Abstract
While the utilization of nuclear medicine methods for the assessment of sleep disorders is still in its infancy, early studies suggest that this is a promising area for future development. The assessment of brain function during sleep introduces a time-of-day variable into a neuroimaging study. Extensive preclinical knowledge of the neural mechanisms of sleep regulation helps to inform models of brain function that may be altered by sleep and by sleep disorders. Early studies show reliable increases in function in limbic and anterior paralimbic cortex in REM sleep and decreases in function in higher order cortical regions in known thalamocortical networks during NREM sleep. While most of the early work in this area has been devoted to the study of normal sleep mechanisms, a collection of studies in diverse sleep disorders such as sleep deprivation, depression, insomnia, dyssomnias, narcolepsy and sleep apnoea suggest that nuclear medicine has great potential in clarifying the pathophysiology of sleep disorders and potentially in guiding treatment strategies.
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References
Albin RL, Koeppe RA, Chervin RD, Consens FB, Wernette K, Frey KA, Aldrich MS (2000) Decreased striatal dopaminergic innervation in REM sleep behavior disorder. Neurology 55: 1410–1412
Alkire MT, Haier RJ, Fallon JH (2000) Towards a unified theory of narcosis: brain imaging evidence for a thalamocortical switch as the neurophysiologic basis of anesthetic-induced unconsciousness. Conscious Cogn 9:370–386
Asenbaum S, Zeithofer J, Saletu B, Frey R, Brucke T, Podreka I, Deecke L (1995) Technetium-99m-HMPAO SPECT imaging of cerebral blood flow during REM sleep in narcoleptics. J Nucl Med 36:1150–1155
Aston-Jones G, Bloom FE (1981) Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle. J Neurosci 1:876–886
Balkin TJ, Braun AR, Wesensten NJ, Jeffries K, Varga M, Baldwin P, Belenky G, Herscovitch P (2002) The process of awakening: a PET study of regional brain activity patterns mediating the re-establishment of alertness and consciousness. Brain 125:2308–2319
Bassetti C, Vella S, Donati F, Wielepp P, Weder B (2000) SPECT during sleepwalking. Lancet 356:484–485.
Benca RM, Obermeyer WH, Thisted RA, Gillin JC (1992) Sleep and psychiatric disorders: a metaanalysis. Arch Gen Psychiatry 49:651–668
Bernard JF, Alden M, Resson JM (1993) The organization of the efferent projections from the pontine parabrachial area to the amygdaloid complex: a phaseolus vulgaris leucoagglutinin (PHA-L) study in rats. J Comp Neurol 329:201–229
Born AP, Law I, Lund TE, Rostrup E, Hanson LG, Wildschiodtz G, Lou HC, Paulson OB (2002) Cortical deactivation induced by visual stimulation in human slow-wave sleep. Neuroimage 17:1325–1335
Braun AR, Balkin TJ, Wesenten NJ, Carson RE, Varga M, Baldwin P, Selbie S, Belenky G, Hersco-vitch P (1997) Regional cerebral blood flow throughout the sleep-wake cycle. An H2(15)0 PET study. Brain 120:1173–1197
Braun AR, Balkin TJ, Wesensten NJ, Gwadry F, Carson RE, Varga M, Baldwin P, Belenky G, Herscovitch P (1998) Dissociated pattern of activity in visual cortices and their projections during human rapid eye movement sleep. Science 279:91–95
Buchsbaum MS, Gillin JC, Wu J, Hazlett E, Sicotte N, DuPont RM, Bunney WE (1989) Regional cerebral glucose metabolic rate in human sleep assessed by positron emission tomography. Life Sci 45:1349–1356
Buchsbaum MS, Hazlett EA, Wu J, Bunney WE (2001) Positron emission tomography with deoxyglucose-F18 imaging of sleep. Neuropsychopharmacology 25[Suppl 5]:S50–S56
Calvo JM, Simon-Arceo K (1999) Cholinergic enhancement of REM sleep from sites in the pons and amygdala. In: Lydic R, Baghdoyan HA (eds) Handbook of behavioral state control: cellular and molecular mechanisms. CRC Press, Boca Raton, pp 391–406
Cape EG, Jones BE (1998) Differential modulation of high-frequency gamma-electroencephalogram activity and sleep-wake state by noradrenaline and serotonin microinjections into the region of cholinergic basalis neurons. J Neurosci 18:2653–2666
Chase MH, Monoson R, Watanabe K, Babb MI (1976) Somatic reflex response-reversal of reticular origin. Exp Neurol 50:561–567
Chou TC, Bjorkum AA, Gaus SE, Lu J, Scammell TE, Saper CB (2002) Afferents to the ventrolateral preoptic nucleus. J Neurosci 22:977–990
Clark C, Dupont R, Lehr P, Yeung D, Halpern S, Golshan S, Gillin JC (1998). Is there a relationship between delta sleep at night and afternoon cerebral blood flow, assessed by HMPAO-SPECT in depressed patients and normal control subjects? Preliminary data. Psychiatry Res 84:89–99
Datta S, Pare D, Oakson G, Steriade M (1989) Thalamic projecting neurons in brainstem cholinergic nuclei increase their firing rates one minute in advance of EEG desynchronization associated with REM sleep. Soc Neurosci Abstr 15:452 (abstract)
Datta S, Calvo JM, Quattrochi J, Hobson JA (1992) Cholinergic microstimulation of the peribra-chial nucleus in the cat. I. Immediate and prolonged increases in ponto-geniculo-occipital waves. Arch Ital Biol 130:263–284
Ebert D, Feistel H, Barocka A (1991) Effects of sleep deprivation on the limbic system and the frontal lobes in affective disorders: a study with Tc-99m-HMPAO SPECT. Psychiatry Res 40: 247–251
Ebert D, Feistel H, Kaschka W, Barocka A, Pirner A (1994) Single photon emission computerized tomography assessment of cerebral dopamine D2 receptor blockade in depression before and after sleep deprivation — preliminary results. Biol Psychiatry 35:880–885
Edgar DM (1994) Sleep-wake circadian rhythms and aging: potential etiologies and relevance to age-related changes in integrated physiological systems. Neurobiol Aging 15:499–501
Eisensehr I, Linke R, Noachtar S, Schwarz J, Gildehaus FJ, Tatsch K (2000) Reduced striatal dopamine transporters in diopathic rapid eye movement sleep behaviour disorder. Comparison with Parkinson’s disease and controls. Brain 123:1155–1160
Ficker JH, Feistel H, Moller C, Merkl M, Dertinger S, Siegfried W, Hahn EG (1997) Changes in regional CNS perfusion in obstructive sleep apnea syndrome: initial SPECT studies with injected nocturnal 99mTc-HMPAO. Pheumologie 51:926–930
Finelli LA, Landolt HP, Buck A, Roth C, Berthold T, Borbely AA, Achermann P (2000) Functional neuroanatomy of human sleep states after Zolpidem and placebo: a H2150-PET study. J Sleep Res 9:161–173
Fiset P, Paus T, Daloze T, Plourde G, Meuret P, Bonhomme V, Hajj-Ali N, Backman SB, Evans AC (1999) Brain mechanisms of propofol-induced loss of consciousness in humans: a positron emission tomographic study. J Neurosci 19:5506–5513
Gadea-Ciria M (1976a) Cerebellar control of activity of the feline oculomotor system during paradoxical sleep. Exp Neurol 51:263–265
Gadea-Ciria M (1976b) Tele-encephalic versus cerebellar control upon ponto-geniculo-occipital waves during paradoxical sleep in the cat. Experientia 32:889–890
Ganguli R, Reynolds CF, Kupfer DJ(1987) Electroencephalographs sleep in young, never medicated schizophrenics. Arch Gen Psychiatry 44:36–44
Gillin JC, Buchsbaum MS, Valladares-Neto DC, Hong CC, Hazlett E, Langer SZ, Wu J (1996) Effects of Zolpidem on local cerebral glucose metabolism during non-REM sleep in normal volunteers: a positron emission tomography study. Neuropsychopharmacology 15:302–313
Heiss WD, Pawlik G, Herholz K, Wagner R, Wienhard K (1985) Regional cerebral glucose metabolism in man during wakefulness, sleep, and dreaming. Brain Res 327:362–366
Ho AP, Gillin JC, Buchsbaum MS, Wu JC, Abel L, Bunney WE Jr (1996) Brain glucose metabolism during non-rapid eye movement sleep in major depression. A positron emission tomography study. Arch Gen Psychiatry 53:645–652
Hobson JA, Stenade M (1986) Neuronal basis of behavioral state control. In: Mountcastle VB, Bloom FE (eds) Handbook of physiology. American Physiological Society, Bethesda, pp 701–823
Hobson JA, McCarley RW, Nelson JP (1983) Location and spike-train characteristics of cells in anterodorsal pons having selective decreases in firing rate during desynchronized sleep. J Neurophysiol 50:770–793
Hobson JA, Datta S, Calvo JM, Quattrochi J (1993) Acetylcholine as a brain state regulator: triggering and long-term regulation of REM sleep. Prog Brain Res 98:389–404
Hobson AJ, Pace-Schott EF, Stickgold R (2003) Dreaming and the brain: toward a cognitive neuroscience of conscious states. In: Pace-Schott EF, Solms M, Blagrove M, Harnad S (eds) Sleep and dreaming. Cambridge University Press, Cambridge, pp 1–50
Hobson JA, Stickgold R, Pace-Schott EF (1997) The neuropsychology of REM sleep dreaming. Neuroreport Rev 9:R1–R14
Hofle N, Paus T, Reutens D, Fiset P, Gotman J, Evans AC, Jones BE (1997) Regional cerebral blood flow changes as a function of delta and spindle activity during slow wave sleep in humans. J Neurosci 17:4800–4808
Hublin C, Launes J, Nikkinen P, Partinen M (1994) Dopamine D2-receptors in human narcolepsy: a SPECT study with 123I-IBZM. Acta Neurol Scand 90:186–189
Jacobs BL, Heym J, Trulson ME (1981) Behavioral and physiological correlates of brain serotonergic unit activity. J Physiol (Lond) 77:431–436
Jones BE (1994) Basic mechanisms of sleep-wake states. In: Kryger MH, Roth T, Dement WC (eds) Principles and practice of sleep medicine. Saunders, Philadelphia, pp 145–162
Kami A, Tanne D, Rubenstein BS, Askenasy JJM, Sagi D (1994) Dependence on REM sleep of overnight improvement of a perceptual skill. Science 265:679–682
Keshavan MS, Anderson S, Pettegrew JW (1994) Is schizophrenia due to excessive synaptic pruning in prefrontal cortex? The Feinberg hypothesis revisited. J Psychiatr Res 28:239–265
Khateb A, Fort P, Pegna A, Jones BE, Winthaler M (1995) Cholinergic nucleus basalis neurons are excited by histamine in vitro. Neuroscience 69:495–506
Kjaer TW, Law I, Wiltschiotz G, Paulson OB, Madsen PL (2002) Regional cerebral blood flow during light sleep-a H (2) (15) O-PET study. Sleep Res 11:201–207
Kloppel S, Pirker W, Brucke T, Kovacs GG, Aimer G (2002) Beta-CIT SPECT demonstrates reduced availability of serotonin transporters in patients with fatal familial insomnia. J Neural Transm 109:1105–1110
Kushida CA, Zoltoski RK, Gillin JC (1995) Expression of m2 muscarinic receptor mRNA in rat brain with REM sleep deprivation. Sleep Res 24:37
Laureys S, Peigneux P, Phillips C, Fuchs S, Degueldre C, Aerts J, Del Fiore G, Petiau C, Luxen A, Van der Linden M, Cleeremans A, Smith C, Maquet P (2001) Experience-dependent changes in cerebral functional connectivity during human rapid eye movement sleep. Neuroscience 105:521–525
Lin JS, Luppi PH, Salvert D, Sakai K, Jouvet M (1986) Histamine-containing neurons in the cat hypothalamus. C R Acad Sci 303:371–376
Lin JS, Sakai K, Jouvet M (1988) Evidence for histaminergic arousal mechanisms in the hypothalamus of cats. Neuropharmacology 27:111–122
Lin JS, Kitahama P, Fort P, Panula P, Denny RM, Jouvet M (1993) Histaminergic system in the cat hypothalamus with reference to type B monoamine oxidase. J Comp Neurol 330:405–420
Lin JS, Sakai K, Jouvet M (1994) Hypothalamo-preoptic histaminergic projections in sleep-wake control in the cat. Eur J Neurosci 6:618–625
Lu J, Bjorkum AA, Xu M, Gaus SE, Shiromani PJ, Saper CB (2002) Selective activation of the extended ventrolateral preoptic nucleus during rapid eye movement sleep. J Neurosci 22:4568–4576
Luebke JI, Greene RW, Semba K, Kamondi A, McCarley RW, Reiner PB (1992) Serotonin hyper-polarizes cholinergic low threshold burst neurons in the rat laterodorsal tegmental nucleus in vitro. Proc Natl Acad Sci U S A 89:743–747
Madsen PL, Holm S, Vorstrup S, Friberg L, Lassen NA, Wildschiodtz G (1991) Human regional cerebral blood flow during rapid-eye-movement sleep. J Cereb Blood Flow Metab 11:502–507
Maquet P (1997) Positron emission tomography studies of sleep and sleep disorders. J Neurol 244[Suppll]:S23–S28
Maquet P (1999) Brain mechanisms of sleep: contribution of neuroimaging techniques. J Psychopharmcol 13[Suppl 1]:S25–S28
Maquet P (2000) Functional neuroimaging of normal human sleep by positron emission tomography. J Sleep Res 9:207–231
Maquet P, Phillips C (1998) Functional brain imaging of human sleep. J Sleep Res 7[Suppl 1]: 42–47
Maquet P, Dive D, Salmon E, Sadzot B, Franco G, Poirrier R, von Frenckell R, Franck G (1990) Cerebral glucose utilization during sleep-wake cycle in man determined by positron emission tomography and [18F]2-fluoro-2-deoxy-D-glucose method. Brain Res 513:136–143
Maquet P, Dive D, Salmon E, Sadzot B, Franco G, Poirrier R, Franck G (1992) Cerebral glucose utilization during stage 2 sleep in man. Brain Res 571:149–153
Maquet P, Peters J, Aerts J, Delfiore G, Degueldre C, Luxen A, Franck G (1996) Functional neuroanatomy of human rapid-eye-movement sleep and dreaming. Nature 383:163–166
Maquet P, Laureys S, Peigneux P, Fuchs S, Petiau C, Phillips C, Aerts J, del Fiore G, Degueldre C, Meulemans T, Luxen A, Franck G, Van der Linden M, Smith C, Cleeremans A (2000) Experience-dependent changes in cerebral activation during human REM sleep. Nature Neurosci 3: 831–836
Massaquoi SG, McCarley RW (1992) Extension of the limit cycle reciprocal interaction model of REM cycle control: an integrated sleep control model. J Sleep Res 1:138–143
McCarley RW, Hobson JA (1975) Neuronal excitability modulation over the sleep cycle: a structural and mathematical model. Science 189:58–60
McCarley RW, Massaquoi SG (1986) A limit cycle mathematical model of the REM sleep oscillator system. Am J Physiol 251:R1011–R1029
McCormick DA (1990) Cellular mechanisms of cholinergic control of neocortical and thalamic neuronal excitability. In: Steriade M, Biesold D (eds) Brain cholinergic systems. Oxford University Press, Oxford
McCormick DA, Williamson A (1991) Modulation of neuronal firing mode in cat and guinea pig LGN by histamine: possible cellular mechanisms of histaminergic control of arousal. J Neurosci 11:3188–3199
McGinty D, Harper RW (1976) Dorsal raphe neurons: depression of firing during sleep in cats. Brain Res 101:569–575
Metherate R, Cox CL, Ashe JH (1992) Cellular bases of neocortical activation: modulation of neural oscillations by the nucleus basalis and endogenous acetylcholine. J Neurosci 12:4701–4711
Meyer JS, Hayman LA, Amano T, Nakajima S, Shaw T, Lauzon P, Derman S, Karacan I, Harati Y (1981) Mapping local blood flow of human brain by CT scanning during stable xenon inhalation. Stroke 12:426–436
Michaud M, Soucy JP, Chabli A, Lavinge G, Montplaisir J (2002) SPECT imaging of striatal pre-and postsynaptic dopaminergic status in restless legs syndrome with periodic leg movements in sleep. J Neurol 249:164–170
Monti JM (1993) Involvement of histamine in the control of the waking state. Life Sci 53:1331–1338
Moore RY, Weis R, Moga MM (2000) Efferent projections of the intergeniculate leaflet and the ventral lateral geniculate nucleus in the rat. J Comp Neurol 420:398–418
Morrison AR, Bowker RM (1975) The biological significance of P60 spikes in the sleeping cat. Acta Neurobiol Exp 35:821–840
Morrison AR, Sanford LD, Ross RJ (1999) Initiation of rapid eye movement sleep: beyond the brainstem. In: Mallcik BN, Inoue S (eds) Rapid eye movement sleep. Dekker, New York
Nofzinger EA, Mintun MA, Wiseman MB, Kupfer DJ, Moore RY (1997) Forebrain activation in REM sleep: an FDG PET study. Brain Res 770:192–201
Nofzinger EA, Mintun MA, Price J, Meltzer CC, Townsend D, Buysse DJ, Reynolds CF, Dachille M, Matzzie J, Kupfer DJ, Moore RY (1998) A method for the assessment of the functional neuroanatomy of human sleep using FDG PET. Brain Res Prot 2:191–198
Nofzinger EA, Nichols TE, Meltzer CC, Price J, Steppe DA, Miewald JM, Kupfer DJ, Moore RY (1999) Changes in forebrain function from waking to REM sleep in depression: preliminary analyses of [18F] FDG PET studies. Psychiatry Res Neuroimaging 91:59–78
Nofzinger EA, Price JC, Meltzer CC, Buysse DJ, villemagne VL, Miewald JM, Sembrat RC, Steppe DA, Kupfer DJ (2000) Towards a neurobiology of dysfunctional arousal in depression: the relationship between beta EEG power and regional cerebral glucose metabolism during NREM sleep. Psychiatry Res Neuroimaging 98:71–91
Nofzinger EA, Berman S, Fasiczka A, Miewald JM, Meltzer CC, Price JC, Sembrat RC, Wood A, Thase ME (2001) Effects of bupropion SR on anterior paralimbic function during waking and REM sleep in depression: preliminary findings using [18F]-FDG PET. Psychiatry Res 106:95–111
Nofzinger EA, Buysse DJ, Miewald JM, Meltzer CC, Price JC, Sembrat RC, Ombao H, Reynolds CF, Monk TH, Hall M, Kupfer DJ, Moore RY (2002) Human regional cerebral glucose metabolism during non-rapid eye movement sleep in relation to waking. Brain 125:1105–1115
Nofzinger EA, Buysse DJ, Germain A, Carter CS, Luna B, Price JC, Meltzer CC, Miewald JM, Reynolds CF, and Kupfer DJ: Increased activation of anterior paralimbic and executive cortex from waking to REM sleep in depression. Archives of General Psychiatry, (in press)
Nose I, Ookawa T, Tanaka J, Yamamoto T, Uchimura N, Maeda H, Kuwahara H (2002) Decreased blood flow of the left thalamus during somnolent episodes in a case of recurrent hypersomnia. Psychiatry Clin Neurosci 56:277–278
Okamura N, Yanai K, Higuchi M, Sakai J, Iwata R, Ido T, Sasaki H, Watanabe T, Itoh M (2000) Functional neuroimaging of cognition impaired by a classical antihistamine, d-chlorpheniramine. Br J Pharmacol 129:115–123
Otte A, Nofzinger EA, Audenaert K, Goethals E, Dietrich AJ (2002) Nuclear medicine asleep in sleep research? Eur J Nucl Med 29:1417–1420
Otte A, Audenaert K, Nofzinger EA, Dierckx RA (2003) Brain SPECT in sleep research. Sleep 26: 227
Panula P, Pirvola U, Auvinen S, Airaksinen MS (1989) Histamine-immunoreactive fibers in the rat brain. Neuroscience 28:585–610
Paus T, Jech R, Thompson CJ, Comeau R, Peters T, Evans AC (1997) Transcranial magnetic stimulation during positron emission tomography: a new method for studying connectivity of the human cerebral cortex. J Neurosci 17:3178–3184
Paus T, Koski L, Caramanos Z, Westbury C (1998) Regional differences in the effects of task difficulty and motor output on blood flow response in the human anterior cingulate cortex: a review of 107 PET activation studies. Neuroreport 9:R37–R47
Peigneux P, Laureys S, Fuchs S, Delbeuck X, Degueldre C, Aerts J, Delfiore G, Luxen A, Maquet P (2001) Generation of rapid eye movements during paradoxical sleep in humans. Neuroimage 14:701–708
Perani D, Cortelli P, Lucignani G, Montagna P, Tinuper P, Gallassi R, Gambetti P, Lenzi GL, Lugaresi E, Fazio F (1993) [18F]FDG PET in fatal familial insomnia: the functional effects of thalamic lesions. Neurology 43:2565–2569
Reinsel RA, Veselis RA, Dnistrian AM, Feshchenko VA, Beattie BJ, Duff MR (2000) Midazolam decreases cerebral blood flow in the left prefrontal cortex in a dose-dependent fashion. Int J Neuropsychopharmacol 3:117–127
Ribeiro S, Goyal V, Mello CV, Pavlides C (1999) Brain gene expression during REM sleep depends on prior waking experience. Learn Mem 6:500–508
Sanford LD, Tejani-Butt SM, Ross RJ, Morrison AR (1995) Amygdaloid control of alerting and behavioral arousal in rats: involvement of serotonergic mechanisms. Arch Ital Biol 134:81–99
Saper CB, Loewy AD (1980) Efferent connections of the parabrachial nucleus in the rat. Brain Res 197:291–317
Saper CB, Sherin JE, Elmquist JK (1997) Role of the ventrolateral preoptic area in sleep induction. In: Hayaishi O, Inoue S (eds) Sleep and sleep disorders: from molecule to behavior. Academic, New York
Saper CB, Chou TC, Scammell TE (2001) The sleep switch: hypothalamic control of sleep and wakefulness. Trends Neurosci 24:726–731
Semba K, Fibiger HC (1992) Afferent connections of the laterodorsal and the pedunculopontine tegmental nuclei in the rat: a retro-and antero-grade transport and immunohistochemical study. J Comp Neurol 323:387–410
Shirakawa S, Takeuchi N, Uchimura N, Ohyama T, Maeda H, Abe T, Ishibashi M, Ohshima Y, Ohshima H (2002) Study of image findings in rapid eye movement sleep behavioural disorder. Psychiatry Clin Neurosci 56:291–292
Shiromani PJ, Gillin JC(1987) Acetylcholine and the regulation of REM sleep: basic mechanisms and clinical implications for affective illness and narcolepsy. Annu Rev Pharmacol Toxicol 27:137–157
Shiromani PJ, Scammell T, Sherin JE, Saper CB (1999) Hypothalamic regulation of sleep. In: Lydic R, Baghdoyan HA (eds) Handbook of behavioral state control: cellular and molecular mechanisms. CRC Press, Boca Raton, pp 311–326
Smith GS, Reynolds CF, Pollock B, Derbyshire S, Nofzinger EA, Dew MA, Houch PR, Milko D, Meltzer CC, Kupfer DJ (1999) Cerebral glucose metabolic response to combined total sleep deprivation and antidepressant treatment in geriatric depression. Am J Psychiatry 156:683–689
Smith MT, Perlis ML, Chengazi VU, Pennington J, Soeffing J, Ryan JM, Giles DE (2002) Neuroimaging of NREM sleep in primary insomnia: a Tc-99-HMPAO single photon emission computed tomography study. Sleep 25:325–335
Staedt J, Stoppe G, Kogler A, Munz D, Riemann H, Emrich D, Ruther E (1993) Dopamine D2 receptor alteration in patients with periodic movements in sleep (nocturnal myoclonus). J Neural Transmitt Gen Sect 93:71–74
Staedt J, Stoppe G, Kogler A, Riemann H, Hajak G, Munz DL, Emrich D, Ruther E (1995a) Nocturnal myoclonus syndrome (periodic movements in sleep) related to central dopamine D2-receptor alteration. Eur Arch Psychiatry Clin Neurosci 245:8–10
Staedt J, Stoppe G, Kogler A, Riemann H, Hajak G, Munz DL, Emrich D, Ruther E (1995b) Single photon emission tomography (SPET) imaging of dopamine D2 receptors in the course of dopamine replacement therapy in patients with nocturnal myoclonus syndrome (NMS). J Neural Transmitt Gen Sect 99:187–193
Steriade M, Buzsaki G (1990) Parallel activation of thalamic and cortical neurons by brainstem and basal forebrain cholinergic systems. In: Steriade M, Biesold D (eds) Brain cholinergic systems, Oxford University Press, Oxford, pp 3–52
Steriade M, McCarley RW (1990) Brainstem mechanisms of dreaming and of disorders of sleep in man. In: Steriade M, McCarley RW (eds) Brainstem control of wakefulness and sleep. Plenum, New York pp 395–482
Sudo Y, Suhara T, Honda Y, Nakajima T, Okubo Y, Suzuki K, Nakashima Y, Yoshikawa K, Okauchi T, Sasaki Y, Matsushita M (1998) Muscarinic cholinergic receptors in human narcolepsy: a PET study. Neurology 51:1297–1302
Szymusiak R (1995) Magnocellular nuclei of the basal forebrain: substrates of sleep and arousal regulation. Sleep 18:478–500
Tandon R, Shipley JE, Taylor S, Greden JF, Eiser A, DeQuardo J, Goodson J (1992) Electroencephalographs sleep abnormalities in schizophrenia: relationship to positive/negative symptoms and prior neuroleptic treatment. Arch Gen Psychiatry 49:185–194
Tashiro M, Mochizuki H, Iwabuchi K, Sakurada Y, Itoh M, Watanabe T, Yanai K (2002) Roles of histamine in regulation of arousal and cognition: functional neuroimaging of histamine HI receptors in human brain. Life Sci 72:409–414
Thomas M, Sing H, Belenky G, Holcomb H, Mayberg H, Dannals R, Wagner H, Thorne D, Popp K, Rowland L, Welsh A, Balwinski S, Redmond D (2000) Neural basis of alertness and cognitive performance impairments during sleepiness. I. Effects of 24 h of sleep deprivation on waking human regional brain activity. J Sleep Res 9:335–352
Volk SA, Kaendler SH, Weber R, Georgi K, Maul F, Hertel A, Pflug B, Hor G (1992) Evaluation of the effects of total sleep deprivation on cerebral blood flow using single photo emission computerized tomography. Acta Psychiatr Scand 86:478–483
Volk SA, Kaendler SH, Hertel A, Maul FD, Manoocheri R, Weber R, Georgi K, Pflug B, Hor G (1997) Can response to partial sleep deprivation in depressed patients be predicted by regional changes of cerebral blood flow? Psychiatry Res 75:67–74
Volkow ND, Wang GJ, Hitzemann R, Fowler JS, Pappas N, Lowrimore P, Burr G, Pascani K, Overall J, Wolf AP (1995) Depression of thalamic metabolism by lorazepam is associated with sleepiness. Neuropsychopharmacology 12:123–132
Wainer BH, Mesulum MM (1990) Ascending cholinergic pathways in the rat brain. In: Steriade M, Biesold D (eds) Brain cholinergic systems. Oxford University Press, Oxford
Weiler MA, Buchsbaum MS, Gillin JC, Tafalla R, Bunney WE (1990) Explorations in the relationship of dream sleep to schizophrenia using positron emission tomography. Neuropsychobiology 23:109–118
Werth E, Achermann P, Borbely AA (1997) Fronto-occipital EEG power gradients in human sleep. J Sleep Res 6:102–112
Williams JA, Reiner PB (1992) Noradrenaline hyperpolarizes cholinergic neurons in rat laterodorsal tegmentum in vitro. Soc Neurosci Abstr 18:975 (abstract)
Wilson MA, McNaughton BL (1994) Reactivation of hippocampal ensemble memories during sleep. Science 265:676–679
Wu JC, Gillin JC, Buchsbaum MS, Hershey T, Hazlett E, Sicotte N, Bunney WE Jr (1991) The effect of sleep deprivation on cerebral glucose metabolic rate in normal humans assessed with positron emission tomography. Sleep 14:155–162
Wu J, Buchsbaum MS, Gillin JC, Tang C, Cadwell S, Wiegand M, Najafi A, Klein E, Hazen K, Bunney WE, Fallon JH, Keator D (1999) Prediction of antidepressant effects of sleep deprivation by metabolic rates in the ventral anterior cingulate and medial prefrontal cortex. Am J Psychiatry 156:1149–1158
Wu JC, Gillin JC, Buchsbaum MS, Hershey T, Johnson JC, Bunney WE Jr (1992) Effect of sleep deprivation on brain metabolism of depressed patients. Am J Psychiatry 149:538–543
Yanai K, Okamura N, Tagawa M, Itoh M, Watanabe T (1999) New findings in pharmacological effects induced by antihistamines: from PET studies to knock-out mice. Clin Exp Allergy 29[Suppl3]:29–36
Zarcone VP, Benson KL (1994) Sleep and schizophrenia. In: Kryger MH, Roth T, Dement WC (eds) Principles and Practice of Sleep Medicine. WB Saunders, Philadelphia
Zoccoli G, Walker AM, Lenzi P, Franzini C (2002) The cerebral circulation during sleep: regulation mechanisms and functional implications. Sleep Med Rev 6:443–455
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Nofzinger, E.A. (2004). Functional Neuroimaging in Sleep Disorders. In: Otte, A., Audenaert, K., Peremans, K., van Heeringen, K., Dierckx, R.A. (eds) Nuclear Medicine in Psychiatry. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-18773-5_26
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