Wang H, Wessendorf M W
Department of Neuroscience, University of Minnesota, Minneapolis, MN 55455, USA.
Neuroscience. 2002;109(3):619-34. doi: 10.1016/s0306-4522(01)00328-1.
Opioid antinociception appears to be mediated at least in part by a pathway that projects from the periaqueductal gray (PAG) to the rostral ventromedial medulla (RVM), but the relationship between opioid receptors and PAG-RVM projection neurons is unclear. Previous electrophysiological studies have suggested that opioids act directly on some PAG neurons projecting to the RVM. However, immunoreactivity for neither the cloned mu-opioid receptor (MOR1) nor the cloned delta-opioid receptor (DOR1) has been observed in PAG cells retrogradely labeled from the RVM. In the present study, we examined the expression of DOR1 and MOR1 mRNAs in PAG neurons projecting to RVM using quantitative in situ hybridization and retrograde tract-tracing. Mesencephalic neurons were labeled in three male Sprague-Dawley rats by microinjection of Fluoro-Gold into the RVM. Five micrometer cryostat sections were cut and in situ hybridization was performed using full-length cRNA probes labeled with 35S-UTP. Retrogradely labeled neurons that were also labeled for MOR1 or DOR1 mRNA were observed in the dorsomedial, lateral, and ventrolateral portions of the PAG. Quantification was performed in the dorsomedial and ventrolateral PAG using the physical disector. We found that of 219 retrogradely labeled neurons, 50 +/- 14% expressed DOR1 mRNA. In a second set of 120 Fluoro-Gold-labeled neurons, 27 +/- 8% expressed MOR1 mRNA. Significantly more PAG-RVM projection neurons were labeled for MOR1 mRNA in the ventrolateral subregion of the PAG than in the dorsomedial subregion. However, no significant difference was observed in the proportions of retrogradely labeled neurons labeled for DOR1 mRNA in the ventrolateral subregion compared to the dorsomedial subregion. We conclude that opioids are likely to exert direct effects on PAG-RVM projection neurons through both delta- and mu-opioid receptors. In addition, direct effects on PAG-RVM projection neurons from activation of MOR1 appear more likely to be exerted in the ventrolateral PAG than in the dorsomedial PAG.
阿片类药物的抗伤害感受作用似乎至少部分是由一条从导水管周围灰质(PAG)投射到延髓头端腹内侧区(RVM)的通路介导的,但阿片受体与PAG-RVM投射神经元之间的关系尚不清楚。以往的电生理研究表明,阿片类药物直接作用于一些投射到RVM的PAG神经元。然而,在从RVM逆向标记的PAG细胞中,未观察到克隆的μ-阿片受体(MOR1)和克隆的δ-阿片受体(DOR1)的免疫反应性。在本研究中,我们使用定量原位杂交和逆向束路追踪技术,检测了投射到RVM的PAG神经元中DOR1和MOR1 mRNA的表达。通过向三只雄性Sprague-Dawley大鼠的RVM微量注射荧光金,标记中脑神经元。切取5微米厚的冰冻切片,使用用35S-UTP标记的全长cRNA探针进行原位杂交。在PAG的背内侧、外侧和腹外侧部分观察到同时被MOR1或DOR1 mRNA标记的逆向标记神经元。使用物理分割器对背内侧和腹外侧PAG进行定量分析。我们发现,在219个逆向标记的神经元中,50±14%表达DOR1 mRNA。在另一组120个荧光金标记的神经元中,27±8%表达MOR1 mRNA。与背内侧亚区相比,PAG腹外侧亚区中被MOR1 mRNA标记的PAG-RVM投射神经元明显更多。然而,腹外侧亚区与背内侧亚区相比,被DOR1 mRNA标记的逆向标记神经元比例没有显著差异。我们得出结论,阿片类药物可能通过δ-和μ-阿片受体对PAG-RVM投射神经元产生直接作用。此外,MOR1激活对PAG-RVM投射神经元的直接作用似乎更可能发生在腹外侧PAG而非背内侧PAG。