TY - JOUR
T1 - Anxiogenic effects of a Lactobacillus, inulin and the synbiotic on healthy juvenile rats
AU - Barrera-Bugueño, Camila
AU - Realini, Ornella
AU - Escobar-Luna, Jorge
AU - Sotomayor-Zárate, Ramón
AU - Gotteland, Martin
AU - Julio-Pieper, Marcela
AU - Bravo, Javier A.
N1 - Publisher Copyright:
© 2017 IBRO
PY - 2017/9/17
Y1 - 2017/9/17
N2 - Gut microbiota interventions, including probiotic and prebiotic use can alter behavior in adult animals and healthy volunteers. However, little is known about their effects in younger individuals. To investigate this, male Sprague–Dawley rats (post-natal day 21, PND21) received Lactobacillus casei 54-2-33 (104 cfu/ml), inulin as prebiotic (16 mg/ml), or both together (synbiotic) via drinking water for 14 days. Control rats received water alone. Open field (OF) and elevated plus maze (EPM) behaviors were evaluated at PND34 and 35, respectively. 30 min after EPM, brains and trunk blood were collected to evaluate hippocampal 5-HT1A (mRNA and protein) and plasma corticosterone (CORT). Lactobacillus, inulin and synbiotic-treated rats had fewer entries to the OF's center and spent more time in its periphery than controls. Synbiotic-fed rats explored the EPM's open arms longer than probiotic and inulin-fed rats. Synbiotic, but not Lactobacillus nor inulin-fed rats had lower levels of EPM-evoked CORT than controls. Basal CORT levels, evaluated in a naïve cohort, were higher in Lactobacillus- and inulin-fed rats than controls. In naïve synbiotic-fed rats, 5-HT1A mRNA levels were higher in dentate gyrus and cornus ammonis 1 layer (CA1), than in all other naïve groups, while hippocampal 5-HT1A protein levels were lower in bacteria-fed rats than controls. 5-HT1A mRNA changes suggest complex effects of gut microbes on hippocampal gene expression machinery, probably involving endogenous/exogenous bacteria and prebiotics interactions. Importantly, age might also influence their behavioral outcomes. Together, these data suggest that interventions in young rat microbiota evoke early behavioral changes upon stress, apparently in a hypothalamus–pituitary–adrenal axis independent fashion.
AB - Gut microbiota interventions, including probiotic and prebiotic use can alter behavior in adult animals and healthy volunteers. However, little is known about their effects in younger individuals. To investigate this, male Sprague–Dawley rats (post-natal day 21, PND21) received Lactobacillus casei 54-2-33 (104 cfu/ml), inulin as prebiotic (16 mg/ml), or both together (synbiotic) via drinking water for 14 days. Control rats received water alone. Open field (OF) and elevated plus maze (EPM) behaviors were evaluated at PND34 and 35, respectively. 30 min after EPM, brains and trunk blood were collected to evaluate hippocampal 5-HT1A (mRNA and protein) and plasma corticosterone (CORT). Lactobacillus, inulin and synbiotic-treated rats had fewer entries to the OF's center and spent more time in its periphery than controls. Synbiotic-fed rats explored the EPM's open arms longer than probiotic and inulin-fed rats. Synbiotic, but not Lactobacillus nor inulin-fed rats had lower levels of EPM-evoked CORT than controls. Basal CORT levels, evaluated in a naïve cohort, were higher in Lactobacillus- and inulin-fed rats than controls. In naïve synbiotic-fed rats, 5-HT1A mRNA levels were higher in dentate gyrus and cornus ammonis 1 layer (CA1), than in all other naïve groups, while hippocampal 5-HT1A protein levels were lower in bacteria-fed rats than controls. 5-HT1A mRNA changes suggest complex effects of gut microbes on hippocampal gene expression machinery, probably involving endogenous/exogenous bacteria and prebiotics interactions. Importantly, age might also influence their behavioral outcomes. Together, these data suggest that interventions in young rat microbiota evoke early behavioral changes upon stress, apparently in a hypothalamus–pituitary–adrenal axis independent fashion.
KW - 5-HT
KW - gut-brain axis
KW - hippocampus
KW - lactobacillus
KW - prebiotic
KW - synbiotic
UR - http://www.scopus.com/inward/record.url?scp=85025708177&partnerID=8YFLogxK
U2 - 10.1016/j.neuroscience.2017.06.064
DO - 10.1016/j.neuroscience.2017.06.064
M3 - Article
C2 - 28694176
AN - SCOPUS:85025708177
SN - 0306-4522
VL - 359
SP - 18
EP - 29
JO - Neuroscience
JF - Neuroscience
ER -