M. Ferreira et al., Evidence of a functional alpha 7-neuronal nicotinic receptor subtype located on motoneurons of the dorsal motor nucleus of the vagus, J PHARM EXP, 296(2), 2001, pp. 260-269
Citations number
40
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
In vitro autoradiography using I-125-alpha -bungarotoxin (alpha -BGTx) and
anti-alpha7 immunohistochemistry were performed on the dorsal motor nucleus
of the vagus (DMV) of sham and chronically vagotomized rats to determine w
hether the alpha7-nicotinic acetylcholine receptor (nAChR) is located posts
ynaptically on DMV neurons whose axons contribute to the vagus nerve. Inten
se bilateral I-125-alpha -BGTx binding and anti-alpha7 immunostaining were
observed in coronal brain sections containing the DMV of sham-vagotomized a
nimals. Unilateral cervical vagotomy resulted in ipsilateral losses of I-12
5-alpha -BGTx binding and anti-alpha7 immunostaining from the DMV. Simultan
eous staining of rat brainstem sections with anti-alpha7 and anti-choline a
cetyltransferase (ChAT) antibodies (to identify cholinergic DMV neurons tha
t project into the vagus nerve) revealed that every DMV neuron that was sta
ined for ChAT showed alpha7-staining as well. In vagotomized animals, no Ch
AT-positive neurons expressing alpha7-nAChRs remained in the ipsilateral DM
V. We conclude that the alpha7-nAChR subtype is located postsynaptically on
DMV neurons. To test whether the alpha7-nAChR is similar to the alpha7-hom
omeric nAChR, experiments were performed in anesthetized rats, and compound
s were microinjected into the DMV while monitoring intragastric pressure (I
GP). alpha -BGTx and strychnine antagonized nicotine-induced increases in I
GP; no antagonism was observed with methyllycaconitine, a compound known to
block the homomeric alpha7-nAChR subtype. Recovery from alpha -BGTx-induce
d antagonism of the nicotine response was observed. We conclude that there
is a nAChR containing the alpha7-subunit in the DMV that is different from
the homomeric alpha7-nAChR subtype.