Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Dec;42(8):e70025.
doi: 10.1002/cbf.70025.

A Recent Update on the Role of Estrogen and Progesterone in Alzheimer's Disease

Affiliations
Review

A Recent Update on the Role of Estrogen and Progesterone in Alzheimer's Disease

S Suganya et al. Cell Biochem Funct. 2024 Dec.

Abstract

Alzheimer's disease (AD), one of the most prevalent neurodegenerative disease responsible for 60%-80% dementia cases globally. The disease is more prevalent among elder females. Female reproductive hormones are found to be essential for cellular activities in brain. The physiological role of neurotrophins and sex hormones in hippocampal region during neurogenesis and neuron differentiation was studied as well. In addition to triggering cellular pathways, estrogen and progesterone carry out a number of biological processes that lead to neuroprotection. They might have an impact on learning and memory. One of estrogen's modest antioxidant properties is its direct scavenging of free radicals. The neurotrophic effect of estrogen and progesterone can be explained by their ability to rise the expression of the brain-derived neurotrophic factor (BDNF) mRNA. Additionally, they have the ability to degrade beta-amyloid and stop inflammation, apoptotic neuronal cell death, and tau protein phosphorylation. To enhance their neuroprotective action, various cross-talking pathways in cells that are mediated by estrogen, progesterone, and BDNF receptors. This include signaling by mitogen-activated protein kinase/extracellular regulated kinase, phosphatidylinositol 3-kinase/protein kinase B, and phospholipase/protein kinase C. Clinical research to establish the significance of these substances are fragmented, despite publications claiming a lower prevalence of AD when medication is started before menopause. This review article emphasizes an update on the role of estrogen, and progesterone in AD.

Keywords: Alzheimer's disease; brain‐derived neurotrophic factor; estrogen; neuropeptides; neurosteroids; progesterone; synaptic plasticity; tauopathies.

PubMed Disclaimer

References

    1. P. M. Maki, “Critical Window Hypothesis of Hormone Therapy and Cognition: A Scientific Update on Clinical Studies,” Menopause 20, no. 6 (2013): 695–709.
    1. N. G. Bazan, A. Halabi, M. Ertel, and N. A. Petasis, “Neuroinflammation,” in Basic Neurochemistry, eds. S. T. Brady, G. J. Siegel, R. W. Albers, and D. L. Price (Elsevier Inc, 2012), 8th ed., 610–620.
    1. D. G. Davis, F. A. Schmitt, D. R. Wekstein, and W. R. Markesbery, “Alzheimer Neuropathologic Alterations in Aged Cognitively Normal Subjects,” Journal of Neuropathology and Experimental Neurology 58, no. 4 (1999): 376–388.
    1. P. Giannakopoulos, P. R. Hof, A. S. Giannakopoulos, F. R. Herrmann, J. P. Michel, and C. Bouras, “Regional Distribution of Neurofibrillary Tangles and Senile Plaques in the Cerebral Cortex of Very Old Patients,” Archives of Neurology 52, no. 12 (1995): 1150–1159.
    1. J. L. Price, P. B. Davis, J. C. Morris, and D. L. White, “The Distribution of Tangles, Plaques and Related Immunohistochemical Markers in Healthy Aging and Alzheimer's Disease,” Neurobiology of Aging 12, no. 4 (1991): 295–312.

LinkOut - more resources