TY - JOUR
T1 - Estrogen Signaling in Alzheimer’s Disease
T2 - Molecular Insights and Therapeutic Targets for Alzheimer’s Dementia
AU - Uddin, Md Sahab
AU - Rahman, Md Motiar
AU - Jakaria, Md
AU - Rahman, Md Sohanur
AU - Hossain, Md Sarwar
AU - Islam, Ariful
AU - Ahmed, Muniruddin
AU - Mathew, Bijo
AU - Omar, Ulfat Mohammed
AU - Barreto, George E.
AU - Ashraf, Ghulam Md
N1 - Publisher Copyright:
© 2020, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - Estrogens play a crucial physiological function in the brain; however, debates exist concerning the role of estrogens in Alzheimer’s disease (AD). Women during pre-, peri-, or menopause periods are more susceptible for developing AD, suggesting the connection of sex factors and a decreased estrogen signaling in AD pathogenesis. Yet, the underlying mechanism of estrogen-mediated neuroprotection is unclarified and is complicated by the existence of estrogen-related factors. Consequently, a deeper analysis of estrogen receptor (ER) expression and estrogen-metabolizing enzymes could interpret the importance of estrogen in age-linked cognitive alterations. Previous studies propose that hormone replacement therapy may attenuate AD onset in postmenopausal women, demonstrating that estrogen signaling is important for the development and progression of AD. For example, ERα exerts neuroprotection against AD by maintaining intracellular signaling cascades and study reported reduced expression of ERα in hippocampal neurons of AD patients. Similarly, reduced expression of ERβ in female AD patients has been associated with abnormal function in mitochondria and improved markers of oxidative stress. In this review, we discuss the critical interaction between estrogen signaling and AD. Moreover, we highlight the potential of targeting estrogen-related signaling for therapeutic intervention in AD.
AB - Estrogens play a crucial physiological function in the brain; however, debates exist concerning the role of estrogens in Alzheimer’s disease (AD). Women during pre-, peri-, or menopause periods are more susceptible for developing AD, suggesting the connection of sex factors and a decreased estrogen signaling in AD pathogenesis. Yet, the underlying mechanism of estrogen-mediated neuroprotection is unclarified and is complicated by the existence of estrogen-related factors. Consequently, a deeper analysis of estrogen receptor (ER) expression and estrogen-metabolizing enzymes could interpret the importance of estrogen in age-linked cognitive alterations. Previous studies propose that hormone replacement therapy may attenuate AD onset in postmenopausal women, demonstrating that estrogen signaling is important for the development and progression of AD. For example, ERα exerts neuroprotection against AD by maintaining intracellular signaling cascades and study reported reduced expression of ERα in hippocampal neurons of AD patients. Similarly, reduced expression of ERβ in female AD patients has been associated with abnormal function in mitochondria and improved markers of oxidative stress. In this review, we discuss the critical interaction between estrogen signaling and AD. Moreover, we highlight the potential of targeting estrogen-related signaling for therapeutic intervention in AD.
KW - Alzheimer’s disease
KW - Estrogen
KW - Estrogen receptors
KW - Estrogen signaling
KW - Estrogen-metabolizing enzymes
KW - Estrogen-related factors
UR - http://www.scopus.com/inward/record.url?scp=85083568563&partnerID=8YFLogxK
U2 - 10.1007/s12035-020-01911-8
DO - 10.1007/s12035-020-01911-8
M3 - Review article
C2 - 32297302
AN - SCOPUS:85083568563
SN - 0893-7648
VL - 57
SP - 2654
EP - 2670
JO - Molecular Neurobiology
JF - Molecular Neurobiology
IS - 6
ER -