Probucol restores the defective leukocyte–endothelial interaction in experimental diabetes

Defective leukocyte–endothelial interactions have been observed in experimental type 1 diabetes. One of the mechanisms involved in the late complications of diabetes mellitus is the formation of free radicals species. Antioxidant treatment has been demonstrated to have beneficial effects on the comp...

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Veröffentlicht in:European journal of pharmacology 2003-10, Vol.478 (2), p.211-219
Hauptverfasser: Zanardo, Renata C.O, Cruz, José W.M.C, Martinez, Luis L, de Oliveira, Maria Ap, Fortes, Zuleica B
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Sprache:eng
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Zusammenfassung:Defective leukocyte–endothelial interactions have been observed in experimental type 1 diabetes. One of the mechanisms involved in the late complications of diabetes mellitus is the formation of free radicals species. Antioxidant treatment has been demonstrated to have beneficial effects on the complications observed in this pathology. Using intravital microscopy to visualize venules of the internal spermatic fascia, we demonstrated that the defective leukocyte–endothelial interactions in alloxan-induced diabetic rats could be corrected by probucol treatment. The defects were quantitated by the number of leukocytes rolling along the venular endothelium, sticking to the venular wall after topical application of zymosan-activated plasma (10%–0.1 ml) or leukotriene B 4 (1 μM/0.1 ml) and migrated after the application of a local irritant stimulus (carrageenan, 100 μg/0.1 ml). Leukocyte counts, erythrocyte velocity and venular shear rate, unaltered in diabetic rats, were not modified by this treatment. Reactive oxygen species formation by endothelial cells increased in diabetic preparations, and the reduced expression of adhesion molecules such as intercellular adhesion molecule-1 (ICAM-1) and P-selectin in cross-sections of the whole testis of the animals, were both restored by the antioxidant agent. Therefore, antioxidant treatment improves leukocyte–endothelial interaction in diabetic rats at least in part by restoring the expression of adhesion molecules in venules of diabetic rats.
ISSN:0014-2999
1879-0712
DOI:10.1016/j.ejphar.2003.08.043