Cargando…
PSUN174 A Microbiome Targeted Nutraceutical that Induces Endogenous Glucoregulatory Peptide Hormones
Maintaining a narrow and healthy blood glucose range is essential for preventing the progression of microvascular and macrovascular complications associated with glucose dysregulation. It has now been established that secondary metabolites derived from colonic microbiota potentially serve as endogen...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624732/ http://dx.doi.org/10.1210/jendso/bvac150.772 |
_version_ | 1784822306541928448 |
---|---|
author | Palmissano, Salvator Ruan, Jingyi Saberi, Maziyar |
author_facet | Palmissano, Salvator Ruan, Jingyi Saberi, Maziyar |
author_sort | Palmissano, Salvator |
collection | PubMed |
description | Maintaining a narrow and healthy blood glucose range is essential for preventing the progression of microvascular and macrovascular complications associated with glucose dysregulation. It has now been established that secondary metabolites derived from colonic microbiota potentially serve as endogenous secretagogues for glucoregulatory hormone peptides. Specifically, metabolites such as short and medium-chain fatty acids and indole derivatives trigger the secretion of GLP-1 and PYY from the colonic L cells that improve gut motility, modulate insulin, and promote anorexigenic effects. However, secondary metabolites are significantly down-regulated in diets that lack complex carbohydrates and polyphenols, leading to hormonal dysbiosis. To address this need, we developed structural, chemical, and cell-based functional assays to screen a library of prebiotic fibers, polyphenols, and probiotics aimed at the induction of glucoregulatory peptides. Precisely, these ingredients were put through a series of microbiological fermentation assays to produce postbiotic secondary metabolites and subsequently tested as secretagogues on specialized human primary enteroendocrine cells. Prebiotics that significantly induced GLP-1 and PYY in these functional cells were formulated into a lead cocktail: JAN-1000. As a proof of concept, JAN-1000 was tested against an equal dose of single fibers to demonstrate superiority in secondary metabolite production and the induction of key metabolic peptides. JAN-1000 increased SCFAs by 7.9-fold (p<0.0001), indoles by 28.4% (p<0.0001), GLP-1 by 4.7-fold (p<0.0001), and PYY by 3.3-fold (p<0.0001). Furthermore, we initiated a pilot clinical study with healthy volunteers to demonstrate tolerability and efficacy on glucose and lipid homeostasis. A one-month supplementation of JAN-1000 lowered fasting glucose by 10% (p<0.001), lowered iAUC postprandial glucose by 42% (p=n.s.), reduced hypo and hyper-glycemic events, and improved HDL cholesterol by 5% (p<0.01). These results suggest that JAN-1000 is an effective and safe nutrition-based intervention that mediates communication between the gut microbiome with colonic cells and effectively improves hallmarks of diabetes complications and comorbidities. Studies are underway to confirm and expand on these results in people with type 2 diabetes and pre-diabetes. Presentation: Sunday, June 12, 2022 12:30 p.m. - 2:30 p.m. |
format | Online Article Text |
id | pubmed-9624732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96247322022-11-14 PSUN174 A Microbiome Targeted Nutraceutical that Induces Endogenous Glucoregulatory Peptide Hormones Palmissano, Salvator Ruan, Jingyi Saberi, Maziyar J Endocr Soc Diabetes & Glucose Metabolism Maintaining a narrow and healthy blood glucose range is essential for preventing the progression of microvascular and macrovascular complications associated with glucose dysregulation. It has now been established that secondary metabolites derived from colonic microbiota potentially serve as endogenous secretagogues for glucoregulatory hormone peptides. Specifically, metabolites such as short and medium-chain fatty acids and indole derivatives trigger the secretion of GLP-1 and PYY from the colonic L cells that improve gut motility, modulate insulin, and promote anorexigenic effects. However, secondary metabolites are significantly down-regulated in diets that lack complex carbohydrates and polyphenols, leading to hormonal dysbiosis. To address this need, we developed structural, chemical, and cell-based functional assays to screen a library of prebiotic fibers, polyphenols, and probiotics aimed at the induction of glucoregulatory peptides. Precisely, these ingredients were put through a series of microbiological fermentation assays to produce postbiotic secondary metabolites and subsequently tested as secretagogues on specialized human primary enteroendocrine cells. Prebiotics that significantly induced GLP-1 and PYY in these functional cells were formulated into a lead cocktail: JAN-1000. As a proof of concept, JAN-1000 was tested against an equal dose of single fibers to demonstrate superiority in secondary metabolite production and the induction of key metabolic peptides. JAN-1000 increased SCFAs by 7.9-fold (p<0.0001), indoles by 28.4% (p<0.0001), GLP-1 by 4.7-fold (p<0.0001), and PYY by 3.3-fold (p<0.0001). Furthermore, we initiated a pilot clinical study with healthy volunteers to demonstrate tolerability and efficacy on glucose and lipid homeostasis. A one-month supplementation of JAN-1000 lowered fasting glucose by 10% (p<0.001), lowered iAUC postprandial glucose by 42% (p=n.s.), reduced hypo and hyper-glycemic events, and improved HDL cholesterol by 5% (p<0.01). These results suggest that JAN-1000 is an effective and safe nutrition-based intervention that mediates communication between the gut microbiome with colonic cells and effectively improves hallmarks of diabetes complications and comorbidities. Studies are underway to confirm and expand on these results in people with type 2 diabetes and pre-diabetes. Presentation: Sunday, June 12, 2022 12:30 p.m. - 2:30 p.m. Oxford University Press 2022-11-01 /pmc/articles/PMC9624732/ http://dx.doi.org/10.1210/jendso/bvac150.772 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Diabetes & Glucose Metabolism Palmissano, Salvator Ruan, Jingyi Saberi, Maziyar PSUN174 A Microbiome Targeted Nutraceutical that Induces Endogenous Glucoregulatory Peptide Hormones |
title | PSUN174 A Microbiome Targeted Nutraceutical that Induces Endogenous Glucoregulatory Peptide Hormones |
title_full | PSUN174 A Microbiome Targeted Nutraceutical that Induces Endogenous Glucoregulatory Peptide Hormones |
title_fullStr | PSUN174 A Microbiome Targeted Nutraceutical that Induces Endogenous Glucoregulatory Peptide Hormones |
title_full_unstemmed | PSUN174 A Microbiome Targeted Nutraceutical that Induces Endogenous Glucoregulatory Peptide Hormones |
title_short | PSUN174 A Microbiome Targeted Nutraceutical that Induces Endogenous Glucoregulatory Peptide Hormones |
title_sort | psun174 a microbiome targeted nutraceutical that induces endogenous glucoregulatory peptide hormones |
topic | Diabetes & Glucose Metabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624732/ http://dx.doi.org/10.1210/jendso/bvac150.772 |
work_keys_str_mv | AT palmissanosalvator psun174amicrobiometargetednutraceuticalthatinducesendogenousglucoregulatorypeptidehormones AT ruanjingyi psun174amicrobiometargetednutraceuticalthatinducesendogenousglucoregulatorypeptidehormones AT saberimaziyar psun174amicrobiometargetednutraceuticalthatinducesendogenousglucoregulatorypeptidehormones |