Literatur 663 Cavus Und Kyphoskoliose Sowie Generalisierten Krampfanfallen Gekennzeichnet

Total Page:16

File Type:pdf, Size:1020Kb

Literatur 663 Cavus Und Kyphoskoliose Sowie Generalisierten Krampfanfallen Gekennzeichnet Literatur 663 cavus und Kyphoskoliose sowie generalisierten Krampfanfallen gekennzeichnet. Die klini­ sche Manifestation der Erkrankung korrelierte mit einem Befall nahezu aller neuronaler Systeme. Intranukleiire eosinophile hyaline Einschliisse lieBen sich in nahezu allen zentralen, peripheren und autonomen Neuronen nachweisen. Die Pathogenese der neuronalen Ein­ schliisse ist unklar, doch vermuten die Autoren, daB es sich urn eine metabolische Starung handelt, die das nukleiire Protein der Neurone betrifft und nicht auf eine Virusinfektion zuriickzufiihren ist. Die hyalinen Einschliisse bestehen allerdings bei dem Fall von SUNG et al. (1980) elektronenmikroskopisch aus geraden Filamenten, die in verschiedenen Richtungen angeordnet sind, bei unserem Fall aber aus granuUiren, nicht fila­ mentosen Substanzen. Literatur Aagard OC (1912/13) Ober die LymphgeniBe der Zunge des quergestreiften Muskelgewebes und der Speicheldriisen des Menschen. Anat Hefte 47, 493-648 Aberfeld DC, Hinterbuchner LP, Schneider M (1965) Myotonia, dwarfism, diffuse bone disease and unusual ocular and facial abnormalities (a new syndrome). Brain 88,313-322 Aberfeld DC, Namba T, Vye M, Grob D (1970) Chondrodystrophic myotonia: Report of two cases. Mytonia, dwarfism, diffuse bone disease, and unusual ocular and facial abnormalities. Arch Neurol 22, 455-462 Abid F, Hudgson P, Hall R, Weiser R (\978) Moebius syndrome, peripheral neuropathy and hypo gonadotrophic hypogonadism. J neurol Sci 35,309-315 Abourizk N, Khalil BA, Bahuth N, Afifi AK (1979) Clofibrate-induced muscular syndrome. Report of a case with clinical, electro myographic and pathologic observations. J neurol Sci 42, 1-9 Abraham W A (1977) Factors in delayed muscle soreness. Med Sci Sports 9, 11-20 Abrikossoff A (1926) Ober Myome, ausgehend von der quergestreiften willkiirlichen Musku­ latur. Arch path Anat 260, 215-233 Acheson GH, Ratnoff OD, Schoenbach ER (1942) Localized action on spinal cord of intramuscularily injected tetanus toxin. J exp Med 75, 465--480 Ackerman LV (1958) Extra-osseous localized nonneoplastic bone and cartilage formation (so-called myositis ossificans). Clinical and pathological confusion with malignant neo­ plasms. J Bone Jt Surg A40, 279 Adachi M, Torii J, Yolk BW, Briet P, Wolnitz A, Schneck L (1973) Electron microscopic and enzyme histochemical studies of cerebellum, ocular and skeletal muscles in chronic progressive ophthalmoplegia with cerebellar ataxia. Acta neuropath (Berl) 23, 300-312 Adal MN (\969) The fine structure of the sensory region of the cat muscle spindles. J Ultrastruct Res 26, 332-354 Adams RD (\969) Pathological reaction of the skeletal muscle fibre in man. In: Walton IN (ed) Disorders of voluntary muscle. Churchill, London pp 143-202 Adams RD (1975) Diseases of muscle. A study in pathology, 3rd edn. Harper & Row, New York 588 p Adams RD, Denny-Brown D, Pearson CM (1962) Diseases of muscle. A study in pathology, 2nd edn. Harper & Row, New York, 735 p. Reprinted 1965 Adams RD, Rebeiz J (1966) Histopathologie der myotonischen Erkrankungen. In: Kuhn E (Hrsg) Progressive Muskeldystrophie, Myotonie, Myasthenie. Springer Berlin Heidel­ berg New York, S 191-203 Adornato BT, Kagen LJ, Garver FA, Engel WK (1978) Depletion of serum hemopexin in fulminant rhabdomyolysis. Arch Neurol 35, 547-548 Adrian ED, Umrath K (1929) The impulse discharge from the Pacinian corpuscle. J Physiol (Lond) 68, 139-154 Afifi AK, Aleu FP, Goodgold J, MacKay B (1966) Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis. Neurology (Minneap) 16, 475--481 664 Literatur Afifi AK, Bergman RA, Zellweger H (1973) A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy. J Neurol Neurosurg Psychiat 36,643-650 Afifi AK, Der Kaloustian VM, Bahuth NB, Mire-Salman J (1974) Concentrically laminated membranous inclusions in myofibres of Dygve-Melchior-Clausen syndrome. J neurol Sci 21, 335-340 Afifi AK, Frayha RA, Bahuth NB, Tekian A (1980) The myopathology of Behcet's disease A histochemical light, and electron-microscopic study. J neurol Sci 48, 333-342 Afifi AK, Ibrahim MZM, Bergman RA, Abu Haydar N, Mire J, Bahuth N, Kaylani F (1972) Morphologic features of hypermetabolic mitochondrial disease. A light micro­ scopic, histochemical and electron microscopic study. J neurol Sci 15, 271-290 Afifi AK, Rebeiz J, Mire J, Andonian SJ, Der Kaloustian VM (1972) The myopathology of the prune belly syndrome. J neurol Sci 15, 153-165 Afifi AK, Smith JW, Zellweger H (1965) Congenital nonprogressive myopathy. Central core disease and nemaline myopathy in one family. Neurology (Minneap) 15, 371-381 Agamanolis DP, Askari AD, Di Mauro S, Hays A, Kumar K, Lipton M, Raynor A (1980) Muscle phosphofructokinase deficiency: Two cases with unusual polysaccharide accumulation and immunologically active enzyme protein. Muscle & Nerve 3, 456-467 Agostini B, Noetzel H (1970) Morphological study of muscle fibres and motor end-plates in tetanus. In: Walton IN, Canal N, Scarlato G (eds) Muscle diseases (Proceedings of an International Congress, Milan 1969). Intern Congr Series No 199. Excerpta Medi­ ca, Amsterdam, pp 123-127 Agostoni A, Vergani C, Villa L (1966) Intracellular distribution of the different forms of lactic dehydrogenases. Nature (Lond) 209, 1024 Aguayo AJ, Hudgson P (1970) Observations on the short-term effects of chloroquine on skeletal muscle. An experimental study in the rabbit. J neurol Sci 11, 301-325 Aharonov A, Abransky 0, Tarrab-Hazdai R, Fuchs S (1975) Humoral antibodies to acetyl­ choline receptor in patients with myasthenia gravis. Lancet II, 340-342 Ahlqvist GBS, Landin D, Wroblewski RBS (1975) Ultrastructure of skeletal muscle in patients with Parkinson's disease and upper motor lesions. Lab Invest 32, 673-679 Aitken JT (1950) Growth of nerve implants in voluntary muscle. J Anat (Lond) 84, 38-49 Aitken RS, Allott EN, Castledern LIM, Walker M (1937) Observations on a case of familial periodic paralysis. Clin Sci 3, 47-57 Alajouanine Th, Nick J (1945). De I'existence d'une myopathie d'origine hypothyroidenne. Paris med 129, 346-351 Aleu FP, Afifi AD (1964) Ultrastructure of muscle in myotonic dystrophy. Preliminary observations. Amer J Path 45,221-223 Alevizos B, Spengos M, Vassilopoulos D, Stefanis C (1976) y-glutamyl transpeptidase. Elevated activity in myotonic dystrophy. J neurol Sci 28,225-231 Allbrook DB, Baker W de C, Kirkaldy-Willis WH (1966) Muscle regeneration in experimen­ tal animals and in man. J Bone Jt Surg B48, 153-169 Allbrook DB, Han MF, Hellmuth AE (1971) Population of satellite cells in relation to age and mitotic activity. Pathology 3, 233-243 Allen ER, Pepe F (1965) Ultrastructure of developing muscle cells in the chick embryo. Amer J Anat 116, 115-147 Allen JE, Rodgin DW (1960) Mental retardation in association with progressive muscular dystrophy. Amer J Dis Child 100, 208-211 Allen PW, Enzinger FM (1972) Hemangioma of skeletal muscle. An analysis of 89 cases. Cancer (Philad) 29, 8-22 Aloisi M (1970) Patterns of muscle regeneration. In: Milhorat AT, Mauro A, Shafiq SA (eds) Regeneration of striated muscle and myogenesis. Intern Congr Series No 218. Excerpta Medica, Amsterdam, p 180 Aloisi M, Margareth A (1976) The question of glycolytic enzyme localization in the skeletal muscle fiber and its bearing upon certain aspects of muscle diseases. In: Milhorat AT (ed) Exploratory concepts in muscular dystrophy and related disorders. Excerpta medica Foundation, Amsterdam, pp 305 Aloisi M, Mussini I, Schiaffino S (1973) Activation of muscle nuclei in denervation and Literatur 665 hypertrophy. In: Kakulas BA (ed) Basic research in myology, part 1, Intern Congr Series No 294. Excerpta Medica, Amsterdam, pp 338-342 Alpert LI, Rule A, Norio M, Kott E, Kornfeld P, Ossermann KE (1972) Studies in myasthenia gravis: cellular hypersensitivity to skeletal muscle. Amer J clin Path 58, 647-653 Altschul R (1942) Atrophy, degeneration and metaplasia in denervated skeletal muscle. Arch Path 34, 982-988 Altschul R (1947) On nuclear division in damaged skeletal muscle. Rev canad Bioi 6, 485 Altschul R (1962) Nuclear proliferation ("nucleosis") in damaged skeletal muscle - a critical review. Z Zellforsch 56, 425--436 Alvira MM, Mendoza M (1975) Reye's syndrome: a viral myopathy. New Engl J Med 292, 1297 Ambache N (1949) The peripheral action of Cl. botulinum toxin. J Physiol (Lond) 108, 127-141 Amici GB (1858) Sulla fibra muscolare. II. Tempo-Giornale Italiano di Medicina, Chirurgia e Scienze affini, Anno I, vol III, p 328 Amick LD, Johnson WH, Smith HL (1967) Electromyographic and histopathologic correla­ tion in arthrogryposis. Arch Neurol 16, 512-523 Andersen DH (1952) Studies on glycogen disease with report of a case in which the glycogen was abnormal. In: Najjar VA (ed) Carbohydrate metabolism. Johns Hopkins, Baltimore, pp 28--42 Andersen DH (1956) Familial cirrhosis of the liver with storage of abnormal glycogen. Lab Invest 5, 11-20 Andersen P, Hendriksson J (1977) Training induced changes in the subgroups of human type II skeletal muscle fibres. Acta physiol scand 99, 123-125 Anderson WR, Richards AM (1968) Evaluation of lower extremity muscle biopsies in the diagnosis of atheroembolism. Arch Path 86, 535-541 Anderson-Cedergren E (1959) Ultrastructure of motor end plate and sarcoplasmic compo­ nents of mouse skeletal muscle fiber as revealed by three-dimensional reconstructions from serial sections. J Ultrastruct Res, Suppll, 1-191 Andrade C (1951) Note preiiminaire sur une forme particuliere de neuropathie peripherique. Rev neurol 85, 301-306 Andrade C (1952) A peculiar form of peripheral neuropathy. Brain 75,408--427 Andrews JM, Johnson RT, Brazier MAB (1976) Amyotrophic lateral sclerosis, 298 p. UCLA Forum in Medical Sciences, No 19. Academic Press, New York San Francisco London Andrus K, Kass EH, Adams RD, Turner FC, Feldman HA (1952) Toxoplasmosis in the human adult. Arch intern Med 89, 759-792 Angelini C, Lucke S, Cantarutti F (1976) Carnitine deficiency of skeletal muscle: Report of a treated case. Neurology (Minneap) 26, 633-637 Angervall L, Moller-Nielsen J, Stener B, Svendsen P (1979) Concomitant arteriovenous vascular malformation in skeletal muscle.
Recommended publications
  • VIEW Open Access Muscle Spindle Function in Healthy and Diseased Muscle Stephan Kröger* and Bridgette Watkins
    Kröger and Watkins Skeletal Muscle (2021) 11:3 https://doi.org/10.1186/s13395-020-00258-x REVIEW Open Access Muscle spindle function in healthy and diseased muscle Stephan Kröger* and Bridgette Watkins Abstract Almost every muscle contains muscle spindles. These delicate sensory receptors inform the central nervous system (CNS) about changes in the length of individual muscles and the speed of stretching. With this information, the CNS computes the position and movement of our extremities in space, which is a requirement for motor control, for maintaining posture and for a stable gait. Many neuromuscular diseases affect muscle spindle function contributing, among others, to an unstable gait, frequent falls and ataxic behavior in the affected patients. Nevertheless, muscle spindles are usually ignored during examination and analysis of muscle function and when designing therapeutic strategies for neuromuscular diseases. This review summarizes the development and function of muscle spindles and the changes observed under pathological conditions, in particular in the various forms of muscular dystrophies. Keywords: Mechanotransduction, Sensory physiology, Proprioception, Neuromuscular diseases, Intrafusal fibers, Muscular dystrophy In its original sense, the term proprioception refers to development of head control and walking, an early im- sensory information arising in our own musculoskeletal pairment of fine motor skills, sensory ataxia with un- system itself [1–4]. Proprioceptive information informs steady gait, increased stride-to-stride variability in force us about the contractile state and movement of muscles, and step length, an inability to maintain balance with about muscle force, heaviness, stiffness, viscosity and ef- eyes closed (Romberg’s sign), a severely reduced ability fort and, thus, is required for any coordinated move- to identify the direction of joint movements, and an ab- ment, normal gait and for the maintenance of a stable sence of tendon reflexes [6–12].
    [Show full text]
  • Multi-Scale Modelling of the Neuromuscular System -- Coupling
    Received: 21 January 2019 Revised: 13 May 2019 Accepted: 14 May 2019 DOI: 10.1002/wsbm.1457 ADVANCED REVIEW Multiscale modeling of the neuromuscular system: Coupling neurophysiology and skeletal muscle mechanics Oliver Röhrle1,2 | Utku S¸. Yavuz1,3 | Thomas Klotz1,2 | Francesco Negro4 | Thomas Heidlauf5 1Institute for Modelling and Simulation of Biomechanical Systems, University of Abstract Stuttgart, Stuttgart, Germany Mathematical models and computer simulations have the great potential to substan- 2Stuttgart Center for Simulation Sciences tially increase our understanding of the biophysical behavior of the neuromuscular (SC SimTech), University of Stuttgart, system. This, however, requires detailed multiscale, and multiphysics models. Stuttgart, Germany Once validated, such models allow systematic in silico investigations that are not 3Biomedical Signals and Systems, Universiteit Twente, Enschede, necessarily feasible within experiments and, therefore, have the ability to provide The Netherlands valuable insights into the complex interrelations within the healthy system and for 4 Department of Clinical and Experimental pathological conditions. Most of the existing models focus on individual parts of Sciences, Universià degli Studi di Brescia, Brescia, Italy the neuromuscular system and do not consider the neuromuscular system as an 5EPS5 – Simulation and System Analysis, integrated physiological system. Hence, the aim of this advanced review is to facili- Hofer pdc GmbH, Stuttgart, Germany tate the prospective development of detailed biophysical models of the entire neu- romuscular system. For this purpose, this review is subdivided into three parts. The Correspondence Oliver Röhrle, Institute for Modelling and first part introduces the key anatomical and physiological aspects of the healthy Simulation of Biomechanical Systems, neuromuscular system necessary for modeling the neuromuscular system.
    [Show full text]
  • Mammalian Muscle Spindles, Which Are Known to Be Sensory Stretch
    Short Communication Japanese Journal of Physiology, 38, 747-751, 1988 Histochemical Properties of Intrafusal Fibers in the Soleus Muscle of the Aged Rat Aklhlko ISHIHARA College of General Education, University of Tokushima, Tokushima, 770 Japan Summary ATPase reaction profiles of intrafusal fibers in the muscle spindle of the soleus muscle of 135-week-old rats were examined. Nuclear bags fibers contained an acid- and alkaline-labile form of the enzyme or an acid-labile and alkaline-stabile form, nuclear bag2 fibers contained an acid- and alkaline-stabile form, and nuclear chain fibers contained an acid- labile and alkaline-stabile form. These results indicate that the enzyme histochemical heterogeneity of intrafusal fibers is well-preserved during ageing. Key words : intrafusal muscle fiber, histochemistry, ageing. Mammalian muscle spindles, which are known to be sensory stretch receptors, contain three types of encapsulated intrafusal muscle fibers, i.e., nuclear bags, nuclear bag2, and nuclear chain fibers (BANKSet al., 1977). These fibers can also be distinguished histochemically on the basis of the myosin ATPase reaction: nuclear bags fibers contain an acid-stabile and base-labile form of the enzyme, nuclear bag2 fibers contain an acid- and base-stabile form, and nuclear chain fibers contain an acid-labile and base-stabile form (OVALLEand SMITH,1972). Despite a number of studies on age-related changes in histochemical properties of extrafusal muscle fibers (CACCIAet al., 1979; LARSSONand EDSTROM,1986; ALNAQEEBand GOLDSPINK,1987; EDSTROMand LARSSON,1987), little is known about the histochemical characteristics of intrafusal muscle fibers in old age. Therefore, this study investigated ATPase reaction in intrafusal muscle fibers of the soleus muscle of aged rats.
    [Show full text]
  • Generating Intrafusal Skeletal Muscle Fibres in Vitro
    TEJ0010.1177/2041731420985205Journal of Tissue EngineeringBarrett et al. 985205review-article2020 Review Journal of Tissue Engineering Volume 11: 1 –15 Generating intrafusal skeletal © The Author(s) 2020 Article reuse guidelines: sagepub.com/journals-permissions muscle fibres in vitro: Current state https://doi.org/10.1177/2041731420985205DOI: 10.1177/2041731420985205 of the art and future challenges journals.sagepub.com/home/tej Philip Barrett1 , Tom J Quick2,3, Vivek Mudera1 and Darren J Player1 Abstract Intrafusal fibres are a specialised cell population in skeletal muscle, found within the muscle spindle. These fibres have a mechano-sensory capacity, forming part of the monosynaptic stretch-reflex arc, a key component responsible for proprioceptive function. Impairment of proprioception and associated dysfunction of the muscle spindle is linked with many neuromuscular diseases. Research to-date has largely been undertaken in vivo or using ex vivo preparations. These studies have provided a foundation for our understanding of muscle spindle physiology, however, the cellular and molecular mechanisms which underpin physiological changes are yet to be fully elucidated. Therefrom, the use of in vitro models has been proposed, whereby intrafusal fibres can be generated de novo. Although there has been progress, it is predominantly a developing and evolving area of research. This narrative review presents the current state of art in this area and proposes the direction of future work, with the aim of providing novel pre-clinical and clinical applications. Keywords Skeletal muscle, muscle spindle, intrafusal fibre, proprioception, tissue engineering Received: 18 August 2020; accepted: 12 December 2020 Introduction main aim is to summarise how our understanding of muscle spindle morphogenesis, has informed the devel- Proprioception is an integrated, multi-system physiological opment of in vitro models of intrafusal fibres.
    [Show full text]
  • Rehabilitation Principles for Motor Dysfunctions According to the Kozyavkin Method
    Kozyavkin V. I. Sak N. N. Kachmar O. O. Babadahly M. O. Rehabilitation principles for motor dysfunctions according to the Kozyavkin Method International Clinic of Rehabilitation www.reha.lviv.ua 2009 1 Universal Decimal classification УДК 616.831 - 009.11 - 053.2 - 085.838 Library and descriptive classifier ББК 57.336.1 Kozyavkin V. I., Sak N. N., Kachmar O. O., Babadagly M. A. Principles of rehabilitation of motor dysfunctions according to Kozyavkin Method. – Lviv: scientific production company ”Ukrayinska tekhnolohiya” (Ukrainian technology), 2007.- 192p. The proposed book is devoted to theoretical principles of motor dysfunction rehabilitation according to Prof. Kozyavkin’s Method and reflects 17 years of experience by the staff at the Institute of Medical Rehabilitation and the International Clinic of Rehabilitation. Readers will be informed about fundamentals related to the organization of human movement systems and rehabilitation principles for disorders of function caused by brain lesions and, in particular, cerebral palsy. They will come to understand how this idea evolved into a fundamentally new tendency in medical treatments and will learn about the effectiveness and application of the given system of rehabilitation. The book will be useful to child neurologists, pediatricians, specialists in medical and physical rehabilitation and students attending related academic institutions. ISBN 978-966-345-118-3 © International Clinic of Rehabilitation 2 Introduction Introduction Motor dysfunctions are one of the main causes of child disabilities and rank the problem of cerebral palsies together with the most important tasks which social pediatrics, child neurology and medical rehabilitation face. For many years, the history of the development of medical treatments for CP was based on attempts to eliminate the most obvious disorders of movement and posture.
    [Show full text]
  • Therapeutic Exercise for Physical Therapist Assistants 2Nd Ed
    LWBK942-FM.qxd 6/25/11 8:45 AM Page x 91537_FM.2 11/30/06 8:30 AM Page i THERAPEUTIC EXERCISE for Physical Therapist Assistants SECOND EDITION 91537_FM.2 11/15/06 4:05 PM Page ii 91537_FM.2 11/30/06 8:38 AM Page iii THERAPEUTIC EXERCISE for Physical Therapist Assistants SECOND EDITION WILLIAM D. BANDY, PT, PhD, SCS, ATC Professor Department of Physical Therapy University of Central Arkansas Conway, Arkansas BARBARA SANDERS, PT, PhD, SCS Professor and Chair Department of Physical Therapy Texas State University—San Marcos Associate Dean College of Health Professions San Marcos, Texas Photography by MICHAEL A. MORRIS, FBCA University of Arkansas for Medical Sciences 91537_FM.2 11/15/06 4:05 PM Page iv Acquisitions Editor: Peter Sabatini Managing Editor: Andrea M. Klingler Marketing Manager: Allison M. Noplock Associate Production Manager: Kevin P. Johnson Creative Director: Doug Smock Compositor: Maryland Composition Printer: Quebecor Dubuque Copyright © 2008 Lippincott Williams & Wilkins 351 West Camden Street Baltimore, MD 21201 530 Walnut Street Philadelphia, PA 19106 All rights reserved. This book is protected by copyright. No part of this book may be reproduced in any form or by any means, including photocopying, or utilized by any information storage and retrieval system without written permis- sion from the copyright owner. The publisher is not responsible (as a matter of product liability, negligence, or otherwise) for any injury resulting from any material contained herein. This publication contains information relating to general principles of medical care that should not be construed as specific instructions for individual patients. Manufacturers’ product information and package inserts should be reviewed for current information, including contraindications, dosages, and precautions.
    [Show full text]
  • Functional Analysis of Human Intrafusal Fiber Innervation by Human Γ-Motoneurons
    www.nature.com/scientificreports OPEN Functional analysis of human intrafusal fber innervation by human γ-motoneurons Received: 25 May 2017 A. Colón, X. Guo, N. Akanda, Y. Cai & J. J. Hickman Accepted: 21 November 2017 Investigation of neuromuscular defcits and diseases such as SMA, as well as for next generation Published: xx xx xxxx prosthetics, utilizing in vitro phenotypic models would beneft from the development of a functional neuromuscular refex arc. The neuromuscular refex arc is the system that integrates the proprioceptive information for muscle length and activity (sensory aferent), to modify motoneuron output to achieve graded muscle contraction (actuation eferent). The sensory portion of the arc is composed of proprioceptive sensory neurons and the muscle spindle, which is embedded in the muscle tissue and composed of intrafusal fbers. The gamma motoneurons (γ-MNs) that innervate these fbers regulate the intrafusal fber’s stretch so that they retain proper tension and sensitivity during muscle contraction or relaxation. This mechanism is in place to maintain the sensitivity of proprioception during dynamic muscle activity and to prevent muscular damage. In this study, a co-culture system was developed for innervation of intrafusal fbers by human γ-MNs and demonstrated by morphological and immunocytochemical analysis, then validated by functional electrophysiological evaluation. This human-based fusimotor model and its incorporation into the refex arc allows for a more accurate recapitulation of neuromuscular function for applications in disease investigations, drug discovery, prosthetic design and neuropathic pain investigations. Tere has been a recent emphasis on the development of in vitro “human-on-a-chip” systems for use in drug discovery studies as well as basic cell biology investigations.
    [Show full text]
  • Ultrastructural Abnormalities of Muscle Spindles in the Rat Masseter Muscle with Malocclusion-Induced Damage
    I Histol Histopathol (2002) 17: 45-54 Histology and http://www.ehu.es/histol-histopathol Histopathology Cellular and Molecular Biology Ultrastructural abnormalities of muscle spindles in the rat masseter muscle with malocclusion-induced damage D. Bani1 and M. Bergamini2 'Department of Human Anatomy, Histology and Forensic Medicine, University of Florence, Florence, ltaly and 2Department of Odontostomatology, School of Dentistry, University of Florence, Florence, ltaly Summary. Human temporomandibular disorders due to resulting in muscular overwork and fatigue (reviewed in disturbed occlusal mechanics are characterized by Simons et al., 1999). Among the possible factors sensory, motor and autonomic symptoms, possibly involved in muscle dysfunction, an abnormal behavior of 1 related to muscle overwork and fatigue. Our previous muscle spindles has been proposed (Hubbard and study in rats with experimentally-induced malocclusion Berkoff, 1993; Hubbard, 1996). Muscle spindles are due to unilateral molar cusp amputation showed that the sense organs located in the skeletal muscles where they ipsilateral masseter muscles undergo morphological and serve as-mechanoreceptors sensitive to muscle length biochemical changes consistent with muscle and its changes. Their principal function is the hypercontraction and ischemia. In the present study, the unconscious control of muscle tone and motor activity masseter muscle spindles of the same malocclusion- (Boyd and Smith, 1984). The idea that muscle spindles bearing rats were examined by electron microscopy. might be involved in the functional derangement of the Sham-operated rats were used as controls. In the treated masticatory muscles of malocclusion-bearing subjects rats, clear-cut alterations of the muscle spindles were also comes from experimental studies in cat limb observed 26 days after surgery, when the extrafusal muscles, in which long-lasting contractions and ischemia muscle showed the more severe damage.
    [Show full text]
  • 07-Control of Movement
    11/13/2009 The Neurological Control of Movement Mary ET Boyle, Ph.D. Department of Cognitive Science UCSD Levels of Control of Movement • A change in the place or position of the Movement bodyyyp or a body part. • When neurological control of movement is working correctly we can … do anything! • If not, movement disorders such as myasthenia gravis, movement apraxia, ALS, Parkinson’s disease, and Huntington’s disease. 1 11/13/2009 Levels of Control of Movement: Simple to Complex The simplest movements are reflexive reactions withdrawing your hand after touching a hot stove or blinking when something gets in your eye more complex than reflexes, but less complex than other skills maintaining posture, sitting, standing, walking, and eye movement complex movements can be learned playing the violin, riding a bike, and operating exercise equipment 2 11/13/2009 Stimulation of Movement Most basic level of control is the spinal cord (e.g., spinal reflexes, such as the withdrawal reflex, are solely controlled by the spinal cord). Next level involves brain stem structures in the hindbrain and midbrain (e.g., visual pursuit of a light stimulus). 3 11/13/2009 Highest level of control involves the cerebral cortex and structures such as the dorsolateral prefrontal cortex, the primary and secondary motor cortex, and the somatosensory cortex. Basal Ganglia (main components: striatum, pallidum, substantia nigra, and subthalamic nucleus) Influences movement by smoothing out and refining it (gets rid of extraneous movement and acts to ensure that the selected movement occurs with sufficient, but not excessive, force); also responsible for muscle tone and postural adjustments.
    [Show full text]
  • Diverse and Complex Muscle Spindle Afferent Firing Properties Emerge
    RESEARCH ARTICLE Diverse and complex muscle spindle afferent firing properties emerge from multiscale muscle mechanics Kyle P Blum1,2*, Kenneth S Campbell3, Brian C Horslen2, Paul Nardelli4, Stephen N Housley4, Timothy C Cope2,4, Lena H Ting2,5* 1Department of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, United States; 2Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, United States; 3Department of Physiology, University of Kentucky, Lexington, United States; 4School of Biological Sciences, Georgia Institute of Technology, Atlanta, United States; 5Department of Rehabilitation Medicine, Emory University, Atlanta, United States Abstract Despite decades of research, we lack a mechanistic framework capable of predicting how movement-related signals are transformed into the diversity of muscle spindle afferent firing patterns observed experimentally, particularly in naturalistic behaviors. Here, a biophysical model demonstrates that well-known firing characteristics of mammalian muscle spindle Ia afferents – including movement history dependence, and nonlinear scaling with muscle stretch velocity – emerge from first principles of muscle contractile mechanics. Further, mechanical interactions of the muscle spindle with muscle-tendon dynamics reveal how motor commands to the muscle (alpha drive) versus muscle spindle (gamma drive) can cause highly variable and complex activity during active muscle contraction and muscle stretch that defy simple explanation. Depending on the neuromechanical conditions, the muscle spindle model output appears to ‘encode’ aspects of muscle force, yank, length, stiffness, velocity, and/or acceleration, providing an extendable, *For correspondence: multiscale, biophysical framework for understanding and predicting proprioceptive sensory signals [email protected] (KPB); in health and disease. [email protected] (LHT) Competing interests: The authors declare that no Introduction competing interests exist.
    [Show full text]
  • Functional Characterization of Murine Muscle Spindles: Modulatory Roles of Acetylcholine Receptors and of the Dystrophin-Associated Protein Complex
    Aus dem Institut für physiologische Genomik – Biomedical Center der Ludwig-Maximilians-Universität München Direktorin: Univ. Prof. Dr. Magdalena Götz Functional Characterization of Murine Muscle Spindles: Modulatory Roles of Acetylcholine Receptors and of the Dystrophin-Associated Protein Complex Dissertation zum Erwerb des Doktorgrades der Naturwissenschaften an der medizinischen Fakultät der Ludwig-Maximilians-Universität zu München vorgelegt von Laura Gerwin aus Starnberg 2019 Mit Genehmigung der Medizinischen Fakultät der Universität München Betreuer : Prof. Dr. Stephan Kröger Zweitgutachter(in): : Prof. Anja Horn-Bochtler Dekan: Prof. Dr. med. dent. Reinhard Hickel Tag der mündlichen Prüfung: 09.04.2020 Eidesstattliche Erklärung Ich, Laura Gerwin, erkläre hiermit an Eides statt, dass ich die vorliegende Dissertation mit dem Titel „Functional Characterization of Murine Muscle Spindles: Modulatory Roles of Acetylcholine Receptors and of the Dystrophin-Associated Protein Complex“ selbständig verfasst, mich außer der angegebenen keiner weiteren Hilfsmittel bedient und alle Erkenntnisse, die aus dem Schrifttum ganz oder annähernd übernommen sind, als solche kenntlich gemacht und nach ihrer Herkunft unter Bezeichnung der Fundstelle einzeln nachgewiesen habe. Ich erkläre des Weiteren, dass die hier vorgelegte Dissertation nicht in gleicher oder in ähnlicher Form bei einer anderen Stelle zur Erlangung eines akademischen Grades eingereicht wurde. München, den 24.04.2020 Laura Gerwin Parts of this thesis have been published: Gerwin L., Haupt C., Wilkinson K.A. and Kröger S. (2019). Acetylcholine receptors in the equatorial region of intrafusal muscle fibres modulate mouse muscle spindle sensitivity. The Journal of Physiology 597: 1993-2006. Gerwin L., Rossmanith S., Haupt C., Schultheiß J., Brinkmeier H., Bittner R.E. and Kröger S. (2020) Impaired Muscle Spindle Function in Murine Models of Muscular Dystrophy manuscript submitted for publication.
    [Show full text]
  • Impaired Muscle Spindle Function in Murine Models of Muscular Dystrophy
    Impaired Muscle Spindle Function in Murine Models of Muscular Dystrophy Laura Gerwin1,2, Sarah Rossmanith1, Corinna Haupt1, Jürgen Schultheiß1, Heinrich Brinkmeier3, Reginald E. Bittner4, Stephan Kröger1 1 Department of Physiological Genomics, Biomedical Center, Ludwig-Maximilians- University, Großhaderner Str. 9, D-82152 Planegg-Martinsried, Germany 2 Institute for Stem Cell Research, German Research Center for Environmental Health, Helmholtz Centre Munich, Ingolstädter Landstraße 1, D-85764 Neuherberg, Germany 3 Institute for Pathophysiology, University Medicine Greifswald, Martin-Luther-Str. 6, 17489 Greifswald 4 Neuromuscular Research Department, Center for Anatomy and Cell Biology, Medical University of Vienna, Waehringerstrasse 13, 1090 Vienna, Austria Corresponding author: Stephan Kröger at above address Email: [email protected] Phone: +49-89-2180-71899 Running title: muscle spindles in dystrophic mice Key words: dystrophin, dysferlin, muscle spindle, proprioception, utrophin, muscular dystrophy 1 Acquisition or analysis or interpretation of data for the work; Final approval of the version to be published Stephan Kroger: Conception or design of the work; Acquisition or analysis or interpretation of data for the work; Drafting the work or revising it critically for important intellectual content; Final approval of the version to be published; Agreement to be accountable for all aspects of the work Running Title: muscle spindles in dystrophic mice Dual Publication: No Funding: Deutsche Forschungsgemeinschaft (DFG): Stephan Kroger,
    [Show full text]