LGN Activity Patterns During Ocular Dominance Plasticity in Vivo

Total Page:16

File Type:pdf, Size:1020Kb

LGN Activity Patterns During Ocular Dominance Plasticity in Vivo LGN Activity Patterns during Ocular Dominance Plasticity in vivo By Monica L. Linden S.B. Mathematics with Computer Science, S.B. Brain and Cognitive Sciences Massachusetts Institute of Technology, 2002 SUBMITTED TO THE DEPARTMENT OF BRAIN AND COGNITIVE SCIENCES IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY IN NEUROSCIENCE AT THE MASSACHUSETTS INSTITUTE OF TECHNOLOGY JUNE 2008 © Massachusetts Institute of Technology All rights reserved Signature of Author: ____________________________________________________________ Department of Brain and Cognitive Sciences May 13, 2008 Certified by: ___________________________________________________________________ Mark F. Bear, Ph.D. Picower Professor of Neuroscience Thesis Supervisor Accepted by: __________________________________________________________________ Matthew A. Wilson, Ph.D. Professor of Neurobiology Chairman, Committee for Graduate Students LGN Activity Patterns during Ocular Dominance Plasticity in vivo By Monica L. Linden Submitted to the Department of Brain and Cognitive Sciences on May 13, 2008 in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Neuroscience ABSTRACT Perturbations of sensory experience in young animals are known to cause lasting changes in adult brain function. For example, monocular visual deprivation by lid closure (MC) leads to a loss of cortical responsiveness of the deprived eye and a concomitant visual impairment. This ocular dominance (OD) plasticity is a well-studied model of experience-dependent cortical plasticity. While much is known about the anatomical, physiological and biochemical changes that occur in primary visual cortex following OD plasticity, the input patterns that lead to these changes have not been characterized. Visual input travels from the retina through the dorsal lateral geniculate nucleus (dLGN) of the thalamus and then into visual cortex. Several models of the thalamic activity patterns which drive OD plasticity have been proposed, but the assumptions about the pattern and amount of input activity from thalamus to cortex during deprivation have not been experimentally validated. Therefore, we performed extracellular recordings from the dLGN of animals during periods of visual manipulation. Contrary to previous hypotheses, the present findings demonstrate that MC does not alter the overall firing rate of neural activity in the dLGN. Instead, MC alters the pattern of neural spike trains such that there is a decrease in simultaneous firing of neighboring neurons. Moreover, the elimination of visual input from the retina, a form of deprivation which does not lead to deprived-eye depression, leads to a dramatic increase in thalamic bursting. Additionally, there are subtle qualitative differences between dLGN activity in juveniles and adults during MC, and this may contribute to differences in OD plasticity with age. These findings substantially alter the interpretation of previous studies and define the activity patterns that govern cortical plasticity in vivo. Furthermore, this work may have important implications for treatments of developmental disorders including ambylopia. Thesis Supervisor: Mark F. Bear, Ph.D. Title: Picower Professor of Neuroscience Monica L. Linden [email protected] Education: Massachusetts Institute of Technology Doctor of Philosophy – June, 2008 Cambridge, MA Ph.D. in Neuroscience, Department of Brain and Cognitive Sciences. Major: Systems Neuroscience, Minor: Computational Neuroscience. Massachusetts Institute of Technology Bachelor of Science – June, 2002 Cambridge, MA Bachelor of Science degrees in Mathematics with Computer Science and Brain and Cognitive Sciences, Minor: Ancient and Medieval Studies. Awards/ Honors: NIH National Research Service Award Predoctoral Fellowship (2007) Walle Nauta Award for Continuing Dedication to Teaching (2006) Dean’s Educational and Student Advising Award (2005) Agnus MacDonald Award for Excellence in Undergraduate Teaching (2005) National Science Foundation Graduate Research Fellowship (2002) MIT Brain and Cognitive Sciences Award for Academic Excellence (2002) Phi Beta Kappa Honor Society Sigma Xi Research Honor Society Teaching Experience: MIT 9.01: Introduction to Neuroscience – Head TA Fall 2004, Fall 2005 Taught one weekly section (~25 students) under Profs. Mark Bear and Sebastian Seung. Coordinated TAs, multiple guest lecturers, and the writing staff. MIT 9.00: Introduction to Psychology – TA Fall 2003 Taught two recitation sections (~25 students) under Prof. Jeremy Wolfe. MIT Orientation for Graduate Teaching Staff – Workshop Facilitator Fall 2005 Co-facilitated “Problems, Pitfalls, Booby Traps and Surprises (in Teaching)” workshop during the fall TA orientation, sponsored by the Teaching and Learning Lab. Research Experience: MIT Picower Center for Learning and Memory – Bear Lab Cambridge, MA June, 2003 – 2008 Graduate Student Researcher: Performing in vivo electrophysiology in awake rodents to understand various aspects of neural plasticity in the visual system. National Security Agency – Students' Summer Program Government Communications Headquarters Cheltenham, UK Summer, 2002 Intern: One of two student liaisons selected to represent the US at this British security agency. Developed mathematical models to analyze systems. Prepared a research report for internal publication and presented results to internal mathematics community. MIT Picower Center for Learning and Memory – Tonegawa Lab Cambridge, MA September, 2001 – March, 2002 Undergraduate Researcher: Data analysis for electrophysiological studies in genetically manipulated mice. National Security Agency – Director's Summer Program Ft. Meade, MD Summer, 2001 Intern: Developed mathematical models to analyze and evaluate data. Prepared a research report for internal publication and briefed the Director of the Agency. Top Secret Clearance. Consulting: Lippincott Williams and Wilkin – Subject Matter Expert Fall 2005 Reviewed manuscripts of ancillary material, specifically “Student Assignments and Activities” for Neuroscience, Exploring the Brain, 3rd Edition by Bear, Connors and Paradiso. This is the textbook used in 9.01 – Introduction to Neuroscience, co-authored by Prof. Bear. Publications & Presentations: M.L. Linden, A.J. Heynen, R. Haslinger, M.F. Bear. (2008) Thalamic activity that drives visual cortical plasticity. Submitted M.L. Linden, A.J. Heynen, R. Haslinger, E.N. Brown, M.F. Bear. LGN activity patterns during ocular dominance plasticity. Picower-RIKEN Symposium, November 8 – 9, 2007. Massachusetts Institute of Technology, Cambridge, MA. Poster Presentation. M.L. Linden, A.J. Heynen, R. Haslinger, E. N. Brown, M. F. Bear. LGN activity patterns during ocular dominance plasticity. Society for Neuroscience, Abstracts, November 3 – 7, 2007. Society for Neuroscience Annual Meeting, San Diego, CA. Poster Presentation. M.L. Linden. LGN activity patterns during ocular dominance plasticity. MIT Brain Lunch Seminar Series, October 15, 2007. Massachusetts Institute of Technology, Cambridge, MA. Lecture. M.L. Linden. LGN activity patterns during ocular dominance plasticity. Picower Institute for Learning and Memory, Annual Retreat, May 30 – June 1, 2007. Cape Cod, MA. Lecture. M.G. Shuler, M.L.Linden, M.Bear. (2004) Learning induced, persistent reward-related activity in the primary visual cortex of adult rodents. Society for Neuroscience, Abstracts, October 23 – 27, 2004. Society for Neuroscience Annual Meeting, San Diego, CA. Acknowledgments “We were but stones, your light made us stars” –Low Light, Pearl Jam There are numerous people whom I’d like to thank, without which my thesis project would not have been as successful. First of all, I’d like to thank Mark Bear. I thoroughly enjoyed working on the fundamental problem which he gave to me, and I was constantly driven to work through my frustrations because I knew there had to be answers. I appreciate all his support throughout the project, even after I upended his hypotheses. I would also like to thank the rest of my thesis committee for their helpful insights: Mriganka Sur, Matthew Wilson and especially Harvey Swadlow, who responded patiently to my emails even when I sent several in the same day. I’d also like to acknowledge my funding sources including a graduate research fellowship from NSF and an NRSA predoctoral fellowship from NINDS/NIH. The Bear Lab provided an incredibly supportive environment throughout my graduate career. Arnie Heynen was a constant source of scientific expertise and emotional support. I couldn’t have done this without him. Marshall Shuler patiently taught me how to be an electrophysiologist and was always there to help me think through my ideas and to challenge my assumptions. Jason Coleman was always willing to help me and provided invaluable knowledge of the dLGN. Sharing lab space with Jonathan Whitlock meant my day in lab would be much more fun. Suzanne Meagher always took care of me, and Erik Sklar fixed everything I managed to break. Our technicians, Caroline Dudley, Cindy Poo, Tina Udaka, and especially Kathleen Oram who did my histology, were wonderful. Gordon Smith always had great answers to questions I asked him, even when they had nothing to do with what he was studying, and even when I asked him quietly during lab meeting. Misha Frenkel, Gül Dölen, Sam Cooke and Emily Osterweil were great sounding-boards for discussing my problems. Lena Khibnik, Rahmat Muhammad, and Wendy Chen were all wonderful friends inside and outside the lab,
Recommended publications
  • 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.
    [Show full text]
  • Single-Cell Reconstruction of Oxytocinergic Neurons Reveals Separate Hypophysiotropic and Encephalotropic Subtypes in Larval Zebrafish
    New Research Development Single-Cell Reconstruction of Oxytocinergic Neurons Reveals Separate Hypophysiotropic and Encephalotropic Subtypes in Larval Zebrafish Ulrich Herget,1 Jose Arturo Gutierrez-Triana,1 Oriana Salazar Thula,1 Boris Knerr,1 and Soojin Ryu1,2 DOI:http://dx.doi.org/10.1523/ENEURO.0278-16.2016 1Developmental Genetics of the Nervous System, Max Planck Institute for Medical Research, 69120 Heidelberg, Germany, 2Focus Program Translational Neuroscience, University Medical Center, Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany Visual Abstract Significance Statement We used the Brainbow technique to reconstruct the morphology and projection patterns of oxytocinergic neurons in larval zebrafish, revealing diverse and complex brainwide innervation patterns originating from a small cluster of cells within the neurosecretory preoptic area. Central target areas include the tectum, hypothalamus, and telencephalon. This is the first comprehensive whole-brain morphology characterization of oxytocinergic neurons, to our knowledge. 3D registration reveals spatially distinct subtypes of oxytocinergic neurons. One group with morphologically complex projections reaches into distinct brain regions, presumably for neuromodulation, whereas another group features simpler projections innervating the pituitary, presumably for endocrine release. These two groups are spatially segregated, suggesting an evolutionarily ancient anatomical separation of oxytocin cell subtypes. January/February 2017, 4(1) e0278-16.2016 1–16 New Research 2 of 16 Oxytocin regulates a diverse set of processes including stress, analgesia, metabolism, and social behavior. How such diverse functions are mediated by a single hormonal system is not well understood. Different functions of oxytocin could be mediated by distinct cell groups, yet it is currently unknown whether different oxytocinergic cell types exist that specifically mediate peripheral neuroendocrine or various central neuromodulatory processes via dedicated pathways.
    [Show full text]
  • Resting State Connectivity of the Human Habenula at Ultra-High Field
    NeuroImage 147 (2017) 872–879 Contents lists available at ScienceDirect NeuroImage journal homepage: www.elsevier.com/locate/neuroimage fi Resting state connectivity of the human habenula at ultra-high eld MARK ⁎ Salvatore Torrisia, , Camilla L. Nordb, Nicholas L. Balderstona, Jonathan P. Roiserb, Christian Grillona, Monique Ernsta a Section on the Neurobiology of Fear and Anxiety, National Institute of Mental Health, Bethesda, MD, United States b Neuroscience and Cognitive Neuropsychiatry group, University of College, London, UK ARTICLE INFO ABSTRACT Keywords: The habenula, a portion of the epithalamus, is implicated in the pathophysiology of depression, anxiety and 7T addiction disorders. Its small size and connection to other small regions prevent standard human imaging from Anxiety delineating its structure and connectivity with confidence. Resting state functional connectivity is an established Depression method for mapping connections across the brain from a seed region of interest. The present study takes Seed-based functional connectivity advantage of 7 T fMRI to map, for the first time, the habenula resting state network with very high spatial resolution in 32 healthy human participants. Results show novel functional connections in humans, including functional connectivity with the septum and bed nucleus of the stria terminalis (BNST). Results also show many habenula connections previously described only in animal research, such as with the nucleus basalis of Meynert, dorsal raphe, ventral tegmental area (VTA), and periaqueductal grey (PAG). Connectivity with caudate, thalamus and cortical regions such as the anterior cingulate, retrosplenial cortex and auditory cortex are also reported. This work, which demonstrates the power of ultra-high field for mapping human functional connections, is a valuable step toward elucidating subcortical and cortical regions of the habenula network.
    [Show full text]
  • The POU Domain Transcription Factor Brn- Is Required for the Determination of Specific Neuronal Lineages M the Hypothalamus of the Mouse
    Downloaded from genesdev.cshlp.org on September 28, 2021 - Published by Cold Spring Harbor Laboratory Press The POU domain transcription factor Brn- is required for the determination of specific neuronal lineages m the hypothalamus of the mouse Shigeyasu Nakai, 1 Hitoshi Kawano, 2 Tamaki Yudate, ~ Miyuki Nishi, 1 Junko Kuno, 1 Aki Nagata, 1 Kou-ichi Jishage, 1 Hiroshi Hamada, ~ Hideta Fujii, 3 Koki Kawamura, 2 Kiyotaka Shiba, 1 and Tetsuo Noda 1'4 1Department of Cell Biology, Cancer Institute, Toshima-ku, Tokyo 170; 2Department of Anatomy, School of Medicine, Keio University, Shinjuku-ku, Tokyo 160; "3Institute for Molecular and Cellular Biology, Osaka University, Suita-shi, Osaka 565, Japan We generated mice carrying a loss-of-function mutation in Brn-2, a gene encoding a nervous system specific POU transcription factor, by gene targeting in embryonic stem cells. In homozygous mutant embryos, migratory precursor cells for neurons of the paraventricular nuclei (PVN) and the supraoptic nuclei (SO) of the hypothalamus die at -E12.5. All homozygous mutants suffered mortality within 10 days after birth, possibly because of a complete deficiency of these neurons in the hypothalamus. Although neither developmental nor histological abnormalities were observed in heterozygous mice, the levels of expression of vasopressin and oxytocin in the hypothalamus of these animals were half these of wild-type mice. These results strongly suggest that Brn-2 plays an essential role in the determination and development of the PVN and SO neuronal lineages in the hypothalamus. [Key Words: POU transcription factor; Brn-2; neuronal development; magnocellular neurons; paraventricular nucleus; supraoptic nucleus] Received August 10, 1995; revised version accepted October 31, 1995.
    [Show full text]
  • Surgical Neurology International
    SSurgicalurgical NNeurologyeurology IInternationalnternational OPEN ACCESS Editor: Antonio A. F. DeSalles, MD SSNI:NI: SStereotactictereotactic, a ssupplementupplement ttoo SSurgicalurgical NNeurologyeurology IInternationalnternational For entire Editorial Board visit : University of California, http://www.surgicalneurologyint.com Los Angeles, CA, USA Maps of the adult human hypothalamus Jean-Jacques Lemaire1,2, Hachemi Nezzar1,3, Laurent Sakka1,2, Yves Boirie4, Denys Fontaine1,5, Aurélien Coste2, Guillaume Coll2, Anna Sontheimer1, Catherine Sarret1,6, Jean Gabrillargues1,7, Antonio De Salles8 1Univ Clermont 1, UFR Médecine, EA 7282, Image-Guided Clinical Neuroscience and Connectomics, Clermont-Ferrand, F-63001, 2Service de Neurochirurgie, 3Service d’Ophtalmologie, 4Service de Nutrition, 6Service de Pédiatrie, 7Unité de Neuroradiologie, CHU Clermont-Ferrand, Clermont-Ferrand, F-63003, 5Service de Neurochirurgie, CHU de Nice, Nice, F-06200, France, 8Department of Neurosurgery, University of California, Los Angeles, USA E-mail: *Jean-Jacques Lemaire - [email protected]; Hachemi Nezzar - [email protected]; Laurent Sakka - [email protected]; Yves Boirie - [email protected]; Denys Fontaine - [email protected]; Aurélien Coste - [email protected]; Guillaume Coll - [email protected]; Anna Sontheimer - [email protected]; Catherine Sarret - [email protected]; Jean Gabrillargues - [email protected]; Antonio De Salles - [email protected] *Corresponding author Received: 01 February 13 Accepted: 01 February 13 Published: 17 April 13 This article may be cited as: Lemaire J, Nezzar H, Sakka L, Boirie Y, Fontaine D, Coste A, et al. Maps of the adult human hypothalamus. Surg Neurol Int 2013;4:156-63. Available FREE in open access from: http://www.surgicalneurologyint.com/text.asp?2013/4/4/156/110667 Copyright: © 2013 Lemaire J.
    [Show full text]
  • Acetylcholine As a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Neuron Review Acetylcholine as a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior Marina R. Picciotto,1,2,3,* Michael J. Higley,2,3 and Yann S. Mineur1 1Department of Psychiatry 2Department of Neurobiology 3Program in Cellular Neuroscience, Neurodegeneration and Repair Yale University School of Medicine, New Haven, CT 06511, USA *Correspondence: [email protected] http://dx.doi.org/10.1016/j.neuron.2012.08.036 Acetylcholine in the brain alters neuronal excitability, influences synaptic transmission, induces synaptic plasticity, and coordinates firing of groups of neurons. As a result, it changes the state of neuronal networks throughout the brain and modifies their response to internal and external inputs: the classical role of a neuro- modulator. Here, we identify actions of cholinergic signaling on cellular and synaptic properties of neurons in several brain areas and discuss consequences of this signaling on behaviors related to drug abuse, attention, food intake, and affect. The diverse effects of acetylcholine depend on site of release, receptor subtypes, and target neuronal population; however, a common theme is that acetylcholine potentiates behaviors that are adaptive to environmental stimuli and decreases responses to ongoing stimuli that do not require immediate action. The ability of acetylcholine to coordinate the response of neuronal networks in many brain areas makes cholinergic modulation an essential mechanism underlying complex behaviors. Acetylcholine (ACh) is a fast-acting, point-to-point neurotrans- ergic activation of interneurons in the auditory cortex that con- mitter at the neuromuscular junction and in the autonomic tribute to learning (Letzkus et al., 2011).
    [Show full text]
  • Saccadic Eye Movements Modulate Visual Responses in the Lateral Geniculate Nucleus
    Neuron, Vol. 35, 961–974, August 29, 2002, Copyright 2002 by Cell Press Saccadic Eye Movements Modulate Visual Responses in the Lateral Geniculate Nucleus John B. Reppas,1 W. Martin Usrey,1,3 and O’Keefe, 1998; Gallant et al., 1998; Gur and Snod- and R. Clay Reid1,2 derly, 1997; Leopold and Logothetis, 1998; Martinez- 1Department of Neurobiology Conde et al., 2000). However, it is not yet generally Harvard Medical School established whether eye movements have an additional Boston, Massachusetts 02115 effect on the organization of visual receptive fields. Ex- periments that have carefully controlled the spatial prop- erties of the retinal stimulus present during saccades Summary have argued both for (Tolias et al., 2001) and against (DiCarlo and Maunsell, 2000; Wurtz, 1969) such an influ- We studied the effects of saccadic eye movements ence on cortical responses to briefly presented stimuli. on visual signaling in the primate lateral geniculate Defining the impact of eye movements on neural re- nucleus (LGN), the earliest stage of central visual pro- sponses is also a requirement for understanding the cessing. Visual responses were probed with spatially well-known effects of saccades on human perception. uniform flickering stimuli, so that retinal processing Eye movements influence many aspects of low-level was uninfluenced by eye movements. Nonetheless, vision, including saccadic suppression of overall sensi- saccades had diverse effects, altering not only re- tivity (reviewed in Volkmann, 1986), as well as spatial sponse strength but also the temporal and chromatic (Cai et al., 1997; Lappe et al., 2000; Ross et al., 1997), properties of the receptive field.
    [Show full text]
  • Segregation Within Afferent Pathways in Primate Vision Sujata Roy March
    Segregation Within Afferent Pathways in Primate Vision Sujata Roy Submitted in total fulfillment of the requirements of the degree of Doctor of Philosophy March 2009 Department of Optometry & Vision Sciences The University of Melbourne Abstract The current knowledge of the visual pathways in primates includes the patterns of projection from the retina through the dorsal lateral geniculate nucleus (dLGN) to the striate cortex (V1) and the extra-striate projections towards the dorsal and ventral streams. Cells with short wavelength sensi- tive cone (S-cone) inputs in the dLGN have been studied extensively in New World marmosets but not in Old World macaques. This thesis presents re- sults from studies in the macaque monkey which are more relevant to humans since humans are closer in evolution to Old World than New World monkeys. The spatial, temporal, chromatic and orientation preferences of neurons in the dLGN of the macaque were investigated by electrophysiological meth- ods. The physiological findings of cells with S-cone inputs were compared to cells with opponent inputs from the long and medium wavelength sensitive cones (L-cones & M-cones, respectively). The cells receiving S-cone inputs (blue-yellow or B-Y cells) preferred lower spatial frequencies than the cells with opponent L-cone and M-cone inputs (red-green or R-G cells). Ortho- dromic latencies from optic chiasm stimulation were measured where possible to distinguish differences in conduction velocity between the cell groups. Al- though the B-Y cells usually had longer latencies than R-G cells, there was considerable overlap between the cell groups. The recorded cells were localised through histological reconstruction of dLGN sections stained for Nissl substance.
    [Show full text]
  • Resting State Functional Connectivity of the Basal Nucleus of Meynert in Humans: in Comparison to the Ventral Striatum and the Effects of Age
    NeuroImage 97 (2014) 321–332 Contents lists available at ScienceDirect NeuroImage journal homepage: www.elsevier.com/locate/ynimg Resting state functional connectivity of the basal nucleus of Meynert in humans: In comparison to the ventral striatum and the effects of age Chiang-shan R. Li a,b,c,⁎, Jaime S. Ide a,d, Sheng Zhang a,SienHua, Herta H. Chao e,f, Laszlo Zaborszky g a Department of Psychiatry, Yale University, New Haven, CT 06519, USA b Department of Neurobiology, Yale University, New Haven, CT 06520, USA c Interdepartmental Neuroscience Program, Yale University, New Haven, CT 06520, USA d Department of Science and Technology, Federal University of Sao Paulo, Sao Jose dos Campos, SP 12231, Brazil e Department of Internal Medicine, Yale University New Haven, CT 06519, USA f Medical Service, VA Connecticut Health Care System, West Haven, CT 06516, USA g Center for Molecular and Behavioral Neuroscience, Rutgers, NJ 07102, USA article info abstract Article history: The basal nucleus of Meynert (BNM) provides the primary cholinergic inputs to the cerebral cortex. Loss of Accepted 6 April 2014 neurons in the BNM is linked to cognitive deficits in Alzheimer's disease and other degenerative conditions. Nu- Available online 13 April 2014 merous animal studies described cholinergic and non-cholinergic neuronal responses in the BNM; however, work in humans has been hampered by the difficulty of defining the BNM anatomically. Here, on the basis of a Keywords: previous study that delineated the BNM of post-mortem human brains in a standard stereotaxic space, we sought Functional connectivity to examine functional connectivity of the BNM, as compared to the nucleus accumbens (or ventral striatum, VS), fMRI Resting state in a large resting state functional magnetic resonance imaging data set.
    [Show full text]
  • Space and Time Maps of Cone Photoreceptor Signals in Macaque Lateral Geniculate Nucleus
    The Journal of Neuroscience, July 15, 2002, 22(14):6158–6175 Space and Time Maps of Cone Photoreceptor Signals in Macaque Lateral Geniculate Nucleus R. Clay Reid1,2 and Robert M. Shapley1 1Center for Neural Science, New York University, New York, New York 10003, and 2Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115 We studied neurons in the central visual field representation of overlapped in space, as sampled by our stimulus grid, but that the lateral geniculate nucleus (LGN) in macaque monkeys by had somewhat different extents. For example, an Lϩ center mapping their receptive fields in space and time. The mapping parvocellular neuron would be Lϩ/MϪ in both center and was performed by reverse correlation of a spike train of a surround, but the Lϩ signal would be stronger in the center and neuron with pseudorandom, binary level stimuli (m-sequence the MϪ signal stronger in the surround. Accordingly, the lumi- grids). Black and white m-sequence grids were used to map the nance receptive field would be spatially antagonistic: on- receptive field for luminance. The locations of receptive field center/off-surround. The space–time maps also characterized center and surround were determined from this luminance map. LGN dynamics. For example, magnocellular responses were To map the contribution of each cone class to the receptive transient, red–green parvocellular responses were more sus- field, we designed red–green or blue–yellow m-sequence grids tained, and blue-on responses were the most sustained for to isolate the influence of that cone (long, middle, or short both luminance and cone-isolating stimuli.
    [Show full text]
  • Hypothalamus
    Hypothalamus Objectives • To learn the general organization of the hypothalamus and the functions of the major nuclei NTA Ch 14, pgs. 419-422 Key Figs: 14-2, 14-3 • To learn how the brain regulates neuroendocrine secretions NTA Ch 14, pgs. 422-427 Key Figs: 14-3; 14-4, • To learn how the hypothalamus regulates the autonomic nervous system and how brain stem and spinal lesions disrupt autonomic functions NTA Ch 14, pgs. 427-433; 440-442 Key Figs: 14-8, 14-9 Clinical Case #14 Menstrual irregularity; CC12-1 Note We will not spend any time on the peripheral organization of the autonomic nervous system. That topic is covered in SPBM. Instead, we focus on the central pathways and how they control autonomic functions. Self evaluation • Be able to identify all structures listed in key terms and describe briefly their principal functions • Use neuroanatomy on the web to test your understanding G-1 Gross anatomy of hypothalamus The ventral view of the brain. Note the relationships of the floor of the hypothalamus to the caudal edge of the chiasm and the basis pedunculi. The caudal hypothalamus lies deep to the mammillary bodies. The middle or tuberal hypothalamus lies deep to the tuber cinereum, the low protuberance extending from the mammillary bodies to the posterior chiasm. SA03 Inferior brain view Identify the mammillary bodies, region of other hypothalamic nuclei, and optic chiasm and tracts SA01 Medial brain view 1 Identify the following landmarks and hypothalamic components: Mammillary body, region of hypothalamus, thalamus, optic nerve and chiasm, and oculomotor nerve. hypothaltrans Hypothalamus (movie) Key: Hypothalamus=yellow Ventricular system=aqua G-3 Hypothalamic nuclei A schematic drawing of a dissected human brain showing the major hypothalamic nuclei in parasagittal section.
    [Show full text]
  • On Cells Are Part of the Third Geniculocortical Pathway in Primates
    European Journal of Neuroscience, Vol. 9, pp. 1536-1541, 1997 0 European Neuroscience Association SHORT COMMUNICATION Evidence that Blue-on Cells are Part of the Third Geniculocortical Pathway in Primates Paul R. Martin, Andrew J. R. White, Ann K. Goodchild, Heath D. Wilder and Ann E. Sefton Department of Physiology and Institute for Biomedical Research, University of Sydney, NSW 2006, Australia Keywords: colour vision, Callithrix jacchus, magnocellular, parvocellular, koniocellular Abstract Colour vision in primates is mediated by cone opponent ganglion cells in the retina, whose axons project to the dorsal lateral geniculate nucleus in the visual thalamus. It has long been assumed that cone opponent ganglion cells project to the parvocellular layers of the geniculate. Here, we examine the role of a third subdivision of the geniculocortical pathway: the interlaminar or koniocellular geniculate relay cells. We made extracellular recordings in the dorsal lateral geniculate nucleus of the common marmoset Callithrix jacchus, a New World monkey in which the interlaminar cells are well segregated from the parvocellular layers. We found that one group of colour opponent cells, the blue-on cells, was largely segregated to the interlaminar zone. This segregation was common to dichromatic (‘red-green colour-blind’) and trichromatic marmosets. The result calls into question the traditional notion that all colour information passes through the parvocellular division of the retino-geniculo-cortical pathway in primates. Introduction The marmoset (CaEZithrix jacchus), in common with several other 1984; Ts’o and Gilbert, 1988; Hendry and Yoshioka, 1994). This species of New World monkeys (Jacobs, 1993), shows sex-linked connectivity has led to speculation about the role of the inter- polymorphism of colour vision.
    [Show full text]