Mogilnicka E, Klimek V, Golembiowska-Nikitin K
J Neural Transm. 1977;40(3):195-204. doi: 10.1007/BF01300134.
Effects of nomifensine (8-amino-1, 2, 3, 4-tetrahydro-2-methyl-4-phenyl-isoquinoline) (NF), an antidepressant drug which inhibits dopamine uptake, on central serotonergic structures were studied in rats. NF affects of 5-hydroxytryptamine (5-HT) and 5-hydroxyindoleacetic acid levels in the whole brain as well as in the separate rat brain structures. The 5-HT turnover is decreased in the whole brain and the striatum but increased in the midbrain and the hippocamp as judged from experiments with tryptophan hydroxylase inhibitor, alpha-propyldopacetamide. Pretreatment with dopamine-receptor blocking agent, spiperone, antagonized the increase of 5-HT turnover rate in brain regions mentioned above. NF stimulates the hind limb flexor reflex in spinal rat, a preparation regarded as a model for evaluation of drug action on central 5-HT neurons. This stimulatory effect was antogonized by cyproheptadine, by reserpine and imipramine. The obtained results indicate that NF activates central 5-HT neurons both directly and indirectly, via stimulation of dopamine receptors as described previously for other dopamine agonists.
对一种抑制多巴胺摄取的抗抑郁药诺米芬辛(8-氨基-1,2,3,4-四氢-2-甲基-4-苯基异喹啉)(NF)对大鼠中枢5-羟色胺能结构的作用进行了研究。NF对全脑以及大鼠各个脑结构中的5-羟色胺(5-HT)和5-羟吲哚乙酸水平均有影响。根据用色氨酸羟化酶抑制剂α-丙基多巴胺酰胺所做的实验判断,全脑和纹状体中的5-HT周转降低,但中脑和海马中的5-HT周转增加。用多巴胺受体阻断剂螺哌隆预处理可拮抗上述脑区中5-HT周转率的增加。NF刺激脊髓大鼠的后肢屈肌反射,该标本被视为评估药物对中枢5-HT神经元作用的模型。这种刺激作用被赛庚啶、利血平和丙咪嗪拮抗。所得结果表明,NF通过刺激多巴胺受体,如先前对其他多巴胺激动剂所描述的那样,直接和间接地激活中枢5-HT神经元。