Abstract
Made up of millions of enteric neurons and glial cells, the enteric nervous system (ENS) is in a key position to modulate the secretomotor function and visceral pain of the gastrointestinal tract. The early life developmental period, through which most of the ENS development occurs, is highly susceptible to microenvironmental perturbation. Over the past decade, accumulating evidence has shown the impact of stress and early life adversity (ELA) on host gastrointestinal pathophysiology. While most of the focus has been on alterations in brain structure and function, limited experimental work in rodents suggest that the enteric nervous system can also be directly affected, as shown by changes in the number, phenotype, and reactivity of enteric nerves. The work of Medland et al. in the current issue of this journal demonstrates that such alterations also occur in pigs, a larger mammalian species with high translational value to human. This work also highlights a sex-differential susceptibility of the ENS to the effect of ELA, which could contribute to the higher prevalence of GI disorders in women. In this mini-review, we will discuss the development and composition of the ENS and related gastrointestinal sensory motor and secretory functions. We will then focus on the influence of stress on the enteric nervous system, with a particular emphasis on neurodevelopmental changes. Finally, we will discuss the influence of sex on those parameters.
The enteric nervous system (ENS) is the key orchestrator of various gastrointestinal functions. The differentiation, organization, and development of the ENS occur throughout the perinatal period which is highly susceptible to microenvironmental changes. Recent evidence supports a role of early life adversity in sex-dependent alterations of ENS development and function, which may have clinical relevance for functional gastrointestinal disorders which have higher prevalence in women.
from #ENT via xlomafota13 on Inoreader http://ift.tt/2bkpylB
via IFTTT
Δεν υπάρχουν σχόλια:
Δημοσίευση σχολίου