Fenofibrate attenuates endothelial monocyte adhesion in chronic heart failure: an in vitro study
Background Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator‐activated receptor‐α (PPARα) activator fenofibrate on monocyte adhesion in CHF patients was investigated in vitro. Materials and methods Isolated peripher...
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Published in | European journal of clinical investigation Vol. 39; no. 9; pp. 775 - 783 |
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Blackwell Publishing Ltd
01.09.2009
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Abstract | Background Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator‐activated receptor‐α (PPARα) activator fenofibrate on monocyte adhesion in CHF patients was investigated in vitro.
Materials and methods Isolated peripheral blood mononuclear cells (PBMCs) were collected from 36 patients (aged 65 ± 8 years) with symptomatic CHF and from 12 healthy control subjects. The cultured human aortic endothelial cells (HAECs) were stimulated with or without 2 ng mL−1 tumour necrosis factor‐alpha (TNF‐α) and the inhibitory effects of fenofibrate at 25, 50, 100 and 200 μM on endothelial mononuclear cell adhesion were tested. Furthermore, the HAECs were stimulated with 70% sera obtained from CHF patients and control individuals, respectively, with or without pretreatments with fenofibrate. The endothelial expression of vascular cell adhesion molecule‐1 (VCAM‐1) and intercellular adhesion molecule‐1 (ICAM‐1) was then confirmed by mRNA expression and Western blot.
Results We found that the increased adhesion of PBMCs to TNF‐α‐stimulated HAECs in CHF patients was reduced when the HAECs were pretreated with fenofibrate (31% inhibition, P = 0·0121). However, pretreatment of the isolated PBMCs collected from CHF patients with fenofibrate failed to suppress their adherence to TNF‐α‐stimulated HAECs. Furthermore, stimulation of cultured HAECs with CHF patient sera significantly increased VCAM‐1 and ICAM‐1 expression, which could also be inhibited by fenofibrate.
Conclusions The fenofibrate directly inhibits monocyte binding by TNF‐α‐activated HAECs, probably through preventing up‐regulation of cell adhesion molecules by endothelial cells in response to inflammatory stimuli. This PPARα activator may have the potential to ameliorate vascular inflammation in patients with CHF. |
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AbstractList | AbstractBackground Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator-activated receptor-a (PPARa) activator fenofibrate on monocyte adhesion in CHF patients was investigated in vitro.Materials and methods Isolated peripheral blood mononuclear cells (PBMCs) were collected from 36 patients (aged 65 c 8 years) with symptomatic CHF and from 12 healthy control subjects. The cultured human aortic endothelial cells (HAECs) were stimulated with or without 2 ng mL-1 tumour necrosis factor-alpha (TNF-a) and the inhibitory effects of fenofibrate at 25, 50, 100 and 200 kM on endothelial mononuclear cell adhesion were tested. Furthermore, the HAECs were stimulated with 70% sera obtained from CHF patients and control individuals, respectively, with or without pretreatments with fenofibrate. The endothelial expression of vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) was then confirmed by mRNA expression and Western blot.Results We found that the increased adhesion of PBMCs to TNF-a-stimulated HAECs in CHF patients was reduced when the HAECs were pretreated with fenofibrate (31% inhibition, P =0.0121). However, pretreatment of the isolated PBMCs collected from CHF patients with fenofibrate failed to suppress their adherence to TNF-a-stimulated HAECs. Furthermore, stimulation of cultured HAECs with CHF patient sera significantly increased VCAM-1 and ICAM-1 expression, which could also be inhibited by fenofibrate.Conclusions The fenofibrate directly inhibits monocyte binding by TNF-a-activated HAECs, probably through preventing up-regulation of cell adhesion molecules by endothelial cells in response to inflammatory stimuli. This PPARa activator may have the potential to ameliorate vascular inflammation in patients with CHF.Eur J Clin Invest 2009; 39(9): 775-783 Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator-activated receptor-alpha (PPARalpha) activator fenofibrate on monocyte adhesion in CHF patients was investigated in vitro.BACKGROUNDInflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator-activated receptor-alpha (PPARalpha) activator fenofibrate on monocyte adhesion in CHF patients was investigated in vitro.Isolated peripheral blood mononuclear cells (PBMCs) were collected from 36 patients (aged 65 +/- 8 years) with symptomatic CHF and from 12 healthy control subjects. The cultured human aortic endothelial cells (HAECs) were stimulated with or without 2 ng mL(-1) tumour necrosis factor-alpha (TNF-alpha) and the inhibitory effects of fenofibrate at 25, 50, 100 and 200 microM on endothelial mononuclear cell adhesion were tested. Furthermore, the HAECs were stimulated with 70% sera obtained from CHF patients and control individuals, respectively, with or without pretreatments with fenofibrate. The endothelial expression of vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) was then confirmed by mRNA expression and Western blot.MATERIALS AND METHODSIsolated peripheral blood mononuclear cells (PBMCs) were collected from 36 patients (aged 65 +/- 8 years) with symptomatic CHF and from 12 healthy control subjects. The cultured human aortic endothelial cells (HAECs) were stimulated with or without 2 ng mL(-1) tumour necrosis factor-alpha (TNF-alpha) and the inhibitory effects of fenofibrate at 25, 50, 100 and 200 microM on endothelial mononuclear cell adhesion were tested. Furthermore, the HAECs were stimulated with 70% sera obtained from CHF patients and control individuals, respectively, with or without pretreatments with fenofibrate. The endothelial expression of vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) was then confirmed by mRNA expression and Western blot.We found that the increased adhesion of PBMCs to TNF-alpha-stimulated HAECs in CHF patients was reduced when the HAECs were pretreated with fenofibrate (31% inhibition, P = 0.0121). However, pretreatment of the isolated PBMCs collected from CHF patients with fenofibrate failed to suppress their adherence to TNF-alpha-stimulated HAECs. Furthermore, stimulation of cultured HAECs with CHF patient sera significantly increased VCAM-1 and ICAM-1 expression, which could also be inhibited by fenofibrate.RESULTSWe found that the increased adhesion of PBMCs to TNF-alpha-stimulated HAECs in CHF patients was reduced when the HAECs were pretreated with fenofibrate (31% inhibition, P = 0.0121). However, pretreatment of the isolated PBMCs collected from CHF patients with fenofibrate failed to suppress their adherence to TNF-alpha-stimulated HAECs. Furthermore, stimulation of cultured HAECs with CHF patient sera significantly increased VCAM-1 and ICAM-1 expression, which could also be inhibited by fenofibrate.The fenofibrate directly inhibits monocyte binding by TNF-alpha-activated HAECs, probably through preventing up-regulation of cell adhesion molecules by endothelial cells in response to inflammatory stimuli. This PPARalpha activator may have the potential to ameliorate vascular inflammation in patients with CHF.CONCLUSIONSThe fenofibrate directly inhibits monocyte binding by TNF-alpha-activated HAECs, probably through preventing up-regulation of cell adhesion molecules by endothelial cells in response to inflammatory stimuli. This PPARalpha activator may have the potential to ameliorate vascular inflammation in patients with CHF. Background Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator‐activated receptor‐α (PPARα) activator fenofibrate on monocyte adhesion in CHF patients was investigated in vitro . Materials and methods Isolated peripheral blood mononuclear cells (PBMCs) were collected from 36 patients (aged 65 ± 8 years) with symptomatic CHF and from 12 healthy control subjects. The cultured human aortic endothelial cells (HAECs) were stimulated with or without 2 ng mL −1 tumour necrosis factor‐alpha (TNF‐α) and the inhibitory effects of fenofibrate at 25, 50, 100 and 200 μM on endothelial mononuclear cell adhesion were tested. Furthermore, the HAECs were stimulated with 70% sera obtained from CHF patients and control individuals, respectively, with or without pretreatments with fenofibrate. The endothelial expression of vascular cell adhesion molecule‐1 (VCAM‐1) and intercellular adhesion molecule‐1 (ICAM‐1) was then confirmed by mRNA expression and Western blot. Results We found that the increased adhesion of PBMCs to TNF‐α‐stimulated HAECs in CHF patients was reduced when the HAECs were pretreated with fenofibrate (31% inhibition, P = 0·0121). However, pretreatment of the isolated PBMCs collected from CHF patients with fenofibrate failed to suppress their adherence to TNF‐α‐stimulated HAECs. Furthermore, stimulation of cultured HAECs with CHF patient sera significantly increased VCAM‐1 and ICAM‐1 expression, which could also be inhibited by fenofibrate. Conclusions The fenofibrate directly inhibits monocyte binding by TNF‐α‐activated HAECs, probably through preventing up‐regulation of cell adhesion molecules by endothelial cells in response to inflammatory stimuli. This PPARα activator may have the potential to ameliorate vascular inflammation in patients with CHF. Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator-activated receptor-alpha (PPARalpha) activator fenofibrate on monocyte adhesion in CHF patients was investigated in vitro. Isolated peripheral blood mononuclear cells (PBMCs) were collected from 36 patients (aged 65 +/- 8 years) with symptomatic CHF and from 12 healthy control subjects. The cultured human aortic endothelial cells (HAECs) were stimulated with or without 2 ng mL(-1) tumour necrosis factor-alpha (TNF-alpha) and the inhibitory effects of fenofibrate at 25, 50, 100 and 200 microM on endothelial mononuclear cell adhesion were tested. Furthermore, the HAECs were stimulated with 70% sera obtained from CHF patients and control individuals, respectively, with or without pretreatments with fenofibrate. The endothelial expression of vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) was then confirmed by mRNA expression and Western blot. We found that the increased adhesion of PBMCs to TNF-alpha-stimulated HAECs in CHF patients was reduced when the HAECs were pretreated with fenofibrate (31% inhibition, P = 0.0121). However, pretreatment of the isolated PBMCs collected from CHF patients with fenofibrate failed to suppress their adherence to TNF-alpha-stimulated HAECs. Furthermore, stimulation of cultured HAECs with CHF patient sera significantly increased VCAM-1 and ICAM-1 expression, which could also be inhibited by fenofibrate. The fenofibrate directly inhibits monocyte binding by TNF-alpha-activated HAECs, probably through preventing up-regulation of cell adhesion molecules by endothelial cells in response to inflammatory stimuli. This PPARalpha activator may have the potential to ameliorate vascular inflammation in patients with CHF. Background Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator‐activated receptor‐α (PPARα) activator fenofibrate on monocyte adhesion in CHF patients was investigated in vitro. Materials and methods Isolated peripheral blood mononuclear cells (PBMCs) were collected from 36 patients (aged 65 ± 8 years) with symptomatic CHF and from 12 healthy control subjects. The cultured human aortic endothelial cells (HAECs) were stimulated with or without 2 ng mL−1 tumour necrosis factor‐alpha (TNF‐α) and the inhibitory effects of fenofibrate at 25, 50, 100 and 200 μM on endothelial mononuclear cell adhesion were tested. Furthermore, the HAECs were stimulated with 70% sera obtained from CHF patients and control individuals, respectively, with or without pretreatments with fenofibrate. The endothelial expression of vascular cell adhesion molecule‐1 (VCAM‐1) and intercellular adhesion molecule‐1 (ICAM‐1) was then confirmed by mRNA expression and Western blot. Results We found that the increased adhesion of PBMCs to TNF‐α‐stimulated HAECs in CHF patients was reduced when the HAECs were pretreated with fenofibrate (31% inhibition, P = 0·0121). However, pretreatment of the isolated PBMCs collected from CHF patients with fenofibrate failed to suppress their adherence to TNF‐α‐stimulated HAECs. Furthermore, stimulation of cultured HAECs with CHF patient sera significantly increased VCAM‐1 and ICAM‐1 expression, which could also be inhibited by fenofibrate. Conclusions The fenofibrate directly inhibits monocyte binding by TNF‐α‐activated HAECs, probably through preventing up‐regulation of cell adhesion molecules by endothelial cells in response to inflammatory stimuli. This PPARα activator may have the potential to ameliorate vascular inflammation in patients with CHF. |
Author | Jen, H. L. Lin, S. J. Yin, W. H. Young, M. S. Huang, W. P. Chen, J. W. |
Author_xml | – sequence: 1 givenname: W. P. surname: Huang fullname: Huang, W. P. organization: Cheng-Hsin Rehabilitation Medical Centre – sequence: 2 givenname: W. H. surname: Yin fullname: Yin, W. H. organization: Cheng-Hsin Rehabilitation Medical Centre – sequence: 3 givenname: J. W. surname: Chen fullname: Chen, J. W. organization: Taipei-Veterans General Hospital – sequence: 4 givenname: H. L. surname: Jen fullname: Jen, H. L. organization: Cheng-Hsin Rehabilitation Medical Centre – sequence: 5 givenname: M. S. surname: Young fullname: Young, M. S. organization: Cheng-Hsin Rehabilitation Medical Centre – sequence: 6 givenname: S. J. surname: Lin fullname: Lin, S. J. organization: Taipei-Veterans General Hospital |
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Keywords | Heart failure Endothelial cell Monocyte Fibrate derivatives Cell adhesion molecule endothelial monocyte adhesion Cardiovascular disease Inflammation chronic heart failure Adhesion In vitro Endothelium Cell adhesion molecules Fenofibrate Medicine Chronic Heart disease peroxisome proliferator-activated receptor Peroxisome proliferator activated receptor Antilipemic agent |
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Snippet | Background Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator‐activated... Background Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator‐activated... Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome proliferator-activated receptor-alpha... AbstractBackground Inflammation is implicated in chronic heart failure (CHF). In this study, the potential inhibitory effect of peroxisome... |
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SubjectTerms | Aged Aorta Biological and medical sciences Blotting, Western Cardiology. Vascular system Cell Adhesion - drug effects Cell adhesion molecules Chronic Disease chronic heart failure Endothelial cells endothelial monocyte adhesion Female Fenofibrate Fenofibrate - pharmacology Gene expression General aspects Heart Heart diseases Heart Failure - pathology Heart failure, cardiogenic pulmonary edema, cardiac enlargement Humans Inflammation Inflammation - pathology intercellular adhesion molecule 1 Leukocytes (mononuclear) Male Medical sciences Middle Aged Monocytes Monocytes - physiology Peripheral blood mononuclear cells peroxisome proliferator-activated receptor Peroxisome proliferator-activated receptor-a Tumor necrosis factor-a vascular cell adhesion molecule 1 Vascular Cell Adhesion Molecule-1 - biosynthesis Vascular Cell Adhesion Molecule-1 - drug effects Vascular system |
Title | Fenofibrate attenuates endothelial monocyte adhesion in chronic heart failure: an in vitro study |
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