Maj J, Kapturkiewicz Z, Michaluk J
Arzneimittelforschung. 1976;26(6):1109-11.
The central action of nomifensine (NF), a new antidepressive drug, was studied in rats and mice. NF stimulates locomotor activity in normal animals as well as in animals whose motor activity has been depressed by reserpine, alpha-methyltyrosine (alpha-MT), bis-(4-methyl-1-homopiperazinyl-thiocarbonyl)-disulfide (Fla-63) or phenoxybenzamine. The sedation produced by alpha-MT plus reserpine or by spiroperidol is not affected by NF. NF induces stereotypy in the rat and antagonizes the catalepsy induced in the rat by neuroleptics, pilocarpine and arecoline. The catalepsy induced by alpha-MT plus reserpine is not influenced. NF elevates the brain levels of serotonin (5-HT) and 5-hydroxyindole acetic acid (5-HIAA) in the rat. These and previous results indicate that the profile of action of NF differs both from that of known tricyclic antidepressive drugs and that of dopaminergic stimulants.
对新型抗抑郁药诺米芬辛(NF)的中枢作用在大鼠和小鼠身上进行了研究。NF可刺激正常动物以及运动活性已被利血平、α-甲基酪氨酸(α-MT)、双-(4-甲基-1-高哌嗪基-硫代羰基)-二硫化物(Fla-63)或酚苄明抑制的动物的运动活性。α-MT加利血平或螺哌啶醇所产生的镇静作用不受NF影响。NF可诱导大鼠出现刻板行为,并拮抗由抗精神病药、毛果芸香碱和槟榔碱在大鼠中诱导产生的僵住症。α-MT加利血平诱导产生的僵住症不受影响。NF可提高大鼠脑内5-羟色胺(5-HT)和5-羟吲哚乙酸(5-HIAA)的水平。这些以及先前的结果表明,NF的作用模式既不同于已知的三环类抗抑郁药,也不同于多巴胺能兴奋剂。