Enteric motor and interneuronal circuits controlling motility

JC Bornstein, M Costa, JR Grider - Neurogastroenterology & …, 2004 - Wiley Online Library
JC Bornstein, M Costa, JR Grider
Neurogastroenterology & Motility, 2004Wiley Online Library
The enteric nervous system regulates intestinal motility. It contains intrinsic sensory
neurones, several types of interneurones and excitatory and inhibitory motor neurones. This
review summarizes our knowledge of motor neurones and interneurones in simple motility
reflex pathways (ascending and descending excitation, descending inhibition) and it focuses
on guinea‐pig ileum. Excitatory circular muscle motor neurones contain choline
acetyltransferase (ChAT) and tachykinins and project orally 0.5–10 mm. They transmit via …
Abstract
The enteric nervous system regulates intestinal motility. It contains intrinsic sensory neurones, several types of interneurones and excitatory and inhibitory motor neurones. This review summarizes our knowledge of motor neurones and interneurones in simple motility reflex pathways (ascending and descending excitation, descending inhibition) and it focuses on guinea‐pig ileum. Excitatory circular muscle motor neurones contain choline acetyltransferase (ChAT) and tachykinins and project orally 0.5–10 mm. They transmit via muscarinic acetylcholine receptors and tachykinins acting at NK1 and NK2 receptors. Inhibitory circular muscle motor neurones contain nitric oxide synthase (NOS), vasoactive intestinal peptide (VIP) and pituitary adenylyl cyclase activating peptide (PACAP), project anally up to 25 mm and transmit via ATP, nitric oxide and/or VIP. Ascending interneurones project up to 10 mm orally and contain ChAT and tachykinins. They transmit to each other via ACh at nicotinic receptors (nAChR), but to excitatory motor neurones via both nAChR and NK3 receptors. There are at least three types of descending interneurones and one transmits to inhibitory motor neurones via ATP acting at P2X receptors. NOS‐containing descending interneurones receive input via P2Y receptors from other interneurones. Transmission to and from the other descending interneurones (ChAT/5‐HT, ChAT/somatostatin) is yet to be characterized.
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