Karinje K U, Ogata M
Department of Public Health, Okayama University Medical School, Japan.
Physiol Chem Phys Med NMR. 1990;22(4):193-8.
The methanol metabolism in acatalasemic mice was studied by administering [14C]methanol and [14C]formic acid to acatalasemic and normal mice and determining the radioactivity of exhaled carbon dioxide. Methanol metabolism was also studied in acatalasemic and normal mice treated with 3-amino-1,2,4-triazole (AT), which is known to be an inhibitor of catalase (EC 1.11.1.6). The metabolism of methanol and formic acid was inhibited in acatalasemic mice as seen by reduced [14C]CO2 production. Similar results were obtained when AT was given prior to the methanol injection into the normal and acatalasemic mice. The results indicate the peroxidative activity of catalase plays the major role in the methanol metabolism in mice. On the other hand similar studies with [1-14C] ethanol showed that the metabolism of ethanol was not inhibited in acatalasemic mice.
通过给无过氧化氢酶血症小鼠和正常小鼠注射[14C]甲醇和[14C]甲酸,并测定呼出二氧化碳的放射性,研究了无过氧化氢酶血症小鼠的甲醇代谢。还在用3-氨基-1,2,4-三唑(AT)处理的无过氧化氢酶血症小鼠和正常小鼠中研究了甲醇代谢,已知3-氨基-1,2,4-三唑是过氧化氢酶(EC 1.11.1.6)的抑制剂。如[14C]CO2生成减少所示,无过氧化氢酶血症小鼠中甲醇和甲酸的代谢受到抑制。在向正常和无过氧化氢酶血症小鼠注射甲醇之前给予AT时,也获得了类似结果。结果表明,过氧化氢酶的过氧化活性在小鼠甲醇代谢中起主要作用。另一方面,用[1-14C]乙醇进行的类似研究表明,无过氧化氢酶血症小鼠中乙醇的代谢未受抑制。