dc.creatorAlonso, Ignacio
dc.creatorSanchez Merlinsky, Agustín
dc.creatorSzczupak, Lidia
dc.date.accessioned2021-10-06T19:40:17Z
dc.date.accessioned2022-10-15T16:45:29Z
dc.date.available2021-10-06T19:40:17Z
dc.date.available2022-10-15T16:45:29Z
dc.date.created2021-10-06T19:40:17Z
dc.date.issued2020-02
dc.identifierAlonso, Ignacio; Sanchez Merlinsky, Agustín; Szczupak, Lidia; Phase-specific motor efference during a rhythmic motor pattern; Society for Neuroscience; Journal of Neuroscience; 40; 9; 2-2020; 1888-1896
dc.identifier0270-6474
dc.identifierhttp://hdl.handle.net/11336/142957
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4411040
dc.description.abstractNeuronal circuits that control motor behaviors orchestrate multiple tasks, including the inhibition of self-generated sensory signals. In the hermaphroditic leech, T and P mechanosensory neurons respond to light touch and pressure on the skin, respectively. We show that the low threshold T cells were also sensitive to topological changes of the animal surface, caused by contraction of the muscles that erect the skin annuli. P cells were unresponsive to this movement. Annuli erection is part of the contraction phase of crawling, a leech locomotive behavior. In isolated ganglia, T cells showed phase-dependent IPSPs during dopamine-induced fictive crawling, whereas P cells were unaffected. The timing and magnitude of the T-IPSPs were highly correlated with the activity of the motoneurons excited during the contraction phase. Together, the results suggest that the central network responsible for crawling sends a reafferent signal onto the T cells, concomitant with the signal to the motoneurons. This reafference is specifically targeted at the sensory neurons that are affected by the movements; and it is behaviorally relevant as excitation of T cells affected the rhythmic motor pattern, probably acting upon the rhythmogenic circuit. Corollary discharge is a highly conserved function of motor systems throughout evolution, and we provide clear evidence of the specificity of its targets and timing and of the benefit of counteracting self-generated sensory input.
dc.languageeng
dc.publisherSociety for Neuroscience
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.1201-19.2020
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1523/JNEUROSCI.1201-19.2020
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectmecanosensorial
dc.subjectdescarga corolaria
dc.subjectosciladores
dc.subjectHirudo
dc.titlePhase-specific motor efference during a rhythmic motor pattern
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


Este ítem pertenece a la siguiente institución