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Milk peptides and immune response in the neonate

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dc.contributor.author Politis, I en
dc.contributor.author Chronopoulou, R en
dc.date.accessioned 2014-06-06T06:48:35Z
dc.date.available 2014-06-06T06:48:35Z
dc.date.issued 2008 en
dc.identifier.issn 00652598 en
dc.identifier.uri http://dx.doi.org/10.1007/978-0-387-74087-4-10 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/4200
dc.subject.other alpha lactalbumin en
dc.subject.other beta casein en
dc.subject.other beta lactoglobulin en
dc.subject.other casein en
dc.subject.other cyclic AMP en
dc.subject.other immunoglobulin en
dc.subject.other lactoferrin en
dc.subject.other milk protein en
dc.subject.other serum albumin en
dc.subject.other transferrin en
dc.subject.other peptide fragment en
dc.subject.other breast milk en
dc.subject.other cow en
dc.subject.other food composition en
dc.subject.other immune response en
dc.subject.other immunocompetence en
dc.subject.other immunomodulation en
dc.subject.other intestine flora en
dc.subject.other intestine function en
dc.subject.other nonhuman en
dc.subject.other piglet en
dc.subject.other priority journal en
dc.subject.other protein analysis en
dc.subject.other protein degradation en
dc.subject.other review en
dc.subject.other animal en
dc.subject.other chemistry en
dc.subject.other drug effect en
dc.subject.other human en
dc.subject.other immune system en
dc.subject.other immunology en
dc.subject.other weaning en
dc.subject.other Animals en
dc.subject.other Caseins en
dc.subject.other Humans en
dc.subject.other Immune System en
dc.subject.other Milk Proteins en
dc.subject.other Peptide Fragments en
dc.subject.other Weaning en
dc.title Milk peptides and immune response in the neonate en
heal.type other en
heal.identifier.primary 10.1007/978-0-387-74087-4-10 en
heal.publicationDate 2008 en
heal.abstract Bioactive peptides encrypted within the native milk proteins can be released by enzymatic proteolysis, food processing, or gastrointestinal digestion. These peptides possess a wide range of properties, including immunomodulatory properties. The first months of life represent a critical period for the maturation of the immune system because a tolerance for nutrient molecules should be developed while that for pathogen-derived antigens is avoided. Evidence has accumulated to suggest that milk peptides may regulate gastrointestinal immunity, guiding the local immune system until it develops its full functionality. Our data using the weaning piglet as the model suggest that several milk peptides can downregulate various immune properties at a time (one to two weeks after weaning) that coincides with immaturity of the immune system. The protein kinase A system and/or the exchange protein directly activated by cyclic AMP (Epac-1) are implicated in the mechanism through which milk peptides can affect immune function in the early postweaning period. Despite the fact that the research in this field is in its infancy, the evidence available suggests that milk protein peptides may promote development of neonatal immune competence. Milk contains a variety of components that provide immunological protection and facilitate the development of neonatal immune competence. Two main categories of milk compounds are thought to be associated with immunological activity. The first category includes cytokines, which neonates do not produce efficiently. Cytokines present in milk are thought to be protected against intestinal proteolysis and could alleviate immunological deficits, aiding immune system maturation (Kelleher&Lonnerdal, 2001; Bryan et al., 2006). The second category of milk compounds includes milk protein peptides. Milk peptides may affect mucosal immunity possibly by guiding local immunity until it develops its full functionality (Baldi et al., 2005). This chapter focuses on the effects of milk peptides on immune function and attempts to provide an overview of the knowledge available in this field. © 2008 Springer Science+Business Media, LLC. en
heal.journalName Advances in Experimental Medicine and Biology en
dc.identifier.volume 606 en
dc.identifier.doi 10.1007/978-0-387-74087-4-10 en
dc.identifier.spage 253 en
dc.identifier.epage 269 en


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