Sodium butyrate (1.2 g/kg BW) in combination with fluoxetine (10 mg/kg BW) |
4 weeks |
C57BL/6J mice |
Histone hyperacetylation in the hippocampus and frontal cortex for short-term, thereby exerted anti-depressant like effects |
Schroeder et al. (2007)
|
Sodium butyrate (1.2 g/kg BW) |
4 weeks |
CK-p25 Tg mice |
Histone hyperacetylation improved learning and memory |
Fischer et al. (2007)
|
Propionic acid (500 mg/kg BW, twice a day) |
3 weeks |
Pregnant Long-Evans rats |
Enhancement in repetitive behavior associated with ASD |
Foley et al. (2014)
|
Sodium butyrate (1.2 g/kg BW) |
5 weeks |
Female ICR (CD1) mice |
Increased histone H4 acetylation in hippocampus facilitated amelioration of memory impairment |
Takuma et al. (2014)
|
GOS (4 g/kg BW) |
Postnatal days (3–21) |
Neonatal rats |
Alterations in BDNF levels, synaptic proteins (synaptophysin, MAP2, and GAP43), and NMDAR subunits (GluN1, GluN2A, GluN2B) |
Williams et al. (2016)
|
E. faecium (4 × 108 CFU) |
5 weeks |
Sprague-Dawley male rats |
Lower levels of pro-inflammatory cytokines and higher levels of BDNF in the hippocampus region of synbiotic and prebiotic treated animals Significant increase in butyrate concentration after synbiotic and prebiotic supplementation |
Araiza et al., 2018 |
Inulin (860 mg/kg BW) |
E. faecium + inulin (4 × 108 CFU + 860 mg/kg BW) |
GOS (15 g/L) |
3 weeks |
SPF Sprague-Dawley male adult rats |
Downregulated activation of microglial cells, thereby reducing surgery-induced cognitive impairments |
Yang et al. (2018)
|
Polydextrose-GOS (7 and 15 g/kg BW for mice and rats, respectively) |
Postnatal days (21–50) |
Weanling male C57BL/6J mice SD rats LE rats |
Improvement of memory and reducing anxiety-related behaviors in normally developing rodents |
Waworuntu et al. (2014)
|
Polydextrose-GOS (2 g/L each) |
Postnatal days (2–33) |
Translational piglet model |
Higher recognition memory |
Fleming et al. (2019)
|
FOS GOS FOS + GOS (0.3–0.4 g/mouse/day) |
10 weeks |
Male C57BL/6J mice |
Improvement in brain chemistry and social behavior related to anxiety and depression Enhanced levels of SCFA in the caecum reduction in stress-induced corticosterone levels in plasma Anti-anxiety levels in open field and elevated plus-maze |
Burokas et al. (2017)
|
XOS (10%) |
12 weeks |
Male Wister rats |
Enhancement in brain mitochondrial function and synaptic plasticity, thereby restoring cognitive function |
Chunchai et al. (2018)
|
L. paracasei HIIO1 (1 × 108 CFU) |
Synbiotics (XOS + L. paracasei HIIO1; 1:1 ratio) |
Lactoferrin (0.3 g/100 g milk powder) |
Postnatal days (2–31) |
Piglets |
Positively influenced brain development as evidenced with neuroimaging outcomes |
Mudd et al. (2016)
|
Milk fat globule membrane (0.25 g/100 g milk powder) |
Blend of polydextrose (1.3 g/100 g milk powder)/GOS (3.5 g/100 g milk powder) |
FOS + XOS (3 g/kg/day) |
Gestation days (0–19) |
Pregnant Wistar rats |
Enhanced exploratory behavior in the open field test Reduction in acrylamide-induced oxidative stress markers level |
Krishna et al. (2015)
|
Inulin (2 g/kg/day) |
Gestation days (0–19) |
Pregnant Wistar rats |
Reduction in acrylamide induced increase in oxidative markers in the fetal and the brain tissues |
Krishna and Muralidhara (2015)
|
Inulin (2 g/kg BW, twice a day) |
Gestation days (6–19) |
Pregnant Wistar rats |
Inulin supplementation diminished gestational rotenone induced increase in oxidative markers in the regions of the maternal brain and affected the whole fetal brain |
Krishna and Muralidhara (2018)
|
FOs (200 ul) |
4 weeks |
Young adult female C57/BL mice |
Ameliorated behavioral recovery following spinal cord injury via modulating the expression of inflammatory mediators |
Li et al. (2020)
|
COS (0.2 mM) |
1 day |
C. elegans
|
Enhancement in the antioxidant potential with an increase in dopamine levels, thereby attenuating monocrotophos induced oxidative stress |
Nidheesh et al. (2016)
|