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The production of free oxygen radicals and nitric oxide in the rat cochlea.

机译:大鼠耳蜗中游离氧自由基和一氧化氮的产生。

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摘要

Rat cochleas were analysed for free oxygen radicals (FOR) and nitric oxide (NO) production by the chemiluminescent oxidation of luminol. 4Beta-phorbol-12beta-myristate-13alpha-acetate (PMA), a well-known agonist of protein kinase C, induced the release of FOR after a time lag close to 30 s and reverted to basal values in approximately 10 min. Sphingosine inhibited by nearly 50% the response to PMA, whereas staurosporine caused an inhibition of 100%. The incubation of rat cochleas with 0.5 mM arginine potentiated the chemiluminescent reaction induced by PMA causing an additional oxidation of luminol that was inhibited by the NO synthase inhibitor N-methyl-arginine (NMA). Our results show for the first time the presence in the cochlea of cell populations producing FOR and NO and the real time production following cell activation. This procedure may help to explain the mechanisms involved in ototoxicity, as in the case of streptomycin and gentamicin that enhanced PMA-dependent production of FOR and NO.
机译:通过鲁米诺的化学发光氧化分析大鼠耳蜗的游离氧自由基(FOR)和一氧化氮(NO)产生。 4Beta-phorbol-12beta-肉豆蔻酸酯-13α-乙酸酯(PMA)是众所周知的蛋白激酶C激动剂,在接近30 s的时间间隔后诱导FOR的释放,并在大约10分钟内恢复为基础值。鞘氨醇抑制了对PMA的响应近50%,而星形孢菌素则引起了100%的抑制。将大鼠耳蜗与0.5 mM的精氨酸一起孵育可增强PMA诱导的化学发光反应,从而引起被NO合酶抑制剂N-甲基-精氨酸(NMA)抑制的鲁米诺进一步氧化。我们的结果首次显示耳蜗中存在产生FOR和NO的细胞群,以及细胞激活后的实时产生。此程序可能有助于解释涉及耳毒性的机制,例如链霉素和庆大霉素可增强PMA依赖性的FOR和NO生成。

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