Cited by 113Alzheimer's disease research and treatmentsCholesterol and Lipid MetabolismCholinesterase and Neurodegenerative Diseases

ACAT1/SOAT1 as a Therapeutic Target for Alzheimer's Disease

Open access
Shibuya, Yohei, Chang, Catherine CY, Chang, Ta-Yuan·2015·Future Medicinal Chemistry

Abstract

Alzheimer's disease (AD) is the most common cause of dementia with no cure at present. Cholesterol metabolism is closely associated with AD at several stages. ACAT1 converts free cholesterol to cholesteryl esters, and plays important roles in cellular cholesterol homeostasis. Recent studies show that in a mouse model, blocking ACAT1 provides multiple beneficial effects on AD. Here we review the current evidence that implicates ACAT1 as a therapeutic target for AD. We also discuss the potential usage of various ACAT inhibitors currently available to treat AD.

Integrity signals

Registry

Crossref · 10.4155/fmc.15.161

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25 of 25 references verified0 citation errors · 0 not checkable

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Authors
Shibuya, Y., Chang, C. C., & Chang, T.-Y.
Affiliations
Dartmouth College (US)
Venue
Future Medicinal Chemistry
Published
2015-12
Volume
7
Issue
18
Pages
2451-2467
ISSN
  • 1756-8919 (ISSN-L)
  • 1756-8927
OpenAlex
W2260642650
Cited by
113
References
25
Citations by year
2026: 5 · 2025: 12 · 2024: 24 · 2023: 11 · 2022: 13 · 2021: 10 · 2020: 16 · 2019: 11 · 2018: 5 · 2017: 4 · 2016: 2
FWCI
0.45
Type
journal article
Language
en
Open access
Locations
  • Future Medicinal Chemistry (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institutes of Health (AG37609)
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
  • Health Sciences › Medicine › Pharmacology › Cholinesterase and Neurodegenerative Diseases
Keywords
ACAT1, SOAT1, Alzheimer's disease, cholesterol metabolism, cholesteryl ester synthesis, cholesterol homeostasis, ACAT inhibitors, therapeutic target, mouse model
MeSH terms
Acetyl-CoA C-Acetyltransferase, Alzheimer Disease, Animals, Sterol O-Acyltransferase, Enzyme Inhibitors, Humans, Mice

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