Journal
GENES & DISEASES
Volume 9, Issue 5, Pages 1315-1331Publisher
ELSEVIER
DOI: 10.1016/j.gendis.2021.01.007
Keywords
Alzheimer?s disease; Estrogen deficiency; Glucose metabolism disorder; GSK-3b; IGF-1; Mitochondria
Funding
- National Natural Science Foundation of China [81671257, 81371221, 31600825]
- Innovation Research Group at Institutions of Higher Education in Chongqing [CXQTP19019019034]
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Alterations in glucose metabolism occur in the early stage of Alzheimer's disease, and estrogen deficiency exacerbates learning and memory deficits while impairing mitochondrial function in glucose metabolism.
Alterations in glucose metabolism occur in the brain in the early stage of Alzhei-mer's disease (AD), and menopausal women have more severe metabolic dysfunction and are more prone to dementia than men. Although estrogen deficiency-induced changes in glucose metabolism have been previously studied in animal models, their molecular mecha-nisms in AD remain elusive. To investigate this issue, double transgenic (APP/PS1) female mice were subjected to bilateral ovariectomy at 3 months of age and were sacrificed 1 week, 1 month and 3 months after surgery to simulate early, middle and late postmenopause, respec-tively. Our analysis demonstrated that estrogen deficiency exacerbates learning and memory deficits in this mouse model of postmenopause. Estrogen deficiency impairs the function of mitochondria in glucose metabolism. It is possible that the occurrence of AD is associated with the aberrant mitochondrial ERI3-mediated IGF-1/IGF-1R/GSK-3 I3 signaling pathway. In this study, we established a potential mechanism for the increased risk of AD in postmenopausal women and proposed a therapeutic target for AD due to postmenopause.Copyright 2022, Chongqing Medical University. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/ by-nc-nd/4.0/).
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