Maprotiline inhibits LPS-induced expression of adhesion molecules (ICAM-1 and VCAM-1) in human endothelial cells

被引:0
|
作者
Rafiee, Laleh [1 ]
Hajhashemi, Valiollah [2 ]
Javanmard, Shaghayegh Haghjooy [3 ,4 ]
机构
[1] Isfahan Univ Med Sci, Appl Physiol Res Ctr, Esfahan, Iran
[2] Isfahan Univ Med Sci, Sch Pharm & Pharmaceut Sci, Dept Pharmacol & Toxicol, Isfahan Pharmaceut Sci Res Ctr, Esfahan, Iran
[3] Isfahan Univ Med Sci, Applied Physiol Res Ctr, Esfahan, Iran
[4] Isfahan Univ Med Sci, Dept Physiol, Esfahan, Iran
关键词
Maprotiline; ICAM-1; VCAM-1; Endothelial cells;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Regardless of the known anti-inflammatory potential of heterocyclic antidepressants, the mechanisms concerning their modulating effects are not completely known. In our earlier work, maprotiline, a heterocyclic antidepressants, considerably inhibited infiltration of polymorphonuclear cell leucocytes into the inflamed paw. To understand the mechanism involved, we evaluated the effect of vascular cell adhesion molecule (VCAM-1), intracellular adhesion molecule (ICAM-1) expression in stimulated endothelial cells. Endothelial cells were stimulated with lipopolysaccharide (LPS) in the presence and absence of maprotiline (10(-8) to 10(-6) M) and ICAM-1 and VCAM-1 expression were measured using real-time quantitative reverse transcription polymerase chain reaction. Maprotiline significantly decreased the LPS-induced expression of VCAM-1 at all applied concentrations. The expression of ICAM-1 decreased in the presence of maprotiline at 10(-6) M concentration (P < 0.05). Since maprotiline inhibits the expression of adhesion molecules, ICAM-1 and VCAM-1 in LPS-stimulated human endothelial cells, it can be a possible way through which maprotiline exerts its anti-inflammatory properties.
引用
收藏
页码:138 / 144
页数:7
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