Coronary Circulation: an Overview Observations About Kugel's Artery Anatomy
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A Direct Examination of Papillary Muscle Function in the Canine Left Ventricle
Loyola University Chicago Loyola eCommons Master's Theses Theses and Dissertations 1968 A Direct Examination of Papillary Muscle Function in the Canine Left Ventricle Robert Emmet Cronin Loyola University Chicago Follow this and additional works at: https://ecommons.luc.edu/luc_theses Part of the Medicine and Health Sciences Commons Recommended Citation Cronin, Robert Emmet, "A Direct Examination of Papillary Muscle Function in the Canine Left Ventricle" (1968). Master's Theses. 2081. https://ecommons.luc.edu/luc_theses/2081 This Thesis is brought to you for free and open access by the Theses and Dissertations at Loyola eCommons. It has been accepted for inclusion in Master's Theses by an authorized administrator of Loyola eCommons. For more information, please contact [email protected]. This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License. Copyright © 1968 Robert Emmet Cronin A DIRECT EXAMINATION OF PAPILLARY MUSCLE FUNCTION IN THE CANINE LEFT VENTRICLE by Robert Emmet Cronin A Thesis Submitted to the Faculty of the Graduate School of Loyola University in Partial Fulfillment of the Requirements for the Degree of Master of Science June 1968 LIFE Robert E. Cronin was born in Chicago, Illinois, on March 26, 1942. He attended St. Ignatius High School, in Chicago, Illinois, and then Holy Cross College in Worcester, Massachusetts, where he received his Bachelor of Arts degree in 1964. Since September, 1964, he has been a medical student at Loyola Uni versity, Stritch School of Medicine, and will receive his M.D. degree in June, 1968. For the past three years he has been enrolled in the combined Master of Science - Medical . -
The Ventricles
Guest Editorial Evolution of the Ventricles Solomon Victor, FRCS, FRCP We studied the evolution of ventricles by macroscopic examination of the hearts of Vijaya M. Nayak, MS marine cartilaginous and bony fish, and by angiocardiography and gross examination of Raveen Rajasingh, MPhil the hearts of air-breathing freshwater fish, frogs, turtles, snakes, and crocodiles. A right-sided, thin-walled ventricular lumen is seen in the fish, frog, turtle, and snake. In fish, there is external symmetry of the ventricle, internal asymmetry, and a thick- walled left ventricle with a small inlet chamber. In animals such as frogs, turtles, and snakes, the left ventricle exists as a small-cavitied contractile sponge. The high pressure generated by this spongy left ventricle, the direction of the jet, the ventriculoarterial ori- entation, and the bulbar spiral valve in the frog help to separate the systemic and pul- monary circulations. In the crocodile, the right aorta is connected to the left ventricle, and there is a complete interventricular septum and an improved left ventricular lumen when compared with turtles and snakes. The heart is housed in a rigid pericardial cavity in the shark, possibly to protect it from changing underwater pressure. The pericardial cavity in various species permits move- ments of the heart-which vary depending on the ventriculoarterial orientation and need for the ventricle to generate torque or spin on the ejected blood- that favor run-off into the appropriate arteries and their branches. In the lower species, it is not clear whether the spongy myocardium contributes to myocardial oxygenation. In human beings, spongy myocardium constitutes a rare form of congenital heart disease. -
Distance Learning Program Anatomy of the Human Heart/Pig Heart Dissection Middle School/ High School
Distance Learning Program Anatomy of the Human Heart/Pig Heart Dissection Middle School/ High School This guide is for middle and high school students participating in AIMS Anatomy of the Human Heart and Pig Heart Dissections. Programs will be presented by an AIMS Anatomy Specialist. In this activity students will become more familiar with the anatomical structures of the human heart by observing, studying, and examining human specimens. The primary focus is on the anatomy and flow of blood through the heart. Those students participating in Pig Heart Dissections will have the opportunity to dissect and compare anatomical structures. At the end of this document, you will find anatomical diagrams, vocabulary review, and pre/post tests for your students. National Science Education (NSES) Content Standards for grades 9-12 • Content Standard:K-12 Unifying Concepts and Processes :Systems order and organization; Evidence, models and explanation; Form and function • Content Standard F, Science in Personal and Social Perspectives: Personal and community health • Content Standard C, Life Science: Matter, energy and organization of living systems • Content Standard A Science as Inquiry National Science Education (NSES) Content Standards for grades 5-8 • Content Standard A Science as Inquiry • Content Standard C, Life Science: Structure and function in living systems; Diversity and adaptations of organisms • Content Standard F, Science in Personal and Social Perspectives: Personal Health Show Me Standards (Science and Health/Physical Education) • Science 3. Characteristics and interactions of living organisms • Health/Physical Education 1. Structures of, functions of and relationships among human body systems Objectives: The student will be able to: 1. -
Prep for Practical II
Images for Practical II BSC 2086L "Endocrine" A A B C A. Hypothalamus B. Pineal Gland (Body) C. Pituitary Gland "Endocrine" 1.Thyroid 2.Adrenal Gland 3.Pancreas "The Pancreas" "The Adrenal Glands" "The Ovary" "The Testes" Erythrocyte Neutrophil Eosinophil Basophil Lymphocyte Monocyte Platelet Figure 29-3 Photomicrograph of a human blood smear stained with Wright’s stain (765). Eosinophil Lymphocyte Monocyte Platelets Neutrophils Erythrocytes "Blood Typing" "Heart Coronal" 1.Right Atrium 3 4 2.Superior Vena Cava 5 2 3.Aortic Arch 6 4.Pulmonary Trunk 1 5.Left Atrium 12 9 6.Bicuspid Valve 10 7.Interventricular Septum 11 8.Apex of The Heart 9. Chordae tendineae 10.Papillary Muscle 7 11.Tricuspid Valve 12. Fossa Ovalis "Heart Coronal Section" Coronal Section of the Heart to show valves 1. Bicuspid 2. Pulmonary Semilunar 3. Tricuspid 4. Aortic Semilunar 5. Left Ventricle 6. Right Ventricle "Heart Coronal" 1.Pulmonary trunk 2.Right Atrium 3.Tricuspid Valve 4.Pulmonary Semilunar Valve 5.Myocardium 6.Interventricular Septum 7.Trabeculae Carneae 8.Papillary Muscle 9.Chordae Tendineae 10.Bicuspid Valve "Heart Anterior" 1. Brachiocephalic Artery 2. Left Common Carotid Artery 3. Ligamentum Arteriosum 4. Left Coronary Artery 5. Circumflex Artery 6. Great Cardiac Vein 7. Myocardium 8. Apex of The Heart 9. Pericardium (Visceral) 10. Right Coronary Artery 11. Auricle of Right Atrium 12. Pulmonary Trunk 13. Superior Vena Cava 14. Aortic Arch 15. Brachiocephalic vein "Heart Posterolateral" 1. Left Brachiocephalic vein 2. Right Brachiocephalic vein 3. Brachiocephalic Artery 4. Left Common Carotid Artery 5. Left Subclavian Artery 6. Aortic Arch 7. -
Physiology of Heart Unit-4 (ZOOA-CC4-9-TH)
Physiology of Heart Unit-4 (ZOOA-CC4-9-TH) Coronary Circulation: The heart muscle, like every other organ or tissue in your body, needs oxygen-rich blood to survive. Blood is supplied to the heart by its own vascular system, called coronary circulation. The aorta (the main blood supplier to the body) branches off into two main coronary blood vessels (also called arteries). These coronary arteries branch off into smaller arteries, which supply oxygen-rich blood to the entire heart muscle. The right coronary artery supplies blood mainly to the right side of the heart. The right side of the heart is smaller because it pumps blood only to the lungs. The left coronary artery, which branches into the left anterior descending artery and the circumflex artery, supplies blood to the left side of the heart. The left side of the heart is larger and more muscular because it pumps blood to the rest of the body. Coronary circulation is the circulation of blood in the blood vessels that supply the heart muscle (myocardium). Coronary arteries supply oxygenated blood to the heart muscle, and cardiac veins drain away the blood once it has been deoxygenated. Because the rest of the body, and most especially the brain, needs a steady supply of oxygenated blood that is free of all but the slightest interruptions, the heart is required to function continuously. Therefore its circulation is of major importance not only to its own tissues but to the entire body and even the level of consciousness of the brain from moment to moment. -
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. -
Blood Vessels
BLOOD VESSELS Blood vessels are how blood travels through the body. Whole blood is a fluid made up of red blood cells (erythrocytes), white blood cells (leukocytes), platelets (thrombocytes), and plasma. It supplies the body with oxygen. SUPERIOR AORTA (AORTIC ARCH) VEINS & VENA CAVA ARTERIES There are two basic types of blood vessels: veins and arteries. Veins carry blood back to the heart and arteries carry blood from the heart out to the rest of the body. Factoid! The smallest blood vessel is five micrometers wide. To put into perspective how small that is, a strand of hair is 17 micrometers wide! 2 BASIC (ARTERY) BLOOD VESSEL TUNICA EXTERNA TUNICA MEDIA (ELASTIC MEMBRANE) STRUCTURE TUNICA MEDIA (SMOOTH MUSCLE) Blood vessels have walls composed of TUNICA INTIMA three layers. (SUBENDOTHELIAL LAYER) The tunica externa is the outermost layer, primarily composed of stretchy collagen fibers. It also contains nerves. The tunica media is the middle layer. It contains smooth muscle and elastic fiber. TUNICA INTIMA (ELASTIC The tunica intima is the innermost layer. MEMBRANE) It contains endothelial cells, which TUNICA INTIMA manage substances passing in and out (ENDOTHELIUM) of the bloodstream. 3 VEINS Blood carries CO2 and waste into venules (super tiny veins). The venules empty into larger veins and these eventually empty into the heart. The walls of veins are not as thick as those of arteries. Some veins have flaps of tissue called valves in order to prevent backflow. Factoid! Valves are found mainly in veins of the limbs where gravity and blood pressure VALVE combine to make venous return more 4 difficult. -
Euler's Elastica-Based Biomechanics of the Papillary Muscle
materials Article Euler’s Elastica-Based Biomechanics of the Papillary Muscle Approximation in Ischemic Mitral Valve Regurgitation: A Simple 2D Analytical Model Francesco Nappi 1,*, Angelo Rosario Carotenuto 2, Sanjeet Singh Avtaar Singh 3, Christos Mihos 4 and Massimiliano Fraldi 2 1 Centre Cardiologique du Nord de Saint-Denis, Paris 36 Rue des Moulins Gmeaux, 93200 Saint-Denis, France 2 Department of Structures for Engineering and Architecture, University of Napoli Federico II, 80125 Naples, Italy; [email protected] (A.R.C.); [email protected] (M.F.) 3 Department of Cardiac Surgery, Golden Jubilee National Hospital, Clydebank G81 4DY, UK; [email protected] 4 Columbia University Division of Cardiology at the Mount Sinai Heart Institute, Miami Beach, FL 33140, USA; [email protected] * Correspondence: [email protected]; Tel.: +33-149-334-104; Fax: +33-149-334-119 Received: 16 March 2019; Accepted: 30 April 2019; Published: 9 May 2019 Abstract: Ischemic mitral regurgitation (IMR) occurs as an adverse consequence of left ventricle remodeling post-myocardial infarction. A change in mitral valve configuration with an imbalance between closing and tethering forces underlie this pathological condition. These abnormalities lead to impaired leaflet coaptation and a variable degree of mitral regurgitation, which can in turn influence the ventricular filling status, the heart rhythm and the afterload regardless of the residual ischemic insult. The IMR correction can be pursued through under-sizing mitral annuloplasty and papillary muscle approximation to restore the mitral valve and left ventricle physiological geometry to, consequently, achieve normalization of the engaged physical forces. Because the structures involved undergo extremely large deformations, a biomechanics model based on the Euler’s Elastica –the mitral leaflet– interlaced with nonlinear chordae tendineae anchored on papillary muscles has been constructed to elucidate the interactions between closing and tethering forces. -
Endocardial Cushion and Myocardial Defects After Cardiac Myocyte-Specific Conditional Deletion of the Bone Morphogenetic Protein Receptor ALK3
Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3 Vinciane Gaussin*†, Tom Van de Putte‡, Yuji Mishina§, Mark C. Hanks¶, An Zwijsen‡, Danny Huylebroeck‡, Richard R. Behringerʈ, and Michael D. Schneider*,** *Center for Cardiovascular Development, Baylor College of Medicine, Houston, TX 77030; ‡Flanders Interuniversity Institute for Biotechnology (VIB07), K.U. Leuven, 3000 Leuven, Belgium; §National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709; ¶Procter and Gamble Pharmaceuticals Health Care Research Center, 8700 Mason Montgomery Road, Mason, OH 45040; and ʈUniversity of Texas–M. D. Anderson Cancer Center, Houston, TX 77030 Edited by Eric N. Olson, University of Texas Southwestern Medical Center, Dallas, TX, and approved December 31, 2001 (received for review July 26, 2001) Receptors for bone morphogenetic proteins (BMPs), members of velopment, whereas ALK6 is absent from the heart at mid- the transforming growth factor- (TGF) superfamily, are persis- gestation (17). The developing heart also expresses ALK2͞ tently expressed during cardiac development, yet mice lacking type ActRIA (5, 18), which can function as a type I BMP receptor II or type IA BMP receptors die at gastrulation and cannot be used with preference for BMP6 and -7 (19). ALK3, ALK2, and to assess potential later roles in creation of the heart. Here, we BMPR-II are each essential for gastrulation and mesoderm used a Cre͞lox system for cardiac myocyte-specific deletion of the formation (18, 20, 21); mice lacking just BMP4 also fail to type IA BMP receptor, ALK3. ALK3 was specifically required at progress, typically, beyond the egg cylinder stage (22). -
In the Pulmonary Arteries, Capillaries, and Veins
Longitudinal Distribution of Vascular Resistance in the Pulmonary Arteries, Capillaries, and Veins JEROME S. BRODY, EDWARD J. STEMMLER, and ARTHu B. DuBois From the Department of Physiology, Division of Graduate Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104 A B S T R A C T A new method has been described monary artery pressure averaged 20.4 cm H2O, for measuring the pressure and resistance to blood and pulmonary vein pressure averaged 9.2 cm flow in the pulmonary arteries, capillaries, and H2O. These techniques also provide a way of ana- veins. Studies were performed in dog isolated lyzing arterial, capillary, and venous responses to lung lobes perfused at constant flow with blood various pharmacologic and physiologic stimuli. from a donor dog. Pulmonary artery and vein volume and total lobar blood volume were mea- INTRODUCTION sured by the ether plethysmograph and dye- dilution techniques. The longitudinal distribution The arterioles are the major resistance vessels in of vascular resistance was determined by analyzing the systemic vascular bed (1, 2), but it is uncer- the decrease in perfusion pressure caused by a tain whether the greatest resistance to blood flow bolus of low viscosity liquid introduced into the in the lungs is in the arteries, capillaries, or veins vascular inflow of the lobe. (1, 3, 4). The pulmonary arteries were responsible for Piiper (5), in 1958, reasoned from Poiseuille's 46% of total lobar vascular resistance, whereas law that, during constant perfusion, injection into the pulmonary capillaries and veins accounted for the bloodstream of a bolus of fluid with viscosity 34 and 20% of total lobar vascular resistance different from that of blood would cause a per- respectively. -
Ventricular Septal Defect (VSD)
Ventricular Septal Defect (VSD) Ventricular Septal Defect. Flow of blood through a normal heart. What is a Ventricular Septal Defect?Your pet has been diagnosed with a Ventricular Septal Defect (VSD). A VSD is a malformation of the wall (interventricular septum) between the two pumping chambers (ventricles) allowing an abnormal communication. A VSD is a type of congenital defect, which means it is present from birth. VSDs are classified based upon whether they are restrictive or non-restrictive. In order to understand how this disease may affect your dog, it is important to understand normal circulation in the heart. Blood drains from the body into the right collecting chamber (called “atrium”) where it passes through the tricuspid valve and into the right pumping chamber (called “ventricle”). From here, blood is pumped into the pulmonary artery and subsequently to the lungs where it picks up oxygen. The oxygenated blood then drains passively into the left atrium, through the mitral valve, and into the left ventricle. The left ventricle then pumps the blood through the aorta and back to the body. Restrictive VSD: A restrictive VSD is a smaller diameter VSD that provides resistance of blood flow. These are the most common VSDs that we diagnose in dogs and cats. Due to normally higher pressures in the left side of the heart compared to the right side of the heart, most have blood flow from left-to-right through the hole. The amount of blood shunted depends on size of the VSD and the pressure difference across the VSD. Therefore, restrictive VSDs are further classified based on whether they are “hemodynamically significant” or not. -
Abnormally Enlarged Singular Thebesian Vein in Right Atrium
Open Access Case Report DOI: 10.7759/cureus.16300 Abnormally Enlarged Singular Thebesian Vein in Right Atrium Dilip Kumar 1 , Amit Malviya 2 , Bishwajeet Saikia 3 , Bhupen Barman 4 , Anunay Gupta 5 1. Cardiology, Medica Institute of Cardiac Sciences, Kolkata, IND 2. Cardiology, North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences, Shillong, IND 3. Anatomy, North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences, Shillong, IND 4. Internal Medicine, North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences, Shillong, IND 5. Cardiology, Vardhman Mahavir Medical College (VMMC) and Safdarjung Hospital, New Delhi, IND Corresponding author: Amit Malviya, [email protected] Abstract Thebesian veins in the heart are subendocardial venoluminal channels and are usually less than 0.5 mm in diameter. The system of TV either opens a venous (venoluminal) or an arterial (arterioluminal) channel directly into the lumen of the cardiac chambers or via some intervening spaces (venosinusoidal/ arteriosinusoidal) termed as sinusoids. Enlarged thebesian veins are reported in patients with congenital heart disease and usually, multiple veins are enlarged. Very few reports of such abnormal enlargement are there in the absence of congenital heart disease, but in all such cases, they are multiple and in association with coronary artery microfistule. We report a very rare case of a singular thebesian vein in the right atrium, which was abnormally enlarged. It is important to recognize because it can be confused with other cardiac structures like coronary sinus during diagnostic or therapeutic catheterization and can lead to cardiac injury and complications if it is attempted to cannulate it or pass the guidewires.