TY - JOUR
T1 - Brain-derived estrogen and neural function
AU - Brann, Darrell W.
AU - Lu, Yujiao
AU - Wang, Jing
AU - Zhang, Quanguang
AU - Thakkar, Roshni
AU - Sareddy, Gangadhara R.
AU - Pratap, Uday P.
AU - Tekmal, Rajeshwar R.
AU - Vadlamudi, Ratna K.
N1 - Funding Information:
The authors research described in this review research was supported by Research Grant NS088058 from the National Institutes of Neurological Disorders and Stroke , National Institutes of Health .
Publisher Copyright:
© 2021 The Author(s)
PY - 2022/1
Y1 - 2022/1
N2 - Although classically known as an endocrine signal produced by the ovary, 17β-estradiol (E2) is also a neurosteroid produced in neurons and astrocytes in the brain of many different species. In this review, we provide a comprehensive overview of the localization, regulation, sex differences, and physiological/pathological roles of brain-derived E2 (BDE2). Much of what we know regarding the functional roles of BDE2 has come from studies using specific inhibitors of the E2 synthesis enzyme, aromatase, as well as the recent development of conditional forebrain neuron-specific and astrocyte-specific aromatase knockout mouse models. The evidence from these studies support a critical role for neuron-derived E2 (NDE2) in the regulation of synaptic plasticity, memory, socio-sexual behavior, sexual differentiation, reproduction, injury-induced reactive gliosis, and neuroprotection. Furthermore, we review evidence that astrocyte-derived E2 (ADE2) is induced following brain injury/ischemia, and plays a key role in reactive gliosis, neuroprotection, and cognitive preservation. Finally, we conclude by discussing the key controversies and challenges in this area, as well as potential future directions for the field.
AB - Although classically known as an endocrine signal produced by the ovary, 17β-estradiol (E2) is also a neurosteroid produced in neurons and astrocytes in the brain of many different species. In this review, we provide a comprehensive overview of the localization, regulation, sex differences, and physiological/pathological roles of brain-derived E2 (BDE2). Much of what we know regarding the functional roles of BDE2 has come from studies using specific inhibitors of the E2 synthesis enzyme, aromatase, as well as the recent development of conditional forebrain neuron-specific and astrocyte-specific aromatase knockout mouse models. The evidence from these studies support a critical role for neuron-derived E2 (NDE2) in the regulation of synaptic plasticity, memory, socio-sexual behavior, sexual differentiation, reproduction, injury-induced reactive gliosis, and neuroprotection. Furthermore, we review evidence that astrocyte-derived E2 (ADE2) is induced following brain injury/ischemia, and plays a key role in reactive gliosis, neuroprotection, and cognitive preservation. Finally, we conclude by discussing the key controversies and challenges in this area, as well as potential future directions for the field.
KW - 17β-Estradiol
KW - Aromatase
KW - Gliosis
KW - Memory
KW - Neuroprotection
KW - Neurosteroid
KW - Sexual behavior
KW - Synaptic plasticity
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U2 - 10.1016/j.neubiorev.2021.11.014
DO - 10.1016/j.neubiorev.2021.11.014
M3 - Review article
C2 - 34823913
AN - SCOPUS:85119652046
SN - 0149-7634
VL - 132
SP - 793
EP - 817
JO - Neuroscience and Biobehavioral Reviews
JF - Neuroscience and Biobehavioral Reviews
ER -