Neuroglial Function and Hormonal Modulation in Neurodegenerative Diseases: The Influence of Sex Hormones

Astrocytes, microglia, and oligodendrocytes, key neuroglial cell types, are essential for central nervous system (CNS) homeostasis, immune regulation, and neuronal support. In neurodegenerative diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease (HD), and amyotrophic lateral sclerosis (ALS), glial dysfunction contributes to pathogenesis via chronic inflammation, synaptic disruption, oxidative stress, and impaired myelination. Growing evidence highlights the regulatory influence of sex hormones on glial function. These hormones modulate inflammatory tone, synaptic remodeling, and remyelination, potentially contributing to sex-based differences in disease incidence, progression, and treatment response. This review synthesizes current understanding of glial involvement in neurodegeneration and examines how gonadal hormones interact with astrocytes, microglia, and oligodendrocytes. By integrating glial biology with neuroendocrinology, we propose that hormone-glia interactions represent promising, personalized targets for sex-informed therapies in CNS disorders.

Authors

Institutions

Publication Details

Journal
Cellular and Molecular Neurobiology
Published
2026-02-05
DOI
https://doi.org/10.1007/s10571-026-01674-1
Citations
1
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
39.15
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Neuroglial Function and Hormonal Modulation in Neurodegenerative Diseases: The Influence of Sex Hormones

Wesam Bassiouni, Hamdan Hamdan, Maitha M. Alhajeri, Zakia Dimassi et al.
1 citations
Cellular and Molecular Neurobiology
Amyotrophic Lateral Sclerosis Research
39.15
article

Neuroglial Function and Hormonal Modulation in Neurodegenerative Diseases: The Influence of Sex Hormones

Wesam Bassiouni, Hamdan Hamdan, Maitha M. Alhajeri, Zakia Dimassi, Rayyah R. Alkhanjari, Amna Baig, Hana Al-Ali, Sara H. Sembaij, Fatima A. Al Muhairi, Khaled S. Abd-Elrahman, Yara Abukhaled
article en
1 citations

Abstract

Astrocytes, microglia, and oligodendrocytes, key neuroglial cell types, are essential for central nervous system (CNS) homeostasis, immune regulation, and neuronal support. In neurodegenerative diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease (HD), and amyotrophic lateral sclerosis (ALS), glial dysfunction contributes to pathogenesis via chronic inflammation, synaptic disruption, oxidative stress, and impaired myelination. Growing evidence highlights the regulatory influence of sex hormones on glial function. These hormones modulate inflammatory tone, synaptic remodeling, and remyelination, potentially contributing to sex-based differences in disease incidence, progression, and treatment response. This review synthesizes current understanding of glial involvement in neurodegeneration and examines how gonadal hormones interact with astrocytes, microglia, and oligodendrocytes. By integrating glial biology with neuroendocrinology, we propose that hormone-glia interactions represent promising, personalized targets for sex-informed therapies in CNS disorders.

Cellular and Molecular NeurobiologyVol. 46(1)
University of British Columbia (CA), University of Tennessee Health Science Center (US), Khalifa University of Science and Technology (AE), Shaikh Khalifa Medical City (AE), Alexandria University (EG)
Good health and well-being
Openalex Percentile: Top 1%
Amyotrophic Lateral Sclerosis Research
39.15
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.