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Resting State Connectivity of the Human Habenula at Ultra-High Field
Author’s Accepted Manuscript Resting State Connectivity of the Human Habenula at Ultra-High Field Salvatore Torrisi, Camilla L. Nord, Nicholas L. Balderston, Jonathan P. Roiser, Christian Grillon, Monique Ernst www.elsevier.com PII: S1053-8119(16)30587-0 DOI: http://dx.doi.org/10.1016/j.neuroimage.2016.10.034 Reference: YNIMG13531 To appear in: NeuroImage Received date: 26 August 2016 Accepted date: 20 October 2016 Cite this article as: Salvatore Torrisi, Camilla L. Nord, Nicholas L. Balderston, Jonathan P. Roiser, Christian Grillon and Monique Ernst, Resting State Connectivity of the Human Habenula at Ultra-High Field, NeuroImage, http://dx.doi.org/10.1016/j.neuroimage.2016.10.034 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting galley proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. 1 Resting State Connectivity of the Human Habenula at Ultra-High Field Salvatore Torrisi1, Camilla L. Nord2, Nicholas L. Balderston1, Jonathan P. Roiser2, Christian Grillon1, Monique Ernst1 Affiliations 1 Section on the Neurobiology of Fear and Anxiety, National Institute of Mental Health, Bethesda, MD 2 Neuroscience and Cognitive Neuropsychiatry group, University of College, London, UK Abstract The habenula, a portion of the epithalamus, is implicated in the pathophysiology of depression, anxiety and addiction disorders. -
From Human Emotions to Robot Emotions
1 American Association for Artificial Intelligence – Spring Symposium 3/2004, Stanford University – Keynote Lecture. From Human Emotions to Robot Emotions Jean-Marc Fellous The Salk Institute for Neurobiological Studies 10010 N. Torrey Pines Road, la Jolla, CA 92037 [email protected] Abstract1 open a new window on the neural bases of emotions that may offer new ways of thinking about implementing robot- The main difficulties that researchers face in understanding emotions. emotions are difficulties only because of the narrow- mindedness of our views on emotions. We are not able to Why are emotions so difficult to study? free ourselves from the notion that emotions are necessarily human emotions. I will argue that if animals have A difficulty in studying human emotions is that here are emotions, then so can robots. Studies in neuroscience have significant individual differences, based on experiential as shown that animal models, though having limitations, have well as genetic factors (Rolls, 1998; Ortony, 2002; significantly contributed to our understanding of the Davidson, 2003a, b; Ortony et al., 2004). My fear at the functional and mechanistic aspects of emotions. I will sight of a bear may be very different from the fear suggest that one of the main functions of emotions is to experienced by a park-ranger who has a better sense for achieve the multi-level communication of simplified but high impact information. The way this function is achieved bear-danger and knows how to react. My fear might also be in the brain depends on the species, and on the specific different from that of another individual who has had about emotion considered. -
What Can Be Learned from White Matter Alterations in Antisocial Girls Willeke M
Menks WM, Raschle NM. J Neurol Neuromedicine (2017) 2(7): 16-20 Neuromedicine www.jneurology.com www.jneurology.com Journal of Neurology & Neuromedicine Mini Review Open Access What can be learned from white matter alterations in antisocial girls Willeke M. Menks1, Christina Stadler1 and Nora M. Raschle1 1Department of Child and Adolescent Psychiatry, University of Basel, Psychiatric University Hospital Basel, Switzerland. Article Info ABSTRACT Article Notes Antisocial behavior in youths constitutes a major public health problem Received: June 17, 2017 worldwide. Conduct disorder is a severe variant of antisocial behavior with higher Accepted: July 31, 2017 prevalence rates for boys (12%) as opposed to girls (7%). A better understanding *Correspondence: of the underlying neurobiological mechanisms of conduct disorder is warranted Dr. Willeke Menks, PhD to improve identification, diagnosis, or treatment. Functional and structural Department of Child and Adolescent Psychiatry (KJPK), neuroimaging studies have indicated several key brain regions within the limbic Psychiatric University Clinics Basel (UPK) system and prefrontal cortex that are altered in youths with conduct disorder. Schanzenstrasse 13, CH-4056 Basel, Switzerland Examining the structural connectivity, i.e. white matter fiber tracts connecting Tel. +41 61 265 89 76 these brain areas, may further inform about the underlying neural mechanisms. Fax +41 61 265 89 61 Diffusion tensor imaging (DTI) is a non-invasive technique that can evaluate the © 2017 Menks WM & Raschle NM. This article is distributed white matter integrity of fiber tracts throughout the brain. To date, DTI studies have under the terms of the Creative Commons Attribution 4.0 found several white matter tracts that are altered in youths with conduct disorder. -
Lesions in the Bed Nucleus of the Stria Terminalis Disrupt
Neuroscience 128 (2004) 7–14 LESIONS IN THE BED NUCLEUS OF THE STRIA TERMINALIS DISRUPT CORTICOSTERONE AND FREEZING RESPONSES ELICITED BY A CONTEXTUAL BUT NOT BY A SPECIFIC CUE-CONDITIONED FEAR STIMULUS G. M. SULLIVAN,a* J. APERGIS,b D. E. A. BUSH,b Activation of the hypothalamic–pituitary–adrenal (HPA) L. R. JOHNSON,b M. HOUb AND J. E. LEDOUXb axis, including release of glucocorticoids, is a central com- aDepartment of Psychiatry, Columbia University College of Physicians ponent of the adaptive response to real or anticipated and Surgeons, 1051 Riverside Drive, Unit #41, New York, NY 10032, aversive physical or psychological challenge. Surprisingly USA little is known about the neural circuits by which environ- bCenter for Neural Science, New York University, 4 Washington Place, mental stimuli come to elicit HPA responses. Fear condi- New York, NY 10003, USA tioning, a behavioral model of emotional stress, is poten- tially useful for exploring this issue since the neural path- Abstract —The bed nucleus of the stria terminalis (BNST) is ways by which stimuli initiate fear behaviors and believed to be a critical relay between the central nucleus of associated autonomic responses have been characterized the amygdala (CE) and the paraventricular nucleus of the in detail (LeDoux, 2000; Davis and Whalen, 2001; Maren, hypothalamus in the control of hypothalamic–pituitary– 2001). adrenal (HPA) responses elicited by conditioned fear stimuli. Through fear conditioning an organism learns that a If correct, lesions of CE or BNST should block expression of simple sensory stimulus (a cue), or more complex environ- HPA responses elicited by either a specific conditioned fear mental representation (a context), predicts imminent ad- cue or a conditioned context. -
The Connexions of the Amygdala
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.28.2.137 on 1 April 1965. Downloaded from J. Neurol. Neurosurg. Psychiat., 1965, 28, 137 The connexions of the amygdala W. M. COWAN, G. RAISMAN, AND T. P. S. POWELL From the Department of Human Anatomy, University of Oxford The amygdaloid nuclei have been the subject of con- to what is known of the efferent connexions of the siderable interest in recent years and have been amygdala. studied with a variety of experimental techniques (cf. Gloor, 1960). From the anatomical point of view MATERIAL AND METHODS attention has been paid mainly to the efferent connexions of these nuclei (Adey and Meyer, 1952; The brains of 26 rats in which a variety of stereotactic or Lammers and Lohman, 1957; Hall, 1960; Nauta, surgical lesions had been placed in the diencephalon and and it is now that there basal forebrain areas were used in this study. Following 1961), generally accepted survival periods of five to seven days the animals were are two main efferent pathways from the amygdala, perfused with 10 % formol-saline and after further the well-known stria terminalis and a more diffuse fixation the brains were either embedded in paraffin wax ventral pathway, a component of the longitudinal or sectioned on a freezing microtome. All the brains were association bundle of the amygdala. It has not cut in the coronal plane, and from each a regularly spaced generally been recognized, however, that in studying series was stained, the paraffin sections according to the Protected by copyright. the efferent connexions of the amygdala it is essential original Nauta and Gygax (1951) technique and the frozen first to exclude a contribution to these pathways sections with the conventional Nauta (1957) method. -
Functional Heterogeneity in the Bed Nucleus of the Stria Terminalis
8038 • The Journal of Neuroscience, August 3, 2016 • 36(31):8038–8049 Dual Perspectives Dual Perspectives Companion Paper: Contributions of the Central Extended Amygdala to Fear and Anxiety, by Alexander J. Shackman and Andrew S. Fox Functional Heterogeneity in the Bed Nucleus of the Stria Terminalis Nur Zeynep Gungor and Denis Pare´ Center for Molecular and Behavioral Neuroscience, Rutgers State University, Newark, New Jersey 07102 Early work stressed the differing involvement of the central amygdala (CeA) and bed nucleus of the stria terminalis (BNST) in the genesis of fear versus anxiety, respectively. In 2009, Walker, Miles, and Davis proposed a model of amygdala-BNST interactions to explain these functional differences. This model became extremely influential and now guides a new wave of studies on the role of BNST in humans. Here, we consider evidence for and against this model, in the process highlighting central principles of BNST organization. This analysis leads us to conclude that BNST’s influence is not limited to the generation of anxiety-like responses to diffuse threats, but that it also shapes the impact of discrete threatening stimuli. It is likely that BNST-CeA interactions are involved in modulating responses to such threats. In addition, whereas current views emphasize the contributions of the anterolateral BNST region in anxiety, accumulating data indicate that the anteromedial and anteroventral regions also play a critical role. The presence of multiple functional subregions within the small volume of BNST raises significant technical obstacles for functional imaging studies in humans. Key words: amygdala; anxiety; BNST; fear Introduction et al., 2003; Xu et al., 2012), and alarm pheromones (Breitfeld In 2009, Walker et al. -
Spinal Cord Organization
Lecture 4 Spinal Cord Organization The spinal cord . Afferent tract • connects with spinal nerves, through afferent BRAIN neuron & efferent axons in spinal roots; reflex receptor interneuron • communicates with the brain, by means of cell ascending and descending pathways that body form tracts in spinal white matter; and white matter muscle • gives rise to spinal reflexes, pre-determined gray matter Efferent neuron by interneuronal circuits. Spinal Cord Section Gross anatomy of the spinal cord: The spinal cord is a cylinder of CNS. The spinal cord exhibits subtle cervical and lumbar (lumbosacral) enlargements produced by extra neurons in segments that innervate limbs. The region of spinal cord caudal to the lumbar enlargement is conus medullaris. Caudal to this, a terminal filament of (nonfunctional) glial tissue extends into the tail. terminal filament lumbar enlargement conus medullaris cervical enlargement A spinal cord segment = a portion of spinal cord that spinal ganglion gives rise to a pair (right & left) of spinal nerves. Each spinal dorsal nerve is attached to the spinal cord by means of dorsal and spinal ventral roots composed of rootlets. Spinal segments, spinal root (rootlets) nerve roots, and spinal nerves are all identified numerically by th region, e.g., 6 cervical (C6) spinal segment. ventral Sacral and caudal spinal roots (surrounding the conus root medullaris and terminal filament and streaming caudally to (rootlets) reach corresponding intervertebral foramina) collectively constitute the cauda equina. Both the spinal cord (CNS) and spinal roots (PNS) are enveloped by meninges within the vertebral canal. Spinal nerves (which are formed in intervertebral foramina) are covered by connective tissue (epineurium, perineurium, & endoneurium) rather than meninges. -
Visualization of the Pyramidal Decussation Utilizing Diffusion
OPEN ACCESS RESEARCH Visualization of the pyramidal decussation utilizing diffusion tensor imaging: a feasibility study utilizing generalized q-sampling imaging Erik H Middlebrooks1,*, Jeffrey A Bennett1, Sharatchandra Bidari1, and Alissa Old Crow1 1Department of Radiology, University of Florida College of Medicine, Gainesville, Florida, USA *corresponding author ([email protected]) Abstract Background: The delineating point of the end of the brainstem and beginning of the spinal cord is known as the cervicomedullary junction (CMJ). This point is defined by the decussation of the pyramidal tracts. Abnormal configuration and location of the CMJ have both been implicated in disease processes such as Chiari malformation. Unfortunately, the CMJ is not directly visualized on contemporary imaging techniques. Diffusion tensor imaging (DTI) has given us the ability to directly visualize white matter tracts, but suffers from difficulties with visualizing crossing fibers. Many advanced techniques for visualizing crossing fibers utilize substantially long imaging times or non-clinical magnet strengths making clinical applicability limited. Objective: This study inves- tigates the use of generalized q-sampling imaging with diffusion decomposition on standard DTI acquisitions at 3 Tesla to demonstrate the pyramidal decussation. Methods: Three differing DTI protocols were analyzed in vivo with scan times of 17 minutes, 10 minutes, and 5.5 minutes. Data was processed with standard DTI post-processing, as well as generalized q-sampling imaging with diffusion decomposition. Results: The results of the study show that the pyramidal decussation can be reliably visualized using generalized q-sampling imaging and diffusion decomposition with scan times as low at 10 minutes. Conclusion: Utilizing generalized q-sampling post-processing, the pyramidal decussation can be reliably visualized using clinically feasible DTI sequences with scan times as low as 10 minutes. -
Andrew Rosen the Architecture of the Nervous System: • Central Nervous
Andrew Rosen The Architecture of the Nervous System: Central Nervous System (CNS) – Includes the brain and spinal cord Peripheral Nervous System (PNS) – All nerves elsewhere and are connected to the CNS via the spinal cord o Composed of the Somatic Nervous System (SNS), which has the efferent nerves that control the skeletal muscles and afferent nerves that carry information from the sense organs to CNS o Also composed of the Autonomous Nervous System (ANS), which has the efferent nerves that regulate the glands and smooth muscles of internal organs and vessels as well as afferent nerves that bring the CNS information about the internal systems . Divided into the sympathetic branch “Revs” body up for an action . Also divided into parasympathetic branch Restores the body’s internal activities to normal after an action Brain is in cerebrospinal fluid that acts as a shock absorber Anatomy of the Brain: Spinal cord that goes into brain forms the brain stem Medulla is at the bottom of the brain stem o Controls breathing, blood circulation, and maintains balance Pons is above the medulla o Controls attentiveness and governs sleep/dreaming Behind the brain stem is the cerebellum o Controls balance, coordination, and spatial reasoning The midbrain and thalamus are on top of the pons o Relay information to the forebrains o Midbrain regulates experience of pain and moods The forebrain is on top of all of these o Outer part of the forebrain is the cerebral cortex . High surface area . Deepest groove is the longitudinal fissure that splits the left cerebral hemisphere from the right . -
Lecture 12 Notes
Somatic regions Limbic regions These functionally distinct regions continue rostrally into the ‘tweenbrain. Fig 11-4 Courtesy of MIT Press. Used with permission. Schneider, G. E. Brain structure and its Origins: In the Development and in Evolution of Behavior and the Mind. MIT Press, 2014. ISBN: 9780262026734. 1 Chapter 11, questions about the somatic regions: 4) There are motor neurons located in the midbrain. What movements do those motor neurons control? (These direct outputs of the midbrain are not a subject of much discussion in the chapter.) 5) At the base of the midbrain (ventral side) one finds a fiber bundle that shows great differences in relative size in different species. Give examples. What are the fibers called and where do they originate? 8) A decussating group of axons called the brachium conjunctivum also varies greatly in size in different species. It is largest in species with the largest neocortex but does not come from the neocortex. From which structure does it come? Where does it terminate? (Try to guess before you look it up.) 2 Motor neurons of the midbrain that control somatic muscles: the oculomotor nuclei of cranial nerves III and IV. At this level, the oculomotor nucleus of nerve III is present. Fibers from retina to Superior Colliculus Brachium of Inferior Colliculus (auditory pathway to thalamus, also to SC) Oculomotor nucleus Spinothalamic tract (somatosensory; some fibers terminate in SC) Medial lemniscus Cerebral peduncle: contains Red corticospinal + corticopontine fibers, + cortex to hindbrain fibers nucleus (n. ruber) Tectospinal tract Rubrospinal tract Courtesy of MIT Press. Used with permission. Schneider, G. -
Basic Organization of Projections from the Oval and Fusiform Nuclei of the Bed Nuclei of the Stria Terminalis in Adult Rat Brain
THE JOURNAL OF COMPARATIVE NEUROLOGY 436:430–455 (2001) Basic Organization of Projections From the Oval and Fusiform Nuclei of the Bed Nuclei of the Stria Terminalis in Adult Rat Brain HONG-WEI DONG,1,2 GORICA D. PETROVICH,3 ALAN G. WATTS,1 AND LARRY W. SWANSON1* 1Neuroscience Program and Department of Biological Sciences, University of Southern California, Los Angeles, California 90089-2520 2Institute of Neuroscience, The Fourth Military Medical University, Xi’an, Shannxi 710032, China 3Department of Psychology, Johns Hopkins University, Baltimore, Maryland 21218 ABSTRACT The organization of axonal projections from the oval and fusiform nuclei of the bed nuclei of the stria terminalis (BST) was characterized with the Phaseolus vulgaris-leucoagglutinin (PHAL) anterograde tracing method in adult male rats. Within the BST, the oval nucleus (BSTov) projects very densely to the fusiform nucleus (BSTfu) and also innervates the caudal anterolateral area, anterodorsal area, rhomboid nucleus, and subcommissural zone. Outside the BST, its heaviest inputs are to the caudal substantia innominata and adjacent central amygdalar nucleus, retrorubral area, and lateral parabrachial nucleus. It generates moderate inputs to the caudal nucleus accumbens, parasubthalamic nucleus, and medial and ventrolateral divisions of the periaqueductal gray, and it sends a light input to the anterior parvicellular part of the hypothalamic paraventricular nucleus and nucleus of the solitary tract. The BSTfu displays a much more complex projection pattern. Within the BST, it densely innervates the anterodorsal area, dorsomedial nucleus, and caudal anterolateral area, and it moderately innervates the BSTov, subcommissural zone, and rhomboid nucleus. Outside the BST, the BSTfu provides dense inputs to the nucleus accumbens, caudal substantia innominata and central amygdalar nucleus, thalamic paraventricular nucleus, hypothalamic paraventricular and periventricular nuclei, hypothalamic dorsomedial nucleus, perifornical lateral hypothalamic area, and lateral tegmental nucleus. -
Remember the Limbic System?: Aftermr the First Generalized Anatomy Seizure Oc- and Pathology Curred
508 THUERL AJNR: 24, March 2003 508 THUERL AJNR: 24, March 2003 FIG 1. Initial MR images obtained 1 day afterF theIG 1. first Initial generalized MR images seizure obtained oc- 1 day Remember the Limbic System?: afterMR the first generalized Anatomy seizure oc- and Pathology curred. A, Axialcurred.fluid-attenuated inversion recov- ery imageA, Axial (9000/110fluid-attenuated [TR/TE]; inversion inversion recov- time,ery 2261 image ms) shows (9000/110 a slightly [TR/TE]; elevated inversion signaltime, intensity 2261 of ms) both shows hippocampal a slightly forma- elevated Review of Structures Involved in Emotiontionssignal (black intensity arrows)andamygdala( of both hippocampalwhite forma-and Memory Formation arrowstions). (black arrows)andamygdala(white B,arrows Coronal). conventional T2-weighted turbo spin-echoB, Coronal image conventional (4462/120/3 T2-weighted [TR/ Jane Ball,BS; David Sawyer,BS; Adam Blanchard,MD; KrystleTE/NEX]) Barhaghi,MDturbo shows spin-echo no signal image intensity (4462/120/3 abnor- [TR/; Enrique Palacios,MD; Jeremy Nguyen,MD. mality.TE/NEX]) shows no signal intensity abnor- Tulane University School of Medicinemality. Department of Radiology Introduction Structural Review Limbic Encephalitis Klüver-Bucy Syndrome Rather than a single, defined structure within the brain, the Klüver-Bucy Syndrome (KBS) is a clinical diagnosis limbic system is a collection of interrelated structures characterized by visual agnosia, hyperorality, involved in learning, memory, emotional responses, hypersexuality, placidity, abnormal dietary changes, homeostasis and primitive drives. Different reference hypermetamorphosis, dementia, and amnesia. Limbic sources include and exclude structures within the limbic encephalitis is the most common cause of KBS, and KBS system. Some structures share formations or groupings has been associated with other neurological disorders and have additional functions beyond their roles in the including traumatic brain injury, anoxia-ischemic limbic system.