally in the LC of the cat produce sleep associated with synchronized brain activity in the electroencephalogram (EEG). Even though much of the research on sleep has been done in the cat, the subcellular location of opioid receptors in the LC and their relationship with LC noradrenergic neurons is not known yet in this species. Therefore, we conducted a study to describe the ultrastructural localization of mu-opioid receptors (MOR), delta-opioid receptors (DOR) and tyrosine hydroxylase (TH) in the cat LC using high resolution electron microscopy double-immunocytochemical detection. MOR and DOR were localized mainly in dendrites (45% and 46% of the total number of profiles respectively), many of which were noradrenergic (35% and 53% for MOR and DOR, respectively). TH immunoreactivity was more frequent in dendrites (65% of the total number of profiles), which mostly also expressed opioid receptors (58% and 73% for MOR and DOR, respectively). Because the distribution of MORs and DORs are similar, it is possible that a substantial sub-population of neurons co-express both receptors, which may facilitate the formation of MOR-DOR heterodimers. Moreover, we found differences in the cat subcellular DOR distribution compared with the rat. This opens the possibility to the existence of diverse mechanisms for opioid modulation of LC activity.

Keywords: Glial opioid receptors; Immunolabeling techniques; Opioid receptors; Transmission electron microscopy; Tyrosine hydroxylase; Ultrastructural localization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic Neurons / metabolism
  • Adrenergic Neurons / ultrastructure*
  • Animals
  • Cats
  • Dendrites / metabolism
  • Dendrites / ultrastructure*
  • Locus Coeruleus / metabolism
  • Locus Coeruleus / ultrastructure*
  • Neuroglia / metabolism
  • Neuroglia / ultrastructure*
  • Receptors, Opioid, delta / metabolism
  • Receptors, Opioid, delta / ultrastructure*
  • Receptors, Opioid, mu / metabolism
  • Receptors, Opioid, mu / ultrastructure*

Substances

  • Receptors, Opioid, delta
  • Receptors, Opioid, mu