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Te2, Part Iii
TERMINOLOGIA EMBRYOLOGICA Second Edition International Embryological Terminology FIPAT The Federative International Programme for Anatomical Terminology A programme of the International Federation of Associations of Anatomists (IFAA) TE2, PART III Contents Caput V: Organogenesis Chapter 5: Organogenesis (continued) Systema respiratorium Respiratory system Systema urinarium Urinary system Systemata genitalia Genital systems Coeloma Coelom Glandulae endocrinae Endocrine glands Systema cardiovasculare Cardiovascular system Systema lymphoideum Lymphoid system Bibliographic Reference Citation: FIPAT. Terminologia Embryologica. 2nd ed. FIPAT.library.dal.ca. Federative International Programme for Anatomical Terminology, February 2017 Published pending approval by the General Assembly at the next Congress of IFAA (2019) Creative Commons License: The publication of Terminologia Embryologica is under a Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0) license The individual terms in this terminology are within the public domain. Statements about terms being part of this international standard terminology should use the above bibliographic reference to cite this terminology. The unaltered PDF files of this terminology may be freely copied and distributed by users. IFAA member societies are authorized to publish translations of this terminology. Authors of other works that might be considered derivative should write to the Chair of FIPAT for permission to publish a derivative work. Caput V: ORGANOGENESIS Chapter 5: ORGANOGENESIS -
Chapter Xi the Circulatory System and Blood
CHAPTER XI THE CIRCULATORY SYSTEM AND BLOOD Page General characterlstlcs______ __ __ _ __ __ __ __ __ __ _ 239 of these organs are independent of the beating of The pericardium ___ __ __ __ 239 the principal heart, and their primary function is The heart. _____ __ __ 240 Physiology of the heart.______________________________________________ 242 to oscillate the blood within the pallial sinuses. Automatism of heart beat. _ 242 The pacemaker system_ 245 THE PERICARDIUM Methods of study of heart beat_____________________________________ 247 Frequency of beat___ __ __ _ 248 Extracardlac regulatlon____ __ __ _ 250 The heart is located in the pericardium, a thin Effects of mineral salts and drugs___________________________________ 251 Blood vessels_ __ ___ _ 253 walled chamber between the visceral mass and the The arterial system______ __ __ ___ __ __ __ __ __ 253 adductor muscle (fig. 71). In a live oyster the The venous system_________________________________________________ 254 location of the heart is indicated by the throbbing The accessory heart._____________ 258 The blood______ __ __ __ __ __ __ __ 259 of the wall of the pericardium on the left side. Color of blood_ __ __ 261 Here the pericardium wall lies directly under the The hyaline cells___________________________________________________ 261 The granular cells .______________________________________ 262 shell. On the right side the promyal chamber Specific gravity of blood____________________________________________ 265 extends down over the heart region and the mantle Serology ___ __________ __________________ ____ __ ______________________ 265 Bibliography __ __ __ __ __ __ __ 266 separates the pericardium wall from the shell. The cavity in which the heart is lodged is slightly A heart, arteries, veins, and open sinuses form asymmetrical; on the right side it extends farther the circulatory system of oysters and other bi along the anterior part of the adductor muscle valves. -
Arterial and Venous Adaptations to Short-Term Handgrip Exercise Training
Louisiana State University LSU Digital Commons LSU Doctoral Dissertations Graduate School 2003 Arterial and venous adaptations to short-term handgrip exercise training Mahmoud Awad Alomari Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_dissertations Part of the Kinesiology Commons Recommended Citation Alomari, Mahmoud Awad, "Arterial and venous adaptations to short-term handgrip exercise training" (2003). LSU Doctoral Dissertations. 188. https://digitalcommons.lsu.edu/gradschool_dissertations/188 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Doctoral Dissertations by an authorized graduate school editor of LSU Digital Commons. For more information, please [email protected]. ARTERIAL AND VENOUS ADAPTATIONS TO SHORT-TERM HANDGRIP EXERCISE TRAINING A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Kinesiology By Mahmoud Alomari B.S., Yarmouk University, Irbid, Jordan, 1990 M.S. Minnesota State University, Mankato, MN, 1995 December, 2003 © Copyright 2003 Mahmoud A. Alomari All right reserved ii DEDICATION I dedicate all of my work to my parents, the love of my life. They feel as though they took every exam with me and were as anxious as I was for each defense. Their confidence in me never wavered and helped me to accomplish the dream of my life. Their motivation made me a better person and they continue to show me what service to others really is. -
St. Lawrence School Subject
St. Lawrence School Subject - Science Class - 4 Chapter - 3 Human Body : Digestive and Excetory System ( Part - 1 ) Learn about * Digestive system * Excretory system * Healthy eating habits Digestive System The process by which food is broken down into a simpler form so that it can be easily taken in or absorbed by our body is called digestion. Many organs work together and help in the process of digestion. The mouth, food pipe, stomach, small and large intestine, liver, rectum, and anus are the main organs of the digestive system. Let us learn about them. Mouth Digestion starts in the mouth. The teeth help to break down and chew food. The chewed food then mixes with a liquid, called saliva, produced in our mouth. It makes the food softer and easier to swallow. The tongue helps in the proper mixing of saliva with the food. Food pipe The food pipe ( oesophagus ) passes the food from the mouth to the stomach. Stomach Inside the stomach, the food is broken down further into smaller pieces by churning and with the help of chemicals called digestive juices. Small intestine From the small intestine, the undigested food passes into the large intestine. The large intestine is a shorter but wider, tube - like structure, which collects the indigestible food from the small intestine. The large intestine absorbs water from this undigested food and forms waste products called faeces. Rectum Rectum is the final part of the large intestine. Faeces are stored in the rectum for a short time before being passed out through anus. Anus Faeces are removed from the body through the anus. -
Urinary Bladder – Proteinaceous Plug
Urinary bladder – Proteinaceous Plug Figure Legend: Figure 1 An eosinophilic amorphous proteinaceous plug in the bladder lumen from a male B6C3F1 mouse in a chronic study. Figure 2 A proteinaceous plug associated with other flocculent, eosinophilic material, from a male F344/N rat in an acute study. Comment: Proteinaceous plugs are commonly noted as a postmortem change resulting from an agonal secretion of accessory sex gland fluids during euthanasia. Proteinaceous plugs vary in size but can be large, filling the urinary bladder (Figure 1 and Figure 2). Microscopically, the plug is composed of a mixture of an amorphous eosinophilic material, sometimes containing desquamated epithelial cells and spermatozoa. Proteinaceous plugs by themselves have no toxicologic importance and are not precursors of calculi. Plugs may be seen with obstructive syndromes associated with bacterial inflammation. They must be differentiated from calculi. Recommendation: Proteinaceous plugs occurring alone and not associated with any pathologic lesions should be recognized as an artifact and should not be diagnosed. Occasionally, proteinaceous plugs are recognized grossly, and the pathologist should use his or her judgment to correlate the gross lesion to an artifactual proteinaceous plug. 1 Urinary bladder – Proteinaceous Plug References: Gaillard ET. 1999. Ureter, urinary bladder and urethra. In: Pathology of the Mouse: Reference and Atlas (Maronpot RR, Boorman GA, Gaul BW, eds). Cache River Press, Vienna, IL, 235– 258. Abstract: http://www.cacheriverpress.com/books/pathmouse.htm Hard GC, Alden CL, Bruner RH, Frith CH, Lewis RM, Owen RA, Krieg K, Durchfeld-Meyer B. 1999. Non-proliferative lesions of the kidney and lower urinary tract in rats. -
Diverse Repertoire of Human Adipocyte Subtypes Develops from Transcriptionally Distinct Mesenchymal Progenitor Cells
Diverse repertoire of human adipocyte subtypes develops from transcriptionally distinct mesenchymal progenitor cells So Yun Mina,b, Anand Desaia, Zinger Yanga,b, Agastya Sharmaa, Tiffany DeSouzaa, Ryan M. J. Gengaa,b,c, Alper Kucukurald, Lawrence M. Lifshitza, Søren Nielsene,f, Camilla Scheelee,f,g, René Maehra,c, Manuel Garbera,d, and Silvia Corveraa,1 aProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655; bGraduate School of Biomedical Sciences, University of Massachusetts Medical School, Worcester, MA 01655; cDepartment of Medicine, Diabetes Center of Excellence, University of Massachusetts Medical School, Worcester, MA 01655; dProgram in Bioinformatics, University of Massachusetts Medical School, Worcester, MA 01655; eCentre of Inflammation and Metabolism, Rigshospitalet, University of Copenhagen, 1165 Copenhagen Denmark; fCentre for Physical Activity Research, Rigshospitalet, University of Copenhagen, 1165 Copenhagen Denmark; and gNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Science, University of Copenhagen, 1165 Copenhagen, Denmark Edited by Rana K. Gupta, University of Texas Southwestern Medical Center, Dallas, TX, and accepted by Editorial Board Member David J. Mangelsdorf July12, 2019 (received for review April 16, 2019) Single-cell sequencing technologies have revealed an unexpectedly UCP1 in response to stimulation. Lineage-tracing and gene- broad repertoire of cells required to mediate complex functions in expression studies point to distinct developmental origins for multicellular organisms. Despite the multiple roles of adipose tissue these adipocyte subtypes (5, 6). In adult humans, no specific depot + in maintaining systemic metabolic homeostasis, adipocytes are is solely composed of UCP1-containing adipocytes, but UCP-1 thought to be largely homogenous with only 2 major subtypes cells can be found interspersed within supraclavicular, para- recognized in humans so far. -
Wound Classification
Wound Classification Presented by Dr. Karen Zulkowski, D.N.S., RN Montana State University Welcome! Thank you for joining this webinar about how to assess and measure a wound. 2 A Little About Myself… • Associate professor at Montana State University • Executive editor of the Journal of the World Council of Enterstomal Therapists (JWCET) and WCET International Ostomy Guidelines (2014) • Editorial board member of Ostomy Wound Management and Advances in Skin and Wound Care • Legal consultant • Former NPUAP board member 3 Today We Will Talk About • How to assess a wound • How to measure a wound Please make a note of your questions. Your Quality Improvement (QI) Specialists will follow up with you after this webinar to address them. 4 Assessing and Measuring Wounds • You completed a skin assessment and found a wound. • Now you need to determine what type of wound you found. • If it is a pressure ulcer, you need to determine the stage. 5 Assessing and Measuring Wounds This is important because— • Each type of wound has a different etiology. • Treatment may be very different. However— • Not all wounds are clear cut. • The cause may be multifactoral. 6 Types of Wounds • Vascular (arterial, venous, and mixed) • Neuropathic (diabetic) • Moisture-associated dermatitis • Skin tear • Pressure ulcer 7 Mixed Etiologies Many wounds have mixed etiologies. • There may be both venous and arterial insufficiency. • There may be diabetes and pressure characteristics. 8 Moisture-Associated Skin Damage • Also called perineal dermatitis, diaper rash, incontinence-associated dermatitis (often confused with pressure ulcers) • An inflammation of the skin in the perineal area, on and between the buttocks, into the skin folds, and down the inner thighs • Scaling of the skin with papule and vesicle formation: – These may open, with “weeping” of the skin, which exacerbates skin damage. -
Carcinomatous Cirrhosis of the Liver with Sarcomatosis of the Peritoneum 1
CARCINOMATOUS CIRRHOSIS OF THE LIVER WITH SARCOMATOSIS OF THE PERITONEUM 1 S. SANES, M.D., AND K. TERPLAN, M.D. (From tile Pathological Laboratory of the Buffalo General Hospital and School of Medicine, University of Buffalo) The following case is reported because of the occurrence of two different types of malignant neoplasm with typical portal cirrhosis of the liver. That a pathogenetic relationship exists between Laennec's cirrhosis and primary carcinoma of the liver is generally recognized. Whether the association of a peritoneal sarcoma with the cirrhosis in this case was more than a coincidence seemed an interesting point for discussion. REPORT OF CASE E. G., 11 white Italian male fifty-seven years old, was admitted to the Buffalo General Hospital on the service of Drs. N. G. Russell and A. H. Aaron, Nov. 25, 1934. He died Nov. 29, 1934. All his adult life he had partaken of large amounts of wine and whiskey daily. At the age of seventeen years he had suffered an attack of jaundice of several weeks' duration. The patient first began to lose weight and strength in 1932 and noticed that his skin was becoming dark. In March 1934 he complained of cramp-like abdominal pain, diarrhea, and bloating. The stools were watery. There was no nausea or vomiting. Upon hos pitalization, April 9, 1934, physical examination revealed that the pupils reacted to light and accommodation. The chest was emphysematous; breath sounds were diminished in both bases. The heart was regular; a systolic murmur was heard. The blood pressure was 118/70. The liver and spleen were palpable three finger breadths below the costal margin. -
The Distribution of Sweat Glands Over the Human Body Has So Far Been In
NOTES ON THE VERTICAL DISTRIBUTION OF THE HUMAN SWEAT GLANDS SHUNZO TAKAGI AND KO TOBARU* Institute of Physiology, School of Medicine, University of Nagoya•õ The distribution of sweat glands over the human body has so far been in- vestigated in the dimension of area, and we have no general idea how deep they are distributed in the skin. In 1943, Kuno and his collaborators (3) expressed the opinion that chloride would be accumulated in the skin during the activity of sweat glands. The truth of this assumption has been confirmed with more certainty by Yoshimura and Chihaya (unpublished), who measured the chloride content in the skin tissue by means of Ag-AgCl electrodes. The chloride may presumably be accumulated in the immediate neighbourhood of the glomeruli of sweat glands, or more diffusely in the layers of skin tissues where the glomeruli are situated. For consideration of the amount of the accumulated chloride, the total volume of these skin layers, which can be estimated by the vertical distribution of the sweat-gland glomeruli, seems to be useful. The fol- lowing investigation was therefore performed. MATERIALS AND METHOD Skin samples of 33 regions of the body, as specified in table 1, were taken from the corpse of a Japanese male of 30 years old, who died an accidental death. The samples were fixed in 10 per cent formalin, embedded in celloidin and cut into sections 15 micra thick. The sections were stained with Delafield's hematoxylin and eosin. Observations of sweat glands were made with 2-3 pieces of the skin about 100 sq. -
7) Anatomy of OMENTUM
OMENTUM ANATOMY DEPARTMENT DR.SANAA AL-SHAARAWY Dr. Essam Eldin Salama OBJECTIVES • At the end of the lecture the students must know: • Brief knowledge about peritoneum as a thin serous membrane and its main parts; parietal and visceral. • The peritonial cavity and its parts the greater sac and the lesser sac (Omental bursa). • The peritoneal folds : omenta, mesenteries, and ligaments. • The omentum, as one of the peritonial folds • The greater omentum, its boundaries, and contents. • The lesser omentum, its boundaries, and contents. • The omental bursa, its boundaries. • The Epiploic foramen, its boundaries. • Mesentery of the small intestine, and ligaments of the liver. • Nerve supply of the peritoneum. • Clinical points. The peritoneum vIs a thin serous membrane, §Lining the wall of the abdominal and pelvic cavities, (the parietal peritoneum). §Covering the existing organs, (the visceral peritoneum). §The potential space between the two layers is the peritoneal cavity. Parietal Visceral The peritoneal Cavity vThe peritoneal cavity is the largest one in the body. vDivisions of the peritoneal cavity : §Greater sac; extends from Lesser Sac diaphragm down to the pelvis. §Lesser sac; lies behind the stomach. §Both cavities are interconnected through the epiploic foramen. §In male : the peritoneum is a closed sac . §In female : the sac is not completely closed because it Greater Sac communicates with the exterior through the uterine tubes, uterus and vagina. The peritoneum qIntraperitoneal and Intraperitoneal viscera retroperitoneal organs; describe the relationship between various organs and their peritoneal covering; §Intraperitonial structure; which is nearly totally covered by visceral peritoneum. §Retroperitonial structure; lies behind the peritoneum, and partially covered by visceral peritoneum. -
Variant Anatomy of the External Jugular Vein
ORIGINAL COMMUNICATION Anatomy Journal of Africa. 2015. 4(1): 518 – 527 VARIANT ANATOMY OF THE EXTERNAL JUGULAR VEIN Beda O. Olabu, Poonamjeet K. Loyal, Bethleen W. Matiko, Joseph M. Nderitu , Musa K. Misiani, Julius A. Ogeng’o Corresponding Author: Beda Otieno Olabu P.O.Box 30197 – 00100 GPO, Nairobi Kenya Email: [email protected] or [email protected]. Cell phone: +254 720 915 805 or +254 736 791 617 ABSTRACT Variant anatomy of the external jugular vein is important when performing invasive procedures in the neck. Although there are a number of case reports on some of these variations, there are few descriptive cross-sectional regarding the same. This study therefore aimed at describing the variant anatomy of the external jugular vein as seen in a sample Kenyan population. One hundred and six (106) sides of the neck from 53 cadaveric specimens (70 males and 36 females) in the Department of Human Anatomy, University of Nairobi, Kenya, were used. Pattern and level of formation, course, communications and termination were studied by dissection. The vein was absent in 14.2% of cases, all males. It was formed within the substance of the parotid gland in 44%, and did not receive posterior auricular vein in 6.6%. Variant communications noted included facial vein, internal jugular, and a presence of a large anastomotic vein connecting it to the anterior jugular. It was duplicated in 2.2% cases and terminated into internal jugular vein in 7.7% of cases. The most common variations were in origin, course, communications and termination. These may limit its clinical utilization, and their awareness is important when considering the vein for any invasive procedure. -
Endotrophin Triggers Adipose Tissue Fibrosis and Metabolic Dysfunction
ARTICLE Received 12 Sep 2013 | Accepted 21 Feb 2014 | Published 19 Mar 2014 DOI: 10.1038/ncomms4485 Endotrophin triggers adipose tissue fibrosis and metabolic dysfunction Kai Sun1,*, Jiyoung Park1,2,*, Olga T. Gupta1, William L. Holland1, Pernille Auerbach3, Ningyan Zhang4, Roberta Goncalves Marangoni5, Sarah M. Nicoloro6, Michael P. Czech6, John Varga5, Thorkil Ploug3, Zhiqiang An4 & Philipp E. Scherer1,7 We recently identified endotrophin as an adipokine with potent tumour-promoting effects. However, the direct effects of local accumulation of endotrophin in adipose tissue have not yet been studied. Here we use a doxycycline-inducible adipocyte-specific endotrophin overexpression model to demonstrate that endotrophin plays a pivotal role in shaping a metabolically unfavourable microenvironment in adipose tissue during consumption of a high-fat diet (HFD). Endotrophin serves as a powerful co-stimulator of pathologically relevant pathways within the ‘unhealthy’ adipose tissue milieu, triggering fibrosis and inflammation and ultimately leading to enhanced insulin resistance. We further demonstrate that blocking endotrophin with a neutralizing antibody ameliorates metabolically adverse effects and effectively reverses metabolic dysfunction induced during HFD exposure. Collectively, our findings demonstrate that endotrophin exerts a major influence in adipose tissue, eventually resulting in systemic elevation of pro-inflammatory cytokines and insulin resistance, and the results establish endotrophin as a potential target in the context of metabolism and cancer. 1 Touchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA. 2 Department of Biological Sciences, School of Life Sciences, Ulsan National Institute of Science and Technology, 50 UNIST street, Ulsan 689-798, Korea.