Ezeamuzie Charles I, Taslim Najla
Department of Pharmacology and Toxicology, Faculty of Medicine, Kuwait University, Kuwait.
Eur J Pharmacol. 2006 Aug 14;543(1-3):174-80. doi: 10.1016/j.ejphar.2006.05.035. Epub 2006 Jun 2.
Recently, we showed that phorbol 12-myristate 13-acetate (PMA) can cause a direct, PKC-dependent, stimulation of intracellular cAMP in human eosinophils. Since PMA also stimulates the release of reactive oxygen species in these cells, we have investigated whether reactive oxygen species are involved in the cAMP response. Provided eosinophils were incubated for <20 min at 37 degrees C before stimulation, PMA potently stimulated cAMP generation that surpassed that of histamine. Pre-treatment of the cells with the NADPH oxidase inhibitors, diphenyleneiodonium (DPI) and apocynin, strongly inhibited the cAMP production induced by PMA, but not that induced by histamine. This treatment also strongly inhibited the release of superoxide anions (O(2)(-)). The cAMP response was also inhibited by pre-treatment with the specific peroxide scavenger, ebselen, but not superoxide dismutase, or NG-nitro-l-arginine methyl ester (L-NAME), thus, suggesting the possible involvement of a peroxide rather than O(2)(-) or nitric oxide (NO). These results reveal a novel involvement of intracellular reactive oxygen species in protein kinase C (PKC)-dependent stimulation of cAMP production in human eosinophils.
最近,我们发现佛波醇12 -肉豆蔻酸酯13 -乙酸酯(PMA)可直接、依赖蛋白激酶C(PKC)刺激人嗜酸性粒细胞内的环磷酸腺苷(cAMP)。由于PMA还能刺激这些细胞释放活性氧,我们研究了活性氧是否参与cAMP反应。如果嗜酸性粒细胞在刺激前于37℃孵育<20分钟,PMA能有效刺激cAMP生成,其生成量超过组胺刺激的。用烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶抑制剂二亚苯基碘鎓(DPI)和夹竹桃麻素预处理细胞,可强烈抑制PMA诱导的cAMP产生,但不抑制组胺诱导的cAMP产生。这种处理还强烈抑制超氧阴离子(O₂⁻)的释放。用特异性过氧化物清除剂依布硒啉预处理也可抑制cAMP反应,但超氧化物歧化酶或NG -硝基-L -精氨酸甲酯(L - NAME)预处理则无此作用,因此表明可能是过氧化物而非O₂⁻或一氧化氮(NO)参与其中。这些结果揭示了细胞内活性氧在蛋白激酶C(PKC)依赖的人嗜酸性粒细胞cAMP产生刺激中的新作用。