“…This type of research has shown a number of actions produced by BS: it was able to inhibit both vascular adhesion and intracellular adhesion molecule 1 expression in TNF-alpha-stimulated human aortic endothelial cells; in 2,4-dinitrofluorobenzene-induced mouse dermatitis, it was able to significantly reduce the clinical severity by inhibiting the infiltration of inflammatory cells, and the levels of IgE, interleukin-4, and histamine in the serum of treated mice; also, in the mouse carrageenan-induced inflammation air pouch model, it was determined that the chemical promoted a time-and dose-dependent increase of the calcium uptake in activated neutrophils, and inhibited myeloperoxidase, adenosine deaminase, interleukin-1 and the tumor necrosis factor. The mentioned effects, as well as the findings of the present report, support the suggested beneficial effects of BS for a number of diseases, which include benign prostatic hyperplasia, colon and breast cancer, atherosclerosis, and gastrointestinal ulceration (Wilt et al, 1999;Choudary and Trans, 2011;Hewing and Fisher, 2012;Tovey, 2015).…”