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Oxysterols: From physiological tuners to pharmacological opportunities

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 178, Issue 16, Pages 3089-3103

Publisher

WILEY
DOI: 10.1111/bph.15073

Keywords

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Funding

  1. National Health and Medical Research Council [APP1139644]
  2. NSW Health [H19/133660]
  3. UNSW Sydney
  4. Australian Research Council [DP170101178]

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Oxysterols are oxygenated forms of cholesterol generated via autooxidation by free radicals and enzymes, playing key roles in health and disease through binding to effector proteins and regulating transcriptional programmes affecting cell metabolism and function at low concentrations in vivo.
Oxysterols are oxygenated forms of cholesterol generated via autooxidation by free radicals and ROS, or formed enzymically by a variety of enzymes such as those involved in the synthesis of bile acids. Although found at very low concentrations in vivo, these metabolites play key roles in health and disease, particularly in development and regulating immune cell responses, by binding to effector proteins such as LXR alpha, ROR gamma and Insig and directly or indirectly regulating transcriptional programmes that affect cell metabolism and function. In this review, we summarise the routes by which oxysterols can be generated and subsequently modified to other oxysterol metabolites and highlight their diverse and profound biological functions and opportunities to alter their levels using pharmacological approaches.

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