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Pentoxifylline in vivo and in vitro down-regulates the expression of the intercellular adhesion molecule-1 in
P Neuner1, G Klosner, M Pourmojib
1Department of Dermatology, University of Vienna, Austria.
Abstract:
Since pentoxifylline (PTX) was recently recognized as a substance with antiinflammatory capacities, we studied the in vivo and in vitro effect of PTX on the expression of the intercellular adhesion molecule-1 (ICAM-1) on human monocytes. For this purpose four healthy volunteers were treated with PTX (5 x 400 mg/day) for 2 days. Monocytes were isolated before and after PTX treatment and ICAM-1 expression was investigated. As shown by fluorescence-activated cell sorter (FACS) analysis, cultured monocytes isolated after oral application of PTX expressed significantly decreased amounts of ICAM-1 when compared with monocytes collected prior to oral PTX application. Northern blot analysis revealed reduced amounts of ICAM-1 mRNA in monocytes derived from volunteers after oral PTX treatment in comparison with monocytes isolated before oral PTX administration. Similarly, in monocytes treated with PTX (200 micrograms/ml) in vitro ICAM-1 was found decreased both at the protein and mRNA level in comparison with untreated cells. The inhibitory effect of PTX on ICAM-1 expression in monocytes could be reversed by the addition of exogenous tumour necrosis factor-alpha (TNF-alpha; 200 U/ml) suggesting that ICAM-1 down-regulation is mediated secondary to TNF-alpha suppression by PTX. The specific role of TNF-alpha in mediating ICAM-1 expression in cultured monocytes could be confirmed by the finding that a neutralizing anti-TNF-alpha antibody partially down-regulated ICAM-1 expression. The observed suppressive in vivo and in vitro effects of PTX on ICAM-1 expression in monocytes may contribute to the recently described antiinflammatory effects of PTX, e.g. in sepsis or allergic contact dermatitis.
Insights
Pentoxifylline (PTX) reduces intercellular adhesion molecule-1 (ICAM-1) expression on human monocytes. This effect, observed both in vivo and in vitro, may explain PTX's anti-inflammatory properties.
Area of Science:
- Immunology
- Pharmacology
Background:
- Pentoxifylline (PTX) is recognized for its anti-inflammatory properties.
- Intercellular adhesion molecule-1 (ICAM-1) plays a role in inflammatory processes.
Purpose of the Study:
- To investigate the in vivo and in vitro effects of PTX on ICAM-1 expression in human monocytes.
- To explore the potential role of tumor necrosis factor-alpha (TNF-alpha) in mediating PTX's effect on ICAM-1.
Main Methods:
- Healthy volunteers received PTX orally; monocytes were isolated before and after treatment.
- Monocyte ICAM-1 expression was analyzed using fluorescence-activated cell sorter (FACS) and Northern blot.
- In vitro studies involved treating monocytes with PTX and measuring ICAM-1 at protein and mRNA levels.
Main Results:
- Oral PTX administration significantly decreased ICAM-1 expression and mRNA levels in monocytes.
- In vitro PTX treatment also reduced both ICAM-1 protein and mRNA in monocytes.
- The inhibitory effect of PTX was reversible by adding TNF-alpha, suggesting TNF-alpha suppression mediates the reduction.
Conclusions:
- PTX effectively down-regulates ICAM-1 expression in human monocytes.
- The anti-inflammatory effects of PTX may be linked to its suppression of TNF-alpha and subsequent reduction of ICAM-1.