Narcoleptic patients suffer from excessive daytime sleepiness, cataplexy, hypnagogic hallucinations and sleep attacks. Another identifying feature of narcolepsy is th entry into REM sleep directly from wakefulness. These symptoms are serious enough to disrupt the patients will being and may also be responsible for life threatening accidents. The disease appears to be a disorder of mechanisms controlling REM sleep because some narcoleptic symptoms, such as cataplexy and hypnagogic hallucinations are components of REM sleep, and in narcolepsy these components inexplicably encroach into the waking state. there is considerable evidence that acetylcholine plays an important role in triggering REM sleep, and the studies proposed in this grant application focus on delineating the cholinergic receptor subtype and neuronal elements related to this phase of sleep. The first experiment will serve to clarify the cholinergic receptor pharmacology involved in REM sleep generation. Pharmacological agents specific to the M1 and non-M1 receptors and nicotinic agents will be infused into the medial pontine reticular formation (mPRF), an area which has been shown to be important for REM sleep generation. The changes in REM sleep will be noted and comparisons between muscarinic and nicotinic mechanisms will be made. The second study will examine the glutaminergic pathway in the pons that along with the cholinergic pathway might represent the final common pathway involved in the atonia of REM sleep. Different retrograde tracers will be injected into the mPRF and the caudal medulla and the presence of the tracer will be examined in chemically identified glutaminergic somata in the dorsolateral pontine tegmentum. The third study will utilize fos-immunohistochemistry to reveal neuronal elements in the brainstem and forebrain related to REM sleep. The fos gene is triggered in response to neuronal stimulation and the presence of the protein allows for mapping of neuronal pathways. The protein might act as a third messenger serving to regulate the functional response of the cell. These studies will establish a groundwork for future work related to the transcriptional processes occuring during REM sleep.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS030140-02
Application #
3417071
Study Section
Special Emphasis Panel (SSS (C))
Project Start
1991-09-30
Project End
1994-09-29
Budget Start
1992-09-30
Budget End
1993-09-29
Support Year
2
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Blanco-Centurion, Carlos; Liu, Meng; Konadhode, RodaRani et al. (2013) Effects of orexin gene transfer in the dorsolateral pons in orexin knockout mice. Sleep 36:31-40
Liu, Meng; Blanco-Centurion, Carlos; Konadhode, RodaRani et al. (2011) Orexin gene transfer into zona incerta neurons suppresses muscle paralysis in narcoleptic mice. J Neurosci 31:6028-40
Thankachan, Stephen; Kaur, Satvinder; Shiromani, Priyattam J (2009) Activity of pontine neurons during sleep and cataplexy in hypocretin knock-out mice. J Neurosci 29:1580-5
Kaur, Satvinder; Thankachan, Stephen; Begum, Suraiya et al. (2009) Hypocretin-2 saporin lesions of the ventrolateral periaquaductal gray (vlPAG) increase REM sleep in hypocretin knockout mice. PLoS One 4:e6346
Liu, Meng; Thankachan, Stephen; Kaur, Satvinder et al. (2008) Orexin (hypocretin) gene transfer diminishes narcoleptic sleep behavior in mice. Eur J Neurosci 28:1382-93
Murillo-Rodriguez, Eric; Liu, Meng; Blanco-Centurion, Carlos et al. (2008) Effects of hypocretin (orexin) neuronal loss on sleep and extracellular adenosine levels in the rat basal forebrain. Eur J Neurosci 28:1191-8
Kaur, Satvinder; Thankachan, Stephen; Begum, Suraiya et al. (2008) Entrainment of temperature and activity rhythms to restricted feeding in orexin knock out mice. Brain Res 1205:47-54
Blanco-Centurion, Carlos; Gerashchenko, Dmitry; Shiromani, Priyattam J (2007) Effects of saporin-induced lesions of three arousal populations on daily levels of sleep and wake. J Neurosci 27:14041-8
Zhang, S; Lin, L; Kaur, S et al. (2007) The development of hypocretin (orexin) deficiency in hypocretin/ataxin-3 transgenic rats. Neuroscience 148:34-43
Blanco-Centurion, Carlos; Xu, Man; Murillo-Rodriguez, Eric et al. (2006) Adenosine and sleep homeostasis in the Basal forebrain. J Neurosci 26:8092-100

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