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首页> 外文期刊>Biological & pharmaceutical bulletin >Effects of the 5-HT1A Receptor Agonist Tandospirone on ACTH-Induced Sleep Disturbance in Rats
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Effects of the 5-HT1A Receptor Agonist Tandospirone on ACTH-Induced Sleep Disturbance in Rats

机译:5-HT1A受体激动剂坦度螺酮对ACTH诱导的大鼠睡眠障碍的影响

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The aim of this study was to compare the effect of the serotonin (5-HT)(1A) receptor agonist tandospirone versus that of the benzodiazepine hypnotic flunitrazepam in a rat model of long-term adrenocorticotropic hormone (ACTH)-induced sleep disturbance. Rats implanted with electrodes for recording electroencephalogram and electromyogram were injected with ACTH once daily at a dose of 100 mu g/rat. Administration of ACTH for 10d caused a significant increase in sleep latency, decrease in non-rapid eye movement (non-REM) sleep time, and increase in wake time. Tandospirone caused a significant decrease in sleep latency and increase in non-REM sleep time in rats treated with ACTH. The effect of tandospirone on sleep patterns was antagonized by the 5-HT1A receptor antagonist WAY-100635. In contrast, flunitrazepam had no significant effect on sleep parameters in ACTH-treated rats. These results clearly indicate that long-term administration of ACTH causes sleep disturbance, and stimulating the 5-HT1A receptor by tandospirone may be efficacious for improving sleep in cases in which benzodiazepine hypnotics are ineffective.
机译:这项研究的目的是比较5-羟色胺(5-HT)(1A)受体激动剂tandospirone与苯二氮卓催眠性氟硝西epa在长期促肾上腺皮质激素(ACTH)诱发的睡眠障碍大鼠模型中的作用。植入用于记录脑电图和肌电图的电极的大鼠每天以100μg /大鼠的剂量注射ACTH。服用ACTH 10d导致睡眠潜伏期显着增加,非快速眼动(non-REM)睡眠时间减少以及唤醒时间增加。在用ACTH治疗的大鼠中,坦度螺环酮导致睡眠潜伏期显着减少,并且非REM睡眠时间增加。 5-HT1A受体拮抗剂WAY-100635拮抗tandospirone对睡眠模式的影响。相比之下,氟尼西AC对ACTH治疗的大鼠的睡眠参数无明显影响。这些结果清楚地表明,长期服用ACTH会导致睡眠障碍,在苯二氮卓类催眠药无效的情况下,通过tandospirone刺激5-HT1A受体可能有效改善睡眠。

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