Descending pathways from the paraventricular nucleus contribute to the recruitment of brainstem nuclei following a systemic immune challenge

[1]  T. Day,et al.  Systemic administration of interleukin‐1β activates select populations of central amygdala afferents , 2002, The Journal of comparative neurology.

[2]  S. Hardy Hypothalamic projections to cardiovascular centers of the medulla , 2001, Brain Research.

[3]  Henrique Sequeira,et al.  Activation of ventrolateral medullary neurons projecting to spinal autonomic areas after chemical stimulation of the central nucleus of amygdala: a neuroanatomical study in the rat , 2001, Brain Research.

[4]  C. Dayas,et al.  Dorsal and Ventral Medullary Catecholamine Cell Groups Contribute Differentially to Systemic Interleukin-1β-Induced Hypothalamic Pituitary Adrenal Axis Responses , 2001, Neuroendocrinology.

[5]  G. Chrousos,et al.  The sympathetic nerve--an integrative interface between two supersystems: the brain and the immune system. , 2000, Pharmacological reviews.

[6]  F. Torrealba,et al.  Anatomical substrate for separate processing of ascending and descending visceral information in the nucleus of the solitary tract of the rat , 2000, Brain Research.

[7]  J. Coote,et al.  Identification of branching paraventricular neurons of the hypothalamus that project to the rostroventrolateral medulla and spinal cord , 2000, Neuroscience.

[8]  C. Saper,et al.  Lipopolysaccharide Activates Specific Populations of Hypothalamic and Brainstem Neurons That Project to the Spinal Cord , 2000, The Journal of Neuroscience.

[9]  M. Palkovits,et al.  Decussations of the descending paraventricular pathways to the brainstem and spinal cord autonomic centers , 1999, The Journal of comparative neurology.

[10]  C. Bergamaschi,et al.  Rostral ventrolateral medulla : A source of sympathetic activation in rats subjected to long-term treatment with L-NAME. , 1999, Hypertension.

[11]  T. Day,et al.  The central amygdala modulates hypothalamic–pituitary–adrenal axis responses to systemic interleukin-1β administration , 1999, Neuroscience.

[12]  R. Stornetta,et al.  Distribution of glutamic acid decarboxylase mRNA‐containing neurons in rat medulla projecting to thoracic spinal cord in relation to monoaminergic brainstem neurons , 1999, The Journal of comparative neurology.

[13]  J. Coote,et al.  Identification of an efferent projection from the paraventricular nucleus of the hypothalamus terminating close to spinally projecting rostral ventrolateral medullary neurons , 1999, Neuroscience.

[14]  T. Lundeberg,et al.  Activation of Vagal Afferents after Intravenous Injection of Interleukin-1β: Role of Endogenous Prostaglandins , 1998, The Journal of Neuroscience.

[15]  A. Shafton,et al.  Neurons in the hypothalamic paraventricular nucleus send collaterals to the spinal cord and to the rostral ventrolateral medulla in the rat , 1998, Brain Research.

[16]  Xu,et al.  Indomethacin Attenuates Oxytocin and Hypothalamic‐Pituitary‐Adrenal Axis Responses to Systemic Interleukin‐1β , 1998, Journal of neuroendocrinology.

[17]  F. Portillo,et al.  Separate populations of neurons within the paraventricular hypothalamic nucleus of the rat project to vagal and thoracic autonomic preganglionic levels and express c-Fos protein induced by lithium chloride , 1998, Journal of Chemical Neuroanatomy.

[18]  S. Maier,et al.  Vagal Paraganglia Bind Biotinylated Interleukin-1 Receptor Antagonist: A Possible Mechanism for Immune-to-Brain Communication , 1997, Brain Research Bulletin.

[19]  P. Sawchenko,et al.  Evidence for an Intramedullary Prostaglandin-Dependent Mechanism in the Activation of Stress-Related Neuroendocrine Circuitry by Intravenous Interleukin-1 , 1997, The Journal of Neuroscience.

[20]  J. Deniau,et al.  Effect of electrical stimulation of the cerebral cortex on the expression of the fos protein in the basal ganglia , 1997, Neuroscience.

[21]  C. Saper,et al.  Intravenous lipopolysaccharide induces cyclooxygenase 2‐like immunoreactivity in rat brain perivascular microglia and meningeal macrophages , 1997, The Journal of comparative neurology.

[22]  H. Kawano,et al.  Synaptic contacts of substance P-immunoreactive axon terminals in the nucleus tractus solitarius onto neurons projecting to the caudal ventrolateral medulla oblongata in the rat , 1997, Brain Research.

[23]  Y. Ishizuka,et al.  Effects of area postrema lesion and abdominal vagotomy on interleukin-1β-induced norepinephrine release in the hypothalamic paraventricular nucleus region in the rat , 1997, Neuroscience Letters.

[24]  R. Dantzer,et al.  Mechanisms of sickness-induced decreases in food-motivated behavior , 1996, Neuroscience & Biobehavioral Reviews.

[25]  H. Kawano,et al.  Neurons in the caudal ventrolateral medulla projecting to the paraventricular hypothalamic nucleus receive synaptic inputs from the nucleus of the solitary tract: a light and electron microscopic double-labeling study in the rat , 1996, Neuroscience Letters.

[26]  Yasuyoshi Watanabe,et al.  Endothelial cells of the rat brain vasculature express cyclooxygenase-2 mRNA in response to systemic interleukin-1β: a possible site of prostaglandin synthesis responsible for fever , 1996, Brain Research.

[27]  J. Pieper,et al.  Subdiaphragmatic vagotomy inhibits intra-abdominal interleukin-1β stimulation of adrenocorticotropin secretion , 1996, Brain Research.

[28]  C. Saper,et al.  Expression of inducible cyclooxygenase mRNA in the mouse brain after systemic administration of bacterial lipopolysaccharide , 1996, Brain Research.

[29]  P. Sawchenko,et al.  Distinct mechanisms underlie activation of hypothalamic neurosecretory neurons and their medullary catecholaminergic afferents in categorically different stress paradigms. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[30]  Y. Ueta,et al.  Activation of sympathetic outflow by recombinant human interleukin-1 beta in conscious rats. , 1996, The American journal of physiology.

[31]  H. D. de Vries,et al.  Interleukin‐1 receptors on rat brain endothelial cells: a role in neuroimmune interaction? , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[32]  H. Besedovsky,et al.  Immune-neuro-endocrine interactions: facts and hypotheses. , 1996, Endocrine reviews.

[33]  S. Maier,et al.  Interleukin-1β induced corticosterone elevation and hypothalamic NE depletion is vagally mediated , 1995, Brain Research Bulletin.

[34]  D. W. Smith,et al.  Role of ventrolateral medulla catecholamine cells in hypothalamic neuroendocrine cell responses to systemic hypoxia , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  P. Sawchenko,et al.  Type 1 interleukin‐1 receptor in the rat brain: Distribution, regulation, and relationship to sites of IL‐1–induced cellular activation , 1995, The Journal of comparative neurology.

[36]  R. Gaykema,et al.  Subdiaphragmatic vagotomy suppresses endotoxin-induced activation of hypothalamic corticotropin-releasing hormone neurons and ACTH secretion. , 1995, Endocrinology.

[37]  G. Aston-Jones,et al.  Evidence that cholera toxin B subunit (CTb) can be avidly taken up and transported by fibers of passage , 1995, Brain Research.

[38]  N. Rothwell,et al.  Cytokines and the nervous system II: actions and mechanisms of action , 1995, Trends in Neurosciences.

[39]  N. Rothwell,et al.  Cytokines and the nervous system I: expression and recognition , 1995, Trends in Neurosciences.

[40]  A. Strack,et al.  Systemic endotoxin induces Fos-like immunoreactivity in rat spinal sympathetic regions. , 1995, Journal of the autonomic nervous system.

[41]  P. Sawchenko,et al.  A1 catecholamine cell group: Fine structure and synaptic input from the nucleus of the solitary tract , 1995, The Journal of comparative neurology.

[42]  M. Satoh,et al.  Localization of type I interleukin-1 receptor mRNA in the rat brain. , 1994, Brain research. Molecular brain research.

[43]  M. Wong,et al.  Localization of interleukin 1 type I receptor mRNA in rat brain. , 1994 .

[44]  H. Nakane,et al.  An Interleukin-1β-Induced Noradrenaline Release in the Spleen Is Mediated by Brain Corticotropin-Releasing Factor: An in Vivo Microdialysis Study in Conscious Rats , 1994, Brain, Behavior, and Immunity.

[45]  P. Sawchenko,et al.  A functional anatomical analysis of central pathways subserving the effects of interleukin-1 on stress-related neuroendocrine neurons , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  Shwun‐De Wang,et al.  Immunohistochemical study of catecholamine enzymes and neuropeptide Y (NPY) in the rostral ventrolateral medulla and bulbospinal projection , 1993, The Journal of comparative neurology.

[47]  A. D. Smith,et al.  Monosynaptic projections from the rostral ventrolateral medulla oblongata to identified sympathetic preganglionic neurons , 1993, Neuroscience.

[48]  Doug W. Smith,et al.  Neurochemical identification of fos-positive neurons using two-colour immunoperoxidase staining , 1993, Journal of Neuroscience Methods.

[49]  C. Saper,et al.  Endogenous pyrogens in the CNS: role in the febrile response. , 1992, Progress in brain research.

[50]  W. Banks,et al.  Human interleukin (IL) 1 alpha, murine IL-1 alpha and murine IL-1 beta are transported from blood to brain in the mouse by a shared saturable mechanism. , 1991, The Journal of pharmacology and experimental therapeutics.

[51]  S. Rivest,et al.  Influence of the paraventricular nucleus of the hypothalamus in the alteration of neuroendocrine functions induced by intermittent footshock or interleukin. , 1991, Endocrinology.

[52]  T. Hori,et al.  Central administration of interferon-α enhances rat sympathetic nerve activity to the spleen , 1991, Neuroscience Letters.

[53]  M. Kluger Fever: Role of Pyrogens and Cryogens , 1991, Physiological reviews.

[54]  T. Curran,et al.  Stimulus-transcription coupling in the nervous system: involvement of the inducible proto-oncogenes fos and jun. , 1991, Annual review of neuroscience.

[55]  L. Renaud,et al.  Oxytocin localization and function in the A1 noradrenergic cell group: Ultrastructural and electrophysiological studies , 1990, Neuroscience.

[56]  M. Jouvet,et al.  Iontophoretic application of unconjugated cholera toxin B subunit (CTb) combined with immunohistochemistry of neurochemical substances: a method for transmitter identification of retrogradely labeled neurons , 1990, Brain Research.

[57]  W. Banks,et al.  Bidirectional transport of interleukin-1 alpha across the blood-brain barrier , 1989, Brain Research Bulletin.

[58]  R. Faull,et al.  The use of c-fos as a metabolic marker in neuronal pathway tracing , 1989, Journal of Neuroscience Methods.

[59]  H. Besedovsky,et al.  Neuroendocrine, sympathetic and metabolic responses induced by interleukin-1. , 1989, Neuroendocrinology.

[60]  T. Curran,et al.  Expression of c-fos protein in brain: metabolic mapping at the cellular level. , 1988, Science.

[61]  H. Besedovsky,et al.  Corticotropin-releasing factor-producing neurons in the rat activated by interleukin-1. , 1987, Science.

[62]  R. Sapolsky,et al.  Interleukin-1 stimulates the secretion of hypothalamic corticotropin-releasing factor. , 1987, Science.

[63]  A. Arimura,et al.  Interleukin-1 stimulates ACTH release by an indirect action which requires endogenous corticotropin releasing factor. , 1987, Endocrinology.

[64]  Michel Jouvet,et al.  Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer , 1987, Brain Research.

[65]  D. Reis,et al.  Projections from the nucleus tractus solitarii to the rostral ventrolateral medulla , 1985, The Journal of comparative neurology.

[66]  E. Sorkin,et al.  Immune-neuroendocrine interactions. , 1985, Journal of immunology.

[67]  P. Luiten,et al.  The course of paraventricular hypothalamic efferents to autonomic structures in medulla and spinal cord , 1985, Brain Research.

[68]  D. Reis,et al.  Rostral ventrolateral medulla: Selective projections to the thoracic autonomic cell column from the region containing C1 adrenaline neurons , 1984, The Journal of comparative neurology.

[69]  D. Pfaff,et al.  Localization of forebrain neurons which project directly to the medulla and spinal cord of the rat by retrograde tracing with wheat germ agglutinin , 1984, The Journal of comparative neurology.

[70]  F E Bloom,et al.  The organization of projections from the cortes, amygdala, and hypothalamus to the nucleus of the solitary tract in rat , 1984, The Journal of comparative neurology.

[71]  P. Voorn,et al.  An immuno-electronmicroscopical study comparing vasopressin, oxytocin, substance P and enkephalin containing nerve terminals in the nucleus of the solitary tract of the rat , 1983, Brain Research.

[72]  R. Schwarcz,et al.  Comparison of ibotenate and kainate neurotoxicity in rat brain: A histological study , 1983, Neuroscience.

[73]  L. Swanson,et al.  The organization of noradrenergic pathways from the brainstem to the paraventricular and supraoptic nuclei in the rat , 1982, Brain Research Reviews.

[74]  I. Kushner THE PHENOMENON OF THE ACUTE PHASE RESPONSE * , 1982, Annals of the New York Academy of Sciences.

[75]  L. Swanson,et al.  Immunohistochemical identification of neurons in the paraventricular nucleus of the hypothalamus that project to the medulla or to the spinal cord in the rat , 1982, The Journal of comparative neurology.

[76]  L. Swanson,et al.  Paraventricular nucleus: a site for the integration of neuroendocrine and autonomic mechanisms. , 1980, Neuroendocrinology.

[77]  H. Kuypers,et al.  The paraventricular nucleus of the hypothalamus: Cytoarchitectonic subdivisions and organization of projections to the pituitary, dorsal vagal complex, and spinal cord as demonstrated by retrograde fluorescence double‐labeling methods , 1980, The Journal of comparative neurology.