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Focusing on the Re-Emergence of Primitive Reflexes Following Acquired Brain Injuries
33 Focusing on The Re-Emergence of Primitive Reflexes Following Acquired Brain Injuries Resiliency Through Reconnections - Reflex Integration Following Brain Injury Alex Andrich, OD, FCOVD Scottsdale, Arizona Patti Andrich, MA, OTR/L, COVT, CINPP September 19, 2019 Alex Andrich, OD, FCOVD Patti Andrich, MA, OTR/L, COVT, CINPP © 2019 Sensory Focus No Pictures or Videos of Patients The contents of this presentation are the property of Sensory Focus / The VISION Development Team and may not be reproduced or shared in any format without express written permission. Disclosure: BINOVI The patients shown today have given us permission to use their pictures and videos for educational purposes only. They would not want their images/videos distributed or shared. We are not receiving any financial compensation for mentioning any other device, equipment, or services that are mentioned during this presentation. Objectives – Advanced Course Objectives Detail what primitive reflexes (PR) are Learn how to effectively screen for the presence of PRs Why they re-emerge following a brain injury Learn how to reintegrate these reflexes to improve patient How they affect sensory-motor integration outcomes How integration techniques can be used in the treatment Current research regarding PR integration and brain of brain injuries injuries will be highlighted Cases will be presented Pioneers to Present Day Leaders Getting Back to Life After Brain Injury (BI) Descartes (1596-1650) What is Vision? Neuro-Optometric Testing Vision writes spatial equations -
Corticospinal Fibers
151 Brain stem Pyramids/Corticospinal Tract 1 PYRAMIDS - CORTICOSPINAL FIBERS The pyramids are two elongated swellings on the ventral aspect of the medulla. Each pyramid contains approximately 1,000,000 CORTICOSPINAL AXONS. As the name suggests, these axons arise from the cerebral cortex and descend to terminate within the spinal cord. The cortical cells that give rise to corticospinal axons are called Betz cells. As corticospinal axons descend from the cortex, they course through the internal capsule, the cerebral peduncle of the midbrain, and the ventral pons (you will learn about these structures later in the course so don’t worry about them now) and onto the ventral surface of the medulla as the pyramids (see below). When corticospinal axons reach the medulla they lie within the pyramids. The pyramids are just big fiber bundles that lie on the ventral surface of the caudal medulla. The fibers in the pyramids are corticospinal. It is important to REMEMBER: THERE HAS BEEN NO CROSSING YET! in this system. The cell bodies of corticospinal axons within the pyramids lie within the IPSILATERAL cerebral cortex. Brain stem 152 Pyramids/Corticospinal Tract At the most caudal pole of the pyramids the corticospinal axons cross over the midline and now continue their descent on the contralateral (to the cell of origin) side. This crossover point is called the PYRAMIDAL DECUSSATION. The crossing fibers enter the lateral funiculus of the spinal cord where they are called the LATERAL CORTICOSPINAL TRACT (“corticospinal” is not good enough, you have to call them lateral corticospinal; LCST - remember this one??). LCST axons exit the tract to terminate upon neurons in the spinal cord gray matter along its entire length. -
Orienting Head Movements Resulting from Electrical Microstimulation of the Brainstem Tegmentum in the Barn Owl
The Journal of Neuroscience, January 1993, 13(l): 351370 Orienting Head Movements Resulting from Electrical Microstimulation of the Brainstem Tegmentum in the Barn Owl Tom Masino and Eric I. Knudsen Department of Neurobiology, Stanford University, Stanford, California 943055401 The size and direction of orienting movements are repre- movement latency, duration, velocity, and size each dem- sented systematically as a motor map in the optic tectum of onstrated dependencies on stimulus amplitude, frequency, the barn owl (du Lac and Knudsen, 1990). The optic tectum and duration. projects to several distinct regions in the medial brainstem The data demonstrate directly that at the level of the mid- tegmentum, which in turn project to the spinal cord (Masino brain tegmentum there exists a three-dimensional Cartesian and Knudsen, 1992). This study explores the hypothesis that representation of head-orienting movements such that hor- a fundamental transformation in the neural representation izontal, vertical, and roll components of movement are en- of orienting movements takes place in the brainstem teg- coded by anatomically distinct neural circuits. The data sug- mentum. Head movements evoked by electrical microstim- gest that in the projection from the optic tectum to these ulation in the brainstem tegmentum of the alert barn owl were medial tegmental regions, the topographic code for orienting cataloged and the sites of stimulation were reconstructed movement that originates in the tectum is transformed into histologically. Movements elicited from the brainstem teg- this Cartesian code. mentum were categorized into one of six different classes: [Key words: optic tectum, superior colliculus, saccadic saccadic head rotations, head translations, facial move- head movement, brainstem tegmentum, interstitial nucleus ments, vocalizations, limb movements, and twitches. -
Optogenetic Activation of Cholinergic Neurons in the PPT Or LDT Induces REM Sleep
Optogenetic activation of cholinergic neurons in the PPT or LDT induces REM sleep Christa J. Van Dorta,b,c,1, Daniel P. Zachsa,b,c, Jonathan D. Kennya,b,c, Shu Zhengb, Rebecca R. Goldblumb,c,d, Noah A. Gelwana,b,c, Daniel M. Ramosb,c, Michael A. Nolanb,c,d, Karen Wangb,c, Feng-Ju Wengb,e, Yingxi Linb,e, Matthew A. Wilsonb,c, and Emery N. Browna,b,d,f,1 aDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114; and bDepartment of Brain and Cognitive Sciences, cPicower Institute for Learning and Memory, eMcGovern Institute for Brain Research, fHarvard-MIT Division of Health Sciences and Technology, and dInstitute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA 02139 Contributed by Emery N. Brown, December 3, 2014 (sent for review September 19, 2014; reviewed by Helen A. Baghdoyan and H. Craig Heller) Rapid eye movement (REM) sleep is an important component of REM sleep regulation, a method that can modulate specific cell the natural sleep/wake cycle, yet the mechanisms that regulate types in the behaving animal is needed. Optogenetics now pro- REM sleep remain incompletely understood. Cholinergic neurons vides this ability to target specific subpopulations of neurons in the mesopontine tegmentum have been implicated in REM sleep and control them with millisecond temporal resolution (30). regulation, but lesions of this area have had varying effects on REM Therefore, we aimed to determine the role of cholinergic sleep. Therefore, this study aimed to clarify the role of cholinergic neurons in the PPT and LDT in REM sleep regulation using neurons in the pedunculopontine tegmentum (PPT) and laterodor- optogenetics. -
Brainstem Dental 2012.Doc
Dental Neuroanatomy January 12 and 19, 10-12, 2012 Suzanne S. Stensaas, Ph.D. Dear Students: Please print these notes and bring them with you. My style is to use a Tablet PC and I draw on either a Word or pdf copy with colors. Be prepared to draw. Have at least 5 colors. Please try to look at the notes AHEAD OF TIME for each lecture in this course. This way you can see the direction and organization of the lecture and be more familiar with the terms. There will be a quiz (that does not count) at the beginning to cover topics in the two gross anatomy lectures by Dr. Morton in Phase 1. They are G 17B and GL 18 Waxman, S Clinical Neuroanatomy, 26th ed.2010. THE OLD EDITION IS FINE TOO. Review Ch 5 on the spinal cord organization, but not the tracts in the middle or lesions at the end of the chapter. Also review the basic concept of a reflex. Review or skim Ch 12 on the vascular supply of the brain. Just look at pictures and legends for the clinical part at the end. NEW material: Chapter 7 Waxman, Brainstem, but not the cerebellum part. NEW material: Chapter 8 Waxman, Cranial nerves, all of it including autonomic. BEWARE THE CRANIAL NERVES ARE KILLERS! There are about 50 copies of the following bright yellow paperback book, which can be checked out from the Eccles Health Sciences Library and kept for the duration of the course. They are on reserve as: Cranial nerves: anatomy and clinical comments Linda Wilson-Pauwels, 1988 Toronto; Philadelphia: B.C. -
Isolated Necrosis of Central Tegmental Tracts Due to Neonatal Hypoxic-Ischemic Encephalopathy: MRI Findings
Journal of Neurology & Stroke Case Report Open Access Isolated necrosis of central tegmental tracts due to neonatal hypoxic-ischemic encephalopathy: MRI findings Abstract Volume 11 Issue 1 - 2021 Perinatal hypoxia is an old entity that still prevails today and may lead to neurological Tomás de Andrade Lourenção Freddi, Luiz sequelae that can go unnoticed until a certain age, generating many costs for public health. In this case report, we demonstrate on magnetic resonance imaging an unusual pattern of Fellipe Curvêlo Ciraulo Santos, Nelson Paes perinatal hypoxia in a preterm 5-month-old infant, involving the central tegmental tracts Fortes Diniz Ferreira, Felipe Diego Gomes and briefly discuss its possible pathophysiology. Dantas Department of Radiology, Hospital do Coração, Brazil Keywords: magnetic resonance imaging, asphyxia, hypoxic-ischemic encephalopathy, tegmentum, neonates, brainstem Correspondence: Tomás de Andrade Lourenção Freddi, Hospital do Coração, 147 Desembargador Eliseu Guilherme Street, São Paulo, SP, 04004-030, Brazil, Tel +5511976059280, Email Received: May 25, 2020 | Published: Febrauary 15, 2021 Abbreviations: MRI, magnetic resonance imaging; HII, that connect the red nucleus and the inferior olivary nucleus, being hypoxic-ischemic injury; FLAIR, fluid-attenuated inversion recovery; part of the dentato-rubro-olivary system, called Guillain–Mollaret CTT, central tegmental tract; VGB, vigabatrin triangle.3–5 Introduction Hypoxic-ischemic injury (HII) is one of the most important causes of encephalopathy in neonates, irrespective of gestational age, and may occur in the uterus or during delivery by different intrapartum conditions. In preterm or very low birth weight infants, brain magnetic resonance imaging (MRI) can demonstrate multiple different findings, which a detailed description is beyond the scope of this article, although being periventricular leukomalacia the most frequent (seen in at least 50% of cases). -
Cerebral Cortex
Cerebral Cortex • Research on the structure and function of the brain reveals that there are both specialized and diffuse areas of function • Motor and sensory areas are localized in discrete cortical areas called domains • Many higher mental functions such as memory and language appear to have overlapping domains and are more diffusely located • Broadmann areas are areas of localized function Cerebral Cortex - Generalizations • The cerebral cortex has three types of functional areas – Motor areas / control voluntary motor function – Sensory areas / provide conscious awareness of sensation – Association areas / act mainly to integrate diverse information for purposeful action • Each hemisphere is chiefly concerned with the sensory and motor functions of the opposite (contralateral) side of the body Motor Areas • Cortical areas controlling motor functions lie in the posterior part of the frontal lobes • Motor areas include the primary motor cortex, the premotor cortex, Broca’s area, and the front eye field Primary Motor Cortex • The primary motor cortex is located in the precentral gyrus of the frontal lobe of each hemisphere • Large neurons (pyramidal cells) in these gyri allow us to consciously control the precise or skill voluntary movements of our skeletal muscles Pyramidal cells • These long axons, which project to the spinal cord, form the massive Dendrites voluntary motor tracts called the pyramidal, or corticospinal tracts • All other descending motor tracts issue from brain stem nuclei and consists of chains of two, three, or -
Amyotrophic Lateral Sclerosis (ALS)
Amyotrophic Lateral Sclerosis (ALS) There are multiple motor neuron diseases. Each has its own defining features and many characteristics that are shared by all of them: Degenerative disease of the nervous system Progressive despite treatments and therapies Begins quietly after a period of normal nervous system function ALS is the most common motor neuron disease. One of its defining features is that it is a motor neuron disease that affects both upper and lower motor neurons. Anatomical Involvement ALS is a disease that causes muscle atrophy in the muscles of the extremities, trunk, mouth and face. In some instances mood and memory function are also affected. The disease operates by attacking the motor neurons located in the central nervous system which direct voluntary muscle function. The impulses that control the muscle function originate with the upper motor neurons in the brain and continue along efferent (descending) CNS pathways through the brainstem into the spinal cord. The disease does not affect the sensory or autonomic system because ALS affects only the motor systems. ALS is a disease of both upper and lower motor neurons and is diagnosed in part through the use of NCS/EMG which evaluates lower motor neuron function. All motor neurons are upper motor neurons so long as they are encased in the brain or spinal cord. Once the neuron exits the spinal cord, it operates as a lower motor neuron. 1 Upper Motor Neurons The upper motor neurons are derived from corticospinal and corticobulbar fibers that originate in the brain’s primary motor cortex. They are responsible for carrying impulses for voluntary motor activity from the cerebral cortex to the lower motor neurons. -
Chapter 128: Basic Mechanisms of Sleep: New Evidence On
128 BASIC MECHANISMS OF SLEEP: NEW EVIDENCE ON THE NEUROANATOMY AND NEUROMODULATION OF THE NREM-REM CYCLE EDWARD F. PACE-SCHOTT J. ALLAN HOBSON The 1990s brought a wealth of new detail to our knowledge NREM sleep (noradrenergic, serotonergic, and cholinergic of the brain structures involved in the control of sleep and systems damped), and REM sleep (noradrenergic and sero- waking and in the cellular level mechanisms that orchestrate tonergic systems off, cholinergic system undamped) (1–4). the sleep cycle through neuromodulation. This chapter pre- sents these new findings in the context of the general history Original Reciprocal Interaction Model: An of research on the brainstem neuromodulatory systems and Aminergic-Cholinergic Interplay the more specific organization of those systems in the con- trol of the alternation of wake, non–rapid eye movement The model of reciprocal interaction (5) provided a theoretic (NREM), and REM sleep. framework for experimental interventions at the cellular and Although the main focus of the chapter is on the our molecular level that has vindicated the notion that waking own model of reciprocal aminergic-cholinergic interaction, and REM sleep are at opposite ends of an aminergically we review new data suggesting the involvement of many dominant to cholinergically dominant neuromodulatory more chemically specific neuronal groups than can be ac- continuum, with NREM sleep holding an intermediate po- commodated by that model. We also extend our purview to sition (Fig. 128.1). The reciprocal interaction hypothesis the way in which the brainstem interacts with the forebrain. (5) provided a description of the aminergic-cholinergic in- These considerations inform not only sleep-cycle control terplay at the synaptic level and a mathematic analysis of per se, but also the way that circadian and ultradian rhythms the dynamics of the neurobiological control system. -
Topographic Organization of Corticospinal Projections from the Frontal Lobe: Motor Areas on the Lateral Surface of the Hemisphere
The Journal of Neuroscience, March 1993, 133): 952-980 Topographic Organization of Corticospinal Projections from the Frontal Lobe: Motor Areas on the Lateral Surface of the Hemisphere San-Qiang He, Richard P. Dum, and Peter L. Strick Research Service, Veterans Affairs Medical Center, and Departments of Neurosurgery and Physiology, SUNY Health Science Center at Syracuse, Syracuse, New York 13210 We examined the topographic organization of corticospinal PMd that project most densely to upper cervical segments neurons in the primary motor cortex and in the two premotor were largely separate from those that project most dense/y areas on the lateral surface of the hemisphere [i.e., the dor- to lower cervical segments. Furthermore, we found two sep- sal premotor area (PMd) and the ventral premotor area (PMv)]. arate regions within area 4 that send corticospinal projec- In two macaques, we labeled corticospinal neurons that pro- tions primarily to the lower cervical segments. One of these ject beyond T7 or S2 by placing crystals of HRP into the regions was located within the classical “hand” area of the dorsolateral funiculus at these segmental levels. In another primary motor cortex. The other was located at the medial seven macaques, we labeled corticospinal neurons that pro- edge of arm representation in the primary motor cortex. ject to specific segmental levels of the spinal cord by in- These results provide new insights into the pattern of body jecting the fluorescent tracers fast blue and diamidino yellow representation in the primary motor cortex, PMd, and PMv. into the gray matter of the cervical and lumbosacral seg- Our findings support the classic distinction between the ments. -
Static Reflexes
Te xt . Important Lecture . Formulas No.16 . Numbers . Doctor notes “Believe In Your Dreams. They . Notes and explanation Were Given To You For A Reason” 1 Physiology of postural reflexes Objectives: 1. Postural reflexes are needed to keep the body in a proper position while standing, moving. When body posture is suddenly altered it is corrected by Sevier reflexes. These reflexes are operating at spinal cord, medulla, mid-brain and cortical levels. To make the reflex movements smooth cerebellum, basal ganglia and vestibular apparatus are needed. Students are required to know posture-regulating parts of CNS. 2 What is posture? ONLY IN MALES’ SLIDES ONLY IN FEMALES’ SLIDES Posture is the attitude taken by the body in any It is maintenance of upright position against gravity particular situation like standing posture, sitting (center of body is needed to be between the legs) it needs posture, etc.. Even during movement, there is a continuously changing posture. anti-garvity muscles (Extensor muscles). Up-right posture need postural reflexes. The basis of posture is the ability to keep certain Posture depends on muscle tone (stretch reflex) ( basic group of muscles in sustained contraction for long periods. Variation in the degree of contraction and postural reflex). tone in different groups of muscle decides the The main pathways concerned with posture are: posture of the individual. Medial tracts: control proximal limbs & axial muscles for posture & gross movements. Lateral pathways: as corticospinal-rubrospinal control distal limbs. 3 ONLY IN MALES’ SLIDES Postural reflex These reflexes resist displacement of the body caused by gravity or acceleratory forces, and they have the following functions: 1. -
A Confocal Microscopic Study of Gene Transfer Into the Mesencephalic Tegmentum of Juvenile Chum Salmon, Oncorhynchus Keta, Using Mouse Adeno-Associated Viral Vectors
International Journal of Molecular Sciences Article A Confocal Microscopic Study of Gene Transfer into the Mesencephalic Tegmentum of Juvenile Chum Salmon, Oncorhynchus keta, Using Mouse Adeno-Associated Viral Vectors Evgeniya V. Pushchina * , Ilya A. Kapustyanov, Ekaterina V. Shamshurina and Anatoly A. Varaksin A.V. Zhirmunsky National Scientific Center of Marine Biology, Far East Branch, Russian Academy of Sciences, 690041 Vladivostok, Russia; [email protected] (I.A.K.); [email protected] (E.V.S.); [email protected] (A.A.V.) * Correspondence: [email protected] Abstract: To date, data on the presence of adenoviral receptors in fish are very limited. In the present work, we used mouse recombinant adeno-associated viral vectors (rAAV) with a calcium indicator of the latest generation GCaMP6m that are usually applied for the dorsal hippocampus of mice but were not previously used for gene delivery into fish brain. The aim of our work was to study the feasibility of transduction of rAAV in the mouse hippocampus into brain cells of juvenile chum salmon and subsequent determination of the phenotype of rAAV-labeled cells by confocal laser scanning microscopy (CLSM). Delivery of the gene in vivo was carried out by intracranial injection of a GCaMP6m-GFP-containing vector directly into the mesencephalic tegmentum region of Citation: Pushchina, E.V.; Kapustyanov, I.A.; Shamshurina, E.V.; juvenile (one-year-old) chum salmon, Oncorhynchus keta. AAV incorporation into brain cells of the Varaksin, A.A. A Confocal juvenile chum salmon was assessed at 1 week after a single injection of the vector. AAV expression in Microscopic Study of Gene Transfer various areas of the thalamus, pretectum, posterior-tuberal region, postcommissural region, medial into the Mesencephalic Tegmentum and lateral regions of the tegmentum, and mesencephalic reticular formation of juvenile O.