Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/39790
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dc.contributor.authorEllery S.J.en
dc.contributor.authorDickinson H.en
dc.contributor.authorWalker D.W.en
dc.date.accessioned2021-05-14T13:35:57Zen
dc.date.available2021-05-14T13:35:57Zen
dc.date.copyright2016en
dc.date.created20160818en
dc.date.issued2016-08-18en
dc.identifier.citationAmino Acids. 48 (8) (pp 1807-1817), 2016. Date of Publication: 01 Aug 2016.en
dc.identifier.issn0939-4451en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/39790en
dc.description.abstractThe creatine/phosphocreatine/creatine kinase circuit is instrumental in regulating high-energy phosphate metabolism, and the maintenance of cellular energy turnover. The mechanisms by which creatine is able to buffer and regulate cellular energy balance, maintain acid-base balance, and reduce the effects of oxidative stress have led to a large number of studies into the use of creatine supplementation in exercise performance and to treat diseases associated with cellular energy depletion. Some of these studies have identified sex-specific responses to creatine supplementation, as such; there is the perception, that females might be less receptive to the benefits of creatine supplementation and therapy, compared to males. This review will describe the differences in male and female physique and physiology that may account for such differences, and discuss the apparent endocrine modulation of creatine metabolism in females. Hormone-driven changes to endogenous creatine synthesis, creatine transport and creatine kinase expression suggest that significant changes in this cellular energy circuit occur during specific stages of a female's reproductive life, including pregnancy and menopause. Recent studies suggest that creatine supplementation may be highly beneficial for women under certain conditions, such as depression. A greater understanding of these pathways, and the consequences of alterations to creatine bioavailability in females are needed to ensure that creatine is used to full advantage as a dietary supplement to optimize and enhance health outcomes for women.Copyright © 2016, Springer-Verlag Wien.en
dc.languageEnglishen
dc.languageenen
dc.publisherSpringer-Verlag Wien (E-mail: michaela.bolli@springer.at)en
dc.relation.ispartofAmino Acidsen
dc.titleCreatine for women: a review of the relationship between creatine and the reproductive cycle and female-specific benefits of creatine therapy.en
dc.typeReviewen
dc.type.studyortrialReview article (e.g. literature review, narrative review)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1007/s00726-016-2199-yen
dc.publisher.placeAustriaen
dc.identifier.pubmedid26898548 [http://www.ncbi.nlm.nih.gov/pubmed/?term=26898548]en
dc.identifier.source608643694en
dc.identifier.institution(Ellery, Walker, Dickinson) Hudson Institute of Medical Research and Department of Obstetrics and Gynaecology, The Ritchie Centre, Monash Medical Centre, Monash University, 27-31 Wright St., Clayton, Melbourne 3168, Australiaen
dc.description.addressH. Dickinson, Hudson Institute of Medical Research and Department of Obstetrics and Gynaecology, The Ritchie Centre, Monash Medical Centre, Monash University, 27-31 Wright St., Clayton, Melbourne 3168, Australia. E-mail: hayley.dickinson@hudson.org.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2017 Elsevier B.V., All rights reserved.en
dc.subect.keywordsNutrition Reproduction Women's healthen
dc.identifier.authoremailDickinson H.; hayley.dickinson@hudson.org.auen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeReview-
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