Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.
Sleep. 2010 Oct;33(10):1295-304. doi: 10.1093/sleep/33.10.1295.
To determine if the dopaminergic system modulates cataplexy, sleep attacks and sleep-wake behavior in narcoleptic mice.
Hypocretin/orexin knockout (i.e., narcoleptic) and wild-type mice were administered amphetamine and specific dopamine receptor modulators to determine their effects on sleep, cataplexy and sleep attacks.
Hypocretin knockout (n = 17) and wild-type mice (n = 21).
Cataplexy, sleep attacks and sleep-wake behavior were identified using electroencephalogram, electromyogram and videography. These behaviors were monitored for 4 hours after an i.p. injection of saline, amphetamine and specific dopamine receptor modulators (D1- and D2-like receptor modulators).
Amphetamine (2 mg/kg), which increases brain dopamine levels, decreased sleep attacks and cataplexy by 61% and 67%, suggesting that dopamine transmission modulates such behaviors. Dopamine receptor modulation also had powerful effects on sleep attacks and cataplexy. Activation (SKF 38393; 20 mg/kg) and blockade (SCH 23390; 1 mg/kg) of D1-like receptors decreased and increased sleep attacks by 77% and 88%, without affecting cataplexy. Pharmacological activation of D2-like receptors (quinpirole; 0.5 mg/kg) increased cataplectic attacks by 172% and blockade of these receptors (eticlopride; 1 mg/kg) potently suppressed them by 97%. Manipulation of D2-like receptors did not affect sleep attacks.
We show that the dopaminergic system plays a role in regulating both cataplexy and sleep attacks in narcoleptic mice. We found that cataplexy is modulated by a D2-like receptor mechanism, whereas dopamine modulates sleep attacks by a D1-like receptor mechanism. These results support a role for the dopamine system in regulating sleep attacks and cataplexy in a murine model of narcolepsy.
确定多巴胺能系统是否调节发作性睡病小鼠的猝倒、睡眠发作和睡眠-觉醒行为。
给予下丘脑分泌素/食欲素敲除(即发作性睡病)和野生型小鼠安非他命和特定多巴胺受体调节剂,以确定它们对睡眠、猝倒和睡眠发作的影响。
下丘脑分泌素敲除(n = 17)和野生型小鼠(n = 21)。
通过脑电图、肌电图和录像确定猝倒、睡眠发作和睡眠-觉醒行为。在腹腔注射生理盐水、安非他命和特定多巴胺受体调节剂(D1-和 D2-样受体调节剂)后 4 小时监测这些行为。
安非他命(2mg/kg)可增加大脑多巴胺水平,使睡眠发作和猝倒减少 61%和 67%,表明多巴胺传递调节此类行为。多巴胺受体调节对睡眠发作和猝倒也有强大的影响。D1-样受体的激活(SKF 38393;20mg/kg)和阻断(SCH 23390;1mg/kg)分别使睡眠发作减少 77%和 88%,而不影响猝倒。D2-样受体的药理学激活(喹吡罗;0.5mg/kg)使猝倒发作增加 172%,而这些受体的阻断(eticlopride;1mg/kg)则强力抑制 97%。D2-样受体的操作不影响睡眠发作。
我们表明,多巴胺能系统在调节发作性睡病小鼠的猝倒和睡眠发作中起作用。我们发现,猝倒受 D2-样受体机制调节,而多巴胺通过 D1-样受体机制调节睡眠发作。这些结果支持多巴胺系统在调节发作性睡病小鼠的睡眠发作和猝倒中的作用。