Vocabulario De Morfoloxía, Anatomía E Citoloxía Veterinaria
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3 Embryology and Development
BIOL 6505 − INTRODUCTION TO FETAL MEDICINE 3. EMBRYOLOGY AND DEVELOPMENT Arlet G. Kurkchubasche, M.D. INTRODUCTION Embryology – the field of study that pertains to the developing organism/human Basic embryology –usually taught in the chronologic sequence of events. These events are the basis for understanding the congenital anomalies that we encounter in the fetus, and help explain the relationships to other organ system concerns. Below is a synopsis of some of the critical steps in embryogenesis from the anatomic rather than molecular basis. These concepts will be more intuitive and evident in conjunction with diagrams and animated sequences. This text is a synopsis of material provided in Langman’s Medical Embryology, 9th ed. First week – ovulation to fertilization to implantation Fertilization restores 1) the diploid number of chromosomes, 2) determines the chromosomal sex and 3) initiates cleavage. Cleavage of the fertilized ovum results in mitotic divisions generating blastomeres that form a 16-cell morula. The dense morula develops a central cavity and now forms the blastocyst, which restructures into 2 components. The inner cell mass forms the embryoblast and outer cell mass the trophoblast. Consequences for fetal management: Variances in cleavage, i.e. splitting of the zygote at various stages/locations - leads to monozygotic twinning with various relationships of the fetal membranes. Cleavage at later weeks will lead to conjoined twinning. Second week: the week of twos – marked by bilaminar germ disc formation. Commences with blastocyst partially embedded in endometrial stroma Trophoblast forms – 1) cytotrophoblast – mitotic cells that coalesce to form 2) syncytiotrophoblast – erodes into maternal tissues, forms lacunae which are critical to development of the uteroplacental circulation. -
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 -
1 Male Checklist Male Reproductive System Components of the Male
Male Checklist Male Reproductive System Components of the male Testes; accessory glands and ducts; the penis; and reproductive system the scrotum. Functions of the male The male reproductive system produces sperm cells that reproductive system can be transferred to the female, resulting in fertilization and the formation of a new individual. It also produces sex hormones responsible for the normal development of the adult male body and sexual behavior. Penis The penis functions as the common outlet for semen (sperm cells and glandular secretions) and urine. The penis is also the male copulatory organ, containing tissue that can fill with blood resulting in erection of the penis. Prepuce A fold of skin over the distal end of the penis. Circumcision is the surgical removal of the prepuce. Corpus spongiosum A spongy body consisting of erectile tissue. It surrounds the urethra. Sexual excitement can cause erectile tissue to fill with blood. As a result, the penis becomes erect. Glans penis The expanded, distal end of the corpus spongiosum. It is also called the head of the penis. Bulb of the penis The proximal end of the corpus spongiosum. Bulbospongiosus muscle One of two skeletal muscles surrounding the bulb of the penis. At the end of urination, contraction of the bulbospongiosus muscles forces any remaining urine out of the urethra. During ejaculation, contractions of the bulbospongiosus muscles ejects semen from the penis. Contraction of the bulbospongiosus muscles compresses the corpus spongiosum, helping to maintain an erection. Corpus cavernosum One of two spongy bodies consisting of erectile tissue that (pl., corpora cavernosa) form the sides and front of the penis. -
HYPOTHALAMUS – PITUITARY-ADRENAL AXIS Learning Objectives OVERVIEW FUNCTIONAL ANATOMY
Introductory Human Physiology ©copyright Emma Jakoi HYPOTHALAMUS – PITUITARY-ADRENAL AXIS Emma R. Jakoi, Ph.D. Learning objectives • Describe the structural and functional organization of the adrenal gland. • Describe the synthesis and secretion of cortical adrenal hormones. • Describe the mechanism of action and physiologic effects of adrenal hormones. • Explain the control of adrenal hormone synthesis and secretion. Describe the major feedback loops that integrate the hypothalamic axis and body homeostasis. • Explain the physiologic roles of the adrenal hormones in normal physiology. OVERVIEW The adrenal glands maintain homeostasis in response to stress. Three major classes of hormones are secreted by these glands: aldosterone (mineralocorticoid), cortisol (glucocorticoid), DHEA (weak androgen), and catecholamines (epinephrine and norepinephrine). FUNCTIONAL ANATOMY The adrenal gland is located on top of the kidney. Like the pituitary, two distinct tissues merge during development to form the adrenal cortex (glandular tissue) and medulla (modified neuronal tissue) (Fig 1). 1 2 cortex 3 medulla Figure 1. Structure of the adrenal gland. The cortex secretes three steroid hormones: 1. aldosterone, 2. cortisol, 3. a weak androgen, DHEA. The medulla secretes epinephrine (Epi) and norepinephrine (NorEpi). 1 Introductory Human Physiology ©copyright Emma Jakoi MINERALOCORTICOIDS The major mineralocorticoid in humans is aldosterone. Aldosterone is NOT under the hypothalamus- pituitary control and does not mediate a negative feedback to this axis. Aldosterone secretion is increased by the vasoconstrictor, angiotensin II, and by elevated plasma K+ concentration. Elevated plasma Na+ inhibits the secretion of aldosterone. Aldosterone, acts in the kidney to promote secretion of K+ into the urine from the blood and the reabsorption of Na+ from the urine into the blood. -
Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-Tailed Opossum (Monodelphis Domestica) and North American Opossum (Didelphis Virginiana)
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 12-2001 Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana) Lee Anne Cope University of Tennessee - Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Animal Sciences Commons Recommended Citation Cope, Lee Anne, "Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana). " PhD diss., University of Tennessee, 2001. https://trace.tennessee.edu/utk_graddiss/2046 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Lee Anne Cope entitled "Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana)." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Animal Science. Robert W. Henry, Major Professor We have read this dissertation and recommend its acceptance: Dr. R.B. Reed, Dr. C. Mendis-Handagama, Dr. J. Schumacher, Dr. S.E. Orosz Accepted for the Council: Carolyn R. -
© Copyright 2016 Wendy Yang
© Copyright 2016 Wendy Yang Role for cell-to-cell communication in stem cell specification toward pancreatic progenitors: relevance to the design of novel therapies for diabetes. Wendy Yang A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy University of Washington 2016 Reading Committee: Vincenzo Cirulli, Chair Laura Crisa Paul D. Lampe Program Authorized to Offer Degree: Pharmacology University of Washington Abstract Role for cell-to-cell communication in stem cell specification toward pancreatic progenitors: relevance to the design of novel therapies for diabetes. Wendy Yang Chair of the Supervisory Committee: Vincenzo Cirulli Metabolism, Endocrinology & Nutrition Pancreatic islets of Langerhans, responsible for the production of hormones such as insulin and glucagon, develop from pluripotent pancreatic progenitors following their specification toward an endocrine phenotype. Based on the established role of cell-to-cell communication as an important mechanism regulating developmental decisions during embryonic life, I investigated the expression pattern of Connexins (Cxs), the building blocks of Gap Junction channels, in the developing human pancreas, and in an in vitro model of pancreatic progenitor differentiation from human embryonic stem cells (hESC). I also investigated the role of β1 integrins and an associated downstream effector, integrin-linked kinase (ILK), on islet development in mice. In a first series of experiments, I investigated the expression pattern of Cxs in the developing human pancreas. Results from these studies revealed that while Cx32 is predominantly expressed in the acinar tissue, Cx36 is primarily expressed in developing islet β- cells. Cx43 exhibited the most interesting expression pattern, being primarily detected in putative islet cell progenitors that delaminate from the pancreatic ductal epithelium and aggregate with developing islet cell clusters. -
ATG9 Regulates Autophagosome Progression from the Endoplasmic Reticulum in Arabidopsis
ATG9 regulates autophagosome progression from the endoplasmic reticulum in Arabidopsis Xiaohong Zhuanga,b,1, Kin Pan Chunga,b,1, Yong Cuia,b,1, Weili Lina,b, Caiji Gaoa,b,2, Byung-Ho Kanga,b, and Liwen Jianga,b,c,3 aCentre for Cell & Developmental Biology, School of Life Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China; bState Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China; and cThe Chinese University of Hong Kong Shenzhen Research Institute, Shenzhen 518057, China Edited by Diane C. Bassham, Iowa State University, Ames, IA, and accepted by Editorial Board Member Maarten J. Chrispeels December 8, 2016 (received for review October 6, 2016) Autophagy is a conserved pathway for bulk degradationofcytoplasmic autophagy pathway because ATG9 was required for the biogenesis material by a double-membrane structure named the autophagosome. of ER-derived compartments during the unfolded protein response The initiation of autophagosome formation requires the recruitment of (9). However, whether ATG9 plays a direct role in the early stages autophagy-related protein 9 (ATG9) vesicles to the preautophagosomal of autophagosome formation or in a specific autophagy process structure. However, the functional relationship between ATG9 vesicles remainstobeinvestigatedinplants.Onemajorchallengeisthelack and the phagophore is controversial in different systems, and the mo- of morphologically informative visualization that might correlate the lecular function of ATG9 remains unknown in plants. Here, we demon- early autophagosomal structures and ATG9 vesicles in real-time and strate that ATG9 is essential for endoplasmic reticulum (ER)-derived in three dimensions. autophagosome formation in plants. -
Liver • Gallbladder
NORMAL BODY Microscopic Anatomy! Accessory Glands of the GI Tract,! lecture 2! ! • Liver • Gallbladder John Klingensmith [email protected] Objectives! By the end of this lecture, students will be able to: ! • trace the flow of blood and bile within the liver • describe the structure of the liver in regard to its functions • indicate the major cell types of the liver and their functions • distinguish the microanatomy of exocrine and endocrine function by the hepatocytes • explain the functional organization of the gallbladder at the cellular level (Lecture plan: overview of structure and function, then increasing resolution of microanatomy and cellular function) Liver and Gallbladder Liver October is “Liver Awareness Month” -- http://www.liverfoundation.org Liver • Encapsulated by CT sheath and mesothelium • Lobes largely composed of hepatocytes in parenchyma • Receives blood from small intestine and general circulation Major functions of the liver • Production and secretion of digestive fluids to small intestine (exocrine) • Production of plasma proteins and lipoproteins (endocrine) • Storage and control of blood glucose • Detoxification of absorbed compounds • Source of embyronic hematopoiesis The liver lobule • Functional unit of the parenchyma • Delimited by CT septa, invisible in humans (pig is shown) • Surrounds the central vein • Bordered by portal tracts Central vein, muralia and sinusoids Parenchyma: Muralia and sinusoids • Hepatocyte basolateral membrane faces sinusoidal lumen • Bile canaliculi occur between adjacent hepatocytes • Cords anastomose Vascularization of the liver • Receives veinous blood from small intestine via portal vein • Receives freshly oxygenated blood from hepatic artery • Discharges blood into vena cava via hepatic vein Blood flow in the liver lobes • flows in via the portal vein and hepatic artery • oozes through the liver lobules to central veins • flows out via the hepatic vein Portal Tract! (aka portal triad) • Portal venule • Hepatic arteriole • Bile duct • Lymph vessel • Nerves • Connective tissue Central vein! (a.k.a. -
Clinical Pelvic Anatomy
SECTION ONE • Fundamentals 1 Clinical pelvic anatomy Introduction 1 Anatomical points for obstetric analgesia 3 Obstetric anatomy 1 Gynaecological anatomy 5 The pelvic organs during pregnancy 1 Anatomy of the lower urinary tract 13 the necks of the femora tends to compress the pelvis Introduction from the sides, reducing the transverse diameters of this part of the pelvis (Fig. 1.1). At an intermediate level, opposite A thorough understanding of pelvic anatomy is essential for the third segment of the sacrum, the canal retains a circular clinical practice. Not only does it facilitate an understanding cross-section. With this picture in mind, the ‘average’ of the process of labour, it also allows an appreciation of diameters of the pelvis at brim, cavity, and outlet levels can the mechanisms of sexual function and reproduction, and be readily understood (Table 1.1). establishes a background to the understanding of gynae- The distortions from a circular cross-section, however, cological pathology. Congenital abnormalities are discussed are very modest. If, in circumstances of malnutrition or in Chapter 3. metabolic bone disease, the consolidation of bone is impaired, more gross distortion of the pelvic shape is liable to occur, and labour is likely to involve mechanical difficulty. Obstetric anatomy This is termed cephalopelvic disproportion. The changing cross-sectional shape of the true pelvis at different levels The bony pelvis – transverse oval at the brim and anteroposterior oval at the outlet – usually determines a fundamental feature of The girdle of bones formed by the sacrum and the two labour, i.e. that the ovoid fetal head enters the brim with its innominate bones has several important functions (Fig. -
Avian Adrenal Medulla: Cytomorphology and Function
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Publications of the IAS Fellows Volume 45(1-4):1-11, 2001 Acta Biologica Szegediensis http://www.sci.u-szeged.hu/ABS REVIEW ARTICLE Avian adrenal medulla: cytomorphology and function Asok Ghosh, Stephen W. Carmichael1*, Monisha Mukherjee Department of Zoology, University of Calcutta, Calcutta, India, 1Department of Anatomy, Mayo Clinic/Foundation, Rochester, Minnesota, USA ABSTRACT The purpose of this review is to explore the world literature on the avian adrenal KEY WORDS medulla from the last 20 years. Unlike the mammalian adrenal medulla, the adrenal gland in adrenal medulla birds has chromaffin cells mixed with cortical cells. Studies have investigated the ultrastructure birds (both transmission and scanning electron microscopy), biochemistry, and physiology (partic- morphology ularly interactions with other endocrine glands) of the avian adrenal medulla. Although function progress has been made, it is apparent that research on the avian adrenal medulla still lags behind work on the mammalian organ. Acta Biol Szeged 45(1-4):1-11 (2001) The adrenal glands of birds, like those in mammals, are in the adrenal medulla. This profound variation of medullary paired yellow- or orange-colored pear- or triangle-shaped E/NE ratio in birds suggests a distinct evolutionary pattern glands that are next to the kidneys. The intermingling nature (Ghosh 1977, 1980). The avian phylogeny used in this study of cortical and medullary components constitutes a major was essentially based on palaeontological evidences (Grego- characteristic of avian adrenal medulla (Vestergaard and ry 1957). We feel that our “claim” of hormonal taxonomy is Willeberg 1978). -
Endocrine Tumors – Adrenal Medulla
Endocrine Tumors – Adrenal Medulla 803-808-7387 www.gracepets.com These notes are provided to help you understand the diagnosis or possible diagnosis of cancer in your pet. For general information on cancer in pets ask for our handout “What is Cancer”. Your veterinarian may suggest certain tests to help confirm or eliminate diagnosis, and to help assess treatment options and likely outcomes. Because individual situations and responses vary, and because cancers often behave unpredictably, science can only give us a guide. However, information and understanding for tumors in animals is improving all the time. We understand that this can be a very worrying time. We apologize for the need to use some technical language. If you have any questions please do not hesitate to ask us. What are the adrenal glands? The adrenal glands are located close to the kidneys. They are part of the body’s endocrine system, the glands of which also include the pituitary (in the brain), thyroid, parathyroid and Islets of Langerhans in the pancreas. Endocrine glands produce specialized chemicals called “hormones”. These regulate and integrate many activities to maintain internal stability of the body. The hormones pass directly into the blood to affect target cells elsewhere. Hormones are also produced by many cells in other tissues. Each of the two adrenal glands has two parts. The outer part (cortex) is controlled by a hormone (adrenocorticotrophic hormone, ACTH) from the pituitary gland. The cortex produces steroid hormones of several types. The inner part (medulla) of the adrenal gland originates from the same cells that in the embryo form the nervous system, and therefore not surprisingly it produces neuroendocrine hormones with effects similar to those of the sympathetic nervous system. -
Roles of Sigma-1 Receptors on Mitochondrial Functions Relevant to Neurodegenerative Diseases Tzu-Yu Weng1,2, Shang-Yi Anne Tsai1 and Tsung-Ping Su1*
Weng et al. Journal of Biomedical Science (2017) 24:74 DOI 10.1186/s12929-017-0380-6 REVIEW Open Access Roles of sigma-1 receptors on mitochondrial functions relevant to neurodegenerative diseases Tzu-Yu Weng1,2, Shang-Yi Anne Tsai1 and Tsung-Ping Su1* Abstract The sigma-1 receptor (Sig-1R) is a chaperone that resides mainly at the mitochondrion-associated endoplasmic reticulum (ER) membrane (called the MAMs) and acts as a dynamic pluripotent modulator in living systems. At the MAM, the Sig-1R is known to play a role in regulating the Ca2+ signaling between ER and mitochondria and in maintaining the structural integrity of the MAM. The MAM serves as bridges between ER and mitochondria regulating multiple functions such as Ca2+ transfer, energy exchange, lipid synthesis and transports, and protein folding that are pivotal to cell survival and defense. Recently, emerging evidences indicate that the MAM is critical in maintaining neuronal homeostasis. Thus, given the specific localization of the Sig-1R at the MAM, we highlight and propose that the direct or indirect regulations of the Sig-1R on mitochondrial functions may relate to neurodegenerative diseases including Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD) and amyotrophic lateral sclerosis (ALS). In addition, the promising use of Sig-1R ligands to rescue mitochondrial dysfunction-induced neurodegeneration is addressed. Keywords: Sigma-1 receptor, Mitochondria, Mitochondrion-associated ER membrane (MAM), Neurodegenerative disorders Background also regulates Ca2+ influx by attenuating the coupling of The sigma-1 receptor (Sig-1R) is an endoplasmic the ER Ca2+ sensor STIM1 to Orai1 [3].