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Modulation of serotonergic projection from dorsal raphe nucleus to basolateral amygdala on sleep-waking cycle of rats.

机译:从大鼠背缝核到基底外侧杏仁核的血清素能投射对大鼠睡眠觉醒周期的调节。

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Putative serotonergic dorsal raphe nucleus (DRN) neurons display a dramatic role in the modulation of behavior. However, it is not clear how this modulation is mediated. The present study investigated the modulatory effects of serotonergic projection of the DRN to the basolateral amygdala (BLA) on the sleep-waking cycle using polysomnograph (PSG) in rats. DRN microinjection of kainic acid (KA) caused insomnia immediately. From the third day, however, slow wave sleep (SWS) and paradoxical sleep (PS) increased markedly. DRN microinjection of p-chlorophenylalanine (PCPA, once a day for 2 days), which inhibits the synthesis of serotonin (5-HT), led to similar effect to KA administration. The percent of sleep-wakefulness began to change on the third day after PCPA microinjection into the DRN, and the effect was most significant on the sixth day. The percent of sleep-wakefulness started to resume on the seventh day. SWS and PS were reduced after excitation of DRN neurons by microinjection of L-glutamate (L-Glu) into the DRN. Preapplication of the nonselective 5-HT receptor antagonist methysergide (MS) into bilateral BLA blocked the effect of DRN microinjection of L-Glu. Furthermore, bilateral BLA microinjection of 5-hydroxytryptophan (5-HTP), the precursor of 5-HT, on the sixth day after microinjection of PCPA into the DRN, could reverse the effect of PCPA microinjection. These results indicate that the modulation of the DRN on sleep is partially mediated by the serotonergic projection of the DRN to the BLA.
机译:假定的血清素能背脊神经元(DRN)神经元在行为调节中显示出重要作用。但是,尚不清楚该调节如何介导。本研究使用多导睡眠监测仪(PSG)研究了DRN的血清素能投射到基底外侧杏仁核(BLA)对睡眠-觉醒周期的调节作用。 DRN微量注射海藻酸(KA)立即导致失眠。从第三天开始,慢波睡眠(SWS)和自相矛盾睡眠(PS)明显增加。对硝基氯苯丙氨酸(PCPA,每天一次,连续2天)的DRN微注射抑制了5-羟色胺(5-HT)的合成,产生了与KA给药相似的效果。 PCPA微量注入DRN后的第三天,睡眠/清醒的百分比开始改变,并且在第六天影响最为明显。睡眠/清醒的百分比在第七天开始恢复。通过将L-谷氨酸(L-Glu)微量注入DRN刺激DRN神经元后,SWS和PS降低。非选择性5-HT受体拮抗剂美塞麦肽(MS)在双边BLA中的预先应用可阻断DRN微量注射L-Glu的作用。此外,在将PCPA微注射到DRN中的第六天,双侧BLA微注射5-羟色氨酸(5-HTP)(5-HT的前体)可以逆转PCPA显微注射的作用。这些结果表明,睡眠中DRN的调节部分是由DRN的血清素能投射到BLA介导的。

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