Fenik Victor B, Ogawa Hiromasa, Davies Richard O, Kubin Leszek
Department of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, 3800 Spruce Street, Philadelphia, PA 19104-6046, USA.
Sleep. 2005 May;28(5):551-9. doi: 10.1093/sleep/28.5.551.
Two pontine reticular regions are implicated in cholinergic triggering of rapid eye movement (REM) sleep: the dorsomedial tegmental region and the ventral nucleus pontis oralis. We previously determined that, in urethane-anesthetized rats, microinjections of a cholinergic agonist, carbachol, into the dorsal region produce REM sleep-like effects comprising cortical activation, hippocampal theta rhythm, suppression of hypoglossal (XII) nerve activity, and silencing of pontine noradrenergic neurons. Our goal was to determine whether carbachol injections into the ventral nucleus pontis oralis elicits comparable effects.
Recording of cortical electroencephalogram, hippocampal activity, XII nerve activity, and discharge of noradrenergic cells of the locus coeruleus.
Basic neurophysiologic research laboratory.
Urethane-anesthetized, paralyzed, and artificially ventilated or nonparalyzed and spontaneously breathing rats with microinjections of carbachol (10 nL, 10 mM) into the ventral nucleus pontis oralis.
In artificially ventilated rats, carbachol injections repeatedly elicited cortical activation and hippocampal theta rhythm. Concomitantly, the activity of locus coeruleus neurons increased from 2.0 per second +/- 0.4 (SE) to 2.6 per second +/- 0.4 (P < .05, n = 8), as did XII nerve activity (by 42.5% +/- 8.8%; P < .01). In spontaneously breathing animals, carbachol similarly activated the cortical electroencephalogram and hippocampal activity, whereas XII nerve activity was reduced by 6.7% +/- 2.5% (P < .05) together with increased ventilation, as indicated by reduced end-expiratory CO2.
Carbachol injections into the ventral nucleus pontis oralis activate, rather than silence, noradrenergic locus coeruleus neurons. This is not compatible with the state of REM sleep.
脑桥网状结构的两个区域与快速眼动(REM)睡眠的胆碱能触发有关:背内侧被盖区和脑桥嘴侧腹侧核。我们之前确定,在乌拉坦麻醉的大鼠中,向背侧区域微量注射胆碱能激动剂卡巴胆碱会产生类似REM睡眠的效应,包括皮质激活、海马θ节律、舌下(XII)神经活动抑制以及脑桥去甲肾上腺素能神经元沉默。我们的目标是确定向脑桥嘴侧腹侧核注射卡巴胆碱是否会引发类似的效应。
记录皮质脑电图、海马活动、XII神经活动以及蓝斑去甲肾上腺素能细胞的放电情况。
基础神经生理学研究实验室。
乌拉坦麻醉、麻痹并人工通气或未麻痹且自主呼吸的大鼠,向脑桥嘴侧腹侧核微量注射卡巴胆碱(10 nL,10 mM)。
在人工通气的大鼠中,注射卡巴胆碱反复引发皮质激活和海马θ节律。同时,蓝斑神经元的活动从每秒2.0次±0.4(标准误)增加到每秒2.6次±0.4(P <.05,n = 8),XII神经活动也增加(增加42.5%±8.8%;P <.01)。在自主呼吸的动物中,卡巴胆碱同样激活了皮质脑电图和海马活动,而XII神经活动减少了6.7%±2.5%(P <.05),同时通气增加,表现为呼气末二氧化碳减少。
向脑桥嘴侧腹侧核注射卡巴胆碱会激活而非使去甲肾上腺素能蓝斑神经元沉默。这与REM睡眠状态不相符。