The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model.

<h4>Introduction</h4>Management of phenylketonuria (PKU) is mainly achieved through dietary control with limited intake of phenylalanine (Phe) from food, supplemented with low protein (LP) food and a mixture of free synthetic (FS) amino acids (AA) (FSAA). Casein glycomacropeptide (CGMP)...

Full description

Bibliographic Details
Main Authors: Kirsten K Ahring, Frederik Dagnæs-Hansen, Annemarie Brüel, Mette Christensen, Erik Jensen, Thomas G Jensen, Mogens Johannsen, Karen S Johansen, Allan M Lund, Jesper G Madsen, Karen Brøndum-Nielsen, Michael Pedersen, Lambert K Sørensen, Mads Kjolby, Lisbeth B Møller
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0261150
_version_ 1818298871395123200
author Kirsten K Ahring
Frederik Dagnæs-Hansen
Annemarie Brüel
Mette Christensen
Erik Jensen
Thomas G Jensen
Mogens Johannsen
Karen S Johansen
Allan M Lund
Jesper G Madsen
Karen Brøndum-Nielsen
Michael Pedersen
Lambert K Sørensen
Mads Kjolby
Lisbeth B Møller
author_facet Kirsten K Ahring
Frederik Dagnæs-Hansen
Annemarie Brüel
Mette Christensen
Erik Jensen
Thomas G Jensen
Mogens Johannsen
Karen S Johansen
Allan M Lund
Jesper G Madsen
Karen Brøndum-Nielsen
Michael Pedersen
Lambert K Sørensen
Mads Kjolby
Lisbeth B Møller
author_sort Kirsten K Ahring
collection DOAJ
description <h4>Introduction</h4>Management of phenylketonuria (PKU) is mainly achieved through dietary control with limited intake of phenylalanine (Phe) from food, supplemented with low protein (LP) food and a mixture of free synthetic (FS) amino acids (AA) (FSAA). Casein glycomacropeptide (CGMP) is a natural peptide released in whey during cheese making by the action of the enzyme chymosin. Because CGMP in its pure form does not contain Phe, it is nutritionally suitable as a supplement in the diet for PKU when enriched with specific AAs. Lacprodan® CGMP-20 (= CGMP) used in this study contained only trace amounts of Phe due to minor presence of other proteins/peptides.<h4>Objective</h4>The aims were to address the following questions in a classical PKU mouse model: Study 1, off diet: Can pure CGMP or CGMP supplemented with Large Neutral Amino Acids (LNAA) as a supplement to normal diet significantly lower the content of Phe in the brain compared to a control group on normal diet, and does supplementation of selected LNAA results in significant lower brain Phe level?. Study 2, on diet: Does a combination of CGMP, essential (non-Phe) EAAs and LP diet, provide similar plasma and brain Phe levels, growth and behavioral skills as a formula which alone consist of FSAA, with a similar composition?.<h4>Material and methods</h4>45 female mice homozygous for the Pahenu2 mutation were treated for 12 weeks in five different groups; G1(N-CGMP), fed on Normal (N) casein diet (75%) in combination with CGMP (25%); G2 (N-CGMP-LNAA), fed on Normal (N) casein diet (75%) in combination with CGMP (19,7%) and selected LNAA (5,3% Leu, Tyr and Trp); G3 (N), fed on normal casein diet (100%); G4 (CGMP-EAA-LP), fed on CGMP (70,4%) in combination with essential AA (19,6%) and LP diet; G5 (FSAA-LP), fed on FSAA (100%) and LP diet. The following parameters were measured during the treatment period: Plasma AA profiles including Phe and Tyr, growth, food and water intake and number of teeth cut. At the end of the treatment period, a body scan (fat and lean body mass) and a behavioral test (Barnes Maze) were performed. Finally, the brains were examined for content of Phe, Tyr, Trp, dopamine (DA), 3,4-dihydroxyphenylacetic acid (DOPAC), serotonin (5-HT) and 5-hydroxyindole-acetic acid (5-HIAA), and the bone density and bone mineral content were determined by dual-energy x-ray absorptiometry.<h4>Results</h4>Study 1: Mice off diet supplemented with CGMP (G1 (N-CGMP)) or supplemented with CGMP in combination with LNAA (G2 (N-CGMP-LNAA)) had significantly lower Phe in plasma and in the brain compared to mice fed only casein (G3 (N)). Extra LNAA (Tyr, Trp and Leu) to CGMP did not have any significant impact on Phe levels in the plasma and brain, but an increase in serotonin was measured in the brain of G2 mice compared to G1. Study 2: PKU mice fed with mixture of CGMP and EAA as supplement to LP diet (G4 (CGMP-EAA-LP)) demonstrated lower plasma-Phe levels but similar brain- Phe levels and growth as mice fed on an almost identical combination of FSAA (G5 (FSAA-LP)).<h4>Conclusion</h4>CGMP can be a relevant supplement for the treatment of PKU.
first_indexed 2024-12-13T04:42:13Z
format Article
id doaj.art-cd95c51ea310445993f44c4034fd8132
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-13T04:42:13Z
publishDate 2022-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-cd95c51ea310445993f44c4034fd81322022-12-21T23:59:17ZengPublic Library of Science (PLoS)PLoS ONE1932-62032022-01-01171e026115010.1371/journal.pone.0261150The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model.Kirsten K AhringFrederik Dagnæs-HansenAnnemarie BrüelMette ChristensenErik JensenThomas G JensenMogens JohannsenKaren S JohansenAllan M LundJesper G MadsenKaren Brøndum-NielsenMichael PedersenLambert K SørensenMads KjolbyLisbeth B Møller<h4>Introduction</h4>Management of phenylketonuria (PKU) is mainly achieved through dietary control with limited intake of phenylalanine (Phe) from food, supplemented with low protein (LP) food and a mixture of free synthetic (FS) amino acids (AA) (FSAA). Casein glycomacropeptide (CGMP) is a natural peptide released in whey during cheese making by the action of the enzyme chymosin. Because CGMP in its pure form does not contain Phe, it is nutritionally suitable as a supplement in the diet for PKU when enriched with specific AAs. Lacprodan® CGMP-20 (= CGMP) used in this study contained only trace amounts of Phe due to minor presence of other proteins/peptides.<h4>Objective</h4>The aims were to address the following questions in a classical PKU mouse model: Study 1, off diet: Can pure CGMP or CGMP supplemented with Large Neutral Amino Acids (LNAA) as a supplement to normal diet significantly lower the content of Phe in the brain compared to a control group on normal diet, and does supplementation of selected LNAA results in significant lower brain Phe level?. Study 2, on diet: Does a combination of CGMP, essential (non-Phe) EAAs and LP diet, provide similar plasma and brain Phe levels, growth and behavioral skills as a formula which alone consist of FSAA, with a similar composition?.<h4>Material and methods</h4>45 female mice homozygous for the Pahenu2 mutation were treated for 12 weeks in five different groups; G1(N-CGMP), fed on Normal (N) casein diet (75%) in combination with CGMP (25%); G2 (N-CGMP-LNAA), fed on Normal (N) casein diet (75%) in combination with CGMP (19,7%) and selected LNAA (5,3% Leu, Tyr and Trp); G3 (N), fed on normal casein diet (100%); G4 (CGMP-EAA-LP), fed on CGMP (70,4%) in combination with essential AA (19,6%) and LP diet; G5 (FSAA-LP), fed on FSAA (100%) and LP diet. The following parameters were measured during the treatment period: Plasma AA profiles including Phe and Tyr, growth, food and water intake and number of teeth cut. At the end of the treatment period, a body scan (fat and lean body mass) and a behavioral test (Barnes Maze) were performed. Finally, the brains were examined for content of Phe, Tyr, Trp, dopamine (DA), 3,4-dihydroxyphenylacetic acid (DOPAC), serotonin (5-HT) and 5-hydroxyindole-acetic acid (5-HIAA), and the bone density and bone mineral content were determined by dual-energy x-ray absorptiometry.<h4>Results</h4>Study 1: Mice off diet supplemented with CGMP (G1 (N-CGMP)) or supplemented with CGMP in combination with LNAA (G2 (N-CGMP-LNAA)) had significantly lower Phe in plasma and in the brain compared to mice fed only casein (G3 (N)). Extra LNAA (Tyr, Trp and Leu) to CGMP did not have any significant impact on Phe levels in the plasma and brain, but an increase in serotonin was measured in the brain of G2 mice compared to G1. Study 2: PKU mice fed with mixture of CGMP and EAA as supplement to LP diet (G4 (CGMP-EAA-LP)) demonstrated lower plasma-Phe levels but similar brain- Phe levels and growth as mice fed on an almost identical combination of FSAA (G5 (FSAA-LP)).<h4>Conclusion</h4>CGMP can be a relevant supplement for the treatment of PKU.https://doi.org/10.1371/journal.pone.0261150
spellingShingle Kirsten K Ahring
Frederik Dagnæs-Hansen
Annemarie Brüel
Mette Christensen
Erik Jensen
Thomas G Jensen
Mogens Johannsen
Karen S Johansen
Allan M Lund
Jesper G Madsen
Karen Brøndum-Nielsen
Michael Pedersen
Lambert K Sørensen
Mads Kjolby
Lisbeth B Møller
The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model.
PLoS ONE
title The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model.
title_full The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model.
title_fullStr The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model.
title_full_unstemmed The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model.
title_short The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model.
title_sort effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model
url https://doi.org/10.1371/journal.pone.0261150
work_keys_str_mv AT kirstenkahring theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT frederikdagnæshansen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT annemariebruel theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT mettechristensen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT erikjensen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT thomasgjensen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT mogensjohannsen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT karensjohansen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT allanmlund theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT jespergmadsen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT karenbrøndumnielsen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT michaelpedersen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT lambertksørensen theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT madskjolby theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT lisbethbmøller theeffectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT kirstenkahring effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT frederikdagnæshansen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT annemariebruel effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT mettechristensen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT erikjensen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT thomasgjensen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT mogensjohannsen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT karensjohansen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT allanmlund effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT jespergmadsen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT karenbrøndumnielsen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT michaelpedersen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT lambertksørensen effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT madskjolby effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel
AT lisbethbmøller effectofcaseinglycomacropeptideversusfreesyntheticaminoacidsforearlytreatmentofphenylketonuriainamicemodel