Mann J J, Aarons S F, Frances A J, Brown R D
J Clin Psychiatry. 1984 Jul;45(7 Pt 2):62-6.
Several selective and reversible monoamine oxidase inhibitors (MAOIs) have recently become available. Preliminary studies suggest that these compounds have antidepressant effects and may offer significant safety and side effect advantages over classical MAOIs. Pilot studies with 1-deprenyl, a selective MAO-B inhibitor, indicate that it may be most effective for patients with nonendogenous depression and for those (endogenous or nonendogenous) who present with certain reverse vegetative signs. The drug appears ineffective in depressed patients with associated panic attacks and phobic symptoms. An alternative approach in the development of safer, effective MAOIs is the use of rapidly reversible MAO-A inhibitors, such as moclobemide, that carry less risk of a hypertensive reaction and yet appear to be effective antidepressants. As selective MAO-A and MAO-B inhibition may be effective in different depressive subtypes and may have different side effects, these drugs are valuable pharmacologic probes for studying the biochemical bases of depressive disorders.
最近有几种选择性且可逆的单胺氧化酶抑制剂(MAOIs)可供使用。初步研究表明,这些化合物具有抗抑郁作用,与传统MAOIs相比,可能具有显著的安全性和副作用优势。对选择性MAO - B抑制剂1 - 司来吉兰的初步研究表明,它可能对非内源性抑郁症患者以及那些(内源性或非内源性)出现某些反向植物神经体征的患者最为有效。该药物对伴有惊恐发作和恐惧症状的抑郁症患者似乎无效。开发更安全、有效的MAOIs的另一种方法是使用快速可逆的MAO - A抑制剂,如吗氯贝胺,其发生高血压反应的风险较低,且似乎是有效的抗抑郁药。由于选择性MAO - A和MAO - B抑制在不同的抑郁亚型中可能有效,且可能有不同的副作用,这些药物是研究抑郁症生化基础的有价值的药理学探针。