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Serotoninergic dorsal raphe neurons possess functional postsynaptic nicotinic acetylcholine receptors
Synapse (New York, N.Y.), 2008-08, Vol.62 (8), p.601-615
Galindo-Charles, Luis
Hernandez-Lopez, Salvador
Galarraga, Elvira
Tapia, Dagoberto
Bargas, José
Garduño, Julieta
Frías-Dominguez, Carmen
Drucker-Colin, René
Mihailescu, Stefan
2008
Volltextzugriff (PDF)
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Autor(en) / Beteiligte
Galindo-Charles, Luis
Hernandez-Lopez, Salvador
Galarraga, Elvira
Tapia, Dagoberto
Bargas, José
Garduño, Julieta
Frías-Dominguez, Carmen
Drucker-Colin, René
Mihailescu, Stefan
Titel
Serotoninergic dorsal raphe neurons possess functional postsynaptic nicotinic acetylcholine receptors
Ist Teil von
Synapse (New York, N.Y.), 2008-08, Vol.62 (8), p.601-615
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2008
Quelle
Wiley-Blackwell Full Collection
Beschreibungen/Notizen
Very few neurons in the telencephalon have been shown to express functional postsynaptic nicotinic acetylcholine receptors (nAChRs), among them, the noradrenergic and dopaminergic neurons. However, there is no evidence for postsynaptic nAChRs on serotonergic neurons. In this study, we asked if functional nAChRs are present in serotonergic (5‐HT) and nonserotonergic (non‐5‐HT) neurons of the dorsal raphe nucleus (DRN). In rat midbrain slices, field stimulation at the tegmental pedunculopontine (PPT) nucleus evoked postsynaptic currents (eEPSCs) with different components in DRN neurons. After blocking the glutamatergic and GABAergic components, the remaining eEPSCs were blocked by mecamylamine and reduced by either the selective α7 nAChR antagonist methyllycaconitine (MLA) or the selective α4β2 nAChR antagonist dihydro‐β‐eritroidine (DHβE). Simultaneous addition of MLA and DHβE blocked all eEPSCs. Integrity of the PPT‐DRN pathway was assessed by both anterograde biocytin tracing and antidromic stimulation from the DRN. Inward currents evoked by the direct application of acetylcholine (ACh), in the presence of atropine and tetrodotoxin, consisted of two kinetically different currents: one was blocked by MLA and the other by DHβE; in both 5‐HT and non‐5‐HT DR neurons. Analysis of spontaneous (sEPSCs) and evoked (eEPSCs) synaptic events led to the conclusion that nAChRs were located at the postsynaptic membrane. The possible implications of these newly described nAChRs in various physiological processes and behavioral events, such as the wake‐sleep cycle, are discussed. Synapse 62:601–615, 2008. © 2008 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 0887-4476
eISSN: 1098-2396
DOI: 10.1002/syn.20526
Titel-ID: cdi_proquest_miscellaneous_71637616
Format
–
Schlagworte
Acetylcholine - metabolism
,
alpha7 Nicotinic Acetylcholine Receptor
,
Animals
,
dorsal raphe nucleus
,
Electric Stimulation
,
Excitatory Postsynaptic Potentials - drug effects
,
Excitatory Postsynaptic Potentials - physiology
,
Mesencephalon - metabolism
,
Neural Pathways - drug effects
,
Neural Pathways - metabolism
,
Neurons - drug effects
,
Neurons - metabolism
,
nicotinic acetylcholine receptor
,
Nicotinic Antagonists - pharmacology
,
Organ Culture Techniques
,
Patch-Clamp Techniques
,
Pedunculopontine Tegmental Nucleus - metabolism
,
Raphe Nuclei - cytology
,
Raphe Nuclei - drug effects
,
Raphe Nuclei - metabolism
,
Rats
,
Rats, Wistar
,
Receptors, Nicotinic - drug effects
,
Receptors, Nicotinic - metabolism
,
serotonergic neurons
,
Serotonin - metabolism
,
Synapses - drug effects
,
Synapses - metabolism
,
Synaptic Membranes - drug effects
,
Synaptic Membranes - metabolism
,
Synaptic Transmission - drug effects
,
Synaptic Transmission - physiology
,
Wakefulness - drug effects
,
Wakefulness - physiology
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