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dc.contributor.authorTitikorn Chunchaien_US
dc.contributor.authorNipon Chattipakornen_US
dc.contributor.authorSiriporn C. Chattipakornen_US
dc.date.accessioned2018-09-05T04:21:32Z-
dc.date.available2018-09-05T04:21:32Z-
dc.date.issued2018-06-01en_US
dc.identifier.issn15737365en_US
dc.identifier.issn08857490en_US
dc.identifier.other2-s2.0-85034651093en_US
dc.identifier.other10.1007/s11011-017-0151-9en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85034651093&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58241-
dc.description.abstract© 2017, Springer Science+Business Media, LLC, part of Springer Nature. Obesity has reached epidemic proportions in many countries around the world. Several studies have reported that obesity can lead to the development of cognitive decline. There is increasing evidence to demonstrate that microglia play a crucial role in cognitive decline in cases of obesity, Alzheimer’s disease and also in the aging process. Although there have been several studies into microglia over the past decades, the mechanistic link between microglia and cognitive decline in obese models is still not fully understood. In this review, the current available evidence from both in vitro and in vivo investigations regarding the association between the alteration in microglial activity in different obese models with respect to cognition are included. The metabolite profiles from obesity, adiposity, dietary and hormone affected microglial activation and its function in the brain are comprehensively summarized. In addition, the possible roles of microglial activation in relation to cognitive dysfunction are also presented and discussed. To ensure a balanced perspective controversial reports regarding these issues are included and discussed.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.subjectNeuroscienceen_US
dc.titleThe possible factors affecting microglial activation in cases of obesity with cognitive dysfunctionen_US
dc.typeJournalen_US
article.title.sourcetitleMetabolic Brain Diseaseen_US
article.volume33en_US
article.stream.affiliationsChiang Mai Universityen_US
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