4.8 Article

Propulsive colonic contractions are mediated by inhibition-driven poststimulus responses that originate in interstitial cells of Cajal

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.2123020119

关键词

colonic motility; enteric nervous system; SIP syncytium; smooth muscle; peristalsis

资金

  1. NIH/National Institute of Diabetes and Digestive and Kidney Diseases [PO1-41315, R01-DK120759, R01-DK-091336, OT2OD024899]

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The peristaltic reflex is a fundamental behavior of the gastrointestinal tract, involving the activation of neurons to produce propulsive contractions. This study found that there are mechanisms other than cholinergic neurons involved in the generation and propagation of colonic migrating motor complexes (CMMCs), and that poststimulus excitations in interstitial cells of Cajal (ICC) play a role in this process. These findings provide alternative insights into the mechanisms of CMMCs in the colon.
The peristaltic reflex is a fundamental behavior of the gastrointestinal (GI) tract in which mucosal stimulation activates propulsive contractions. The reflex occurs by stim-ulation of intrinsic primary afferent neurons with cell bodies in the myenteric plexus and projections to the lamina propria, distribution of information by interneurons, and activation of muscle motor neurons. The current concept is that excitatory cholinergic motor neurons are activated proximal to and inhibitory neurons are activated distal to the stimulus site. We found that atropine reduced, but did not block, colonic migrating motor complexes (CMMCs) in mouse, monkey, and human colons, suggesting a mech-anism other than one activated by cholinergic neurons is involved in the generation/ propagation of CMMCs. CMMCs were activated after a period of nerve stimulation in colons of each species, suggesting that the propulsive contractions of CMMCs may be due to the poststimulus excitation that follows inhibitory neural responses. Blocking nitrergic neurotransmission inhibited poststimulus excitation in muscle strips and blocked CMMCs in intact colons. Our data demonstrate that poststimulus excitation is due to increased Ca2+ transients in colonic interstitial cells of Cajal (ICC) following cessation of nitrergic, cyclic guanosine monophosphate (cGMP)-dependent inhibitory responses. The increase in Ca2+ transients after nitrergic responses activates a Ca2+- activated Cl2 conductance, encoded by Ano1, in ICC. Antagonists of ANO1 channels inhibit poststimulus depolarizations in colonic muscles and CMMCs in intact colons. The poststimulus excitatory responses in ICC are linked to cGMP-inhibited cyclic adenosine monophosphate (cAMP) phosphodiesterase 3a and cAMP-dependent effects. These data suggest alternative mechanisms for generation and propagation of CMMCs in the colon.

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