Food safety assessment and 28-day toxicity study of the synbiotic medical food consortium SBD121

Food Chem Toxicol. 2024 Sep:191:114839. doi: 10.1016/j.fct.2024.114839. Epub 2024 Jun 26.

Abstract

The human gut microbiome plays a crucial role in immune function. The synbiotic consortium or Defined Microbial Assemblage™ (DMA™) Medical Food product, SBD121, consisting of probiotic microbes and prebiotic fibers was designed for the clinical dietary management of rheumatoid arthritis. A 28-day repeated administration study was performed to evaluate the oral toxicity of SBD121 in male and female rats (age/weight at study start: 60 days/156-264 g) administered levels of 0, 4.96 x 1010, 2.48 x 1011, or 4.96 x 1011 colony forming units (CFU)/kg-bw. No treatment related changes were observed in ophthalmological effects, mortality, morbidity, general health and clinical observations, urinalysis, hematology, serum chemistry, absolute or relative organ weights, gross necropsy, or histopathology. A significant decrease in body weight was reported in females in the low and high-concentration groups, which corresponded in part with a significant decrease in food consumption. Results of the functional observation battery indicated front grip strength was significantly greater in the high-concentration males compared to the controls; however, this effect was not considered adverse. Based on these findings, the administration of the Medical Food SBD121 to male and female rats has a no-observable adverse effect level (NOAEL) at the highest level tested of 4.96 x 1011 CFU/kg-bw.

Keywords: Bacillus; Gut; Inflammation; Lactobacillus; Lactococcus; Microbiome; Rheumatoid arthritis; Safety.

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Female
  • Food Safety*
  • Male
  • No-Observed-Adverse-Effect Level
  • Organ Size / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Synbiotics* / administration & dosage