Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/30218
Title: Serotonergic neurons activate chemosensitive retrotrapezoid nucleus neurons by a pH-independent mechanism
Authors: Mulkey, Daniel K.
Rosin, Diane L.
West, Gavin
Takakura, Ana C. [UNIFESP]
Moreira, Thiago S. [UNIFESP]
Bayliss, Douglas A.
Guyenet, Patrice G.
Univ Virginia
Universidade Federal de São Paulo (UNIFESP)
Keywords: chemosensitivity
raphe
central respiratory control
ventral medullary surface
pH signaling
brain slice
Issue Date: 19-Dec-2007
Publisher: Soc Neuroscience
Citation: Journal of Neuroscience. Washington: Soc Neuroscience, v. 27, n. 51, p. 14128-14138, 2007.
Abstract: Serotonin activates respiration and enhances the stimulatory effect of CO2 on breathing. the present study tests whether the mechanism involves the retrotrapezoid nucleus (RTN), a group of medullary glutamatergic neurons activated by extracellular brain pH and presumed to regulate breathing. We show that the RTN is innervated by both medullary and pontine raphe and receives inputs from thyrotropin-releasing hormone (TRH) and substance P-expressing neurons. Coexistence of serotonin and substance P in terminals within RTN confirmed that lower medullary serotonergic neurons innervate RTN. in vivo, unilateral injection of serotonin into RTN stimulated inspiratory motor activity, and pH-sensitive RTN neurons were activated by iontophoretic application of serotonin or substance P. in brain slices, pH-sensitive RTN neurons were activated by serotonin, substance P, and TRH. the effect of serotonin in slices was ketanserin sensitive and persisted in the presence of glutamate, GABA, glycine, and purinergic ionotropic receptor antagonists. Serotonin and pH had approximately additive effects on the discharge rate of RTN neurons, both in slices and in vivo. in slices, serotonin produced an inward current with little effect on conductance and had no effect on the pH-induced current. We conclude that (1) RTN receives input from multiple raphe nuclei, (2) serotonin, substance P, and TRH activate RTN chemoreceptors, and (3) excitatory effects of serotonin and pH are mediated by distinct ionic conductances. Thus, RTN neurons presumably contribute to the respiratory stimulation caused by serotonergic neurons, but serotonin seems without effect on the cellular mechanism by which RTN neurons detect pH.
URI: http://repositorio.unifesp.br/handle/11600/30218
ISSN: 0270-6474
Other Identifiers: http://dx.doi.org/10.1523/JNEUROSCI.4167-07.2007
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