Ultrastructural localization of mu-1 opioid receptor in the dorsal raphe nucleus of the rat

✍ Scribed by Qing-Ping Wang; Hidehiko Ochiai; Jian-Lian Guan; Yasumitsu Nakai

• Publisher: John Wiley and Sons
• Year: 1998
• Tongue: English
• Weight: 702 KB
• Volume: 29
• Category: Article
• ISSN: 0887-4476
• DOI: 10.1002/(sici)1098-2396(199807)29:3<240::aid-syn6>3.0.co;2-6

✦ Synopsis

A simple pre-embedding avidin-biotin-peroxidase complex technique was used to study the ultrastructural localization of mu-1 opioid receptor in the rat dorsal raphe nucleus. Using low concentrations of the first antiserum for incubation with a short reaction time to 3,3'-diaminobenzidine, the immunostaining was faint at the light microscopic level. However, at the electron microscopic level strong immunoreaction was observed. Mu-1 opioid receptors were found to be localized on the postsynaptic membrane of dendrites, extra-synaptic plasma membrane, and the surface of the small, clear vesicles in axon terminals. Of the total 407 immunopositive profiles observed, 76.4% (311/407) were dendrites and 18.9% (77/407) were axon terminals. The immunostained myelinated axons and perikarya were relatively rare, with frequencies of 1.0% (4/407) and 3.7% (15/407), respectively. About 50.8% of the immunopositive dendrites (158/311) were immunostained having their MOR-LI results beneath the postsynaptic membrane, although about 19.6% of them (31/158) also exhibited MOR-LI on other components, including the extrasynaptic plasma membrane. Other immunopositive dendrites showed staining in some other contents, including extrasynaptic plasma membrane (82/311, 26.4%) or not on the plasma membranes (71/311, 22.8%). Less than half of the immunopositive axon terminals (35/77, 45.5%) were found to make synapses with nonimmunoreactive dendrites (31/77, 40.3%) or immunopositive dendrites (4/77, 5.2%); none were found to make synapses with immunoreactive perikarya. The present study shows that mu-1 opioid receptor in the dorsal raphe nucleus plays a role at both synapse or not.