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A ganglionic intestinointestinal reflex activated by acute noxious challenge.
Stebbing, Martin J; Shafton, Anthony D; Davey, Catherine E; Di Natale, Madeleine R; Furness, John B; McAllen, Robin M.
Afiliação
  • Stebbing MJ; Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
  • Shafton AD; Department of Anatomy and Physiology, University of Melbourne, Parkville, Victoria, Australia.
  • Davey CE; Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
  • Di Natale MR; Department of Biomedical Engineering, University of Melbourne, Parkville, Victoria, Australia.
  • Furness JB; Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
  • McAllen RM; Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
Am J Physiol Gastrointest Liver Physiol ; 326(4): G360-G373, 2024 Apr 01.
Article em En | MEDLINE | ID: mdl-38226653
ABSTRACT
To investigate noxious stimulation-responsive neural circuits that could influence the gut, we recorded from intestinally directed (efferent) nerve filaments dissected from mesenteric nerves close to the small intestine in anesthetized rats. These exhibited baseline multiunit activity that was almost unaffected by vagotomy (VagX) and reduced only slightly by cutting the splanchnic nerves. The activity was halved by hexamethonium (Hex) treatment. When an adjacent gut segment received an intraluminal stimulus 2,4,6-trinitrobenzenesulfonate (TNBS) in 30% ethanol, mesenteric efferent nerve activity increased for more than 1 h. The increased activity was almost unaffected by bilateral vagotomy or splanchnic nerve section, indicating a lack of central nervous involvement, but it was 60% reduced by hexamethonium. Spike sorting discriminated efferent single and predominantly single-unit spike trains that responded to TNBS, were unaffected by splachnectomy but were silenced by hexamethonium. After noxious stimulation of one segment, the adjacent segment showed no evidence of suppression of gut motility or vasoconstriction. We conclude that luminal application of a noxious stimulus to the small intestine activates an entirely peripheral, intestinointestinal reflex pathway. This pathway involves enteric intestinofugal neurons that excite postganglionic sympathetic neurons via a nicotinic synapse. We suggest that the final sympathetic efferent neurons that respond to a tissue damaging stimulus are distinct from vasoconstrictor, secretomotor, and motility inhibiting neurons.NEW & NOTEWORTHY An intraluminal noxious chemical stimulus applied to one segment of small intestine increased mesenteric efferent nerve activity to an adjacent segment. This was identified as a peripheral ganglionic reflex that did not require vagal or spinal connections. Hexamethonium blocked most, but not all, ongoing and reflex mesenteric efferent activity. The prevertebral sympathetic efferent neurons that are activated likely affect inflammatory and immune functions of other gut segments.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reflexo / Nervos Esplâncnicos Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reflexo / Nervos Esplâncnicos Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article