Higashi Tatsuya, Yokoi Hiroyuki, Nagura Yukiko, Nishio Tadashi, Shimada Kazutake
Division of Pharmaceutical Sciences, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.
Biomed Chromatogr. 2008 Dec;22(12):1434-41. doi: 10.1002/bmc.1078.
The development and validation of liquid chromatography-electrospray ionization-tandem mass spectrometric (LC-ESI-MS/MS) methods that enable the quantification of neuroactive androgens, androsterone (5alpha-androstan-3alpha-ol-17-one, 3alpha,5alpha-A) and 5alpha-androstane-3alpha,17beta-diol (3alpha,5alpha-Adiol), in the rat brain and serum are presented. The androgens were extracted with methanol-acetic acid, purified using solid-phase extraction cartridges, derivatized with an ESI-active reagent, isonicotinoyl azide (INA), and then subjected to LC-ESI-MS/MS. The quantifications were based on selected reaction monitoring mode using the characteristic transitions of the INA derivatives. The methods allowed the reproducible and accurate quantification of the brain and serum neuroactive androgens using a 100 mg or 100 microL sample; the intra- and inter-assay relative standard deviations were below 3.6%, and the percentage accuracy values were 97.1-103.7% for both androgens. The animal study using the methods suggests that most of 3alpha,5alpha-Adiol found in the brain is derived from the periphery, while 3alpha,5alpha-A is not only transported from the periphery into the brain, but also synthesized in the brain by the oxidation of 3alpha,5alpha-Adiol. The androgens in the rats intraperitoneally administered finasteride, a 5alpha-reductatse inhibitor, were also measured; this treatment significantly reduced the brain 3alpha,5alpha-A and 3alpha,5alpha-Adiol levels and increased only the brain level of androstenedione, the precursor of 3alpha,5alpha-A.
本文介绍了液相色谱 - 电喷雾电离 - 串联质谱(LC - ESI - MS/MS)方法的开发与验证,该方法能够对大鼠脑和血清中的神经活性雄激素、雄甾酮(5α - 雄甾烷 - 3α - 醇 - 17 - 酮,3α,5α - A)和5α - 雄甾烷 - 3α,17β - 二醇(3α,5α - 阿二醇)进行定量分析。这些雄激素用甲醇 - 乙酸提取,通过固相萃取柱纯化,用一种电喷雾电离活性试剂异烟酰叠氮(INA)衍生化,然后进行LC - ESI - MS/MS分析。定量分析基于选择反应监测模式,使用INA衍生物的特征性跃迁。这些方法允许使用100 mg或100 μL样品对脑和血清中的神经活性雄激素进行可重复且准确的定量分析;批内和批间相对标准偏差均低于3.6%,两种雄激素的百分准确度值为97.1 - 103.7%。使用这些方法进行的动物研究表明,脑中发现的大部分3α,5α - 阿二醇来源于外周,而3α,5α - A不仅从外周转运至脑内,还可通过3α,5α - 阿二醇的氧化在脑内合成。还测定了腹腔注射5α - 还原酶抑制剂非那雄胺的大鼠体内的雄激素;这种处理显著降低了脑内3α,5α - A和3α,5α - 阿二醇的水平,且仅提高了3α,5α - A的前体雄烯二酮的脑内水平。