Organization of hypocretin/orexin efferents to locus coeruleus and basal forebrain arousal‐related structures

Hypocretin/orexin neurons give rise to an extensive projection system, portions of which innervate multiple regions associated with the regulation of behavioral state. These regions include the locus coeruleus, medial septal area, medial preoptic area, and substantia innominata. Evidence indicates that hypocretin modulates behavioral state via actions within each of these terminal fields. To understand better the circuitry underlying hypocretin‐dependent modulation of behavioral state, the present study characterized the degree to which there exists: 1) lateralization of hypocretin efferents to basal forebrain and brainstem arousal‐related regions, 2) topographic organization of basal forebrain‐ and brainstem‐projecting hypocretin neurons, and 3) collateralization of individual hypocretin neurons to these arousal‐related terminal fields. These studies utilized combined immunohistochemical identification of hypocretin neurons with single or double retrograde tracing from the locus coeruleus, medial preoptic area, medial septal area, and substantia innominata. Results indicate that approximately 80% of hypocretin efferents to basal forebrain regions project ipsilaterally, whereas projections to the locus coeruleus are more bilateral (65%). There was a slight preference for basal forebrain‐projecting hypocretin neurons to be distributed within the medial half of the hypocretin cell group. In contrast, hypocretin neurons projecting to the locus coeruleus were located primarily within the dorsal half of the hypocretin cell group. Finally, a large proportion of hypocretin neurons appear to project simultaneously to at least two of the examined terminal fields. These latter observations suggest coordinated actions of hypocretin across multiple arousal‐related regions. J. Comp. Neurol. 481:160–178, 2005. © 2004 Wiley‐Liss, Inc.

[1]  C. Berridge,et al.  Fos immunoreactivity in hypocretin-synthesizing and hypocretin-1 receptor-expressing neurons: effects of diurnal and nocturnal spontaneous waking, stress and hypocretin-1 administration , 2003, Neuroscience.

[2]  C. Berridge,et al.  Additive wake-promoting actions of medial basal forebrain noradrenergic α1- and β-receptor stimulation. , 2003 .

[3]  C. Berridge,et al.  Circadian-dependent and circadian-independent behavioral actions of hypocretin/orexin , 2002, Brain Research.

[4]  Jun Lu,et al.  Selective Activation of the Extended Ventrolateral Preoptic Nucleus during Rapid Eye Movement Sleep , 2002, The Journal of Neuroscience.

[5]  S. Shioda,et al.  Orexin-1 receptor immunoreactivity in chemically identified target neurons in the rat hypothalamus , 2002, Neuroscience Letters.

[6]  G. Hervieu,et al.  Protein distribution of the orexin-2 receptor in the rat central nervous system , 2002, Regulatory Peptides.

[7]  G. Hervieu,et al.  Orexin receptor‐1 (OX‐R1) immunoreactivity in chemically identified neurons of the hypothalamus: focus on orexin targets involved in control of food and water intake , 2002, The European journal of neuroscience.

[8]  A. Kelley,et al.  Wake-promoting and sleep-suppressing actions of hypocretin (orexin): basal forebrain sites of action , 2001, Neuroscience.

[9]  C. Saper,et al.  Differential expression of orexin receptors 1 and 2 in the rat brain , 2001, The Journal of comparative neurology.

[10]  R. McCarley,et al.  Microdialysis perfusion of orexin-A in the basal forebrain increases wakefulness in freely behaving rats. , 2001, Archives italiennes de biologie.

[11]  P. Shiromani,et al.  Hypocretin receptor protein and mRNA expression in the dorsolateral pons of rats. , 2001, Brain research. Molecular brain research.

[12]  J. Roberts,et al.  Gene expression and protein distribution of the orexin-1 receptor in the rat brain and spinal cord , 2001, Neuroscience.

[13]  C. Berridge,et al.  Differential sensitivity to the wake-promoting actions of norepinephrine within the medial preoptic area and the substantia innominata. , 2001, Behavioral neuroscience.

[14]  R. Szymusiak,et al.  Effects of lateral preoptic area application of orexin‐A on sleep–wakefulness , 2000, Neuroreport.

[15]  Luis de Lecea,et al.  Hypocretin-1 Modulates Rapid Eye Movement Sleep through Activation of Locus Coeruleus Neurons , 2000, The Journal of Neuroscience.

[16]  Michael Aldrich,et al.  Reduced Number of Hypocretin Neurons in Human Narcolepsy , 2000, Neuron.

[17]  C. Saper,et al.  Effect of Lesions of the Ventrolateral Preoptic Nucleus on NREM and REM Sleep , 2000, The Journal of Neuroscience.

[18]  A. Hunter,et al.  The novel brain neuropeptide, orexin‐A, modulates the sleep–wake cycle of rats , 2000, The European journal of neuroscience.

[19]  Sebastiaan Overeem,et al.  Hypocretin (orexin) deficiency in human narcolepsy , 2000, The Lancet.

[20]  E. V. Bockstaele,et al.  Anatomic basis for differential regulation of the rostrolateral peri–locus coeruleus region by limbic afferents , 1999, Biological Psychiatry.

[21]  E. V. Van Bockstaele,et al.  Efferent projections of the nucleus of the solitary tract to peri‐locus coeruleus dendrites in rat brain: Evidence for a monosynaptic pathway , 1999, The Journal of comparative neurology.

[22]  M. I. Smith,et al.  Orexin A activates locus coeruleus cell firing and increases arousal in the rat. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[23]  M. Ghatei,et al.  Distribution and quantification of immunoreactive orexin A in rat tissues , 1999, FEBS letters.

[24]  Emmanuel Mignot,et al.  The Sleep Disorder Canine Narcolepsy Is Caused by a Mutation in the Hypocretin (Orexin) Receptor 2 Gene , 1999, Cell.

[25]  C. Berridge,et al.  Amphetamine acts within the medial basal forebrain to initiate and maintain alert waking , 1999, Neuroscience.

[26]  Jon T. Willie,et al.  Narcolepsy in orexin Knockout Mice Molecular Genetics of Sleep Regulation , 1999, Cell.

[27]  Takeshi Sakurai,et al.  Distribution of orexin neurons in the adult rat brain 1 Published on the World Wide Web on 17 March 1999. 1 , 1999, Brain Research.

[28]  M. Nakazato,et al.  Effect of lateral cerebroventricular injection of the appetite-stimulating neuropeptide, orexin and neuropeptide Y, on the various behavioral activities of rats , 1999, Brain Research.

[29]  T. Sakurai,et al.  Orexins, orexigenic hypothalamic peptides, interact with autonomic, neuroendocrine and neuroregulatory systems. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[30]  A. N. van den Pol,et al.  Neurons Containing Hypocretin (Orexin) Project to Multiple Neuronal Systems , 1998, The Journal of Neuroscience.

[31]  E. V. Van Bockstaele,et al.  Amygdaloid Corticotropin‐Releasing Factor Targets Locus Coeruleus Dendrites: Substrate for the Co‐ordination of Emotional and Cognitive Limbs of the Stress Response , 1998, Journal of neuroendocrinology.

[32]  S. Carr,et al.  Orexins and Orexin Receptors: A Family of Hypothalamic Neuropeptides and G Protein-Coupled Receptors that Regulate Feeding Behavior , 1998, Cell.

[33]  F. Perler,et al.  Protein Splicing of Inteins and Hedgehog Autoproteolysis: Structure, Function, and Evolution , 1998, Cell.

[34]  R C Lin,et al.  Lateralization and functional organization of the locus coeruleus projection to the trigeminal somatosensory pathway in rat , 1997, The Journal of comparative neurology.

[35]  S. Foote,et al.  Enhancement of Behavioral and Electroencephalographic Indices of Waking following Stimulation of Noradrenergic β-Receptors within the Medial Septal Region of the Basal Forebrain , 1996, The Journal of Neuroscience.

[36]  S. Foote,et al.  Modulation of Forebrain Electroencephalographic Activity in Halothane-Anesthetized Rat via Actions of Noradrenergic β-Receptors within the Medial Septal Region , 1996, The Journal of Neuroscience.

[37]  G. Aston-Jones,et al.  Evidence for divergent projections to the brain noradrenergic system and the spinal parasympathetic system from Barrington's nucleus , 1996, Brain Research.

[38]  M Ennis,et al.  Dendrites of locus coeruleus neurons extend preferentially into two pericoerulear zones , 1996, The Journal of comparative neurology.

[39]  E. V. Van Bockstaele,et al.  Corticotropin‐releasing factor‐containing axon terminals synapse onto catecholamine dendrites and may presynaptically modulate other afferents in the rostral pole of the nucleus locus coeruleus in the rat brain , 1996, The Journal of comparative neurology.

[40]  R. McCarley,et al.  Activation of Ventrolateral Preoptic Neurons During Sleep , 1996, Science.

[41]  G. Aston-Jones,et al.  Evidence for widespread afferents to barrington's nucleus, a brainstem region rich in corticotropin-releasing hormone neurons , 1994, Neuroscience.

[42]  Larry W. Swanson,et al.  Brain Maps: Structure of the Rat Brain , 1992 .

[43]  C. L. Cox,et al.  Cellular bases of neocortical activation: modulation of neural oscillations by the nucleus basalis and endogenous acetylcholine , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[44]  B. Mallick,et al.  Different types of norepinephrinergic receptors are involved in preoptic area mediated independent modulation of sleep-wakefulness and body temperature , 1992, Brain Research.

[45]  G. Aston-Jones,et al.  Robust enkephalin innervation of the locus coeruleus from the rostral medulla , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  G. Aston-Jones,et al.  Corticotropin-releasing factor innervation of the locus coeruleus region: Distribution of fibers and sources of input , 1992, Neuroscience.

[47]  Gary Aston-Jones,et al.  The iontophoretic application of Fluoro-Gold for the study of afferents to deep brain nuclei , 1988, Brain Research.

[48]  G. Buzsáki,et al.  Nucleus basalis and thalamic control of neocortical activity in the freely moving rat , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[49]  A I Basbaum,et al.  Wheat germ agglutinin‐apoHRP gold: A new retrograde tracer for light‐ and electron‐microscopic single‐ and double‐label studies , 1987, The Journal of comparative neurology.

[50]  K. Kitahama,et al.  Effects of electrolytic lesion of hypothalamic paraventricular nucleus and its related areas on the sleep waking cycle in the cat. , 1987, Archives italiennes de biologie.

[51]  S. Datta,et al.  Alpha adrenergic system in medial preoptic area involved in sleep-wakefulness in rats , 1986, Brain Research Bulletin.

[52]  P. Goldman-Rakic,et al.  Selective prefrontal cortical projections to the region of the locus coeruleus and raphe nuclei in the rhesus monkey , 1984, Brain Research.

[53]  M. Mesulam,et al.  Central cholinergic pathways in the rat: An overview based on an alternative nomenclature (Ch1–Ch6) , 1983, Neuroscience.

[54]  D. Woodward,et al.  The distribution of neocortical projection neurons in the locus coeruleus , 1983, The Journal of comparative neurology.

[55]  S. Foote,et al.  Corticotropin-releasing factor activates noradrenergic neurons of the locus coeruleus , 1983, Brain Research.

[56]  Dennis A. Steindler,et al.  Locus coerules neurons have axons that branch to the forebrain and cerebellum , 1981, Brain Research.

[57]  F. Bloom,et al.  Impulse activity of locus coeruleus neurons in awake rats and monkeys is a function of sensory stimulation and arousal. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[58]  Virginia M. Pickel,et al.  A serotonergic innervation of noradrenergic neurons in nucleus locus coeruleus: Demonstration by immunocytochemical localization of the transmitter specific enzymes tyrosine and tryptophan hydroxylase , 1977, Brain Research.

[59]  J A Hobson,et al.  Sleep cycle oscillation: reciprocal discharge by two brainstem neuronal groups. , 1975, Science.

[60]  J. Korf,et al.  Bilaterally diverging axon collaterals and contralateral projections from rat locus coeruleus neurons, demonstrated by fluorescent retrograde double labeling and norepinephrine metabolism , 2005, Journal of Neural Transmission.

[61]  D. Menétrey Retrograde tracing of neural pathways with a protein-gold complex , 2004, Histochemistry.

[62]  C. Berridge,et al.  Additive wake-promoting actions of medial basal forebrain noradrenergic alpha1- and beta-receptor stimulation. , 2003, Behavioral neuroscience.

[63]  S. Carr,et al.  Orexins and orexin receptors: a family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior. , 1998, Cell.