Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55238
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dc.contributor.authorHiranya Pintanaen_US
dc.contributor.authorWasana Pratchayasakulen_US
dc.contributor.authorPiangkwan Sa-Nguanmooen_US
dc.contributor.authorWanpitak Pongkanen_US
dc.contributor.authorRungroj Tawinvisanen_US
dc.contributor.authorNipon Chattipakornen_US
dc.contributor.authorSiriporn C. Chattipakornen_US
dc.date.accessioned2018-09-05T02:53:28Z-
dc.date.available2018-09-05T02:53:28Z-
dc.date.issued2016-02-01en_US
dc.identifier.issn15328600en_US
dc.identifier.issn00260495en_US
dc.identifier.other2-s2.0-84959522822en_US
dc.identifier.other10.1016/j.metabol.2015.10.015en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84959522822&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55238-
dc.description.abstract© 2015 Elsevier Inc. All rights reserved. Objective Previous studies demonstrated a correlation between cognitive decline and either testosterone deprivation or obesity. However, the effect of obesity combined with testosterone deprivation on cognitive function has not been investigated. This study investigated the effects of obesity on brain insulin sensitivity, brain mitochondrial function, hippocampal synaptic plasticity and cognitive function in testosterone-deprived male rats. Materials/Methods Male Wistar rats were divided into sham-operated (control) and bilateral orchiectomized (ORX) groups. Rats in each group were further divided into two subgroups to receive either a normal diet (ND) or a high fat diet (HFD) for 4, 8 or 12 weeks. Blood samples were collected to determine metabolic parameters. Cognitive function was tested using the Morris Water Maze Test. At the end of the study, brains were removed to investigate brain insulin sensitivity, brain mitochondrial function and hippocampal synaptic plasticity. Results Both control-obese and ORX-obese rats developed peripheral insulin resistance at week eight, and brain insulin resistance as well as brain mitochondrial dysfunction at week 12. However, the ORX-obese rats developed cognitive impairment and decreased hippocampal synaptic plasticity beginning at week eight, whereas the control-obese rats developed these impairments later at week 12. Although both peripheral and brain insulin resistance were not observed in both the control-lean and ORX-lean rats, impaired cognition and decreased hippocampal synaptic plasticity were found in the ORX-lean rats beginning at week eight. Conclusion These findings suggest that testosterone deprivation has neither additive nor synergistic effects over obesity in the development of cognitive dysfunction in orchiectomized-obese male rats.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleTestosterone deprivation has neither additive nor synergistic effects with obesity on the cognitive impairment in orchiectomized and/or obese male ratsen_US
dc.typeJournalen_US
article.title.sourcetitleMetabolism: Clinical and Experimentalen_US
article.volume65en_US
article.stream.affiliationsChiang Mai Universityen_US
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