Golembiowska-Nikitin K, Wiszniowska G, Marchaj J
Pol J Pharmacol Pharm. 1977 Sep-Oct;29(5):485-95.
Cyproheptadine (CPH), 0.5 mg/kg ip, did not affect the cerebral serotonin (5-HT) level, but elevated the level of 5-hydroxyindoleacetic acid (5-HIAA). Danitracen (DN), 1 mg/kg ip, depressed the cerebral 5-HT level and elevated the 5-HIAA level, but at a dose 10 mg/kg did not affect the levels of either the amine, or its metabolite. Both CPH and DN, 1 mg/kg, significantly potentiated the disappearance of 5-HT after administration of p-chlorophenylalanine. DN, in a low dose, accelerated the disappearance of 5-HT after inhibition of 5-HT synthesis by alpha-propyldopacetamide. The rate of accumulation of 5-HIAA after probenecid, was increased only by CPH. CPH did not affect the 5-HT accumulation after pargyline, while DN depressed its accumulation. The results of experiments on the levels of 5-HT and 5-HIAA, and on the rate of disappearance of 5-HT after inhibition of tryptophan decarboxylase suggest that CPH and DN increase the 5-HT turnover. The results of studies on the turnover rate of 5-HT after administration of probenecid and parygline do not corroborate fully this assumption. Possibly, this discrepancy may depend on differences in the action of 5-HT in various brain areas and interaction of serotoninolytics tested with effects of the MAO inhibitor.
赛庚啶(CPH),腹腔注射剂量为0.5毫克/千克,不影响大脑中血清素(5-羟色胺,5-HT)水平,但会提高5-羟吲哚乙酸(5-HIAA)水平。丹曲林(DN),腹腔注射剂量为1毫克/千克,会降低大脑5-HT水平并提高5-HIAA水平,但剂量为10毫克/千克时,对胺及其代谢产物的水平均无影响。CPH和1毫克/千克的DN在给予对氯苯丙氨酸后均显著增强了5-HT的消失。低剂量的DN在α-丙基多巴胺酰胺抑制5-HT合成后加速了5-HT的消失。丙磺舒给药后5-HIAA的积累速率仅因CPH而增加。CPH不影响帕吉林给药后5-HT的积累,而DN则抑制其积累。关于5-HT和5-HIAA水平以及色氨酸脱羧酶抑制后5-HT消失速率的实验结果表明,CPH和DN增加了5-HT的周转率。丙磺舒和帕吉林给药后关于5-HT周转率的研究结果并未完全证实这一假设。这种差异可能取决于5-HT在不同脑区的作用差异以及所测试的血清素分解剂与单胺氧化酶抑制剂作用之间的相互作用。