Yoshida T, Oguro T, Numazawa S, Kuroiwa Y
Biochem Biophys Res Commun. 1987 May 29;145(1):502-8. doi: 10.1016/0006-291x(87)91349-0.
Concomitant with the depletion of glutathione content, phorone (250 mg/kg, ip.) produced a marked increase in heme oxygenase activity, biphasic effect on delta-aminolevulinic acid synthetase activity, and slight decreases in cytochrome P-450 content and aminopyrine demethylase activity in the liver of rats. The increase in heme oxygenase activity evoked by phorone was almost completely blocked by pretreatment of rats with actinomycin D and cycloheximide. Phorone was able to produce the changes in these parameters in a dose-dependent manner. Buthionine sulfoximine, a GSH depletor by inhibition of biosynthesis, failed to affect these hepatic parameters.
伴随着谷胱甘肽含量的耗尽,佛尔酮(250毫克/千克,腹腔注射)使大鼠肝脏中的血红素加氧酶活性显著增加,对δ-氨基-γ-酮戊酸合成酶活性产生双相效应,并使细胞色素P-450含量和氨基比林脱甲基酶活性略有降低。放线菌素D和环己酰亚胺预处理大鼠几乎完全阻断了佛尔酮引起的血红素加氧酶活性增加。佛尔酮能够以剂量依赖的方式引起这些参数的变化。丁硫氨酸亚砜胺,一种通过抑制生物合成来消耗谷胱甘肽的物质,未能影响这些肝脏参数。