Screening and validation of probiotics to relieve cathartic colon based on enteric glial cells

  • ZHU Shengnan ,
  • XUE Yifan ,
  • HUANG Yin ,
  • LI Jiazhen ,
  • LIU Wenxu ,
  • WANG Linlin ,
  • CHEN Wei
Expand
  • (School of Food Science and Technology, Jiangnan University, Wuxi 214122, China)

Received date: 2024-01-22

  Revised date: 2025-03-18

  Online published: 2025-08-01

Abstract

Cathartic colon is primarily characterized by substantial damage to the enteric nervous system (ENS).Probiotics have demonstrated the ability to repair the ENS and enhance gut motility.However, existing probiotic screening methods predominantly rely on animal models or clinical trials, both of which are inefficient and costly.This study aimed to develop a rapid and efficient in vitro screening method to identify probiotics capable of alleviating the cathartic colon.Probiotic lysates, dead bacterial components, and fermentation supernatants were co-cultured with enteric glial cells (EGCs) in vitro, and the expression levels of neurotrophic factors Bdnf, Gdnf, and S100β were measured.Principal component analysis (PCA) was employed to identify three probiotic strains with high, medium, and low in vitro scores, which were subsequently validated in vivo.Results showed that the trends in the in vivo efficacy of the three strains were consistent with their in vitro scores.Notably, Bifidobacterium bifidum BB5 significantly upregulated the expression of neurotrophic factors in vitro, indicating its potential for modulating the ENS.In vivo, Bifidobacterium bifidum BB5 increased stool water content, enhanced fecal pellet count, and reduced intestinal transit time, thereby alleviating the cathartic colon.The in vitro screening method developed based on EGCs was efficient, cost-effective, and reliable.It provided a novel scientific approach for probiotic screening and functional evaluation, offering promising probiotic intervention strategies for the treatment of the cathartic colon.This method establishe an important theoretical foundation for the screening and clinical application of probiotics and holds considerable potential for broad application.

Cite this article

ZHU Shengnan , XUE Yifan , HUANG Yin , LI Jiazhen , LIU Wenxu , WANG Linlin , CHEN Wei . Screening and validation of probiotics to relieve cathartic colon based on enteric glial cells[J]. Food and Fermentation Industries, 2025 , 51(14) : 1 -8 . DOI: 10.13995/j.cnki.11-1802/ts.042193

References

[1] MENG Y Y, LI Q D, FENG Y, et al. Animal models of cathartic colon[J]. World Journal of Clinical Cases, 2021, 9(6):1251-1258.
[2] LI H Y, YAN X, XUE Q L, et al. Effects of nociceptin/orphanin FQ on rats with cathartic colon[J]. World Journal of Gastroenterology, 2007, 13(1):141-145.
[3] LIU B H, MO P, ZHANG S B. Effects of mu and kappa opioid receptor agonists and antagonists on contraction of isolated colon strips of rats with cathartic colon[J]. World Journal of Gastroenterology, 2004, 10(11):1672-1674.
[4] SEGUELLA L, GULBRANSEN B D. Enteric glial biology, intercellular signalling and roles in gastrointestinal disease[J]. Nature Reviews. Gastroenterology & Hepatology, 2021, 18(8):571-587.
[5] HANSEBOUT C R, SU C X, REDDY K, et al. Enteric glia mediate neuronal outgrowth through release of neurotrophic factors[J]. Neural Regeneration Research, 2012, 7(28):2165-2175.
[6] BOESMANS W, HAO M M, FUNG C, et al. Structurally defined signaling in neuro-glia units in the enteric nervous system[J]. Glia, 2019, 67(6):1167-1178.
[7] BOHÓRQUEZ D V, LIDDLE R A. The gut connectome: Making sense of what you eat[J]. The Journal of Clinical Investigation, 2015, 125(3):888-890.
[8] CHOW A K, GULBRANSEN B D. Potential roles of enteric glia in bridging neuroimmune communication in the gut[J]. American Journal of Physiology. Gastrointestinal and Liver Physiology, 2017, 312(2): G145-G152.
[9] NEUNLIST M, ROLLI-DERKINDEREN M, LATORRE R, et al. Enteric glial cells: Recent developments and future directions[J]. Gastroenterology, 2014, 147(6):1230-1237.
[10] SHARKEY K A. Emerging roles for enteric glia in gastrointestinal disorders[J]. The Journal of Clinical Investigation, 2015, 125(3):918-925.
[11] POPOVA N K, ILCHIBAEVA T V, NAUMENKO V S. Neurotrophic factors (BDNF and GDNF) and the serotonergic system of the brain[J]. Biochemistry. Biokhimiia, 2017, 82(3):308-317.
[12] OBATA Y, CASTAÑO Á, BOEING S, et al. Neuronal programming by microbiota regulates intestinal physiology[J]. Nature, 2020, 578(7794):284-289.
[13] VICENTINI F A, KEENAN C M, WALLACE L E, et al. Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia[J]. Microbiome, 2021, 9(1):210.
[14] WANG H Y, LEE I S, BRAUN C, et al. Effect of probiotics on central nervous system functions in animals and humans: A systematic review[J]. Journal of Neurogastroenterology and Motility, 2016, 22(4):589-605.
[15] FUYUKI A, HIGURASHI T, KESSOKU T, et al. Efficacy of Bifidobacterium bifidum G9-1 in improving quality of life in patients with chronic constipation: A prospective intervention study[J]. Bioscience of Microbiota, Food and Health, 2021, 40(2):105-114.
[16] TANG N, YU Q Q, MEI C X, et al. Bifidobacterium bifidum CCFM1163 alleviated cathartic colon by regulating the intestinal barrier and restoring enteric nerves[J]. Nutrients, 2023, 15(5):1146.
[17] GE X L, DING C, ZHAO W, et al. Antibiotics-induced depletion of mice microbiota induces changes in host serotonin biosynthesis and intestinal motility[J]. Journal of Translational Medicine, 2017, 15(1):13.
[18] STORR M A, BASHASHATI M, HIROTA C, et al. Differential effects of CB(1) neutral antagonists and inverse agonists on gastrointestinal motility in mice[J]. Neurogastroenterology and Motility, 2010, 22(7):787-796; e223.
[19] KOBAYASHI M, YAMAGUCHI T, ODAKA T, et al. Regionally differential effects of sennoside A on spontaneous contractions of colon in mice[J]. Basic & Clinical Pharmacology & Toxicology, 2007, 101(2):121-126.
[20] IZZY M, MALIECKAL A, LITTLE E, et al. Review of efficacy and safety of laxatives use in geriatrics[J]. World Journal of Gastrointestinal Pharmacology and Therapeutics, 2016, 7(2):334-342.
[21] SINGH A. Brain-derived neurotrophic factor-a key player in the gastrointestinal system[J]. Przeglad Gastroenterologiczny, 2023, 18(4):380-392.
[22] SUDA K, MATSUDA K. How microbes affect depression: Underlying mechanisms via the gut-brain axis and the modulating role of probiotics[J]. International Journal of Molecular Sciences, 2022, 23(3):1172.
[23] MOLSKA M, MRUCZYK K, CISEK-WOźNIAK A, et al. The influence of intestinal microbiota on BDNF levels[J]. Nutrients, 2024, 16(17):2891.
[24] LIU W, ZHOU T T, TIAN J Q, et al. Role of GDNF, GFRα1 and GFAP in a Bifidobacterium-intervention induced mouse model of intestinal neuronal dysplasia[J]. Frontiers in Pediatrics, 2022, 9:795678.
Outlines

/