Pal Dinesh, Mallick Birendra Nath
School of Life Sciences, Jawaharlal Nehru University, New Delhi 110 067, India.
Neurosci Lett. 2004 Jul 29;365(3):200-4. doi: 10.1016/j.neulet.2004.04.080.
REM-OFF and REM-ON neurons in the brainstem are reported to regulate REM sleep, however, the detailed mechanism of generation of REM sleep is unknown. The former are continuously active except during REM sleep and an inhibitory neurotransmitter, GABA, has been implicated in mediating the inhibition for the generation of REM sleep. The REM-ON neurons, on the other hand, remain inactive throughout but increase firing during REM sleep. This study was conducted to investigate if GABA in the brain area rich in cholinergic REM-ON neurons would modulate REM sleep as proposed earlier. Rats were surgically prepared for sleep-wake recording and two cannulae aiming pedunculopontine areas in the brainstem that are rich in REM-ON neurons, were implanted bilaterally. After recovery, picrotoxin, a GABA(A) antagonist, was simultaneously microinjected bilaterally into the pedunculopontine area in freely moving normally behaving rats using a remote dual syringe pump and the effects were studied on electrophysiological sleep and waking parameters. The results showed that picrotoxin significantly reduced REM sleep for 6h and the effect was due to reduction in the frequency of generation of REM sleep.
据报道,脑干中的快速眼动睡眠关闭(REM-OFF)神经元和快速眼动睡眠开启(REM-ON)神经元调节快速眼动睡眠,然而,快速眼动睡眠产生的详细机制尚不清楚。前者在快速眼动睡眠期间除外持续活跃,一种抑制性神经递质γ-氨基丁酸(GABA)被认为参与介导对快速眼动睡眠产生的抑制作用。另一方面,REM-ON神经元在整个过程中保持不活跃,但在快速眼动睡眠期间放电增加。本研究旨在调查富含胆碱能REM-ON神经元的脑区中的GABA是否如先前提出的那样调节快速眼动睡眠。对大鼠进行手术准备以记录睡眠-觉醒情况,并在双侧植入两个套管,目标是脑干中富含REM-ON神经元的脚桥核区域。恢复后,使用远程双注射器泵将GABA(A)拮抗剂印防己毒素同时双侧微量注射到自由活动的正常行为大鼠的脚桥核区域,并研究其对电生理睡眠和觉醒参数的影响。结果表明,印防己毒素使快速眼动睡眠显著减少6小时,且该效应是由于快速眼动睡眠产生频率降低所致。