Nakagawa H, Endo Y, Ohtaki S
Endocrinol Jpn. 1981 Aug;28(4):409-17. doi: 10.1507/endocrj1954.28.409.
The lipid materials extracted from hog thyroid microsomes were found to contain factors which stimulated both the NADPH oxidation by NADPH-cytochrome c reductase and PBI formation by a reconstituted system containing the reductase as a hydrogen peroxide generator and thyroid peroxidase. For both reactions, the stimulating activity in the extracts from the other subcellular fractions was less than that observed in the extracts from microsomal fraction. Lipids extracted from hog liver microsomes did not show any NADPH oxidation stimulating activity. Thin-layer chromatography of the lipid extracts from thyroid microsomes revealed the presence of at least two stimulating factors differing in chromatographic behaviour. At least one of the stimulating factors separated on TLC stimulated the oxygen consumption accompanied by generation of hydrogen peroxide due to the NADPH oxidation by NADPH-cytochrome c reductase. From these results it was suggested that in thyroid microsomes, but not in liver microsomes, there were stimulating factors extractable by chloroform-methanol. The factors could stimulate NADPH oxidation by NADPH-cytochrome c reductase followed by generation of hydrogen peroxide, resulting in the enhancement of PBI formation coupled with thyroid peroxidase.
从猪甲状腺微粒体中提取的脂质材料被发现含有一些因子,这些因子既能刺激NADPH - 细胞色素c还原酶对NADPH的氧化,又能刺激由包含该还原酶作为过氧化氢生成剂和甲状腺过氧化物酶的重组系统形成PBI。对于这两个反应,其他亚细胞组分提取物中的刺激活性低于微粒体组分提取物中观察到的活性。从猪肝微粒体中提取的脂质未显示出任何刺激NADPH氧化的活性。对甲状腺微粒体脂质提取物进行的薄层色谱分析表明,存在至少两种色谱行为不同的刺激因子。在薄层层析上分离出的至少一种刺激因子,能刺激因NADPH - 细胞色素c还原酶氧化NADPH而伴随过氧化氢生成的耗氧量。从这些结果推测,在甲状腺微粒体中而非肝微粒体中,存在可被氯仿 - 甲醇提取的刺激因子。这些因子能刺激NADPH - 细胞色素c还原酶对NADPH的氧化,随后生成过氧化氢,从而增强与甲状腺过氧化物酶相关的PBI形成。