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In Vivo Metabolic Responses to Different Formulations of Amino Acid Mixtures for the Treatment of Phenylketonuria (PKU)

dc.contributor.authorGiarratana, N
dc.contributor.authorGiardino, L
dc.contributor.authorBighinati, A
dc.contributor.authorReiner, G
dc.contributor.authorCésar Rocha, J
dc.date.accessioned2023-07-26T15:03:27Z
dc.date.available2023-07-26T15:03:27Z
dc.date.issued2022-02
dc.description.abstractPhenylketonuria (PKU) is a rare autosomal recessive inborn error of metabolism where the mainstay of treatment is a Phe restricted diet consisting of a combination of limited amounts of natural protein with supplementation of Phe-free or low-Phe protein substitutes and special low protein foods. Suboptimal outcomes may be related to the different absorption kinetics of free AAs, which have lower biological efficacy than natural proteins. Physiomimic TechnologyTM is a technology engineered to prolong AA (AA-PT) release allowing physiological absorption and masking the odor and taste of free AAs. The aim of these studies was to assess the impact of AA-PT formulation on selected functional and metabolic parameters both in acute and long-term experimental studies. Adult rats in fasting conditions were randomized in different groups and treated by oral gavage. Acute AA-PT administration resulted in significantly lower BUN at 90 min versus baseline. Both BUN and glycemia were modulated in the same direction as intact casein protein. Long-term treatment with AA-PT significantly reduces the protein expression of the muscle degradation marker Bnip3L (-46%) while significantly increasing the proliferation of market myostatin (+58%). Animals dosed for 15 days with AA-PT had significantly stronger grip strength (+30%) versus baseline. In conclusion, the results suggest that the AA-PT formulation may have beneficial effects on both AA oxidation and catabolism with a direct impact on muscle as well as on other metabolic pathways.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationInt J Mol Sci. 2022 Feb 17;23(4):2227.pt_PT
dc.identifier.doi10.3390/ijms23042227pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4619
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.subjectHCC ENDpt_PT
dc.subjectMalept_PT
dc.subjectAmino Acids / metabolism*pt_PT
dc.subjectAnimalspt_PT
dc.subjectAmino Acids / pharmacology*pt_PT
dc.subjectBiomarkers / metabolismpt_PT
dc.subjectCaseins / metabolismpt_PT
dc.subjectDiet, Protein-Restricted / methodspt_PT
dc.subjectMembrane Proteins / metabolismpt_PT
dc.subjectMyostatin / metabolismpt_PT
dc.subjectPhenylketonurias / drug therapy*pt_PT
dc.subjectPhenylketonurias / metabolism*pt_PT
dc.subjectRatspt_PT
dc.subjectRats, Wistarpt_PT
dc.titleIn Vivo Metabolic Responses to Different Formulations of Amino Acid Mixtures for the Treatment of Phenylketonuria (PKU)pt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue4pt_PT
oaire.citation.startPage2227pt_PT
oaire.citation.titleInternational Journal of Molecular Sciencespt_PT
oaire.citation.volume23pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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