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大鼠体内及体外由吗啡生成吗啡酮的过程

In vivo and in vitro formation of morphinone from morphine in rat.

作者信息

Yamano S, Takahashi A, Todaka T, Toki S

机构信息

Faculty of Pharmaceutical Sciences, Fukuoka University, Japan.

出版信息

Xenobiotica. 1997 Jul;27(7):645-56. doi: 10.1080/004982597240244.

Abstract
  1. Morphinone, a toxic metabolite, and its glutathione adduct (MO-GSH) were identified in the bile of rat after subcutaneous injection of morphine (25 mg/kg) by hplc procedures. The amounts of morphinone and MO-GSH excreted in the 12-h bile were 0.8 +/- 0.3 and 8.4 +/- 4.3% respectively. 2. The 9000 g supernatants of rat, guinea pig, rabbit, mouse, hamster and bovine livers produced morphinone from morphine in the presence of either NAD+ or NADP+, NAD+ was a more efficient cofactor than NADP+ except in the guinea pig which equally utilized both cofactors. With NAD+ as cofactor, the amounts of morphinone formed in rat and guinea pig were 5.70 and 5.82 mumol/g liver/30 min respectively and were three-to-four times those in other species. 3. The enzyme activity responsible for formation of morphinone from morphine in the rat was almost exclusively distributed in the microsomal fraction, whereas guinea pig, hamster and bovine expressed the enzyme activity mainly in the cytosolic fraction. Rabbit and mouse gave higher activity in the cytosolic and microsomal fractions respectively, but other fractions of both species contained considerable activity. 4. The enzyme activities in male and female rat microsomes were characterized with respect to developmental pattern, kinetic parameters, pH dependency and susceptibility to inhibitors. 5. In conclusion the metabolism of morphine to morphinone in rat was confirmed by in vivo and in vitro experiments. It is also suggested that this pathway is a common route in morphine metabolism in several mammalian species.
摘要
  1. 通过高效液相色谱法在皮下注射吗啡(25毫克/千克)的大鼠胆汁中鉴定出了有毒代谢物吗啡酮及其谷胱甘肽加合物(MO - GSH)。12小时胆汁中排泄的吗啡酮和MO - GSH量分别为0.8±0.3%和8.4±4.3%。2. 在存在NAD⁺或NADP⁺的情况下,大鼠、豚鼠、兔子、小鼠、仓鼠和牛肝脏的9000克上清液可由吗啡生成吗啡酮,除豚鼠能同等利用这两种辅因子外,NAD⁺作为辅因子比NADP⁺更有效。以NAD⁺为辅因子时,大鼠和豚鼠中形成的吗啡酮量分别为5.70和5.82微摩尔/克肝脏/30分钟,是其他物种的三到四倍。3. 大鼠中负责由吗啡生成吗啡酮的酶活性几乎完全分布在微粒体部分,而豚鼠、仓鼠和牛主要在胞质部分表达该酶活性。兔子和小鼠分别在胞质和微粒体部分具有较高活性,但这两个物种的其他部分也含有相当的活性。4. 对雄性和雌性大鼠微粒体中的酶活性进行了发育模式、动力学参数、pH依赖性和对抑制剂敏感性方面的表征。5. 总之,体内和体外实验证实了大鼠体内吗啡代谢为吗啡酮的过程。还表明该途径是几种哺乳动物物种中吗啡代谢的常见途径。

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