Kitchen E A, Dawson W
J Pharm Pharmacol. 1984 May;36(5):300-4. doi: 10.1111/j.2042-7158.1984.tb04378.x.
The chemotactic response, towards zymosan activated serum (ZAS), of elicited peritoneal exudate leucocytes was assessed in-vitro after treatment with inhibitors of the lipoxygenase enzyme pathway. Leucocytes from both rat and guinea-pig were used. BW755C and benoxaprofen reduced the chemotaxis of mononuclear cells from both species at 10(-4) M. Nordihydroguaiaretic acid (NDGA) at 7.5 X 10(-6) M depressed the chemotaxis of rat mononuclear cells but failed to modify the response of guinea-pig mononuclear cells. NDGA, BW755C and benoxaprofen, at concentrations that inhibit the lipoxygenase enzyme pathway in-vitro, were ineffective in reducing the chemotactic response of rat PMN. All three agents potentiated guinea-pig PMN chemotaxis, to a greater or lesser extent, the most pronounced effect being with NDGA when increased PMN migration was accompanied by an increased detachment of cells from the lower surface of the filters. The effects of these agents on both cellular chemotaxis and adherence are not necessarily related to their inhibitory effects on the lipoxygenase enzyme pathway.
在用脂氧合酶途径抑制剂处理后,体外评估了诱导的腹膜渗出白细胞对酵母聚糖激活血清(ZAS)的趋化反应。使用了大鼠和豚鼠的白细胞。BW755C和苯恶洛芬在10(-4)M时降低了两种物种单核细胞的趋化性。7.5×10(-6)M的去甲二氢愈创木酸(NDGA)抑制了大鼠单核细胞的趋化性,但未能改变豚鼠单核细胞的反应。NDGA、BW755C和苯恶洛芬在体外抑制脂氧合酶途径的浓度下,对降低大鼠PMN的趋化反应无效。所有三种药物在不同程度上增强了豚鼠PMN的趋化性,最明显的作用是NDGA,此时PMN迁移增加伴随着细胞从滤器下表面的脱离增加。这些药物对细胞趋化性和黏附的影响不一定与其对脂氧合酶途径的抑制作用相关。