TABLE 1.
Host | SCFAs | Administered via | Dose | Duration | Main results | References |
Mice mesenteric adipocytes | Acetate; butyrate | Incubation | Acetate (0.1 and 0.2 mM); Butyrate (0.2 mM) | – | • Acetate but not butyrate stimulated leptin secretion in wild-type mesenteric adipocytes | Zaibi et al., 2010 |
Human white adipocytes | Acetate; propionate; butyrate | Incubation | Ranging between 1 μmol/L and 1 mmol/L | – | • Acetate suppressed while butyrate increased basal and the β-adrenergic receptor-mediated glycerol release and propionate did not affect their release | Jocken et al., 2018 |
Mice | Acetate | Oral | 0, 0.3, or 1.5% acetic acid at 10 mL/kg BW | 6 weeks | • Acetate increased the expressions of genes for fatty-acid-oxidation- and thermogenesis-related proteins in the liver • No effect on FI | Kondo et al., 2009 |
Mice | Acetate; propionate; butyrate | Oral | Butyrate (5% w/w); propionate (4.3%); acetate (3.7%) | 9 days | • Butyrate and propionate supplementation reduced FI • Acetate increased FI | Lin et al., 2012 |
Mice | Butyrate | Oral or IV injection | 6 M, 0.15 mL for oral 15 mM or 150 mM, 0.1 mL for IV | 9 weeks | • Oral rather than intravenous butyrate decreased FI and inhibited orexigenic neuron activity | Li et al., 2018 |
Mice or rats | Acetate | IP or ICV | IP: 500 mg/kg BW; ICV: 2.5 μmol | Acute | • Significant reduction in acute FI • Acetate may modulate FI through direct impact on the CNS | Frost et al., 2014 |
Rats | Propionate; butyrate | Oral | 5% w/w | 10–14 days | • Butyrate and propionate induced IGN via different mechanisms | De Vadder et al., 2014 |
Rats | Acetate | AT or ICV infusion | AT: 20 μmol kg–1min–1; ICV: 200 μM; | 3 days or 4 weeks | • High fat diet induced acetate production • Increased acetate concentrations have been associated with obesity, insulin resistance | Perry et al., 2016b |
Pigs | Acetate; propionate; butyrate | Dietary supplementation | 0.1% in the diet | 28 days | • Acetate reduced FI and body weight gain • SCFAs reduced lipogenesis, enhanced lipolysis via regulating related hormones and genes | Jiao et al., 2020 |
Humans | IPE | Dietary supplementation | 10 g/day | Acute or 24 weeks | • Acute ingestion significantly reduced FI • 24 weeks supplementation reduced weight gain, intrahepatocellular lipid content | Chambers et al., 2015 |
Humans | Acetate | Distal or proximal colonic supplementation | 100 or 180 mmol/l dissolved in 120 ml 0.9% NaCl | 3 days | • Distal, but not proximal colonic acetate administration increased fat oxidation and fasting plasma PYY | van der Beek et al., 2016 |
Humans | IPE | Dietary supplementation | 20 g/day | 42 days | • IPE supplementation decreased proinflammatory interleukin-8 levels | Chambers et al., 2019 |
AT, arterial; CNS, central nervous system; FI, food intake; ICV, intracerebroventricular; IGN, intestinal gluconeogenesis; IP, intraperitoneal; IPE, inulin-propionate ester; IV, intravenous; PYY, gut hormones peptide YY.