Article Text
Abstract
Statins reduce cholesterol levels by inhibiting 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase and have an established role in the treatment of atherosclerotic disease. Recent research has identified anti-inflammatory properties of statins. Statins appear to reduce the stability of lipid raft formation with subsequent effects on immune activation and regulation, and also prevent the prenylation of signalling molecules with subsequent downregulation of gene expression. Both these effects result in reduced cytokine, chemokine, and adhesion molecule expression, with effects on cell apoptosis or proliferation. This review considers the evidence for the anti-inflammatory properties of statins in the lung, and how these effects are being applied to research into the role of statins as a novel treatment of respiratory diseases.
- CCL2, chemoattractant chemokine ligand 2
- COPD, chronic obstructive pulmonary disease
- CRP, C-reactive protein
- CTGF, connective tissue growth factor
- HMG-CoA, 3-hydroxy-3-methylglutaryl coenzyme A
- IFN-γ, interferon γ
- ICAM-1, intercellular adhesion molecule 1
- IL, interleukin
- IPF, idiopathic pulmonary fibrosis
- LFA-1, lymphocyte function associated antigen 1
- LPS, lipopolysaccharide
- MHC-II, major histocompatibility complex class II
- MMP, metalloprotease
- NF-κB, nuclear factor κB
- NK, natural killer
- TGF-β, transforming growth factor β
- TNF-α, tumour necrosis factor α
- asthma
- chronic obstructive pulmonary disease
- statins
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- CCL2, chemoattractant chemokine ligand 2
- COPD, chronic obstructive pulmonary disease
- CRP, C-reactive protein
- CTGF, connective tissue growth factor
- HMG-CoA, 3-hydroxy-3-methylglutaryl coenzyme A
- IFN-γ, interferon γ
- ICAM-1, intercellular adhesion molecule 1
- IL, interleukin
- IPF, idiopathic pulmonary fibrosis
- LFA-1, lymphocyte function associated antigen 1
- LPS, lipopolysaccharide
- MHC-II, major histocompatibility complex class II
- MMP, metalloprotease
- NF-κB, nuclear factor κB
- NK, natural killer
- TGF-β, transforming growth factor β
- TNF-α, tumour necrosis factor α