HMO compositions and methods for reducing detrimental proteolytic metabolites
A method and a composition comprising human milk oligosaccharides for decreasing the production of detrimental proteolytic metabolites such as ammonia and branched chain fatty acids in the intestinal microbiota of humans, which is useful for the treatment of brain-gut disorders like autism, stress, anxiety, and depressive disorders, are disclosed. Methods of treatment of colon cancer and liver damage are also disclosed.
1. A method comprising:
selecting a non-infant human with elevated concentrations of detrimental proteolytic metabolites selected from ammonia, branched short chain fatty acids, and combinations thereof;
selecting an effective amount of a composition consisting essentially of one or more synthetic human milk oligosaccharides (HMOs) chosen from the group consisting of 2′-fucosyllactose (2′-FL), 3-fucosyllactose (3-FL), difucosyllactose (DFL), lacto-N-fucopentaose I (LNFP-I), lacto-N-tetraose (LNT), lacto-N-neotetraose (LNnT), and combinations thereof, the amount effective for increasing a relative abundance of Bifidobacterium adolescentis in the gastrointestinal microbiota of a non-infant human;
shifting the gastrointestinal microbiota of the non-infant human away from a proteolytic metabolism toward a saccharolytic metabolism by increasing the relative abundance of Bifidobacterium adolescentis and causing a delayed increase of butyrate in colon of the non-infant human by administering the effective amount of the chosen HMOs to the non-infant human, wherein during an initial treatment phase, the effective amount is a daily dosage for non-infants of from about 3 g to about 10 g per day; and
decreasing the elevated concentrations of the detrimental proteolytic metabolites in the gastrointestinal tract of the non-infant human.
2. The method of claim 1 , further comprising increasing the relative abundance of Bifidobacterium longum and/or Bifidobacterium bifidum concurrently with the delayed increase in colonic butyrate by administering the effective amount of the chosen HMOs to the non-infant human.
3. The method of claim 1 , wherein the condition associated with an elevated concentration of the detrimental proteolytic metabolites is a gut-brain disorder.
4. The method of claim 3 , wherein the gut-brain disorder is selected from stress, anxiety, and combinations thereof.
5. The method of claim 1 , wherein during a maintenance phase following the initial treatment phase, the daily dosage for non-infants is reduced from about 3 g to 10 g per day to about 1 g to 3 g per day.
6. The method of claim 1 , wherein the one or more synthetic HMOs consists essentially of a mixture of one or more neutral fucosylated HMOs selected from 2′-FL, 3-FL, DFL, and LNFP-I and one or more neutral non-fucosylated HMOs selected from LNT and LNnT.
7. The method of claim 1 , wherein composition consists essentially of a mixture of two or more HMOs selected from 2′-FL, DFL, 3-FL, LNT, LNnT.
8. The method of claim 7 , wherein the composition consists essentially of 2′-FL, LNnT, or the combination thereof.
9. A method comprising:
selecting a non-infant human with elevated concentrations of gut-derived ammonia associated with liver dysfunction;
selecting an effective amount of a composition consisting essentially of one or more synthetic human milk oligosaccharides (HMOs) chosen from the group consisting of 2′-fucosyllactose (2′-FL), 3-fucosyllactose (3-FL), difucosyllactose (DFL), lacto-N-fucopentaose I (LNFP-I), lacto-N-tetraose (LNT), lacto-N-neotetraose (LNnT), and combinations thereof, the amount effective for increasing a relative abundance of Bifidobacterium adolescentis in the gastrointestinal microbiota of a non-infant human; and
reducing the elevated concentrations of gut-derived ammonia by increasing the relative abundance of Bifidobacterium adolescentis and causing a delayed increase of butyrate in colon of the non-infant human by administering the effective amount of the chosen HMOs to the non-infant human, wherein during an initial treatment phase, the effective amount is a daily dosage for non-infants of from about 3 g to about 10 g per day.
10. The method of claim 9 , wherein the liver dysfunction is select from acute liver failure and chronic liver disease.
11. The method of claim 10 , wherein the concentration of ammonia or branched short chain fatty acids in the colon is decreased by at least 10% as compared to the concentration prior to the administration of the selected one or more HMOs.
12. The method of claim 10 , wherein the initial treatment phase is at least 14 days.
13. The method of claim 12 , further comprising increasing the relative abundance of Bifidobacterium longum and/or Bifidobacterium bifidum concurrently with the delayed increase in colonic butyrate by administering the effective amount of the chosen HMOs to the non-infant human.
14. The method of claim 13 , wherein the level of butyrate produced in the proximal colon is increased by at least 50% in response to the administration of the effective amount of the chosen one or more HMOs during the initial treatment phase.
15. A method comprising:
selecting a non-infant human with elevated concentrations of gut-derived ammonia associated with development of colon cancer;
selecting an effective amount of a composition consisting essentially of one or more synthetic human milk oligosaccharides (HMOs) chosen from the group consisting of 2′-fucosyllactose (2′-FL), 3-fucosyllactose (3-FL), difucosyllactose (DFL), lacto-N-fucopentaose I (LNFP-I), lacto-N-tetraose (LNT), lacto-N-neotetraose (LNnT), and combinations thereof, the amount effective for increasing a relative abundance of Bifidobacterium adolescentis in the gastrointestinal microbiota of a non-infant human; and
reducing the elevated concentrations of gut-derived ammonia by increasing the relative abundance of Bifidobacterium adolescentis and causing a delayed increase of butyrate in colon of the non-infant human by administering the effective amount of the chosen HMOs to the non-infant human, wherein during an initial treatment phase, the effective amount is a daily dosage for non-infants of from about 3 g to about 10 g per day.
16. The method of claim 15 , further comprising, causing a delayed increase inthe relative abundance of Bifidobacterium longum and/or Bifidobacterium bifidum by administering the effective amount of the chosen HMOs to the non-infant human.
17. The method of claim 15 , wherein during a maintenance phase following the initial treatment phase, the daily dosage for non-infants is reduced from about 3 g to 10 g per day to about 1 g to 3 g per day.
18. The method of claim 15 , wherein the composition consists essentially of neutral HMOs chosen from 2′-FL, DFL, LNnT, LNT, and combinations thereof.