Muscle Contraction

Total Page:16

File Type:pdf, Size:1020Kb

Muscle Contraction 10/19/2009 CONTROL OF MOVEMENT: STRIATED MUSCLES SKELETAL (STRIATED) MUSCLE: - each muscle = ____________________________________lots of muscle cells (muscle fibers) - each muscle cell =packed _______________________________________ with myosin and actin filament proteins -Myosin: Filamentous___________________________________________ protein with cross bridges -Actin: _________________________________________________Filamentous protein where cross bridges of myosin bind ANATOMY OF SKELETAL MUSCLE Axon______________ of alpha motor_____________ neuron Endplate________ Extrafusal muscle fiber ________Muscle Tendon_________ Myofibril Actin_____________ filament __________________Myosin filament ___________Z discs (bands) MUSCLE CONTRACTION Watch muscle contraction movie Myosin Myosin cross bridges filament Actin filaments Actin MtfMovement of filament actin filament Myosin cross bridge Movement of myosin filament Heads of cross bridges: 1. Attach to active sites on actin filaments 2. “Ratchet” forward 3. Release 4. Repeat -Onlyoccurs in the presence of calcium How is calcium released? From___________________________ activity at neuromuscular ________junction 1 10/19/2009 NEUROMUSCULAR JUNCTION Synapse between terminal of alpha_________________ motor neuron and a muscle___________ fiber is called a neuromuscular junction; Terminals of alpha motor neurons synapse on motor_____________ enplates - grooves along the surface of muscle fibers; When motor neuron fires, _____________acetylcholine is liberated from terminals at the endplate and depolarizes muscle fibers - endplate________________; potentials Depolarization of muscle fiber opens ________voltage- dependent_________________________ calcium channels , producing a large _______calcium influx into the fiber; Calcium triggers the actin-myosin “rowing” action leading to the contraction__________ of muscle fibers; Calcium is extruded from fiber by “pump”; Endplate potential ______always cause muscle fiber to fire = contraction or “twitch” of fiber. MOTOR UNITS Motor unit: _______________________________________One alpha motor neuron + its axon + all the ___________________________________muscle fibers it innervates (contacts) Motor pool: All______________________________________ motor neurons that innervate fibers of __________________a single muscle Muscle fibers Alpha motor neurons Axons - weak muscular contraction = ______________________few motor units activated _ - strong contraction = lots_______________________ of motor units activated - discrete/fine movements = __________________________small motor units – few fibers ____________activated - crude/gross movements = big__________________________ motor units – lots of units ____________activated 2 10/19/2009 Localization and distribution of motor neurons in the spinal cord Somatosensory (mechano) and nociceptive (pain) receptors Glabrous skin: skin_________________________________ that does not have hair follicles (hairless) Hairy skin: skin__________________________________ that covers the rest of the body There are 3 groups of somatosensory receptors: 1. ______________Nociception 2. ______________Hapsis 3. ______________ Proprioception Epidermis Dermis 3 10/19/2009 Somatosensory pathway from receptors to somatosensory (primary) cortex: How pain reaches the somatosensory cortex 4 10/19/2009 How is the phenomenon of “referred pain” produced? Arm and shoulder pain “referred” from heart pain receptors during heart attack. MONOSYNAPTIC STRETCH REFLEX Involves: - _________________intrafusal muscle - _________________________________muscle spindle receptor (signals stretch) - ________________________________________spindle afferent neuron (pseudounipolar __________________________sensory neuron) - ______________________________intrafusal (gamma) motor neuron - ____________________________________extrafusal muscle and motor neuron Watch stretch reflex movie 5 10/19/2009 How muscle spindles work! - Gamma motor neurons provide the ________overall ________________________________sensitivity of the muscle spindles - without gamma motor neurons, the spindles would become __________________________“slack” and unresponsive to_______________ stretch. - gamma motor neurons function __________to adjust the length_______________________ of intrafusal muscles titto an appropriate degree of tension Gamma motor neurons Muscle spindles Extrafusal muscle Spindle “slack” - insensitive to strech Spindle “tight” - ready to respond to strech POLYSYNAPTIC REFLEXES: EXAMPLE OF WITHDRAWAL FROM PAIN - reflexes requiring interneurons_________________________ in the spinal cord - concept of _______________________________antagonistic muscles (flexor vs. ____________________________extensor muscles) - ex., biceps vs. triceps of arms - reciprocal innervation (excitatory vs. inhibitory) -excitatory ________________________________________ and inhibitory interneurons work ____________________________________together to withdraw limb from pain. 6 10/19/2009 CROSSED EXTENSOR REFLEX Think of this reflex as being ____________“connected” with previous polysynaptic withdrawal reflex For example, if flexion reflex triggered in one leg, extensor___________________________________ reflex is triggered in other leg All thi s h appens _________________________;attht the leve l o fthf the sp ina l cor d the brain has nothing to do with it. This serves to: - _______________________________________help remove or push entire body away from _______________________painful stimulus; - _______________________________________help restore balance when flexed leg is _____________________withdrawn. An example of a complex sensorimotor reflex is ________.walking - spinal cat when placed on a treadmill can ______________________________________initiate normal walking when provided with ______________________________________somatosensory feedback of treadmill. GOLGI TENDON REFLEX or how not to shred your muscles and bones! Golgi Tendon Organ: ______________________receptor organ sensitive ________________________________________to stretch and located at the junction of the _____________________________tendon and muscle. - only contacts ________________________inhibitory interneurons. - if maximally activated, completely___________________ inhibits ________________________________alppyha motor neuron activity. - helps prevent tearing of muscles and tendons from bone Golgi____________ tendon organ_______ ____________________Pseudounipolar _________neuron alpha______________________ motor neuron inhibitory_________________________ interneuron 7.
Recommended publications
  • Of 100 1. the Golgi Tendon Organ Is an Essential Component of Static
    1. The Golgi tendon organ is an essential component of static stretching because it A. increases muscle spindle activity in a tight muscle. Rationale A. Golgi tendon organs decrease muscle spindle activity. B. prevents muscles from stretching too far or too fast. Rationale B. Muscle spindles prevent muscles from stretching too far or too fast. C. increases contraction rate in muscle fibers. Rationale C. Holding a stretch creates tension in the muscle, which stimulates the Golgi tendon organ, causes relaxation of an overactive muscle, and allows optimal lengthening of tissue. D. prevents muscle from being placed under excessive tension.(correct) Rationale D. The Golgi tendon organ prevents muscles from being placed under excessive tension (autogenic inhibition). Question Name 1-1 Certification Thinking Skills Foundational Thinking Current Forms 2011 Practice A Primary Reference Chapter 7, Task 1A1 Page 1 of 100 2. Which of the following is the correct force-couple relationship that allows for the upward rotation of the scapula? A. Longus capitus and brachialis Rationale A. The longus capitus concentrically accelerates cervical flexion and lateral flexion, while the brachialis concentrically accelerates elbow flexion. B. Rhomboid minor and anterior scalenes Rationale B. The rhomboid minor concentrically accelerates scapular retraction and downward rotation, while the anterior scalenes concentrically accelerates cervical flexion, rotation, and lateral flexion. C. Sternocleidomastoid and longus coli Rationale C. The sternocleidomastoid concentrically accelerates cervical flexion, rotation, and lateral flexion while the longus coli concentrically accelerate cervical flexion, lateral flexion, and ipsilateral rotation. D. Upper trapezius and lower portions of the serratus anterior (correct) Rationale D. The upper trapezius and the lower portion of the serratus anterior are muscle groups that move together to produce upward rotation of the scapula.
    [Show full text]
  • Microanatomy of Muscles
    Microanatomy of Muscles Anatomy & Physiology Class Three Main Muscle Types Objectives: By the end of this presentation you will have the information to: 1. Describe the 3 main types of muscles. 2. Detail the functions of the muscle system. 3. Correctly label the parts of a myocyte (muscle cell) 4. Identify the levels of organization in a skeletal muscle from organ to myosin. 5. Explain how a muscle contracts utilizing the correct terminology of the sliding filament theory. 6. Contrast and compare cardiac and smooth muscle with skeletal muscle. Major Functions: Muscle System 1. Moving the skeletal system and posture. 2. Passing food through the digestive system & constriction of other internal organs. 3. Production of body heat. 4. Pumping the blood throughout the body. 5. Communication - writing and verbal Specialized Cells (Myocytes) ~ Contractile Cells Can shorten along one or more planes because of specialized cell membrane (sarcolemma) and specialized cytoskeleton. Specialized Structures found in Myocytes Sarcolemma: The cell membrane of a muscle cell Transverse tubule: a tubular invagination of the sarcolemma of skeletal or cardiac muscle fibers that surrounds myofibrils; involved in transmitting the action potential from the sarcolemma to the interior of the myofibril. Sarcoplasmic Reticulum: The special type of smooth endoplasmic Myofibrils: reticulum found in smooth and a contractile fibril of skeletal muscle, composed striated muscle fibers whose function mainly of actin and myosin is to store and release calcium ions. Multiple Nuclei (skeletal) & many mitochondria Skeletal Muscle - Microscopic Anatomy A whole skeletal muscle (such as the biceps brachii) is considered an organ of the muscular system. Each organ consists of skeletal muscle tissue, connective tissue, nerve tissue, and blood or vascular tissue.
    [Show full text]
  • 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]
  • Neural Control of Movement: Motor Neuron Subtypes, Proprioception and Recurrent Inhibition
    List of Papers This thesis is based on the following papers, which are referred to in the text by their Roman numerals. I Enjin A, Rabe N, Nakanishi ST, Vallstedt A, Gezelius H, Mem- ic F, Lind M, Hjalt T, Tourtellotte WG, Bruder C, Eichele G, Whelan PJ, Kullander K (2010) Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as mark- ers for fast motor neurons and partition cells. J Comp Neurol 518:2284-2304. II Wootz H, Enjin A, Wallen-Mackenzie Å, Lindholm D, Kul- lander K (2010) Reduced VGLUT2 expression increases motor neuron viability in Sod1G93A mice. Neurobiol Dis 37:58-66 III Enjin A, Leao KE, Mikulovic S, Le Merre P, Tourtellotte WG, Kullander K. 5-ht1d marks gamma motor neurons and regulates development of sensorimotor connections Manuscript IV Enjin A, Leao KE, Eriksson A, Larhammar M, Gezelius H, Lamotte d’Incamps B, Nagaraja C, Kullander K. Development of spinal motor circuits in the absence of VIAAT-mediated Renshaw cell signaling Manuscript Reprints were made with permission from the respective publishers. Cover illustration Carousel by Sasha Svensson Contents Introduction.....................................................................................................9 Background...................................................................................................11 Neural control of movement.....................................................................11 The motor neuron.....................................................................................12 Organization
    [Show full text]
  • Interpretation of Sensory Information from Skeletal Muscle Receptors for External Control Milan Djilas
    Interpretation of Sensory Information From Skeletal Muscle Receptors For External Control Milan Djilas To cite this version: Milan Djilas. Interpretation of Sensory Information From Skeletal Muscle Receptors For External Control. Automatic. Université Montpellier II - Sciences et Techniques du Languedoc, 2008. English. tel-00333530 HAL Id: tel-00333530 https://tel.archives-ouvertes.fr/tel-00333530 Submitted on 23 Oct 2008 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. UNIVERSITE MONTPELLIER II SCIENCES ET TECHNIQUES DU LANGUEDOC T H E S E pour obtenir le grade de DOCTEUR DE L'UNIVERSITE MONTPELLIER II Formation doctorale: SYSTEMES AUTOMATIQUES ET MICROELECTRONIQUES Ecole Doctorale: INFORMATION, STRUCTURES ET SYSTEMES présentée et soutenue publiquement par Milan DJILAS le 13 octobre 2008 Titre: INTERPRETATION DES INFORMATIONS SENSORIELLES DES RECEPTEURS DU MUSCLE SQUELETTIQUE POUR LE CONTROLE EXTERNE INTERPRETATION OF SENSORY INFORMATION FROM SKELETAL MUSCLE RECEPTORS FOR EXTERNAL CONTROL JURY Jacques LEVY VEHEL Directeur de Recherches, INRIA Rapporteur
    [Show full text]
  • Characterization of Cecal Smooth Muscle Contraction in Laying Hens
    veterinary sciences Communication Characterization of Cecal Smooth Muscle Contraction in Laying Hens Katrin Röhm 1, Martin Diener 2 , Korinna Huber 1 and Jana Seifert 1,* 1 Institute of Animal Science, University of Hohenheim, 70593 Stuttgart, Germany; [email protected] (K.R.); [email protected] (K.H.) 2 Institute of Veterinary Physiology and Biochemistry, Justus-Liebig University, 35392 Gießen, Germany; [email protected] * Correspondence: [email protected] Abstract: The ceca play an important role in the physiology of the gastrointestinal tract in chickens. Nevertheless, there is a gap of knowledge regarding the functionality of the ceca in poultry, especially with respect to physiological cecal smooth muscle contraction. The aim of the current study is the ex vivo characterization of cecal smooth muscle contraction in laying hens. Muscle strips of circular cecal smooth muscle from eleven hens are prepared to investigate their contraction ex vivo. Contraction is detected using an isometric force transducer, determining its frequency, height and intensity. Spontaneous contraction of the chicken cecal smooth muscle and the influence of buffers (calcium-free buffer and potassium-enriched buffer) and drugs (carbachol, nitroprusside, isoprenaline and Verapamil) affecting smooth muscle contraction at different levels are characterized. A decrease in smooth muscle contraction is observed when a calcium-free buffer is used. Carbachol causes an increase in smooth muscle contraction, whereas atropine inhibits contraction. Nitroprusside, isoprenaline and Verapamil result in a depression of smooth muscle contraction. In conclusion, the present results confirm a similar contraction behavior of cecal smooth muscles in laying hens as Citation: Röhm, K.; Diener, M.; shown previously in other species.
    [Show full text]
  • ALS and Other Motor Neuron Diseases Can Represent Diagnostic Challenges
    Review Article Address correspondence to Dr Ezgi Tiryaki, Hennepin ALS and Other Motor County Medical Center, Department of Neurology, 701 Park Avenue P5-200, Neuron Diseases Minneapolis, MN 55415, [email protected]. Ezgi Tiryaki, MD; Holli A. Horak, MD, FAAN Relationship Disclosure: Dr Tiryaki’s institution receives support from The ALS Association. Dr Horak’s ABSTRACT institution receives a grant from the Centers for Disease Purpose of Review: This review describes the most common motor neuron disease, Control and Prevention. ALS. It discusses the diagnosis and evaluation of ALS and the current understanding of its Unlabeled Use of pathophysiology, including new genetic underpinnings of the disease. This article also Products/Investigational covers other motor neuron diseases, reviews how to distinguish them from ALS, and Use Disclosure: Drs Tiryaki and Horak discuss discusses their pathophysiology. the unlabeled use of various Recent Findings: In this article, the spectrum of cognitive involvement in ALS, new concepts drugs for the symptomatic about protein synthesis pathology in the etiology of ALS, and new genetic associations will be management of ALS. * 2014, American Academy covered. This concept has changed over the past 3 to 4 years with the discovery of new of Neurology. genes and genetic processes that may trigger the disease. As of 2014, two-thirds of familial ALS and 10% of sporadic ALS can be explained by genetics. TAR DNA binding protein 43 kDa (TDP-43), for instance, has been shown to cause frontotemporal dementia as well as some cases of familial ALS, and is associated with frontotemporal dysfunction in ALS. Summary: The anterior horn cells control all voluntary movement: motor activity, res- piratory, speech, and swallowing functions are dependent upon signals from the anterior horn cells.
    [Show full text]
  • Innovations Present in the Primate Interneuron Repertoire
    Article Innovations present in the primate interneuron repertoire https://doi.org/10.1038/s41586-020-2781-z Fenna M. Krienen1,2 ✉, Melissa Goldman1,2, Qiangge Zhang2,3, Ricardo C. H. del Rosario2, Marta Florio1,2, Robert Machold4, Arpiar Saunders1,2, Kirsten Levandowski2,3, Heather Zaniewski2,3, Received: 19 July 2019 Benjamin Schuman4, Carolyn Wu3, Alyssa Lutservitz1,2, Christopher D. Mullally1,2, Nora Reed1,2, Accepted: 1 July 2020 Elizabeth Bien1,2, Laura Bortolin1,2, Marian Fernandez-Otero2,5, Jessica D. Lin2, Alec Wysoker2, James Nemesh2, David Kulp2, Monika Burns5, Victor Tkachev6,7,8, Richard Smith9,10, Published online: xx xx xxxx Christopher A. Walsh9,10, Jordane Dimidschstein2, Bernardo Rudy4,11, Leslie S. Kean6,7,8, Check for updates Sabina Berretta5,12,13, Gord Fishell2,14, Guoping Feng2,3 & Steven A. McCarroll1,2 ✉ Primates and rodents, which descended from a common ancestor around 90 million years ago1, exhibit profound diferences in behaviour and cognitive capacity; the cellular basis for these diferences is unknown. Here we use single-nucleus RNA sequencing to profle RNA expression in 188,776 individual interneurons across homologous brain regions from three primates (human, macaque and marmoset), a rodent (mouse) and a weasel (ferret). Homologous interneuron types—which were readily identifed by their RNA-expression patterns—varied in abundance and RNA expression among ferrets, mice and primates, but varied less among primates. Only a modest fraction of the genes identifed as ‘markers’ of specifc interneuron subtypes in any one species had this property in another species. In the primate neocortex, dozens of genes showed spatial expression gradients among interneurons of the same type, which suggests that regional variation in cortical contexts shapes the RNA expression patterns of adult neocortical interneurons.
    [Show full text]
  • Muscle Histology
    Muscle Histology Dr. Heba Kalbouneh Functions of muscle tissue ▪ Movement ▪ Maintenance of posture ▪ Joint stabilization ▪ Heat generation Types of Muscle Tissue ▪ Skeletal muscle ▪ Cardiac muscle ▪ Smooth muscle Types of Muscle Tissue Skeletal •Attach to and move skeleton •40% of body weight •Fibers = multinucleate cells (embryonic cells fuse) •Cells with obvious striations •Contractions are voluntary Cardiac: only in the wall of the heart •Cells are striated •Contractions are involuntary (not voluntary) Smooth: walls of hollow organs •Lack striations •Contractions are involuntary (not voluntary) Similarities… ▪ Their cells are called fibers because they are elongated ▪ Contraction depends on myofilaments ▪ Actin ▪ Myosin ▪ Plasma membrane is called sarcolemma ▪ Sarcos = flesh ▪ Lemma = sheath SKELETAL MUSCLES Epimysium: surrounds whole muscle Endomysium is around each muscle fiber Perimysium is around fascicle = muscle cell= myofiber Skeletal muscle This big cylinder is a fiber: a cell ▪ Fibers (each is one cell) have striations ▪ Myofibrils are organelles of the cell: these are made -an organelle up of myofilaments ▪ Sarcomere ▪ Basic unit of contraction ▪ Myofibrils are long rows of repeating sarcomeres ▪ Boundaries: Z discs (or lines) Sarcomere M line provides an attachment to myosin filaments Z line provides an attachment to actin filaments A band is the darker band of the myofibril containing myosin filaments H band is the lighter section in the middle of the A band where only myosin is present I band is the lighter band containing
    [Show full text]
  • Fine Structure of the Receptors at the Myotendinous Junction of Human Extraocular Muscles
    Histol Histopath (1 988) 3: 103-113 Histology and Fine structure of the receptors at the myotendinous junction of human extraocular muscles A. Sodii, M. Corsii, M.S. Faussone Pellegrini2and G. Salvii 'Eye Clinic, Chair of Physiopathological Optics and Departrnent of Hurnan Anatorny and Histology, Section of Histology, University of Florence, ltaly Summary. The myotendinous junction of the human lntroduction extraocular muscles was studied by electron microscopy. Some peculiar receptorial structures have been found in The proprioceptors known as tendon organs were first the majority of the samples examined. These structures identified by Golgi in 1880 in skeletal muscles. They were are very small and consist of 1) the terminal portion of first described at electron microscope level by Merrillees one muscle fibre, 2) the tendon into which it inserts and in 1962 and later by other authors (Schoultz and Swett, y), within the tendon, a rich nerve arborization, whose 1972, 1974; Barker, 1974: Zelena and Soukup, 1977; branches are always very close to the rnuscle component. Soukup and Zelena, 1985; Ovalle and Dow, 1983). In the Only one discontinuous layer, made up of tlat cells. extraocular muscles (EOM) the presence of tendon which lack a basa1 lamina and often show pinocytotic organs was first excluded by Golgi himself, but further vesicles, encapsules every musculo-tendinous complex. investigations (Dogiel. 1906: Loffredo-Sampaolo, 1952; The tendinous component consists of amorphous ground Bonavolonta, 1956, 1958) led to their identification and substance of different electron density. of collagen and description at light microscopy level in several animal elastic fibres and is divided in compartments by ramified species.
    [Show full text]
  • Tissue Engineered Myelination and the Stretch Reflex Arc Sensory Circuit: Defined Medium Ormulation,F Interface Design and Microfabrication
    University of Central Florida STARS Electronic Theses and Dissertations, 2004-2019 2009 Tissue Engineered Myelination And The Stretch Reflex Arc Sensory Circuit: Defined Medium ormulation,F Interface Design And Microfabrication John Rumsey University of Central Florida Part of the Biology Commons Find similar works at: https://stars.library.ucf.edu/etd University of Central Florida Libraries http://library.ucf.edu This Doctoral Dissertation (Open Access) is brought to you for free and open access by STARS. It has been accepted for inclusion in Electronic Theses and Dissertations, 2004-2019 by an authorized administrator of STARS. For more information, please contact [email protected]. STARS Citation Rumsey, John, "Tissue Engineered Myelination And The Stretch Reflex Arc Sensory Circuit: Defined Medium Formulation, Interface Design And Microfabrication" (2009). Electronic Theses and Dissertations, 2004-2019. 3826. https://stars.library.ucf.edu/etd/3826 TISSUE ENGINEERED MYELINATION AND THE STRETCH REFLEX ARC SENSORY CIRCUIT: DEFINED MEDIUM FORMULATION, INTERFACE DESIGN AND MICROFABRICATION by JOHN WAYNE RUMSEY B.S. University of Florida, 2001 M.S. University of Central Florida, 2004 A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Burnett School of Biomedical Sciences in the College of Medicine at the University of Central Florida Orlando, Florida Fall Term 2009 Major Professor: James J. Hickman ABSTRACT The overall focus of this research project was to develop an in vitro tissue- engineered system that accurately reproduced the physiology of the sensory elements of the stretch reflex arc as well as engineer the myelination of neurons in the systems. In order to achieve this goal we hypothesized that myelinating culture systems, intrafusal muscle fibers and the sensory circuit of the stretch reflex arc could be bioengineered using serum-free medium formulations, growth substrate interface design and microfabrication technology.
    [Show full text]
  • Skeletal Muscle Physiology
    This document was created by Alex Yartsev ([email protected]); if I have used your data or images and forgot to reference you, please email me. Skeletal Muscle Physiology First of all, which muscle is which - Skeletal muscle: o Well-developed cross-striations o Does not contract in absence of a nerve stimulus o The individual muscle fibers DO NOT connect functionally or anatomically (i.e. they don’t form a single sheet of cells, and one fiber’s action potential wont get transmitted to the next) o Generally, skeletal muscle is under voluntary control - Cardiac muscle: o Also has cross-striations o Is functionally syncytial: cells are connected well enough to conduct action potentials to one another o Can contract on its own, without stimulus (but this is under some control via the autonomic nervous system, which modulates its activity) - Smooth muscle: o Has no cross-striations o Two broad types: . VISCERAL or “unitary” smooth muscle: Functionally syncytial, action potentials propagate from cell to cell Contains pacemakers which discharge irregularly, but remains under control of the autonomic nervous system Found in most hollow viscera . MULTI-UNIT SMOOTH MUSCLE Found in the eye and some other locations Does NOT activate spontaneously SKELETAL MUSCLE ORGANIZATION - Each muscle is a bundle of fibers - Each fiber is a long, multinucleated single cell - Each fiber is surrounded by a SARCOLEMMA- the cell membrane - There are NO SYNCYTIAL BRIDGES between the cells. When one cell goes off, the others don’t follow. TRANSVERSE TUBULES: T-tubules, invaginations of SARCOLEMMA: the muscle cell membrane the sarcolemma, they form part of the T-system; the space inside is an extension of the extracellular space.
    [Show full text]