Chemical Inhibition of Sterol Biosynthesis.


Journal

Biomolecules
ISSN: 2218-273X
Titre abrégé: Biomolecules
Pays: Switzerland
ID NLM: 101596414

Informations de publication

Date de publication:
28 Mar 2024
Historique:
received: 25 02 2024
revised: 22 03 2024
accepted: 26 03 2024
medline: 27 4 2024
pubmed: 27 4 2024
entrez: 27 4 2024
Statut: epublish

Résumé

Cholesterol is an essential molecule of life, and its synthesis can be inhibited by both genetic and nongenetic mechanisms. Hundreds of chemicals that we are exposed to in our daily lives can alter sterol biosynthesis. These also encompass various classes of FDA-approved medications, including (but not limited to) commonly used antipsychotic, antidepressant, antifungal, and cardiovascular medications. These medications can interfere with various enzymes of the post-lanosterol biosynthetic pathway, giving rise to complex biochemical changes throughout the body. The consequences of these short- and long-term homeostatic disruptions are mostly unknown. We performed a comprehensive review of the literature and built a catalogue of chemical agents capable of inhibiting post-lanosterol biosynthesis. This process identified significant gaps in existing knowledge, which fall into two main areas: mechanisms by which sterol biosynthesis is altered and consequences that arise from the inhibitions of the different steps in the sterol biosynthesis pathway. The outcome of our review also reinforced that sterol inhibition is an often-overlooked mechanism that can result in adverse consequences and that there is a need to develop new safety guidelines for the use of (novel and already approved) medications with sterol biosynthesis inhibiting side effects, especially during pregnancy.

Identifiants

pubmed: 38672427
pii: biom14040410
doi: 10.3390/biom14040410
pii:
doi:

Substances chimiques

Sterols 0
Cholesterol 97C5T2UQ7J
Lanosterol 1J05Z83K3M

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH110636
Pays : United States

Auteurs

Eric S Peeples (ES)

Department of Pediatrics, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Child Health Research Institute, Omaha, NE 68198, USA.
Division of Neonatology, Children's Nebraska, Omaha, NE 68114, USA.

Karoly Mirnics (K)

Child Health Research Institute, Omaha, NE 68198, USA.
Department of Biochemistry & Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Department of Pharmacology & Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Munroe-Meyer Institute, University of Nebraska Medical Center, Omaha, NE 68198, USA.

Zeljka Korade (Z)

Department of Pediatrics, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Child Health Research Institute, Omaha, NE 68198, USA.
Department of Biochemistry & Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198, USA.

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Classifications MeSH