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Spreading the Love: the Circulatory System
Chapter 10 Spreading the Love: The Circulatory System In This Chapter ᮣ Understanding the heart’s rhythm and structure ᮣ Identifying the heart’s chambers and valves ᮣ Tracing arteries, veins, and capillaries ᮣ Touching on fetal circulation his chapter gets to the heart of the well-oiled human machine to see how its central Tpump is the hardest-working muscle in the entire body. From a month after you’re con- ceived to the moment of your death, this phenomenal powerhouse pushes a liquid connec- tive tissue — blood — and its precious cargo of oxygen and nutrients to every nook and cranny of the body, and then it keeps things moving to bring carbon dioxide and waste products back out again. In the first seven decades of human life, the heart beats roughly 2.5 billion times. Do the math: How many pulses has your ticker clocked if the average heart keeps up a pace of 72 beats per minute, 100,000 per day, or roughly 36 million per year? Moving to the Beat of a Pump Also called the cardiovascular system, the circulatory system includes the heart, all blood vessels, and the blood that moves endlessly through it all (see Figure 10-1). It’s what’s referred to as a closed double system; the term “closed” is used for three reasons: because the blood is contained in the heart and its vessels; because the vessels specifically target the blood to the tissues; and because the heart critically regulates blood flow to the tissues. The system is called “double” because there are two distinct circuits and cavities within the heart separated by a wall of muscle called the septum. -
The Myosin Interacting-Heads Motif Present in Live Tarantula Muscle Explains Tetanic and Posttetanic INAUGURAL ARTICLE Phosphorylation Mechanisms
The myosin interacting-heads motif present in live tarantula muscle explains tetanic and posttetanic INAUGURAL ARTICLE phosphorylation mechanisms Raúl Padróna,1,2, Weikang Mab,1, Sebastian Duno-Mirandac,3, Natalia Koubassovad, Kyoung Hwan Leea,4, Antonio Pintoc, Lorenzo Alamoc, Pura Bolañose, Andrey Tsaturyand, Thomas Irvingb, and Roger Craiga aDivision of Cell Biology and Imaging, Department of Radiology, University of Massachusetts Medical School, Worcester, MA 01655; bBiophysics Collaborative Access Team, Department of Biological Sciences, Illinois Institute of Technology, Chicago, IL 60616; cCentro de Biología Estructural, Instituto Venezolano de Investigaciones Científicas, Caracas 1020A, Venezuela; dInstitute of Mechanics, Moscow State University, 119992 Moscow, Russia; and eCentro de Biofísica y Bioquímica, Instituto Venezolano de Investigaciones Científicas, Caracas 1020A, Venezuela This contribution is part of the special series of Inaugural Articles by members of the National Academy of Sciences elected in 2018. Contributed by Raúl Padrón, April 7, 2020 (sent for review December 6, 2019; reviewed by H. Lee Sweeney and Rene Vandenboom) Striated muscle contraction involves sliding of actin thin filaments frozen-hydrated tarantula thick filaments showed that the helices along myosin thick filaments, controlled by calcium through thin of heads on the filaments were formed by a two-headed assem- filament activation. In relaxed muscle, the two heads of myosin blage that we called the myosin interacting-heads motif (IHM) interact with each other on the filament surface to form the (8, 9), formed by the interaction of a blocked head (BH) and a interacting-heads motif (IHM). A key question is how both heads free head (FH) (10) with the subfragment-2 (8) (Fig. -
16 the Heart
Physiology Unit 3 CARDIOVASCULAR PHYSIOLOGY: THE HEART Cardiac Muscle • Conducting system – Pacemaker cells – 1% of cells make up the conducting system – Specialized group of cells which initiate the electrical current which is then conducted throughout the heart • Myocardial cells (cardiomyocytes) • Autonomic Innervation – Heart Rate • Sympathetic and Parasympathetic regulation • �1 receptors (ADRB1), M-ACh receptors – Contractility • Sympathetic stimulus • Effects on stroke volume (SV) Electrical Synapse • Impulses travel from cell to cell • Gap junctions – Adjacent cells electrically coupled through a channel • Examples – Smooth and cardiac muscles, brain, and glial cells. Conducting System of the Heart • SA node is the pacemaker of the heart – Establishes heart rate – ANS regulation • Conduction Sequence: – SA node depolarizes – Atria depolarize – AV node depolarizes • Then a 0.1 sec delay – Bundle of His depolarizes – R/L bundle branches depolarize – Purkinje fibers depolarize Sinus Rhythm: – Ventricles depolarize Heartbeat Dance Conduction Sequence Electrical Events of the Heart • Electrocardiogram (ECG) – Measures the currents generated in the ECF by the changes in many cardiac cells • P wave – Atrial depolarization • QRS complex – Ventricular depolarization – Atrial repolarization • T wave – Ventricular repolarization • U Wave – Not always present – Repolarization of the Purkinje fibers AP in Myocardial Cells • Plateau Phase – Membrane remains depolarized – L-type Ca2+ channels – “Long opening” calcium channels – Voltage gated -
4B. the Heart (Cor) 1
Henry Gray (1821–1865). Anatomy of the Human Body. 1918. 4b. The Heart (Cor) 1 The heart is a hollow muscular organ of a somewhat conical form; it lies between the lungs in the middle mediastinum and is enclosed in the pericardium (Fig. 490). It is placed obliquely in the chest behind the body of the sternum and adjoining parts of the rib cartilages, and projects farther into the left than into the right half of the thoracic cavity, so that about one-third of it is situated on the right and two-thirds on the left of the median plane. Size.—The heart, in the adult, measures about 12 cm. in length, 8 to 9 cm. in breadth at the 2 broadest part, and 6 cm. in thickness. Its weight, in the male, varies from 280 to 340 grams; in the female, from 230 to 280 grams. The heart continues to increase in weight and size up to an advanced period of life; this increase is more marked in men than in women. Component Parts.—As has already been stated (page 497), the heart is subdivided by 3 septa into right and left halves, and a constriction subdivides each half of the organ into two cavities, the upper cavity being called the atrium, the lower the ventricle. The heart therefore consists of four chambers, viz., right and left atria, and right and left ventricles. The division of the heart into four cavities is indicated on its surface by grooves. The atria 4 are separated from the ventricles by the coronary sulcus (auriculoventricular groove); this contains the trunks of the nutrient vessels of the heart, and is deficient in front, where it is crossed by the root of the pulmonary artery. -
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. -
Back-To-Basics: the Intricacies of Muscle Contraction
Back-to- MIOTA Basics: The CONFERENCE OCTOBER 11, Intricacies 2019 CHERI RAMIREZ, MS, of Muscle OTRL Contraction OBJECTIVES: 1.Review the anatomical structure of a skeletal muscle. 2.Review and understand the process and relationship between skeletal muscle contraction with the vital components of the nervous system, endocrine system, and skeletal system. 3.Review the basic similarities and differences between skeletal muscle tissue, smooth muscle tissue, and cardiac muscle tissue. 4.Review the names, locations, origins, and insertions of the skeletal muscles found in the human body. 5.Apply the information learned to enhance clinical practice and understanding of the intricacies and complexity of the skeletal muscle system. 6.Apply the information learned to further educate clients on the importance of skeletal muscle movement, posture, and coordination in the process of rehabilitation, healing, and functional return. 1. Epithelial Four Basic Tissue Categories 2. Muscle 3. Nervous 4. Connective A. Loose Connective B. Bone C. Cartilage D. Blood Introduction There are 3 types of muscle tissue in the muscular system: . Skeletal muscle: Attached to bones of skeleton. Voluntary. Striated. Tubular shape. Cardiac muscle: Makes up most of the wall of the heart. Involuntary. Striated with intercalated discs. Branched shape. Smooth muscle: Found in walls of internal organs and walls of vascular system. Involuntary. Non-striated. Spindle shape. 4 Structure of a Skeletal Muscle Skeletal Muscles: Skeletal muscles are composed of: • Skeletal muscle tissue • Nervous tissue • Blood • Connective tissues 5 Connective Tissue Coverings Connective tissue coverings over skeletal muscles: .Fascia .Tendons .Aponeuroses 6 Fascia: Definition: Layers of dense connective tissue that separates muscle from adjacent muscles, by surrounding each muscle belly. -
Structure of a Skeletal Muscle
STRUCTURE OF A SKELETAL MUSCLE Skeletal muscles are not made of muscle cells alone • Skeletal muscle contains blood vessels that supply muscle cells with oxygen and glucose, and remove wastes, and nerves that coordinate muscle contraction • 1 § Each individual muscle cell (fiber) is surrounded by the _____________ § Several muscle cells are bundled together into a _________ by the _____________ § All fascicles that make up a muscle are, in turn, enclosed by the _____________ § Interconnected connective tissues taper down and connect to tendons or other connective tissues; attach muscle to bone or other structure to be moved Figure 9.1 Position and structure of a skeletal muscle. 2 FUNCTIONS OF SKELETAL MUSCLES • Muscle contractions are involved in more than just movement of bones at a joint: § § Contraction of diaphragm muscle is a vital function associated with respiratory system § _________________ – sitting, standing, holding head upright § Skeletal muscles attached to facial skin allow for facial expression; muscles in throat assist with swallowing § Sphincters composed of skeletal muscle allow conscious control over opening and closing of body openings § Support of soft tissue – abdominal walls, pelvic floor 3 • Functional groups of muscles: generally takes cooperation of several individual muscles working as a group to perform a movement or action § __________________ provide most force for a given muscle action § _____________have opposite action of agonist; allows for modulation and control of agonist movement § _____________aid agonists by supplying supplemental force, minimizing unwanted movement, and by helping to stabilize joints § _____________also provide stabilizing force that anchors a bone; protection from injury due to unnecessary movements Figure 9.3 Functional groups of muscles. -
Basic ECG Interpretation
12/2/2016 Basic Cardiac Anatomy Blood Flow Through the Heart 1. Blood enters right atrium via inferior & superior vena cava 2. Right atrium contracts, sending blood through the tricuspid valve and into the right ventricle 3. Right ventricle contracts, sending blood through the pulmonic valve and to the lungs via the pulmonary artery 4. Re-oxygenated blood is returned to the left atrium via the right and left pulmonary veins 5. Left atrium contracts, sending blood through the mitral valve and into the left ventricle 6. Left ventricle contracts, sending blood through the aortic Septum valve and to the body via the aorta 1 http://commons.wikimedia.org/wiki/File:Diagram_of_the_human_heart 2 _(cropped).svg Fun Fact….. Layers of the Heart Pulmonary Artery – The ONLY artery in the body that carries de-oxygenated blood Pulmonary Vein – The ONLY vein in the body that carries oxygenated blood 3 4 Layers of the Heart Endocardium Lines inner cavities of the heart & covers heart valves (Supplies left ventricle) Continuous with the inner lining of blood vessels Purkinje fibers located here; (electrical conduction system) Myocardium Muscular layer – the pump or workhorse of the heart “Time is Muscle” Epicardium Protective outer layer of heart (Supplies SA node Pericardium in most people) Fluid filled sac surrounding heart 5 6 http://stanfordhospital.org/images/greystone/heartCenter/images/ei_0028.gif 1 12/2/2016 What Makes the Heart Pump? Electrical impulses originating in the right atrium stimulate cardiac muscle contraction Your heart's -
Genome-Wide Identification, Characterization and Expression
G C A T T A C G G C A T genes Article Genome-Wide Identification, Characterization and Expression Profiling of myosin Family Genes in Sebastes schlegelii Chaofan Jin 1, Mengya Wang 1,2, Weihao Song 1 , Xiangfu Kong 1, Fengyan Zhang 1, Quanqi Zhang 1,2,3 and Yan He 1,2,* 1 MOE Key Laboratory of Molecular Genetics and Breeding, College of Marine Life Sciences, Ocean University of China, Qingdao 266003, China; [email protected] (C.J.); [email protected] (M.W.); [email protected] (W.S.); [email protected] (X.K.); [email protected] (F.Z.); [email protected] (Q.Z.) 2 Laboratory of Tropical Marine Germplasm Resources and Breeding Engineering, Sanya Oceanographic Institution, Ocean University of China, Sanya 572000, China 3 Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266003, China * Correspondence: [email protected]; Tel.: +86-0532-82031986 Abstract: Myosins are important eukaryotic motor proteins that bind actin and utilize the energy of ATP hydrolysis to perform a broad range of functions such as muscle contraction, cell migration, cytokinesis, and intracellular trafficking. However, the characterization and function of myosin is poorly studied in teleost fish. In this study, we identified 60 myosin family genes in a marine teleost, black rockfish (Sebastes schlegelii), and further characterized their expression patterns. myosin showed divergent expression patterns in adult tissues, indicating they are involved in different types and Citation: Jin, C.; Wang, M.; Song, W.; compositions of muscle fibers. Among 12 subfamilies, S. schlegelii myo2 subfamily was significantly Kong, X.; Zhang, F.; Zhang, Q.; He, Y. -
Ventricular Anatomy for the Electrophysiologist (Part
Ventricular Anatomy for the REVIEW Electrophysiologist (Part II) SPECIAL 서울대학교 의과대학 병리학교실 서정욱 이화여자대학교 의학전문대학원 김문영 ABSTRACT The conduction fibers and Purkinje network of the ventricular myocardium have their peculiar location and immuno-histochemical characteristics. The bundle of His is located at the inferior border of the membranous septum, where the single trunk ramifies into the left and right bundle branches. The left bundle branches are clearly visible at the surface. The right bundles are hidden in the septal myocardium and it is not easy to recognize them. The cellular characters of the conduction bundles are modified myocardial cells with less cytoplasmic filaments. Myoglobin is expressed at the contractile part, whereas CD56 is expressed at the intercalated disc. A fine meshwork of synaptophysin positive processes is noted particularly at the nodal tissue. C-kit positive cells are scattered, but their role is not well understood. Purkinje cells are a peripheral continuation of bundles seen at the immediate subendocardium of the left ventricle. Key words: ■ conduction system ■ Purkinje network ■ pathology ■ arrhythmia ■ electrophysiology Introduction human heart. In this brief review, the histological characteristics of conduction cells, stained by The functional assessment of abnormal cardiac conventional and immuno-histochemical staining, are 3 rhythm and a targeted treatment based on demonstrated in the second part of the review. electrophysiologic studies are successful advances in cardiology.1 Morphological assessment or confirmation The characteristic location of the ventricular of hearts with such abnormalities is rare, not only due conduction system to the limited availability of human hearts but also inherent technological limitations of existing The atrioventricular node is situated in its technology.2 Classical morphological approaches and subendocardial location at the triangle of Koch. -
The Ubiquitin Proteasome System in Neuromuscular Disorders: Moving Beyond Movement
International Journal of Molecular Sciences Review The Ubiquitin Proteasome System in Neuromuscular Disorders: Moving Beyond Movement 1, , 2, 3,4 Sara Bachiller * y , Isabel M. Alonso-Bellido y , Luis Miguel Real , Eva María Pérez-Villegas 5 , José Luis Venero 2 , Tomas Deierborg 1 , José Ángel Armengol 5 and Rocío Ruiz 2 1 Experimental Neuroinflammation Laboratory, Department of Experimental Medical Science, Lund University, Sölvegatan 19, 221 84 Lund, Sweden; [email protected] 2 Departamento de Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad de Sevilla/Instituto de Biomedicina de Sevilla-Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, 41012 Sevilla, Spain; [email protected] (I.M.A.-B.); [email protected] (J.L.V.); [email protected] (R.R.) 3 Unidad Clínica de Enfermedades Infecciosas, Hospital Universitario de Valme, 41014 Sevilla, Spain; [email protected] 4 Departamento de Especialidades Quirúrgicas, Bioquímica e Inmunología, Facultad de Medicina, 29071 Universidad de Málaga, Spain 5 Departamento de Fisiología, Anatomía y Biología Celular, Universidad Pablo de Olavide, 41013 Sevilla, Spain; [email protected] (E.M.P.-V.); [email protected] (J.Á.A.) * Correspondence: [email protected] These authors contributed equally to the work. y Received: 14 July 2020; Accepted: 31 August 2020; Published: 3 September 2020 Abstract: Neuromuscular disorders (NMDs) affect 1 in 3000 people worldwide. There are more than 150 different types of NMDs, where the common feature is the loss of muscle strength. These disorders are classified according to their neuroanatomical location, as motor neuron diseases, peripheral nerve diseases, neuromuscular junction diseases, and muscle diseases. Over the years, numerous studies have pointed to protein homeostasis as a crucial factor in the development of these fatal diseases. -
Primary Human Chondrocytes Respond to Compression with Phosphoproteomic Signatures That Include Microtubule Activation ⇑ Donald L
Journal of Biomechanics 97 (2019) 109367 Contents lists available at ScienceDirect Journal of Biomechanics journal homepage: www.elsevier.com/locate/jbiomech www.JBiomech.com Primary human chondrocytes respond to compression with phosphoproteomic signatures that include microtubule activation ⇑ Donald L. Zignego a, Jonathan K. Hilmer b, Brian Bothner b, William J. Schell a, Ronald K. June a, a Department of Mechanical & Industrial Engineering, Montana State University, United States b Department of Chemistry and Biochemistry, Montana State University, United States article info abstract Article history: Chondrocytes are responsible for maintaining the cartilage that helps joints bear load and move Accepted 22 September 2019 smoothly. These cells typically respond to physiological compression with pathways consistent with matrix synthesis, and chondrocyte mechanotransduction is essential for homeostasis. In osteoarthritis (OA), chondrocyte mechanotransduction appears to be dysregulated, yet the mechanisms remain poorly Keywords: understood. The objective of this study is to document the phosphoproteomic responses of primary Chondrocyte biology osteoarthritic chondrocytes to physiological sinusoidal compression. We show that OA chondrocytes Cartilage biomechanics respond to physiological compression by first activating proteins consistent with cytoskeletal remodeling Mechanobiology and decreased transcription, and then later activating proteins for transcription. These results show that Mechanotransduction Cartilage repair several microtubule-related proteins respond to compression. Our results demonstrate that compression Osteoarthritis is a relevant physiological stimulus for osteoarthritic chondrocytes. Future analyses may build on these results to find differences in compression-induced phosphoproteins between normal and OA cells that lead to druggable targets to restore homeostasis to diseased joints. Ó 2019 Elsevier Ltd. All rights reserved. 1. Introduction (Jaalouk and Lammerding, 2009).