EphrinB2/ephB2‐mediated myenteric synaptic plasticity: mechanisms underlying the persistent muscle hypercontractility and pain in postinfectious IBS

Patients with irritable bowel syndrome (IBS) show pain hypersensitivity and smooth muscle hypercontractility in response to colorectal distension (CRD). Synaptic plasticity, a key process of memory formation, in the enteric nervous system may be a novel explanation. This study aimed to explore the regulatory role of ephrinB2/ephB2 in enteric synaptic plasticity and colonic hyperreactive motility in IBS. Postinfectious (PI)‐IBS was induced by Trichinella spiralis infection in rats. Isometric contractions of colonic circular muscle strips, particularly neural‐mediated contractions, were recorded ex vivo. Meanwhile, ephrinB2/ephB2‐mediated enteric structural and functional synaptic plasticity were assessed in the colonic muscularis, indicating that ephrinB2 and ephB2 were located on enteric nerves and up‐regulated in the colonic muscularis of PI‐IBS rats. Colonic hypersensitivity to CRD and neural‐mediated colonic hypercontractility were present in PI‐IBS rats, which were correlated with increased levels of cellular homologous fos protein ( c‐fos ) and activity‐regulated cystoskeleton‐associated protein (arc), the synaptic plasticity‐related immediate early genes, and were ameliorated by ephB2Fc (an ephB2 receptor blocker) or MK801 (an NMDA receptor inhibitor) exposure. EphrinB2/ephB2 facilitated synaptic sprouting and NMDA receptor‐mediated synaptic potentiation in the colonic muscularis of PI‐IBS rats and in the longitudinal muscle‐myenteric plexus cultures, involving the Erk‐MAPK and PI3K‐protein kinase B pathways. In conclusion, ephrinB2/ephB2 promoted the synaptic sprouting and potentiation of myenteric nerves involved in persistent muscle hypercontractility and pain in PI‐IBS. Hence, ephrinB2/ephB2 may be an emerging target for the treatment of IBS.—Zhang, L., Wang, R., Bai, T., Xiang, X., Qian, W., Song, J., Hou, X. EphrinB2/ephB2‐mediated myenteric synaptic plasticity: mechanisms underlying the persistent muscle hypercontractility and pain in postinfectious IBS. FASEB J. 33, 13644‐13659 (2019). www.fasebj.org