TY - JOUR
T1 - Acute stress-induced alterations in short-chain fatty acids
T2 - Implications for the intestinal and blood brain barriers
AU - Rosell-Cardona, Cristina
AU - Leigh, Sarah Jane
AU - Knox, Emily
AU - Tirelli, Emanuela
AU - Lyte, Joshua M.
AU - Goodson, Michael S.
AU - Kelley-Loughnane, Nancy
AU - Aburto, Maria R.
AU - Cryan, John F.
AU - Clarke, Gerard
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/7
Y1 - 2025/7
N2 - Unravelling the features of the whole-body response to acute stress exposures is critical to understand this neglected building block of chronic stress. A single acute stress exposure rapidly modulates gut-brain axis signalling including intestinal permeability, but the mechanisms are unclear. Microbially-produced metabolites such as short-chain fatty acids (SCFA) are key effectors within the gut-brain axis which can affect gut and brain function. The aim of this work is to determine if acute stress regulates SCFA production in the gut and to understand the associated implications for gastrointestinal and brain barrier function. Stress reduced caecal SCFA concentrations, primarily butyrate and acetate. These SCFAs prevented LPS-induced disruption of gut and brain barrier function in a dose-dependent manner in in vitro models. This functional protection was associated with altered tight-junction abundance and morphology. These results provide a better understanding of the role SCFAs have on barriers following acute stress.
AB - Unravelling the features of the whole-body response to acute stress exposures is critical to understand this neglected building block of chronic stress. A single acute stress exposure rapidly modulates gut-brain axis signalling including intestinal permeability, but the mechanisms are unclear. Microbially-produced metabolites such as short-chain fatty acids (SCFA) are key effectors within the gut-brain axis which can affect gut and brain function. The aim of this work is to determine if acute stress regulates SCFA production in the gut and to understand the associated implications for gastrointestinal and brain barrier function. Stress reduced caecal SCFA concentrations, primarily butyrate and acetate. These SCFAs prevented LPS-induced disruption of gut and brain barrier function in a dose-dependent manner in in vitro models. This functional protection was associated with altered tight-junction abundance and morphology. These results provide a better understanding of the role SCFAs have on barriers following acute stress.
KW - Acute stress
KW - Barriers
KW - Microbial metabolites
KW - Microbiota-gut-brain axis
KW - Short-chain fatty acids
UR - https://www.scopus.com/pages/publications/105006659383
U2 - 10.1016/j.bbih.2025.100992
DO - 10.1016/j.bbih.2025.100992
M3 - Article
AN - SCOPUS:105006659383
SN - 2666-3546
VL - 46
JO - Brain, Behavior, and Immunity - Health
JF - Brain, Behavior, and Immunity - Health
M1 - 100992
ER -