Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/65407
Title: Comparative effects of sex hormone deprivation on the brain of insulin-resistant rats
Authors: Jirapas Sripetchwandee
Hiranya Pintana
Piangkwan Sanguanmoo
Chiraphat Boonnag
Wasana Pratchayasakul
Nipon Chattipakorn
Siriporn C. Chattipakorn
Authors: Jirapas Sripetchwandee
Hiranya Pintana
Piangkwan Sanguanmoo
Chiraphat Boonnag
Wasana Pratchayasakul
Nipon Chattipakorn
Siriporn C. Chattipakorn
Keywords: Biochemistry, Genetics and Molecular Biology;Medicine
Issue Date: 1-Jan-2019
Abstract: © 2019 Society for Endocrinology Published by Bioscientifica Ltd. Obese-insulin resistance following chronic high-fat diet consumption led to cognitive decline through several mechanisms. Moreover, sex hormone deprivation, including estrogen and testosterone, could be a causative factor in inducing cognitive decline. However, comparative studies on the effects of hormone deprivation on the brain are still lacking. Adult Wistar rats from both genders were operated upon (sham operations or orchiectomies/ovariectomies) and given a normal diet or high-fat diet for 4, 8 and 12 weeks. Blood was collected to determine the metabolic parameters. At the end of the experiments, rats were decapitated and their brains were collected to determine brain mitochondrial function, brain oxidative stress, hippocampal plasticity, insulin-induced long-term depression, dendritic spine density and cognition. We found that male and female rats fed a high-fat diet developed obese-insulin resistance by week 8 and brain defects via elevated brain oxidative stress, brain mitochondrial dysfunction, impaired insulin-induced long-term depression, hippocampal dysplasticity, reduced dendritic spine density and cognitive decline by week 12. In normal diet-fed rats, estrogen deprivation, not testosterone deprivation, induced obese-insulin resistance, oxidative stress, brain mitochondrial dysfunction, impaired insulin-induced long-term depression, hippocampal dysplasticity and reduced dendritic spine density. In high-fat-diet-fed rats, estrogen deprivation, not testosterone deprivation, accelerated and aggravated obese-insulin resistance and brain defects at week 8. In conclusion, estrogen deprivation aggravates brain dysfunction more than testosterone deprivation through increased oxidative stress, brain mitochondrial dysfunction, impaired insulin-induced long-term depression and dendritic spine reduction. These findings may explain clinical reports which show more severe cognitive decline in aging females than males with obese-insulin resistance.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85063964195&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/65407
ISSN: 14796805
00220795
Appears in Collections:CMUL: Journal Articles

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