4.5 Article

Distribution of delta and mu opioid receptor mRNA in rodent dorsal root ganglia neurons

期刊

EUROPEAN JOURNAL OF NEUROSCIENCE
卷 56, 期 3, 页码 4031-4044

出版社

WILEY
DOI: 10.1111/ejn.15733

关键词

delta opioid receptor; dorsal root ganglia; in situ hybridization; mu opioid receptor; primary afferent fibres; rodents

资金

  1. Canadian Institutes of Health Research [PJT-162103]
  2. Fond de la Recherche du Quebec - Sante
  3. Natural Sciences and Engineering Research Council of Canada [RGPIN-2018-06100]

向作者/读者索取更多资源

This study aimed to assess the distribution of MOP and DOP in the dorsal root ganglia of mice and rats. The results showed that both receptors are expressed in all types of neurons to different extents. DOP is mainly expressed in large and medium myelinated neurons, while MOP is mainly found in C fibres. The distribution slightly differs between rats and mice.
Primary afferents are responsible for transmitting signals produced by noxious stimuli from the periphery to the spinal cord. Mu and delta opioid receptors (MOP and DOP) have analgesic properties and are highly expressed in dorsal root ganglia (DRG) neurons. In humans, spinal DOP is almost exclusively located on central terminals of DRG neurons, whereas in rodents, it is expressed both on presynaptic terminals and spinal neurons. In this study, we aimed to assess the distribution of MOP and DOP in the DRGs of mice and rats. Using in situ hybridization and immunofluorescence, we visualized MOP and DOP mRNA together with various neuronal markers. In rats and mice, we show that both receptors are expressed, albeit to different extents, in all types of neurons, namely, large and medium myelinated neurons (NF200-positive), small nonpeptidergic (IB4- or P2X3R-positive) and peptidergic C fibres (Tac1-positive). Overall, DOP mRNA was found to be mainly expressed in large and medium myelinated neurons, whereas MOP mRNA was mainly found in C fibres. The distribution of MOP and DOP, however, slightly differs between rats and mice, with a higher proportion of small nonpeptidergic C fibres expressing DOP mRNA in mice than in rats. We further found that neither morphine nor inflammation affected the distribution of the receptor mRNA. Because of their location, our results confirm that MOP and DOP have the potential to alleviate similar types of pain and that this effect could slightly differ between species.

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