Sugden D, Fletcher A
Psychopharmacology (Berl). 1981;74(4):369-73. doi: 10.1007/BF00432750.
DL-6-Fluorotryptophan (6-FT), a competitive inhibitor of tryptophan hydroxylase, produced a transient disruption of sleep in rats chronically implanted with EEG recording electrodes. In the 4 h period following the administration of 6-FT (120 mg/kg) awake time was increased, paradoxical sleep time was decreased and slow-wave sleep remained unchanged. These sleep changes were accompanied by significant reductions in brain 5-HT levels. L-Tryptophan (100 mg/kg) co-administration with 6-FT prevented the major sleep changes whereas L-leucine (100 mg/kg) was without effect. The major sleep changes produced by 6-FT were prevented by the pineal indole melatonin (20 mg/kg) but not by L-5-hydroxytryptophan (5 mg/kg). These neurochemical and drug interaction data raise the possibility that 5-hydroxytryptamine is involved in the control of paradoxical rather than slow-wave sleep in the rat.
DL-6-氟色氨酸(6-FT)是色氨酸羟化酶的竞争性抑制剂,它会使长期植入脑电图记录电极的大鼠的睡眠产生短暂紊乱。在给予6-FT(120毫克/千克)后的4小时内,清醒时间增加,异相睡眠时间减少,慢波睡眠保持不变。这些睡眠变化伴随着大脑5-羟色胺水平的显著降低。与6-FT共同给予L-色氨酸(100毫克/千克)可防止主要的睡眠变化,而L-亮氨酸(100毫克/千克)则无作用。松果体吲哚褪黑素(20毫克/千克)可防止6-FT引起的主要睡眠变化,但L-5-羟色氨酸(5毫克/千克)则不能。这些神经化学和药物相互作用数据增加了5-羟色胺参与大鼠异相睡眠而非慢波睡眠控制的可能性。