Blood Vessels: Part A
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Chapter 20 *Lecture Powerpoint the Circulatory System: Blood Vessels and Circulation
Chapter 20 *Lecture PowerPoint The Circulatory System: Blood Vessels and Circulation *See separate FlexArt PowerPoint slides for all figures and tables preinserted into PowerPoint without notes. Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Introduction • The route taken by the blood after it leaves the heart was a point of much confusion for many centuries – Chinese emperor Huang Ti (2697–2597 BC) believed that blood flowed in a complete circuit around the body and back to the heart – Roman physician Galen (129–c. 199) thought blood flowed back and forth like air; the liver created blood out of nutrients and organs consumed it – English physician William Harvey (1578–1657) did experimentation on circulation in snakes; birth of experimental physiology – After microscope was invented, blood and capillaries were discovered by van Leeuwenhoek and Malpighi 20-2 General Anatomy of the Blood Vessels • Expected Learning Outcomes – Describe the structure of a blood vessel. – Describe the different types of arteries, capillaries, and veins. – Trace the general route usually taken by the blood from the heart and back again. – Describe some variations on this route. 20-3 General Anatomy of the Blood Vessels Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Capillaries Artery: Tunica interna Tunica media Tunica externa Nerve Vein Figure 20.1a (a) 1 mm © The McGraw-Hill Companies, Inc./Dennis Strete, photographer • Arteries carry blood away from heart • Veins -
Physiology Lessons for Use with the Biopac Student Lab Lesson 5
Physiology Lessons Lesson 5 for use with the ELECTROCARDIOGRAPHY I Biopac Student Lab Components of the ECG Richard Pflanzer, Ph.D. Associate Professor Emeritus Indiana University School of Medicine Purdue University School of Science William McMullen Vice President BIOPAC Systems, Inc. BIOPAC® Systems, Inc. 42 Aero Camino, Goleta, CA 93117 (805) 685-0066, Fax (805) 685-0067 Email: [email protected] Web: www.biopac.com Manual Revision PL3.7.5 03162009 BIOPAC Systems, Inc. Page 2 Biopac Student Lab 3.7.5 I. INTRODUCTION The main function of the heart is to pump blood through two circuits: 1. Pulmonary circuit: through the lungs to oxygenate the blood and remove carbon dioxide; and 2. Systemic circuit: to deliver oxygen and nutrients to tissues and remove carbon dioxide. Because the heart moves blood through two separate circuits, it is sometimes described as a dual pump. In order to beat, the heart needs three types of cells: 1. Rhythm generators, which produce an electrical signal (SA node or normal pacemaker); 2. Conductors to spread the pacemaker signal; and 3. Contractile cells (myocardium) to mechanically pump blood. The Electrical and Mechanical Sequence of a Heartbeat The heart has specialized pacemaker cells that start the electrical sequence of depolarization and repolarization. This property of cardiac tissue is called inherent rhythmicity or automaticity. The electrical signal is generated by the sinoatrial node (SA node) and spreads to the ventricular muscle via particular conducting pathways: internodal pathways and atrial fibers, the atrioventricular node (AV node), the bundle of His, the right and left bundle branches, and Purkinje fibers (Fig 5.1). -
The Circulatory System
TheThe CirculatoryCirculatory SystemSystem Xue Hui DepartmentDepartment ofof HistologyHistology && EmbryologyEmbryology TheThe CirculatoryCirculatory SystemSystem Cardiovascular system (blood vascular system) Heart Artery Capillary Vein Lymphatic vascular system Lymphatic capillary Lymphatic vessel Lymphatic duct II GeneralGeneral structurestructure ofof thethe bloodblood vesselsvessels Tunica intima Tunica media Tunica adventitia Drawing of a medium-sized muscular artery, showing its layers. II GeneralGeneral structurestructure ofof thethe bloodblood vesselsvessels IIII ArteryArtery Large artery Medium-sized artery Small artery Arteriole II Artery LargeLarge arteryartery Structure Tunica intima Tunica media 40-70 layers of elastic lamina Smooth muscle cells, collagenous fibers Tunica adventitia Function Carry the blood from the heart to the middle arteries Tunica Tunica intima intima Tunica Tunica media media Tunica Tunica adventitia adventitia Transverse sections showing part of a large elastic artery showing a well developed tunica media containing several elastic laminas. II Artery MediumMedium--sizedsized arteryartery Structure Tunica intima: clear internal elastic membrane Tunica media: 10-40 layers of smooth muscle cells Tunica adventitia: external elastic membrane Function Regulate the distribution of the blood to various parts of the body Tunica Internal intima elastic membrane Tunica media External elastic membrane Tunica adventitia II Artery SmallSmall arteryartery Structure characteristic Diameter:0.3-1mm Tunica intima: clear -
Infliximab, a TNF-Α Inhibitor, Reduces 24-H Ambulatory
Journal of Human Hypertension (2014) 28, 165–169 & 2014 Macmillan Publishers Limited All rights reserved 0950-9240/14 www.nature.com/jhh ORIGINAL ARTICLE Infliximab, a TNF-a inhibitor, reduces 24-h ambulatory blood pressure in rheumatoid arthritis patients S Yoshida1, T Takeuchi1, T Kotani1, N Yamamoto1, K Hata1, K Nagai1, T Shoda1,STakai2, S Makino1 and T Hanafusa1 Tumour necrosis factor-alpha (TNF-a) is an important mediator in the pathogenesis of rheumatoid arthritis (RA) and hypertension. TNF-a inhibitors improve clinical symptoms and inhibit joint destruction in RA, but their effect on blood pressure (BP) has not been fully investigated. We measured 24-h BP using an ambulatory BP monitor in 16 RA patients treated with a TNF-a inhibitor, infliximab, to investigate its influence on BP and its association with the regulatory factors of BP and renin-angiotensin-aldosterone and sympathetic nervous systems. Infliximab significantly reduced the 24-h systolic BP (SBP) from 127.4±21.8 to 120.1±23.4 mm Hg (Po0.0001). Particularly, morning BP (0600–0800 h) decreased from 129.7±19.7 to 116.9±13.4 mm Hg (Po0.0001), and daytime BP decreased from 131.8±15.1 to 122.5±13.7 mm Hg (Po0.0001). Infliximab significantly reduced the plasma level of norepinephrine and plasma renin activity (PRA) (from 347.5±180.7 to 283.0±181.8 pg ml À 1 and 2.6±2.7 to 2.1±2.9 ng ml À 1 h À 1, respectively) but did not significantly reduce the plasma levels of dopamine and epinephrine. -
Anatomy Review: Blood Vessel Structure & Function
Anatomy Review: Blood Vessel Structure & Function Graphics are used with permission of: Pearson Education Inc., publishing as Benjamin Cummings (http://www.aw-bc.com) Page 1. Introduction • The blood vessels of the body form a closed delivery system that begins and ends at the heart. Page 2. Goals • To describe the general structure of blood vessel walls. • To compare and contrast the types of blood vessels. • To relate the blood pressure in the various parts of the vascular system to differences in blood vessel structure. Page 3. General Structure of Blood Vessel Walls • All blood vessels, except the very smallest, have three distinct layers or tunics. The tunics surround the central blood-containing space - the lumen. 1. Tunica Intima (Tunica Interna) - The innermost tunic. It is in intimate contact with the blood in the lumen. It includes the endothelium that lines the lumen of all vessels, forming a smooth, friction reducing lining. 2. Tunica Media - The middle layer. Consists mostly of circularly-arranged smooth muscle cells and sheets of elastin. The muscle cells contract and relax, whereas the elastin allows vessels to stretch and recoil. 3. Tunica Adventitia (Tunica Externa) - The outermost layer. Composed of loosely woven collagen fibers that protect the blood vessel and anchor it to surrounding structures. Page 4. Comparison of Arteries, Capillaries, and Veins • Let's compare and contrast the three types of blood vessels: arteries, capillaries, and veins. • Label the artery, capillary and vein. Also label the layers of each. • Arteries are vessels that transport blood away from the heart. Because they are exposed to the highest pressures of any vessels, they have the thickest tunica media. -
Vocabulario De Morfoloxía, Anatomía E Citoloxía Veterinaria
Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) Servizo de Normalización Lingüística Universidade de Santiago de Compostela COLECCIÓN VOCABULARIOS TEMÁTICOS N.º 4 SERVIZO DE NORMALIZACIÓN LINGÜÍSTICA Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) 2008 UNIVERSIDADE DE SANTIAGO DE COMPOSTELA VOCABULARIO de morfoloxía, anatomía e citoloxía veterinaria : (galego-español- inglés) / coordinador Xusto A. Rodríguez Río, Servizo de Normalización Lingüística ; autores Matilde Lombardero Fernández ... [et al.]. – Santiago de Compostela : Universidade de Santiago de Compostela, Servizo de Publicacións e Intercambio Científico, 2008. – 369 p. ; 21 cm. – (Vocabularios temáticos ; 4). - D.L. C 2458-2008. – ISBN 978-84-9887-018-3 1.Medicina �������������������������������������������������������������������������veterinaria-Diccionarios�������������������������������������������������. 2.Galego (Lingua)-Glosarios, vocabularios, etc. políglotas. I.Lombardero Fernández, Matilde. II.Rodríguez Rio, Xusto A. coord. III. Universidade de Santiago de Compostela. Servizo de Normalización Lingüística, coord. IV.Universidade de Santiago de Compostela. Servizo de Publicacións e Intercambio Científico, ed. V.Serie. 591.4(038)=699=60=20 Coordinador Xusto A. Rodríguez Río (Área de Terminoloxía. Servizo de Normalización Lingüística. Universidade de Santiago de Compostela) Autoras/res Matilde Lombardero Fernández (doutora en Veterinaria e profesora do Departamento de Anatomía e Produción Animal. -
Blood and Lymph Vascular Systems
BLOOD AND LYMPH VASCULAR SYSTEMS BLOOD TRANSFUSIONS Objectives Functions of vessels Layers in vascular walls Classification of vessels Components of vascular walls Control of blood flow in microvasculature Variation in microvasculature Blood barriers Lymphatic system Introduction Multicellular Organisms Need 3 Mechanisms --------------------------------------------------------------- 1. Distribute oxygen, nutrients, and hormones CARDIOVASCULAR SYSTEM 2. Collect waste 3. Transport waste to excretory organs CARDIOVASCULAR SYSTEM Cardiovascular System Component function Heart - Produce blood pressure (systole) Elastic arteries - Conduct blood and maintain pressure during diastole Muscular arteries - Distribute blood, maintain pressure Arterioles - Peripheral resistance and distribute blood Capillaries - Exchange nutrients and waste Venules - Collect blood from capillaries (Edema) Veins - Transmit blood to large veins Reservoir Larger veins - receive lymph and return blood to Heart, blood reservoir Cardiovascular System Heart produces blood pressure (systole) ARTERIOLES – PERIPHERAL RESISTANCE Vessels are structurally adapted to physical and metabolic requirements. Vessels are structurally adapted to physical and metabolic requirements. Cardiovascular System Elastic arteries- conduct blood and maintain pressure during diastole Cardiovascular System Muscular Arteries - distribute blood, maintain pressure Arterioles - peripheral resistance and distribute blood Capillaries - exchange nutrients and waste Venules - collect blood from capillaries -
The Icefish (Chionodraco Hamatus)
The Journal of Experimental Biology 207, 3855-3864 3855 Published by The Company of Biologists 2004 doi:10.1242/jeb.01180 No hemoglobin but NO: the icefish (Chionodraco hamatus) heart as a paradigm D. Pellegrino1,2, C. A. Palmerini3 and B. Tota2,4,* Departments of 1Pharmaco-Biology and 2Cellular Biology, University of Calabria, 87030, Arcavacata di Rende, CS, Italy, 3Department of Cellular and Molecular Biology, University of Perugia, 06126, Perugia, Italy and 4Zoological Station ‘A. Dohrn’, Villa Comunale, 80121, Napoli, Italy *Author for correspondence (e-mail: [email protected]) Accepted 13 July 2004 Summary The role of nitric oxide (NO) in cardio-vascular therefore demonstrate that under basal working homeostasis is now known to include allosteric redox conditions the icefish heart is under the tonic influence modulation of cell respiration. An interesting animal for of a NO-cGMP-mediated positive inotropism. We also the study of this wide-ranging influence of NO is the cold- show that the working heart, which has intracardiac adapted Antarctic icefish Chionodraco hamatus, which is NOS (shown by NADPH-diaphorase activity and characterised by evolutionary loss of hemoglobin and immunolocalization), can produce and release NO, as multiple cardio-circulatory and subcellular compensations measured by nitrite appearance in the cardiac effluent. for efficient oxygen delivery. Using an isolated, perfused These results indicate the presence of a functional NOS working heart preparation of C. hamatus, we show that system in the icefish heart, possibly serving a both endogenous (L-arginine) and exogenous (SIN-1 in paracrine/autocrine regulatory role. presence of SOD) NO-donors as well as the guanylate cyclase (GC) donor 8Br-cGMP elicit positive inotropism, while both nitric oxide synthase (NOS) and sGC Key words: nitric oxide, heart, Antarctic teleost, icefish, Chionodraco inhibitors, i.e. -
A Review of the Stroke Volume Response to Upright Exercise in Healthy Subjects
190 Br J Sports Med: first published as 10.1136/bjsm.2004.013037 on 25 March 2005. Downloaded from REVIEW A review of the stroke volume response to upright exercise in healthy subjects C A Vella, R A Robergs ............................................................................................................................... Br J Sports Med 2005;39:190–195. doi: 10.1136/bjsm.2004.013037 Traditionally, it has been accepted that, during incremental well trained athletes (subject sex was not stated). Unfortunately, these findings were exercise, stroke volume plateaus at 40% of VO2MAX. largely ignored and it became accepted that However, recent research has documented that stroke stroke volume plateaus during exercise of increasing intensity. volume progressively increases to VO2MAX in both trained More recent investigations have reported that and untrained subjects. The stroke volume response to stroke volume progressively increases in certain 7–12 incremental exercise to VO2MAX may be influenced by people. The mechanisms for the continual training status, age, and sex. For endurance trained increase in stroke volume are not completely understood. Gledhill et al7 proposed that subjects, the proposed mechanisms for the progressive enhanced diastolic filling and subsequent increase in stroke volume to VO2MAX are enhanced diastolic enhanced contractility are responsible for the filling, enhanced contractility, larger blood volume, and increased stroke volume in trained subjects. However, an increase in stroke volume with an decreased cardiac afterload. For untrained subjects, it has increase in exercise intensity has also been been proposed that continued increases in stroke volume reported in untrained subjects.89Table 1 presents may result from a naturally occurring high blood volume. a summary of the past research that has quantified stroke volume during exercise. -
Bio 104 Cardiovascular System
29 Bio 104 Cardiovascular System Lecture Outline: Cardiovascular System Hole’s HAP [Chapters 14, 15, 16] Blood: Introduction (Chapter 14) - - - - A. Characteristics of Blood 1. Blood Volume - - - 2. Blood Composition a. Blood Cells Red blood cells White blood cells Platelets b. Plasma 3. Origin of Blood Cells - - 30 Bio 104 Cardiovascular System B. Red Blood Cells 1. Characteristics - - - oxyhemoglobin - deoxyhemoglobin - 2. Red Blood Cell Counts 4.6 – 6.2 4.2. – 5.4 reflects blood’s ___________________________ 3. Red Blood Cell Production low blood oxygen ________________________ RBC production vitamin B12, folic acid, Fe are necessary Dietary Factors Affecting RBC Production 31 Bio 104 Cardiovascular System 4. Life Cycle of RBC lifespan worn out RBCs destroyed by Hb heme and globin 5. Anemia Def. = C. White Blood Cells 1. Functions & Types diapedesis positive chemotaxis granulocytes - - - agranulocytes - - 32 Bio 104 Cardiovascular System 2. White Blood Cell Counts 5, 000 - 10,000 leukopenia leukocytosis differential WBC count Granulocytes Agranulocytes Neutrophils (segs, PMNs, bands) Monocytes Eosinophils Lymphocytes Basophils D. Platelets - cell fragments -130,000 - 360,000 - helps control _______________ Plasma A. Characteristics 33 Bio 104 Cardiovascular System B. Plasma Proteins C. Gases and Nutrients Gases Nutrients - - - - - - D. Nonprotein Nitrogenous Substances Urea - Uric acid - Amino acids – Creatine – Creatinine – BUN – E. Plasma Electrolytes Absorbed from the _____________ or released as by-products -
Effects of Vasodilation and Arterial Resistance on Cardiac Output Aliya Siddiqui Department of Biotechnology, Chaitanya P.G
& Experim l e ca n i t in a l l C Aliya, J Clinic Experiment Cardiol 2011, 2:11 C f a Journal of Clinical & Experimental o r d l DOI: 10.4172/2155-9880.1000170 i a o n l o r g u y o J Cardiology ISSN: 2155-9880 Review Article Open Access Effects of Vasodilation and Arterial Resistance on Cardiac Output Aliya Siddiqui Department of Biotechnology, Chaitanya P.G. College, Kakatiya University, Warangal, India Abstract Heart is one of the most important organs present in human body which pumps blood throughout the body using blood vessels. With each heartbeat, blood is sent throughout the body, carrying oxygen and nutrients to all the cells in body. The cardiac cycle is the sequence of events that occurs when the heart beats. Blood pressure is maximum during systole, when the heart is pushing and minimum during diastole, when the heart is relaxed. Vasodilation caused by relaxation of smooth muscle cells in arteries causes an increase in blood flow. When blood vessels dilate, the blood flow is increased due to a decrease in vascular resistance. Therefore, dilation of arteries and arterioles leads to an immediate decrease in arterial blood pressure and heart rate. Cardiac output is the amount of blood ejected by the left ventricle in one minute. Cardiac output (CO) is the volume of blood being pumped by the heart, by left ventricle in the time interval of one minute. The effects of vasodilation, how the blood quantity increases and decreases along with the blood flow and the arterial blood flow and resistance on cardiac output is discussed in this reviewArticle. -
Electrical Activity of the Heart: Action Potential, Automaticity, and Conduction 1 & 2 Clive M
Electrical Activity of the Heart: Action Potential, Automaticity, and Conduction 1 & 2 Clive M. Baumgarten, Ph.D. OBJECTIVES: 1. Describe the basic characteristics of cardiac electrical activity and the spread of the action potential through the heart 2. Compare the characteristics of action potentials in different parts of the heart 3. Describe how serum K modulates resting potential 4. Describe the ionic basis for the cardiac action potential and changes in ion currents during each phase of the action potential 5. Identify differences in electrical activity across the tissues of the heart 6. Describe the basis for normal automaticity 7. Describe the basis for excitability 8. Describe the basis for conduction of the cardiac action potential 9. Describe how the responsiveness relationship and the Na+ channel cycle modulate cardiac electrical activity I. BASIC ELECTROPHYSIOLOGIC CHARACTERISTICS OF CARDIAC MUSCLE A. Electrical activity is myogenic, i.e., it originates in the heart. The heart is an electrical syncitium (i.e., behaves as if one cell). The action potential spreads from cell-to-cell initiating contraction. Cardiac electrical activity is modulated by the autonomic nervous system. B. Cardiac cells are electrically coupled by low resistance conducting pathways gap junctions located at the intercalated disc, at the ends of cells, and at nexus, points of side-to-side contact. The low resistance pathways (wide channels) are formed by connexins. Connexins permit the flow of current and the spread of the action potential from cell-to-cell. C. Action potentials are much longer in duration in cardiac muscle (up to 400 msec) than in nerve or skeletal muscle (~5 msec).