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Study Design

Population
primary mouse stomach cells; rats
Methods
Treating cultured cells and experimental animals with heat-killed Lactobacillus brevis SBC8803 (hk-SBC8803) and assessing ghrelin secretion, expression of ghrelin-related genes, and food intake; oral administration of 500 mg/kg hk-SBC8803 to rats
  • Rigorous Journal
  • Animal Study
It is known that gastrointestinal microbiota, probiotics and heat-killed microbes can regulate intestinal immunity; however, their effect on the secretion of gastrointestinal hormones is unclear. The secretion of gastrointestinal hormones can be mediated by the elevation of intracellular Ca2+ concentration, suggesting that these hormones may act through common mechanisms. We have previously shown that heat-killed Lactobacillus brevis SBC8803 (hk-SBC8803) induced the secretion of serotonin and elevated intracellular Ca2+ concentration in serotonin-producing RIN-14B cells, suggesting that hk-SBC8803 could potentially cause the same effect on other gastrointestinal hormones, including hunger hormone ghrelin. Here, we tested this hypothesis by treating cultured cells and experimental animals with hk-SBC8803 and assessing ghrelin secretion, expression of ghrelin-related genes, and food intake. The results indicated that hk-SBC8803 treatment for 30 min significantly upregulated the secretion of acyl ghrelin (active form) (P=0.046) and mRNA expression of the Syt3 (synaptotagmin 3) gene related to ghrelin exocytosis (P<0.05) in primary mouse stomach cells. In addition, oral administration of 500 mg/kg hk-SBC8803 to rats tended to upregulate acyl ghrelin concentration (P=0.10) and significantly increased the ratio of acyl to des-acyl (inactive) ghrelin (P=0.027) in blood, which corresponded to a tendency of stimulating food intake (P=0.087) at 30 min post-treatment. However, when in order to minimise individual differences we normalised the data on food intake to those on one-day food intake prior to food deprivation, the resultant food intake ratio showed a significant increase (by 5% compared to control; P=0.032) at 30 min after hk-SBC8803 treatment, indicating that hk-SBC8803 administration stimulated rats to take more food during the first meal after fasting. These results suggest that hk-SBC8803 induces short-term ghrelin secretion and transiently increases appetite, which is an important effect for individuals with low energy intake.

Research Insights

SupplementDoseHealth OutcomeEffect TypeEffect SizeSource
Lactobacillus brevis SBC8803Increased Acyl Ghrelin SecretionBeneficial
Small
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hk-SBC8803 treatment for 30 min significantly upregulated the secretion of acyl ghrelin (active form) ... in primary mouse stomach cells

Lactobacillus brevis SBC8803Increased Acyl/Des-Acyl Ghrelin RatioBeneficial
Small
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significantly increased the ratio of acyl to des-acyl (inactive) ghrelin in blood

Lactobacillus brevis SBC8803Increased AppetiteBeneficial
Small
View source

oral administration of 500 mg/kg hk-SBC8803 to rats tended to upregulate acyl ghrelin concentration ... and significantly increased the ratio of acyl to des-acyl (inactive) ghrelin ... which corresponded to a tendency of stimulating food intake ... at 30 min post-treatment

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