Ungar F, Callaghan O H
Res Commun Chem Pathol Pharmacol. 1977 Jun;17(2):191-9.
The in vivo and in vitro effects of various monoamine oxidase inhibitors (MAOI) on the borohydride stabilizable finding of serotonin (5-HT) or tryptamine in brain was investigated. A significant correlation between the extent of Mao inhibition and the amount of stabilized binding of the indolealkylamines was demonstrated. All hydrazine-type MAOI and harmine, a reversible nonhydrazine-type MAOI, employed in vitro, were shown to decrease the binding. beta-Phenylisopropylhydrazine apparently blocks the receptor carbonyl groups in the brain in vitro as well as in vivo.
研究了各种单胺氧化酶抑制剂(MAOI)在体内和体外对大脑中硼氢化物稳定的血清素(5-HT)或色胺的影响。结果表明,单胺氧化酶抑制程度与吲哚烷基胺的稳定结合量之间存在显著相关性。体外使用的所有肼类MAOI和一种可逆的非肼类MAOI——骆驼蓬碱,均显示出能减少结合。β-苯异丙基肼在体内和体外均能明显阻断大脑中的受体羰基。