4.6 Article

Nitric Oxide Is Essential for Generating the Minute Rhythm Contraction Pattern in the Small Intestine, Likely via ICC-DMP

期刊

FRONTIERS IN NEUROSCIENCE
卷 14, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fnins.2020.592664

关键词

gap junction; nitric oxide; gastrointestinal motility; small intestine; slow waves; coupled oscillators; interstitial cells of cajal

资金

  1. Canadian Institutes of Health Research [12874, 152942]
  2. Natural Sciences and Engineering Research Council [386877, 1293408]
  3. Farncombe Family Digestive Health Research Institute

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The study explores the role of nitric oxide in peristaltic activity in the ex vivo mouse intestine using spatiotemporal mapping. It identifies a propulsive motor pattern dependent on nitric oxide and reveals that cluster formation is inhibited by neural activity and nitric oxide synthesis blockade but restored by a constant level of nitric oxide. The presence of rhythmic inhibitions not dependent on nitrergic nerves and the involvement of ICC network synchronization in cluster and contraction wave formation are also noted.
Nitrergic nerves have been proposed to play a critical role in the orchestration of peristaltic activities throughout the gastrointestinal tract. In the present study, we investigated the role of nitric oxide, using spatiotemporal mapping, in peristaltic activity of the whole ex vivo mouse intestine. We identified a propulsive motor pattern in the form of propagating myogenic contractions, that are clustered by the enteric nervous system into a minute rhythm that is dependent on nitric oxide. The cluster formation was abolished by TTX, lidocaine and nitric oxide synthesis inhibition, whereas the myogenic contractions, occurring at the ICC-MP initiated slow wave frequency, remained undisturbed. Cluster formation, inhibited by block of nitric oxide synthesis, was fully restored in a highly regular rhythmic fashion by a constant level of nitric oxide generated by sodium nitroprusside; but the action of sodium nitroprusside was inhibited by lidocaine indicating that it was relying on neural activity, but not rhythmic nitrergic nerve activity. Hence, distention-induced activity of cholinergic nerves and/or a co-factor within nitrergic nerves such as ATP is also a requirement for the minute rhythm. Cluster formation was dependent on distention but was not evoked by a distention reflex. Block of gap junction conductance by carbenoxolone, dose dependently inhibited, and eventually abolished clusters and contraction waves, likely associated, not with inhibition of nitrergic innervation, but by abolishing ICC network synchronization. An intriguing feature of the clusters was the presence of bands of rhythmic inhibitions at 4-8 cycles/min; these inhibitory patches occurred in the presence of tetrodotoxin or lidocaine and hence were not dependent on nitrergic nerves. We propose that the minute rhythm is generated by nitric oxide-induced rhythmic depolarization of the musculature via ICC-DMP.

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