Buczko W, De Blasi A
Pol J Pharmacol Pharm. 1983;35(1):45-7.
No effect of fibrinogen degradation products on specific binding of [3H]spiroperidol and [3H]ADTN was observed. Low molecular weight peptides derived from fibrinogen degradation by plasmin (FDP) increase the motor activity of rats [7] augment apomorphine- and amphetamine-induced stereotypy and diminish haloperidol catalepsy [2]. It has been suggested that FDP interact with central dopamine receptor [2]. Taking the above considerations into account it was decided to investigate the effect of FDP on specific binding of [3H] spiroperidol and 2-amino-6,7-dihydroxy-1,2,3,4-tetrahydronaphthalene ([3H]ADTN).
未观察到纤维蛋白原降解产物对[3H]螺哌啶醇和[3H]ADTN特异性结合的影响。纤溶酶降解纤维蛋白原产生的低分子量肽(FDP)可增加大鼠的运动活性[7],增强阿扑吗啡和苯丙胺诱导的刻板行为,并减轻氟哌啶醇诱导的僵住症[2]。有人提出FDP与中枢多巴胺受体相互作用[2]。考虑到上述因素,决定研究FDP对[3H]螺哌啶醇和2-氨基-6,7-二羟基-1,2,3,4-四氢萘([3H]ADTN)特异性结合的影响。