2 Cholesterol crystal secretion of IL-1β from PBMCS is reduced with simvastatin treatment. (26th March 2018)
- Record Type:
- Journal Article
- Title:
- 2 Cholesterol crystal secretion of IL-1β from PBMCS is reduced with simvastatin treatment. (26th March 2018)
- Main Title:
- 2 Cholesterol crystal secretion of IL-1β from PBMCS is reduced with simvastatin treatment
- Authors:
- Gangadharan, N
Kavanagh, P
Wash, PT
Hemeryck, L
Kieran, J
Barry, M
Lucitt, M - Abstract:
- Abstract : Considerable evidence implicates a role for interleukin-1 beta (IL-1β) in the pathogenesis of atherosclerosis 1 revealing its potential as a novel therapeutic target. Statins are known to have anti-inflammatory effects, 2 however the specific mechanisms remain to be established. To test the anti-inflammatory effects of simvastatin, PBMCs were isolated from healthy donors and treated in vitro with simvastatin (100 µM) or from hyperlipidaemic patients at baseline and following 8 weeks simvastatin (10–20 mg) daily treatment. PBMCs were then stimulated with LPS (100 ng/ml) for 3 hour followed by cholesterol crystal (CC) (1 mg/ml) stimulation overnight to activate the NLRP3 inflammasome complex involved in processing IL-1β to its mature secreted form. IL-Iβ levels in the supernatants form PBMCs was measured by ELISA. All experiments carried out were approved by the Medical Research Ethics Committees at St James Hospital/AMNCH, Dublin 8, Ireland and comply fully with the Declaration of Helsinki. Patients (n=9) taking simvastatin (10–20 mg daily) over 8 weeks exhibited reduced LDL cholesterol, (4.87±0.76 mmol/L) pre vs (3.78±0.67 mmol/L) post statin treatment. Simvastatin treatment also reduced levels of IL-1β secretion by PBMCs, when stimulated with LPS and CC, (5.27±0.6 ng/ml) pre vs (4.27±0.5 ng/ml) post statin treatment. Similarly, in vitro treatment of PBMCs with simvastatin (100 µM) reduced IL-1β secretion upon activation with LPS and CC, (2.37±0.17 ng/ml) controlAbstract : Considerable evidence implicates a role for interleukin-1 beta (IL-1β) in the pathogenesis of atherosclerosis 1 revealing its potential as a novel therapeutic target. Statins are known to have anti-inflammatory effects, 2 however the specific mechanisms remain to be established. To test the anti-inflammatory effects of simvastatin, PBMCs were isolated from healthy donors and treated in vitro with simvastatin (100 µM) or from hyperlipidaemic patients at baseline and following 8 weeks simvastatin (10–20 mg) daily treatment. PBMCs were then stimulated with LPS (100 ng/ml) for 3 hour followed by cholesterol crystal (CC) (1 mg/ml) stimulation overnight to activate the NLRP3 inflammasome complex involved in processing IL-1β to its mature secreted form. IL-Iβ levels in the supernatants form PBMCs was measured by ELISA. All experiments carried out were approved by the Medical Research Ethics Committees at St James Hospital/AMNCH, Dublin 8, Ireland and comply fully with the Declaration of Helsinki. Patients (n=9) taking simvastatin (10–20 mg daily) over 8 weeks exhibited reduced LDL cholesterol, (4.87±0.76 mmol/L) pre vs (3.78±0.67 mmol/L) post statin treatment. Simvastatin treatment also reduced levels of IL-1β secretion by PBMCs, when stimulated with LPS and CC, (5.27±0.6 ng/ml) pre vs (4.27±0.5 ng/ml) post statin treatment. Similarly, in vitro treatment of PBMCs with simvastatin (100 µM) reduced IL-1β secretion upon activation with LPS and CC, (2.37±0.17 ng/ml) control vs (0.64±0.06 ng/ml) simvastatin treatment. Values presented are mean ±sem. We have demonstrated that CC induced IL-1β release by PBMCs from hyperlipidaemic patients, is reduced after treatment with simvastatin. These data identify a previously unappreciated beneficial role for statin therapy in atherosclerotic patients. References: . Duewell P, et al. Nature2010;464:1357–61. . Arslan F, et al. Circ Res2008;103:334–6. … (more)
- Is Part Of:
- Heart. Volume 104(2018)Supplement 4
- Journal:
- Heart
- Issue:
- Volume 104(2018)Supplement 4
- Issue Display:
- Volume 104, Issue 4 (2018)
- Year:
- 2018
- Volume:
- 104
- Issue:
- 4
- Issue Sort Value:
- 2018-0104-0004-0000
- Page Start:
- A5
- Page End:
- A5
- Publication Date:
- 2018-03-26
- Subjects:
- Heart -- Diseases -- Treatment -- Periodicals
Cardiology -- Periodicals
616.12 - Journal URLs:
- http://www.bmj.com/archive ↗
http://heart.bmj.com ↗
http://www.heartjnl.com ↗ - DOI:
- 10.1136/heartjnl-2018-SCF.12 ↗
- Languages:
- English
- ISSNs:
- 1355-6037
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 18521.xml