Buckpitt A R, Bahnson L S
Toxicology. 1986 Nov;41(3):333-41. doi: 10.1016/0300-483x(86)90186-1.
In the presence of glutathione and glutathione transferases, microsomal fractions prepared from fresh samples of human lung tissue obtained at resection metabolized naphthalene to naphthalene dihydrodiol and 3 glutathione conjugates at easily measurable rates. Addition of varying amounts of human lung microsomal protein markedly inhibited mouse liver microsome-catalyzed naphthalene metabolism in one sample but not the other. These data show that naphthalene is a good substrate for human pulmonary microsomal monooxygenases. In addition, these studies suggest that there may be an inhibitor, potentially released during tissue homogenization, that makes measurement of human lung xenobiotic metabolism difficult.
在谷胱甘肽和谷胱甘肽转移酶存在的情况下,从切除时获取的新鲜人肺组织样本制备的微粒体组分,能以易于测量的速率将萘代谢为萘二氢二醇和3种谷胱甘肽结合物。在一个样本中加入不同量的人肺微粒体蛋白,显著抑制了小鼠肝微粒体催化的萘代谢,但在另一个样本中则没有。这些数据表明,萘是人肺微粒体单加氧酶的良好底物。此外,这些研究表明,可能存在一种在组织匀浆过程中潜在释放的抑制剂,这使得测量人肺外源性物质代谢变得困难。