Organization of Brainstem Nuclei
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Distribution of Neurotransmitters in the Sheep Brain
Journal of Reproduction and Fertility Supplement 49, 199-220 Distribution of neurotransmitters in the sheep brain Y. Tillet Laborcttoirede NeuroendocrinologieSexuelle, Station de Physiologiede la Reproductiondes Mammiferes Domestiques, INRA, 37380 Nouzilly, France Although the general organization of the sheep brain is similar to that of other mammals, there are species differences in the fine architecture and neurotransmitter distribution. In sheep, perikarya are generally scattered, unlike the situation in rodents where they are clustered. The same organization is observed in cows and primates. The density of neurones immunoreactive for tyrosine hydroxylase in the dorsorostral diencephalon of sheep is lower than in rodents; A14 and A15 dopaminergic cell groups do not present a dorsal part. Only one adrenergic group, C2, is observed in the dorsomedial medulla oblongata. GnRH-immunoreactive neurones are mainly found in the anterior hypothalamic—preoptic areas, a few being present in the mediobasal hypothalamus. The density of several neurones contain- ing neuropeptides (for example vasoactive intestinal polypeptide, cholecystokinin and somatostatin) in the caudal brain of sheep is lower than in other species and in the forebrain of sheep. These differences contribute to different patterns of innervation of brain areas compared with other species. For example, the supra- chiasmatic nucleus does not present a dense network of fibres immunoreactive for 5-hydroxytryptamine and neuropeptide Y as observed in rats. These morphological studies constitute information necessary for further physiological investigations. Introduction In sheep, as in other species, neurotransmitters in the brain are involved in the control of physiological cues through endocrine and autonomic regulation. Among the species used to study endocrine regulation, sheep present interesting and specific physiological characteristics. -
Deconstructing Arousal Into Wakeful, Autonomic and Affective Varieties
Neuroscience Letters xxx (xxxx) xxx–xxx Contents lists available at ScienceDirect Neuroscience Letters journal homepage: www.elsevier.com/locate/neulet Review article Deconstructing arousal into wakeful, autonomic and affective varieties ⁎ Ajay B. Satputea,b, , Philip A. Kragelc,d, Lisa Feldman Barrettb,e,f,g, Tor D. Wagerc,d, ⁎⁎ Marta Bianciardie,f, a Departments of Psychology and Neuroscience, Pomona College, Claremont, CA, USA b Department of Psychology, Northeastern University, Boston, MA, USA c Department of Psychology and Neuroscience, University of Colorado Boulder, Boulder, USA d The Institute of Cognitive Science, University of Colorado Boulder, Boulder, USA e Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA f Department of Radiology, Harvard Medical School, Boston, MA, USA g Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA ARTICLE INFO ABSTRACT Keywords: Arousal plays a central role in a wide variety of phenomena, including wakefulness, autonomic function, affect Brainstem and emotion. Despite its importance, it remains unclear as to how the neural mechanisms for arousal are or- Arousal ganized across them. In this article, we review neuroscience findings for three of the most common origins of Sleep arousal: wakeful arousal, autonomic arousal, and affective arousal. Our review makes two overarching points. Autonomic First, research conducted primarily in non-human animals underscores the importance of several subcortical Affect nuclei that contribute to various sources of arousal, motivating the need for an integrative framework. Thus, we Wakefulness outline an integrative neural reference space as a key first step in developing a more systematic understanding of central nervous system contributions to arousal. -
The Role of the Parabrachial/Kolliker Fuse Respiratory Complex in the Control of Respiration
THE ROLE OF THE PARABRACHIAL/KOLLIKER FUSE RESPIRATORY COMPLEX IN THE CONTROL OF RESPIRATION by JOYCE A. BOON B.Sc. Honors The University of Alberta, 1967 M.Sc. The University of British Columbia, 1970 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in THE FACULTY OF GRADUATE STUDIES ZOOLOGY THE UNIVERSITY OF BRITISH COLUMBIA DECEMBER 2004 ©Joyce A. Boon, 2004 Abstract: My goal was to explore the role of the parabrachial/Kolliker Fuse region (PBrKF) of the pons in the production of "state-related" changes in breathing in rats. I hypothesized that the effects of changes in cortical activation state on breathing and respiratory sensitivity are relayed from the pontine reticular formation to the respiratory centres of the medulla via the PBrKF. I found that urethane anaesthetized Sprague Dawley rats spontaneously cycled between a cortically desynchronized state (State I) and a cortically synchronized state (State III), which were very similar to awake and slow wave sleep (SWS) states in unanaesthetized animals, based on EEG criteria. Urethane produced no significant respiratory depression or reduction in sensitivity to hypoxia or hypercapnia. However, breathing frequency (TR), tidal volume (VT) and total ventilation (V TOT) all increased on cortical activation, and changes in the relative sensitivity to hypoxia and hypercapnia with changes in state were similar to those seen in unanaesthetized rats. This indicated that the urethane model of sleep and wakefulness could be used to investigate the effects of cortical activation state on respiration. Since NMDA-type glutamate receptor mediated processes in the PBrKF are known to be important in respiratory control, I examined the role of the PBrKF as a relay site for state effects on respiration by blocking neurons with NMDA-type glutamate receptors with MK-801. -
Brainstem and Its Associated Cranial Nerves
Brainstem and its Associated Cranial Nerves Anatomical and Physiological Review By Sara Alenezy With appreciation to Noura AlTawil’s significant efforts Midbrain (Mesencephalon) External Anatomy of Midbrain 1. Crus Cerebri (Also known as Basis Pedunculi or Cerebral Peduncles): Large column of descending “Upper Motor Neuron” fibers that is responsible for movement coordination, which are: a. Frontopontine fibers b. Corticospinal fibers Ventral Surface c. Corticobulbar fibers d. Temporo-pontine fibers 2. Interpeduncular Fossa: Separates the Crus Cerebri from the middle. 3. Nerve: 3rd Cranial Nerve (Oculomotor) emerges from the Interpeduncular fossa. 1. Superior Colliculus: Involved with visual reflexes. Dorsal Surface 2. Inferior Colliculus: Involved with auditory reflexes. 3. Nerve: 4th Cranial Nerve (Trochlear) emerges caudally to the Inferior Colliculus after decussating in the superior medullary velum. Internal Anatomy of Midbrain 1. Superior Colliculus: Nucleus of grey matter that is associated with the Tectospinal Tract (descending) and the Spinotectal Tract (ascending). a. Tectospinal Pathway: turning the head, neck and eyeballs in response to a visual stimuli.1 Level of b. Spinotectal Pathway: turning the head, neck and eyeballs in response to a cutaneous stimuli.2 Superior 2. Oculomotor Nucleus: Situated in the periaqueductal grey matter. Colliculus 3. Red Nucleus: Red mass3 of grey matter situated centrally in the Tegmentum. Involved in motor control (Rubrospinal Tract). 1. Inferior Colliculus: Nucleus of grey matter that is associated with the Tectospinal Tract (descending) and the Spinotectal Tract (ascending). Tectospinal Pathway: turning the head, neck and eyeballs in response to a auditory stimuli. 2. Trochlear Nucleus: Situated in the periaqueductal grey matter. Level of Inferior 3. -
Qt59x2b1ds.Pdf
UCLA UCLA Previously Published Works Title Efferent projections of excitatory and inhibitory preBötzinger Complex neurons. Permalink https://escholarship.org/uc/item/59x2b1ds Journal The Journal of comparative neurology, 526(8) ISSN 0021-9967 Authors Yang, Cindy F Feldman, Jack L Publication Date 2018-06-01 DOI 10.1002/cne.24415 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Received: 28 September 2017 | Revised: 4 February 2018 | Accepted: 9 February 2018 DOI: 10.1002/cne.24415 RESEARCH ARTICLE Efferent projections of excitatory and inhibitory preBotzinger€ Complex neurons Cindy F. Yang | Jack L. Feldman Department of Neurobiology, David Geffen School of Medicine, UCLA, Los Angeles, Abstract California 90095-1763 The preBotzinger€ Complex (preBotC),€ a compact medullary region essential for generating normal breathing rhythm and pattern, is the kernel of the breathing central pattern generator (CPG). Exci- Correspondence tatory preBotC€ neurons in rats project to major breathing-related brainstem regions. Here, we Jack L. Feldman, Box 951763, Department € of Neurobiology, David Geffen School of provide a brainstem connectivity map in mice for both excitatory and inhibitory preBotC neurons. Medicine, UCLA, Los Angeles, Using a genetic strategy to label preBotC€ neurons, we confirmed extensive projections of preBotC€ CA 90095-1763. excitatory neurons within the brainstem breathing CPG including the contralateral preBotC,€ Email: [email protected] Botzinger€ Complex (BotC),€ ventral respiratory group, nucleus of the solitary tract, parahypoglossal € € Funding information nucleus, parafacial region (RTN/pFRG or alternatively, pFL/pFV), parabrachial and Kolliker-Fuse A.P. Giannini Foundation and the National nuclei, as well as major projections to the midbrain periaqueductal gray. -
Parabrachial Complex: a Hub for Pain and Aversion
The Journal of Neuroscience, October 16, 2019 • 39(42):8225–8230 • 8225 Mini-Symposium Parabrachial Complex: A Hub for Pain and Aversion Michael C. Chiang,1 Anna Bowen,2 Lindsey A. Schier,3 Domenico Tupone,4,6 Olivia Uddin,5 and Mary M. Heinricher6,7 1Department Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania, 15213, 2Graduate Program in Neuroscience, University of Washington, Seattle, Washington, 98195, 3Department Biological Sciences, University of Southern California, Los Angeles, California, 90089, 4Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy, 5Department of Anatomy and Neurobiology, University of Maryland, Baltimore, Maryland, 21201, 6Department Neurological Surgery, Oregon Health and Science University, Portland, Oregon, 97239, and 7Department Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon, 97239 The parabrachial nucleus (PBN) has long been recognized as a sensory relay receiving an array of interoceptive and exteroceptive inputs relevant to taste and ingestive behavior, pain, and multiple aspects of autonomic control, including respiration, blood pressure, water balance, and thermoregulation. Outputs are known to be similarly widespread and complex. How sensory information is handled in PBN and used to inform different outputs to maintain homeostasis and promote survival is only now being elucidated. With a focus on taste and ingestive behaviors, pain, and thermoregulation, this review is intended to provide a context for analysis of PBN circuits -
NIH Public Access Author Manuscript Neuromodulation
NIH Public Access Author Manuscript Neuromodulation. Author manuscript; available in PMC 2015 June 01. NIH-PA Author ManuscriptPublished NIH-PA Author Manuscript in final edited NIH-PA Author Manuscript form as: Neuromodulation. 2014 June ; 17(4): 312–319. doi:10.1111/ner.12141. Surgical Neuroanatomy and Programming in Deep Brain Stimulation for Obsessive Compulsive Disorder Takashi Morishita, M.D., Ph.D.1, Sarah M. Fayad, M.D.2, Wayne K. Goodman, M.D.3, Kelly D. Foote, M.D.1, Dennis Chen, B.S.2, David A. Peace, M.S., CMI1, Albert L. Rhoton Jr.1, and Michael S. Okun, M.D.1,2 1Department of Neurosurgery, University of Florida College of Medicine/Shands Hospital, Center for Movement Disorders and Neurorestoration, McKnight Brain Institute, Gainesville, FL Corresponding Author: Takashi Morishita, M.D., Ph.D., Department of Neurosurgery, Mcknight Brain Institute Room L2-100, 1149 South Newell Drive, Gainesville, FL 32611, 352-273-9000, 352-392-8413 FAX, [email protected]. Authorship Statement: Drs. Morishita and Okun deigned and conducted the study, including patient recruitment, data collection and data analysis. Drs. Morishita and Fayad prepared the manuscript draft with important intellectual input from Drs. Okun, Rhoton, Goodman and Foote. Mr. Peace provided his illustration into this manuscript. Mr. Chen contributed to collect the data. All authors approved the final manuscript. Author disclosures 1. Takashi Morishita, M.D., Ph.D. Disclosures: Dr. Morishita has received grant support from Nakatomi foundation, St. Luke’s Life Science Institute of Japan, and Japan Society for Promotion of Science in Japan. 2. Sarah M. -
The Three-Dimensional Architecture of the Internal Capsule of the Human Brain Demonstrated by Fiber Dissection Technique
ARS Medica Tomitana - 2014; 3(78): 115 -122 10.2478/arsm-2014-0021 Goga Cristina1,2,3, Brinzaniuc Klara1, Florian I.S.2, Rodriguez Mena R.3 The three-dimensional architecture of the internal capsule of the human brain demonstrated by fiber dissection technique 1. University of Medicine and Pharmacy Tirgu Mures, Tirgu Mures, Romania, Department of Anatomy 2. Cluj County Emergency Hospital, Cluj Napoca, Romania, Department of Neurosurgery 3. Yeditepe University School of Medicine, Istanbul, Turkey, Department of Neurosurgery ABSTRACT Introduction The fiber dissection technique involves peeling away white matter fiber tracts of the brain to display its three-dimensional anatomic arrangement. The intricate three-dimensional configuration and structure of the internal capsule (IC) is not well defined. By using The white matter of the brain consists of the fiber dissection technique, our aim was to expose bundles of myelinated nerve fibers known as and study the IC to achieve a clearer conception of its fascicles or fiber tracts. There are three groups of configuration and relationships with neighboring white nerve fibers: association, connection and projection matter fibers and central nuclei. fibers. Association fibers connect neighboring The lateral and medial aspects of the temporal lobes of and distal cortical region in the same hemisphere. twenty, previously frozen, formalin-fixed human brains Commissural fibers connect homologues regions in were dissected under the operating microscope using the two hemispheres. Projection fibers connect the the fiber dissection technique. The details of the three-dimensional arrangement of the cerebral cortex with subcortical structures such as fibers within the IC were studied and a comprehensive thalamus, basal ganglia, brainstem and spinal cord. -
Enkephalin Systems in Diencephalon and Brainstem of the Rat
THE JOURNAL OF COMPARI1TIVE NEUROLOGY 220:310-320 (19113) Enkephalin Systems in Diencephalon and Brainstem of the Rat HENRY KHACHATURIAN, MICHAEL E. LEWIS, AND STANLEY J. WATSON Mental Health Research Institute, University of Michigan, Ann Arbor, Michigan 48105 ABSTRACT The immunocytochemical distribution of [Leulenkephalin and an adre- nal enkephalin precursor fragment (BAM-22P)immunoreactivity was inves- tigated in the diencephalon and brainstem of rats pretreated with relatively high doses of colchicine (300-400 pgil0 pl intracerebroventricularly). The higher ranges of colchicine pretreatment allowed the visualization of exten- sive enkephalincontaining systems in these brain regions, some of which are reported for the first time. Immunoreactive perikarya were found in many hypothalamic and thalamic nuclei, interpeduncular nucleus, substan- tia nigra, the colliculi, periaqueductal gray, parabrachial nuclei, trigeminal motor and spinal nuclei, nucleus raphe magnus and other raphe nuclei, nu- cleus reticularis paragigantocellularis, vestibular nuclei, several nor- adrenergic cell groups, nucleus tractus solitarius, as well as in the spinal cord dorsal horn. In addition to the above regions, immunoreactive fibers were also noted in the habenular nuclei, trigeminal sensory nuclei, locus coeruleus, motor facial nucleus, cochlear nuclei, dorsal motor nucleus of the vagus, and hypoglossal nucleus. When adjacent sections to those stained for Peulenkephalin were processed for BAM-22P immunoreactivity, it was found that these two immunoreactivities were distributed identically at almost all anatomical locations. BAM-22P immunoreactivity was generally less pronounced and was preferentially localized to neuronal perikarya. The results of the present as well as the preceding studies (Khachaturian et al., '83) strongly suggest substantial structural similarity between the adrenal proenkephalin precursor and that which occurs in the brain. -
Morphological and Physiological Evidence of a Synaptic Connection
Liu et al. Journal of Biomedical Science (2015) 22:79 DOI 10.1186/s12929-015-0179-2 RESEARCH Open Access Morphological and physiological evidence of a synaptic connection between the lateral parabrachial nucleus and neurons in the A7 catecholamine cell group in rats Chia-Yi Liu1,2†, Meng-Lam Lee3,4†, Chi-Sheng Yang5, Chuan-Mu Chen1,6, Ming-Yuan Min7 and Hsiu-Wen Yang3,4* Abstract Background: The descending noradrenergic (NAergic) system is one of the important endogenous analgesia systems. It has been suggested that noxious stimuli could activate descending NAergic system; nevertheless, the underlying neuronal circuit remains unclear. As NAergic neurons in the A7 catecholamine cell group (A7) are a part of the descending NAergic system and the lateral parabrachial nucleus (LPB) is an important brainstem structure that relays ascending nociceptive signal, we aimed to test whether LPB neurons have direct synaptic contact with NAergic A7 neurons. Results: Stereotaxic injections of an anterograde tracer, biotinylated dextran-amine (BDA), were administered to LPB in rats. The BDA-labeled axonal terminals that have physical contacts with tyrosine hydroxylase-positive (presumed noadrenergic) neurons were identified in A7. Consistent with these morphological observations, the excitatory synaptic currents (EPSCs) were readily evoked in NAergic A7 neurons by extracellular stimulation of LPB. The EPSCs evoked by LPB stimulation were blocked by CNQX, a non-NMDA receptor blocker, and AP5, a selective NMDA receptor blocker, showing that LPB-A7 synaptic transmission is glutamatergic. Moreover, the amplitude of LPB-A7 EPSCs was significantly attenuated by DAMGO, a selective μ-opioid receptor agonist, which was associated with an increase in paired-pulse ratio. -
The Parabrachial Nucleus in the Rat: an Immunhistochemical Study of Its Forebrain Neural Input
Loyola University Chicago Loyola eCommons Dissertations Theses and Dissertations 1988 The Parabrachial Nucleus in the Rat: An Immunhistochemical Study of Its Forebrain Neural Input Margaret M. Moga Loyola University Chicago Follow this and additional works at: https://ecommons.luc.edu/luc_diss Part of the Anatomy Commons Recommended Citation Moga, Margaret M., "The Parabrachial Nucleus in the Rat: An Immunhistochemical Study of Its Forebrain Neural Input" (1988). Dissertations. 2681. https://ecommons.luc.edu/luc_diss/2681 This Dissertation is brought to you for free and open access by the Theses and Dissertations at Loyola eCommons. It has been accepted for inclusion in Dissertations by an authorized administrator of Loyola eCommons. For more information, please contact [email protected]. This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License. Copyright © 1988 Margaret M. Moga THE PARABRACHIAL NUCLEUS IN THE RAT: AN IMMUNHISTOCHEMICAL STUDY OF ITS FOREBRAIN NEURAL INPUT By Margaret M.\Moga A Dissertation Submitted to the Faculty of the Graduate School of Loyola University of Chicago in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Hay 1988 ACKNOWLEDGEMENTS I would like to thank my family, especially my mother, for their tremendous support during this venture; my advisor, Dr. Thackery S. Gray, for his support and advice; my co-workers, Andrea Zardetto-Smith and Debra Magnuson, for their help, and my lab-mates at the University of Chicago, Karen Hurley, Rodney Holmes, Horst Herbert, Quan Ha and Chris Breder, for their friendship and interest. I would also like to thank my committee members, Dr. -
Parabrachial Internal Lateral Neurons Convey Nociceptive Messages from the Deep Laminas of the Dorsal Horn to the Intralaminar Thalamus
The Journal of Neuroscience, March 15, 2001, 21(6):2159–2165 Parabrachial Internal Lateral Neurons Convey Nociceptive Messages from the Deep Laminas of the Dorsal Horn to the Intralaminar Thalamus Laurence Bourgeais, Le´ naı¨c Monconduit, Luis Villanueva, and Jean-Franc¸ ois Bernard Institut National de la Sante´ et de la Recherche Me´ dicale U-161, F-75014 Paris, France This study investigates the physiological properties of parabra- which in turn projects to the prefrontal cortex. Recent clinical chial internal lateral (PBil) neurons that project to the paracen- imaging studies showed the important participation of prefron- tral thalamic (PC) nucleus using antidromic activation and tal cortex in emotional response to pain. This spino–PBil–PC single-unit recording techniques in anesthetized rat. We re- pathway may explain how nociceptive messages reach the ported here that most of these neurons responded exclusively prefrontal cortex and thus trigger unbearable aversive aspects to the nociceptive stimulation of large receptive fields with a of pain. sustained firing that often outlasted the stimulus up to several minutes. These responses were depressed by intravenous Key words: parabrachial area; thalamus; intralaminar nuclei; morphine. paracentral nucleus; dorsal horn; nociception Our results demonstrated a novel spino–PBil–PC pathway, which transmits nociceptive messages to the PC nucleus, Old clinical reports (Freeman and Watts, 1948), as well as more V/VI of the spinal cord (Kitamura et al., 1993; Bernard et al., recent brain imaging studies (Rainville et al., 1997), demon- 1995; Feil and Herbert, 1995); it projects to the PC and to a lesser strated that the prefrontal cortex plays an important role in the extent in other intralaminar thalamic nuclei (see also Fulwiler processing of aversive component of pain.