Ilarionov I, Todorova P
Eksp Med Morfol. 1980;19(1):41-6.
The authors used the compounds 2-methyl-3)2-phenyl-3-methyl tetrahydroxasino)-propiophenone hydrochloriad (code PsI) and 1-phenoxycarboxy-1-phenyl-2-methyl-3 (2-phenyl-3-methyl-tetrahydroxasino-propan hydrochlorid(code P3) and carried out the following studies: influence of tripamine, corasol and strichnine seizures 1-phenoxycarboxy--1-phenyl-2-methyl--3 (2-phenyl--3-methyl-tetrahydroxasino) propar hydrochlor (Code P8) in white mice, effect on the hypertensive action of reserpine in white rats, investigations on the analeptic action in urethanized cats as well as on the analgetic effect, examined both by the test of "hot plate" and the method of Hendreshot-Forsaith. The examined compounds, administered in a dose of 1/6 of LD50, showed analgetic effect weaker than that of the preparations Morphinum hydrochloricum and Analigin, but their analeptic effect was less manifested that of of corasol. Similar to MAO-inhibitor-oproniazid although in smaller degree the compound PS1 potentiated tripamine seizures and inverted the hypotensive effect of Reserpine into hypertensive.
作者使用了化合物2-甲基-3-(2-苯基-3-甲基四氢吖辛因基)-苯丙酮盐酸盐(代码PsI)和1-苯氧基羰基-1-苯基-2-甲基-3-(2-苯基-3-甲基-四氢吖辛因基)丙烷盐酸盐(代码P3),并进行了以下研究:在小白鼠中研究曲帕明、可拉佐和士的宁惊厥对1-苯氧基羰基-1-苯基-2-甲基-3-(2-苯基-3-甲基-四氢吖辛因基)丙烷盐酸盐(代码P8)的影响;对大白鼠中利血平的降压作用的影响;对乌拉坦麻醉猫的苏醒作用以及镇痛作用的研究,镇痛作用通过“热板”试验和亨德肖特-福赛思方法进行检测。所检测的化合物以半数致死量的1/6剂量给药时,其镇痛作用比盐酸吗啡和安乃近制剂弱,但其苏醒作用比利血平的表现程度低。与单胺氧化酶抑制剂优降宁类似,尽管程度较小,但化合物PS1增强了曲帕明惊厥作用,并将利血平的降压作用转变为升压作用。