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The phospholipids of cell membrane can be metabolized to form arachidonic acid by phospholipase A2. Arachidonic acid then produces different metabolites, including prostaglandins, thromboxanes and leukotrienes by three distinct pathways. These products have potent biological functions, particularly leukotrienes, related with allergy and inflammation. Asthma is a disease that bronchia are stimulated by allergens resulting in inflammatory reactions with contraction of brochi and dyspnea. In some studies, it has been found that the major cells involved in inflammatory reactions are mast cell and monocyte- macrophage. When these cells are challenged by allergens, they can release different mediators such as leukotrienes to induce asthma. If we understand the regulatory mechanisms of leukotriene production in mast cell and monocyte-macrophages, we may be able to control the asthma. In this study, we investigated the effects of three different Chinese herbs, Schisandra chinensis Baill, Citrus tangerina Hort. et Tanaka and Prunus armeniaca L., on the leukotriene production in mouse mastocytoma cell line P815 and mouse monocyte-macrophage cell line P388D1. Furthermore, regulation of leukotriene production by PKC and Ca2+ in these cell lines was also studied. These Chinese herbs, PKC activators and inhibitors, and Ca2+ ionophore A23187 were used to study the effects on arachidonic acid metabolism. Test cells were resuspended in buffer (pH = 7.4) and incubated with 0.1 mCi 14C-arachidonic acid and above agents for 2 hr at 37℃. The products of arachidonic acid metabolism were extracted and then identified by HPLC. Results show that these three Chinese herbs have inhibitory effects on the production of LTC4/D4 in P815 and P388D1 cells. The inhibitory effects of Schisandra chinensis Baill is shown to be the highest, and Citrus tangerina Hort. et Tanaka and Prunus armeniaca L. were the next. In P815 cells, it has been found that activation of PKC contains position effect on the regulation of leukotriene production. However, high concentration of Ca2+ did not affect leukotriene production. In P388D1 cells, both PKC and Ca2+ show no effect on leukotriene production.
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