scholarly journals Ca2+transients in myenteric glial cells during the colonic migrating motor complex in the isolated murine large intestine

2012 ◽  
Vol 590 (2) ◽  
pp. 335-350 ◽  
Author(s):  
Matthew J. Broadhead ◽  
Peter O. Bayguinov ◽  
Takanobu Okamoto ◽  
Dante J. Heredia ◽  
Terence K. Smith
Keyword(s):  
Glial Cells ◽  
Large Intestine ◽  
Migrating Motor Complex ◽  
Motor Complex ◽  
Colonic Migrating Motor Complex

scholarly journals Critical role of 5-HT1A, 5-HT3, and 5-HT7 receptor subtypes in the initiation, generation, and propagation of the murine colonic migrating motor complex

2010 ◽  
Vol 299 (1) ◽  
pp. G144-G157 ◽  
Author(s):  
Eamonn J. Dickson ◽  
Dante J. Heredia ◽  
Terence K. Smith
Keyword(s):  
Critical Role ◽  
Circular Muscle ◽  
Migrating Motor Complex ◽  
Receptor Subtypes ◽  
Type Ii ◽  
Motor Complex ◽  
Intracellular Microelectrodes ◽  
Dogiel Type Ii ◽  
Colonic Migrating Motor Complex

The colonic migrating motor complex (CMMC) is necessary for fecal pellet propulsion in the murine colon. We have previously shown that 5-hydroxytryptamine (5-HT) released from enterochromaffin cells activates 5-HT3 receptors on the mucosal processes of myenteric Dogiel type II neurons to initiate the events underlying the CMMC. Our aims were to further investigate the roles of 5-HT1A, 5-HT3, and 5-HT7 receptor subtypes in generating and propagating the CMMC using intracellular microelectrodes or tension recordings from the circular muscle (CM) in preparations with and without the mucosa. Spontaneous CMMCs were recorded from the CM in isolated murine colons but not in preparations without the mucosa. In mucosaless preparations, ondansetron (3 μM; 5-HT3 antagonist) plus hexamethonium (100 μM) completely blocked spontaneous inhibitory junction potentials, depolarized the CM. Ondansetron blocked the preceding hyperpolarization associated with a CMMC. Spontaneous CMMCs and CMMCs evoked by spritzing 5-HT (10 and 100 μM) or nerve stimulation in preparations without the mucosa were blocked by SB 258719 or SB 269970 (1–5 μM; 5-HT7 antagonists). Both NAN-190 and (S)-WAY100135 (1–5 μM; 5-HT1A antagonists) blocked spontaneous CMMCs and neurally evoked CMMCs in preparations without the mucosa. Both NAN-190 and (S)-WAY100135 caused an atropine-sensitive depolarization of the CM. The precursor of 5-HT, 5-hydroxytryptophan (5-HTP) (10 μM), and 5-carboxamidotryptamine (5-CT) (5 μM; 5-HT1/5/7 agonist) increased the frequency of spontaneous CMMCs. 5-HTP and 5-CT also induced CMMCs in preparations with and without the mucosa, which were blocked by SB 258719. 5-HT1A, 5-HT3, and 5-HT7 receptors, most likely on Dogiel Type II/AH neurons, are important in initiating, generating, and propagating the CMMC. Tonic inhibition of the CM appears to be driven by ongoing activity in descending serotonergic interneurons; by activating 5-HT7 receptors on AH neurons these interneurons also contribute to the generation of the CMMC.

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