首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Involvement of secretory phospholipase A2 activity in the zymosan rat air pouch model of inflammation.
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Involvement of secretory phospholipase A2 activity in the zymosan rat air pouch model of inflammation.

机译:分泌型磷脂酶A2活性参与炎症的zymosan大鼠气袋模型。

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摘要

1. In the zymosan rat air pouch model of inflammation we have assessed the time dependence of phospholipase A2 (PLA2) accumulation in the inflammatory exudates as well as cell migration, myeloperoxidase activity, prostaglandin E2 (PGE2) and leukotriene B4 (LTB4) levels. 2. A significant increase in PLA2 activity was detected in 1,200 g supernatants of exudates 8 h after injection of zymosan into rat air pouch. This event coincided with peaks in cell accumulation (mainly neutrophils) and myeloperoxidase activity in exudates and was preceded by a rise in eicosanoid levels. 3. This enzyme (without further purification) behaved as a secretory type II PLA2 with an optimum pH at 7-8 units, lack of selectivity for arachidonate release and dependence on mM calcium concentrations for maximal activity. 4. The PLA2 inhibitors manoalide and scalaradial inhibited this enzyme activity in vitro in a concentration-dependent manner. Scalaradial also inhibited zymosan stimulated myeloperoxidase release in vitro. 5. Injection of the marine PLA2 inhibitor scalaradial together with zymosan into the pouch at doses of 0.5, 1 and 5 mumol per pouch resulted in a dose-dependent inhibition of PLA2 activity in exudates collected 8 h later. Myeloperoxidase levels and cell migration were also decreased, while eicosanoid levels were not modified. 6. Colchicine administration to rats prevented infiltration and decreased PLA2 levels in the 8 h zymosan-injected air pouch. 7. These results indicate that during inflammatory response to zymosan in the rat air pouch a secretory PLA2 activity is released into the exudates. The source of this activity is mainly the neutrophil which migrates into the pouch. 8. Scalaradial exerts anti-inflammatory effects in the zymosan air pouch.
机译:1.在酵母菌的大鼠气囊模型中,我们评估了磷脂酶A2(PLA2)在炎性渗出液中积累的时间依赖性以及细胞迁移,髓过氧化物酶活性,前列腺素E2(PGE2)和白三烯B4(LTB4)的水平。 2.将zymosan注入大鼠气囊后8 h,在1200 g渗出液的上清液中检测到PLA2活性显着增加。该事件与渗出液中细胞积累(主要是中性粒细胞)和髓过氧化物酶活性达到峰值,并在类花生酸水平升高之前发生。 3.该酶(无需进一步纯化)表现为分泌型II PLA2,最适pH为7-8单位,对花生四烯酸释放没有选择性,并且对最大活性的mM钙浓度没有依赖性。 4. PLA2抑制剂manoalide和scalaradial在体外以浓度依赖的方式抑制了这种酶的活性。 ala骨还抑制了酵母聚糖刺激的髓过氧化物酶的体外释放。 5.以每袋0.5、1和5μmol的剂量向袋中注入海洋PLA2抑制剂sc放射酶和酵母聚糖,导致剂量依赖性抑制8小时后收集的分泌物中的PLA2活性。髓过氧化物酶水平和细胞迁移也降低,而类花生酸水平未改变。 6.向大鼠施用秋水仙碱可防止在注入酵母聚糖8小时后的气囊中渗透并降低PLA2水平。 7.这些结果表明,在大鼠气袋中对酵母聚糖的炎症反应期间,分泌型PLA2活性释放到渗出液中。这种活动的来源主要是嗜中性粒细胞,它会迁移到囊袋中。 8. radi骨在酵母聚糖气囊中发挥抗炎作用。

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