Kong L D, Tan R X, Woo A Y, Cheng C H
State Key Laboratory of Pharmaceutical Biotechnology, Institute of Pharmaceutical Biology and Phytochemistry, Nanjing University, NT, Hong Kong, China.
Pharmacol Toxicol. 2001 Feb;88(2):75-80. doi: 10.1034/j.1600-0773.2001.d01-86.x.
Psoralen and isopsoralen, furocoumarins isolated from the plant Psoralea corylifolia L., were demonstrated to exhibit in vitro inhibitory actions on monoamine oxidase (MAO) activities in rat brain mitochondria, preferentially inhibiting MAO-A activity over MAO-B activity. This inhibition of enzyme activities was found to be dose-dependent and reversible. For MAO-A, the IC50 values are 15.2 +/- 1.3 microM psoralen and 9.0 +/- 0.6 microM isopsoralen. For MAO-B, the IC50 values are 61.8 +/- 4.3 microM psoralen and 12.8 +/- 0.5 microM isopsoralen. Lineweaver-Burk transformation of the inhibition data indicates that inhibition by both psoralen and isopsoralen is non-competitive for MAO-A. The Ki values were calculated to be 14.0 microM for psoralen and 6.5 microM for isopsoralen. On the other hand, inhibition by both psoralen and isopsoralen is competitive for MAO-B. The Ki values were calculated to be 58.1 microM for psoralen and 10.8 microM for isopsoralen. These inhibitory actions of psoralen and isopsoralen on rat brain mitochondrial MAO activities are discussed in relation to their toxicities and their potential applications to treat affective disorders.
补骨脂素和异补骨脂素是从植物补骨脂中分离得到的呋喃香豆素,已证明它们在体外对大鼠脑线粒体中的单胺氧化酶(MAO)活性具有抑制作用,相对于MAO - B活性,它们优先抑制MAO - A活性。发现这种酶活性抑制具有剂量依赖性且是可逆的。对于MAO - A,补骨脂素的IC50值为15.2±1.3微摩尔,异补骨脂素的IC50值为9.0±0.6微摩尔。对于MAO - B,补骨脂素的IC50值为61.8±4.3微摩尔,异补骨脂素的IC50值为12.8±0.5微摩尔。抑制数据的Lineweaver - Burk转换表明,补骨脂素和异补骨脂素对MAO - A的抑制是非竞争性的。计算得出补骨脂素的Ki值为14.0微摩尔,异补骨脂素的Ki值为6.5微摩尔。另一方面,补骨脂素和异补骨脂素对MAO - B的抑制是竞争性的。计算得出补骨脂素的Ki值为58.1微摩尔,异补骨脂素的Ki值为10.8微摩尔。本文讨论了补骨脂素和异补骨脂素对大鼠脑线粒体MAO活性的这些抑制作用与其毒性以及它们在治疗情感障碍方面的潜在应用之间的关系。