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 inEuropean journal of clinical investigation Vol. 39; no. 9; pp. 775 - 783
Main Authors Huang, W. P., Yin, W. H., Chen, J. W., Jen, H. L., Young, M. S., Lin, S. J.
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Published Oxford, UK 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.
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.
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IsPeerReviewed true
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Issue 9
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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Yin WH, Jen HL, Chiang MC, Huang WP, Feng AN, Young MS. Circulating soluble tumor necrosis factor-α and cell adhesion molecules in patients with acute cardiogenic pulmonary edema. J Emerg Crit Care Med 2004;15:9-19.
Marx N, Sukhova GK, Collins T, Libby P, Plutzky J. PPARalpha activators inhibit cytokine-induced vascular cell adhesion molecule-1 expression in human endothelial cells. Circulation 1999;99:3125-31.
Anker SD, Von Haehling S. Inflammatory mediators in chronic heart failure: an overview. Heart 2004;90:464-70.
Tousoulis D, Homaei H, Ahmed N, Asimakopoulos G, Zouridakis E, Toutouzas P et al. Increased plasma adhesion molecule levels in patients with heart failure who have ischemic heart disease and dilated cardiomyopathy. Am Heart J 2001;141:277-80.
Ogata T, Miyauchi T, Sakai S, Irukayama-Tomobe Y, Goto K, Yamaguchi I. Stimulation of peroxisome-proliferator-activated receptor alpha (PPAR alpha) attenuates cardiac fibrosis and endothelin-1 production in pressure-overloaded rat hearts. Clin Sci (Lond) 2002;103(Suppl. 48):284S-8S.
Lebrasseur NK, Duhaney TA, De Silva DS, Cui L, Ip PC, Joseph L et al. Effects of fenofibrate on cardiac remodeling in aldosterone-induced hypertension. Hypertension 2007;50:489-96.
Ichihara S, Obata K, Yamada Y, Nagata K, Noda A, Ichihara G et al. Attenuation of cardiac dysfunction by a PPAR-alpha agonist is associated with down-regulation of redox-regulated transcription factors. J Mol Cell Cardiol 2006;41:318-29.
Ogata T, Miyauchi T, Sakai S, Takanachi M, Irukayama-Tomobe Y, Yamaguchi I. Myocardial fibrosis and diastolic dysfunction in deoxycorticosterone acetate-salt hypertensive rats is ameliorated by the peroxisome proliferator-activated receptor alpha activator fenofibrate, partly by suppressing inflammatory response associated with the nuclear factor-kappa B pathway. J Am Coll Cardiol 2004;43:1481-8.
Kronke G, Kadl A, Ikonomu E, Bluml S, Furnkranz A, Sarembock IJ et al. Expression of heme oxygenase-1 in human vascular cells is regulated by peroxisome proliferator-activated receptors. Arterioscler Thromb Vasc Biol 2007;27:1276-82.
Sweets PJ, Teunissen BE, Willemsen PH, Van Nieuwenhoven FA, Brouns AE, Janssen BJ et al. Cardiac hypertrophy is enhanced in PPAR alpha −/− mice in response to chronic pressure overload. Cardiovasc Res 2008;78:79-89.
Barger PM, Kelly DP. Fatty acid utilization in the hypertrophied and failing heart: molecular regulatory mechanisms. Am J Med Sci 1999;318:36-42.
Devaux B, Scholz D, Hirche A, Klovekorn WP, Schaper J. Upregulation of cell adhesion molecules and the presence of low grade inflammation in human chronic heart failure. Eur Heart J 1997;18:470-9.
Geppert A, Zorn G, Heinz G, Huber K, Siostrzonek P. Soluble selectins in the pulmonary and systemic circulation in acute cardiogenic and non-cardiogenic pulmonary failure. Intensive Care Med 2001;27:521-7.
Duhaney TA, Cui L, Rude MK, Lebrasseur NK, Ngoy S, De Silva DS et al. Peroxisome proliferator-activated receptor alpha-independent actions of fenofibrate exacerbates left ventricular dilation and fibrosis in chronic pressure overload. Hypertension 2007;49:1084-94.
Morgan EE, Rennison JH, Young ME, McElfresh TA, Kung TA, Tserng KY et al. Effects of chronic activation of peroxisome proliferator-activated receptor-alpha or high-fat feeding in a rat infarct model of heart failure. Am J Physiol Heart Circ Physiol 2006;290:H1899-904.
Maruyama S, Kato K, Kodama M, Hirono S, Fuse K, Nakagawa O et al. Fenofibrate, a peroxisome proliferator-activated receptor alpha activator, suppresses experimental autoimmune myocarditis by stimulating the interleukin-10 pathway in rats. J Atheroscler Thromb 2002;9:87-92.
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Sweets PJ, De Vogel-van den Bosch HM, Willensen PH, Stassen AP, Ayoubi T, Van Der Vusse GJ et al. Transcriptomic analysis of PPARalpha-dependent alterations during cardiac hypertrophy. Physiol Genomics 2008;36:15-23.
Diep QN, Benkirane K, Amiri F, Cohn JS, Endemann D, Schiffrin EL. PPAR alpha activator fenofibrate inhibits myocardial inflammation and fibrosis in angiotensin II-infused rats. J Mol Cell Cardiol 2004;36:295-304.
Wayman NS, Hattori Y, McDonald MC, Mota-Filipe H, Cuzzocrea S, Pisano B et al. Ligands of the peroxisome proliferator-activated receptors (PPAR-gamma and PPAR-alpha) reduce myocardial infarct size. FASEB J 2002;16:1027-40.
Campbell FM, Kozak R, Wagner A, Altarejos JY, Dyck JR, Belke DD et al. A role for peroxisome proliferator-activated receptor alpha (PPARalpha) in the control of cardiac malonyl-CoA levels: reduced fatty acid oxidation rates and increased glucose oxidation rates in the hearts of mice lacking PPARalpha are associated with higher concentrations of malonyl-CoA and reduced expression of malonyl-CoA decarboxylase. J Biol Chem 2002;277:4098-103.
Luptak I, Balschi JA, Xing Y, Leone TC, Kelly DP, Tian R. Decreased contractile and metabolic reserve in peroxisome proliferator-activated receptor-alpha-null hearts can be rescued by increasing glucose transport and utilization. Circulation 2005;112:2339-46.
Yin WH, Chen JW, Jen HL, Chiang MC, Huang WP, Feng AN et al. The prognostic value of circulating soluble cell adhesion molecules in patients with chronic congestive heart failure. Eur J Heart Fail 2003;5:507-16.
Schiffrin EL. Peroxisome proliferator-activated receptors and cardiovascular remodeling. Am J Physiol Heart Circ Physiol 2005;288:H1037-43.
2004; 43
2002; 16
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2005; 288
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2002; 103
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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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StartPage 775
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
URI https://api.istex.fr/ark:/67375/WNG-65VL6ZGX-S/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1365-2362.2009.02176.x
https://www.ncbi.nlm.nih.gov/pubmed/19531154
https://www.proquest.com/docview/20702202
https://www.proquest.com/docview/733965410
Volume 39
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