Background: Besides its role in neuronal growth and differentiation, brain-derived neurotrophic factor (BDNF) has been implicated in the control of peristalsis where it serves to enhance gastrointestinal motility. Aim: To unravel the cellular mechanisms governing BDNF’s effect on motility. Methods: Studies were performed in primary myenteric neuron cultures and whole mount preparations derived from guinea pig ileum. Expression of BDNF and its TrkB receptor was assessed by immunohistochemistry. Intracellular Ca2+ concentration ([Ca2+]i) changes in myenteric neurons were monitored using Fluo-4 and neurotransmitter release kinetics at enteric synapses were evaluated with FM1-43 imaging. Results: Immunohistochemistry revealed the presence of BDNF and TrkB in mucosa, submucosal plexus and myenteric ganglia. Primary cultures also expressed BDNF and TrkB and were used to study the physiological effects of BDNF. None of the neurons studied, displayed a [Ca2+]i change when challenged with BDNF. However, BDNF exposure caused an enhancement of Ca2+ transients induced by serotonin and substance P, which was reversed by the Trk receptor blocker K-252a (0.1 µM). BDNF incubation also resulted in an amplification of spontaneous network activity which was reflected in an increased number of synaptic vesicle clusters. Furthermore, BDNF treatment facilitated FM1-43 labelled vesicle destaining in enteric terminals during field stimulation. Conclusions: Our findings demonstrate that BDNF is able to enhance rather than directly activate enteric nervous system signalling. Therefore, the promotion of motility by BDNF seems to result from its potent modulating role on enteric neuronal activity and synaptic communication.
- calcium imaging
- enteric neurone
- synaptic transmission
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