dc.creatorVillalobos Hernandéz, Egina Criseida
dc.creatorBarajas López, Carlos
dc.creatorMartínez Salazar, Elizabeth Aurelia
dc.creatorSalgado Delgado, Roberto Carlos
dc.creatorMiranda Morales, Marcela
dc.date2019-08-09T22:23:00Z
dc.date2019-08-09T22:23:00Z
dc.date2017
dc.date.accessioned2023-07-17T22:03:52Z
dc.date.available2023-07-17T22:03:52Z
dc.identifierEgina C. Villalobos-Hernández, Carlos Barajas-López, Elizabeth A. Martínez-Salazar, Roberto C. Salgado-Delgado, Marcela Miranda-Morales, Cholinergic signaling plasticity maintains viscerosensory responses during Aspiculuris tetraptera infection in mice small intestine, Autonomic Neuroscience, Volume 206, 2017, Pages 8-18.
dc.identifierhttp://hdl.handle.net/11627/5077
dc.identifierhttps://doi.org/10.1016/j.autneu.2017.06.001
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/7543709
dc.description"Intestinal parasites alter gastrointestinal (GI) functions like the cholinergic function. Aspiculuris tetraptera is a pinworm frequently observed in laboratory facilities, which infests the mice cecum and proximal colon. However, little is known about the impact of this infection on the GI sensitivity. Here, we investigated possible changes in spontaneous mesenteric nerve activity and on the mechanosensitivity function of worm-free regions of naturally infected mice with A. tetraptera. Infection increased the basal firing of mesenteric afferent nerves in jejunum. Our findings indicate that nicotinic but not muscarinic receptors, similarly affect spontaneous nerve firing in control and infected animals; these axons are mainly vagal. No difference between groups was observed on spontaneous activity after nicotinic receptor inhibition. However, and contrary to the control group, during infection, the muscarinic signaling was shown to be elevated during mechanosensory experiments. In conclusion, we showed for the first time that alterations induced by infection of the basal afferent activity were independent of the cholinergic function but changes in mechanosensitivity were mediated by muscarinic, but not nicotinic, receptors and specifically by high threshold nerve fibers (activated above 20 mm Hg), known to play a role in nociception. These plastic changes within the muscarinic signaling would function as a compensatory mechanism to maintain a full mechanosensory response and the excitability of nociceptors during infection. These changes indicate that pinworm colonic infection can target other tissues away from the colon."
dc.formatapplication/pdf
dc.publisherElsevier
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rightsAcceso Abierto
dc.subjectMechanosensitive response
dc.subjectAfferent multifiber recordings
dc.subjectGastrointestinal sensory fibers
dc.subjectAcetylcholine responses
dc.subjectAspiculuris tetraptera
dc.subjectNEUROCIENCIAS
dc.titleCholinergic signaling plasticity maintains viscerosensory responses during Aspiculuris tetraptera infection in mice small intestine
dc.typearticle


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