Neuro-Endocrine System
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Thyroid Gland Parathyroid Glands
Human Physiology Course Thyroid Gland Parathyroid Glands Assoc. Prof. Mária Pallayová, MD, PhD [email protected] Department of Human Physiology, UPJŠ LF April 13, 2020 (10th week – Summer Semester 2019/2020) Hormones and Functions Thyroid gland Parathyroids Thymus Adrenal glands Endocrine pancreas Ovaries, Testes Pineal Pituitary Hypothalamus-Pituitary Axis GIT, adipose tissue, brain, heart, kidney, ... Hormones and Functions Thyroid gland Parathyroids Thymus Adrenal glands Endocrine pancreas Ovaries, Testes Pineal Pituitary Hypothalamus-Pituitary Axis GIT, adipose tissue, brain, heart, kidney, ... Lecture Outline Functional anatomy of the thyroid gland Synthesis, secretion, and metabolism of the thyroid hormones The mechanism of thyroid action Role of the thyroid hormones in development, growth, and metabolism Thyroid hormone deficiency and excess in adults Physiology of the parathyroids Functional Anatomy of the Thyroid Gland two lobes + isthmus (just below the cricoid cartilage) attached to the trachea by connective tissue A normal THGL in a healthy adult weighs about 15-20 g. Functional Anatomy of the Thyroid Gland arterial blood supply: from a superior and an inferior thyroid a., which arise from the external carotid and subclavian a., respectively. venous blood supply: a series of thyroid veins drain into the ext. jugular and innominate vv. ( a rich blood supply to the thyroid gland w/ a higher rate of blood flow per gram than even that of the kidneys). innervation: adrenergic innervation from the cervical ganglia; cholinergic innervation from the n. vagus (regulation of vasomotor function to increase the delivery of TSH, iodide, and metabolic substrates to the THGL). Functional Anatomy of the Thyroid Gland The colloid (a thick, gel-like substance) is a solution composed primarily of thyroglobulin (10-25% the high viscosity), a large protein that is a storage form of the thyroid hormones. -
The Potential Therapeutic Effect of Melatonin in Gastro-Esophageal Reflux Disease Tharwat S Kandil1*, Amany a Mousa2, Ahmed a El-Gendy3, Amr M Abbas3
Kandil et al. BMC Gastroenterology 2010, 10:7 http://www.biomedcentral.com/1471-230X/10/7 RESEARCH ARTICLE Open Access The potential therapeutic effect of melatonin in gastro-esophageal reflux disease Tharwat S Kandil1*, Amany A Mousa2, Ahmed A El-Gendy3, Amr M Abbas3 Abstract Background: Gastro-Esophageal Reflux Disease (GERD) defined as a condition that develops when the reflux of stomach contents causes troublesome symptoms and/or complications. Many drugs are used for the treatment of GERD such as omeprazole (a proton pump inhibitor) which is a widely used antiulcer drug demonstrated to protect against esophageal mucosal injury. Melatonin has been found to protect the gastrointestinal mucosa from oxidative damage caused by reactive oxygen species in different experimental ulcer models. The aim of this study is to evaluate the role of exogenous melatonin in the treatment of reflux disease in humans either alone or in combination with omeprazole therapy. Methods: 36 persons were divided into 4 groups (control subjects, patients with reflux disease treated with melatonin alone, omeprazole alone and a combination of melatonin and omeprazole for 4 and 8 weeks) Each group consisted of 9 persons. Persons were subjected to thorough history taking, clinical examination, and investigations including laboratory, endoscopic, record of esophageal motility, pH-metry, basal acid output and serum gastrin. Results: Melatonin has a role in the improvement of Gastro-esophageal reflux disease when used alone or in combination with omeprazole. Meanwhile, omeprazole alone is better used in the treatment of GERD than melatonin alone. Conclusion: The present study showed that oral melatonin is a promising therapeutic agent for the treatment of GERD. -
07. Endocrine, Reproductive and Urogenital Pharmacology 07.001
07. Endocrine, Reproductive and Urogenital Pharmacology 07.001 Mirabegron relaxes urethral smooth muscle by a dual mechanism involving β3-Adrenoceptor activation and α1-adrenoceptor blockade. Alexandre EC1, Kiguti LR2, Calmasini FB1, Ferreira R3, Silva FH1, Silva KP2, Ribeiro CA2, Mónica FZ1, Pupo AS2, Antunes E1 1FCM-Unicamp – Farmacologia, 2IBB-Unesp, 3FCM- Unicamp – Hematologia e Hemoterapia Introduction: Overactive bladder syndrome (OAB) is a subset of storage LUTS (lower urinary tract symptoms) highly prevalent in diabetes, obesity and hypertension. Benign prostatic hyperplasia (BPH) in aging men is another pathological condition highly associated with OAB secondary to bladder outlet obstruction (BOO). The β3- adrenoceptor apparently is the major receptor to induce bladder relaxations. Mirabegron is the first β3-adrenoceptor (β3-AR) agonist approved for OAB treatment (Chapple et al., 2014). Urethral smooth muscle plays a critical role to urinary continence, but no studies have examined the mirabegron-induced urethral relaxations. Aims: This study was designed to investigate the mirabegron-induced mouse urethral relaxations. In preliminary assays, mirabegron showed an unexpected action by competitively antagonizing the urethral contractions induced by the α1-AR agonist phenylephrine. Therefore, this study also aimed to characterize the α1-AR blockade by mirabegron, focusing on the α1-AR subtypes in rat vas deferens and prostate (α1A- AR), spleen (α1B-AR) and aorta (α1D-AR) preparations. Methods: Functional assays were carried out in mouse urethra rings, and rat vas deferens, prostate, aorta and spleen. β3-AR expression (mRNA and immunohistochemistry) and cyclic AMP levels were determined in mouse urethra. Competition assays for the specific binding of [3H]Prazosin to membrane preparations of HEK 293 cells expressing each of the human α1-ARs subtypes were performed. -
Chapter 45-Hormones and the Endocrine System Pathway Example – Simple Hormone Pathways Stimulus Low Ph in Duodenum
Chapter 45-Hormones and the Endocrine System Pathway Example – Simple Hormone Pathways Stimulus Low pH in duodenum •Hormones are released from an endocrine cell, S cells of duodenum travel through the bloodstream, and interact with secrete secretin ( ) Endocrine the receptor or a target cell to cause a physiological cell response Blood vessel A negative feedback loop Target Pancreas cells Response Bicarbonate release Insulin and Glucagon: Control of Blood Glucose Body cells •Insulin and glucagon are take up more Insulin antagonistic hormones that help glucose. maintain glucose homeostasis Beta cells of pancreas release insulin into the blood. The pancreas has clusters of endocrine cells called Liver takes islets of Langerhans up glucose and stores it as glycogen. STIMULUS: Blood glucose Blood glucose level level declines. rises. Target Tissues for Insulin and Glucagon Homeostasis: Blood glucose level Insulin reduces blood glucose levels by: (about 90 mg/100 mL) Promoting the cellular uptake of glucose Blood glucose STIMULUS: Slowing glycogen breakdown in the liver level rises. Blood glucose level falls. Promoting fat storage Alpha cells of pancreas release glucagon. Liver breaks down glycogen and releases glucose. Glucagon Glucagon increases blood glucose levels by: Stimulating conversion of glycogen to glucose in the liver Stimulating breakdown of fat and protein into glucose Diabetes Mellitus Type I diabetes mellitus (insulin-dependent) is an autoimmune disorder in which the immune system destroys pancreatic beta cells Type II diabetes -
2018 Camp Lesson Book
Arkansas 4-H Veterinary Science Urinalysis 1 Why Urine? Urine is the end product of a filtering process that removes waste from the body The color of urine can give you information about hydration level as well as possible underlying disease A urinalysis should be performed at least yearly for healthy pets, and more often for older animals and those with existing or chronic health issues Important elements of a urinalysis include a visual inspection of the urine sample, a dipstick test, and microscopic evaluation of urine sediment 2 The Urinary System The urinary tract consists of the kidneys, the ureters, the bladder, the urethra, and finally, the urethral opening at either the end of the penis or just within the vagina Kidneys filter out waste products from the blood Ureters connect the kidneys to the bladder The urethra is a tube that is controlled by a sphincter muscle that empties the bladder to the outside world 3 The Bladder Detrusor muscle Ureter Bladder Ureteral Opening Bladder Neck Sphincter Muscles Trigone Urethra 4 Urinary Tract Problems Inflammation of bladder caused by stress Bacterial or fungal bladder infections Inflammation of bladder from urinary crystals Inflammation of bladder from bladder stones Inflammation of the urethra Damage to ureters by trauma, passing kidney stones, surgical accident or cancer Damage to kidneys by dehydration, infection, toxins or cancer 5 Feline Idiopathic Cystitis Inflammation of the bladder with an unknown cause Can quickly lead to kidney and heart problems Can lead to -
The Third Eye and Pineal Gland Connection
D.U.Quark Volume 5 Issue 1 Fall 2020 Article 2 12-27-2020 Rolling My Third Eye: The Third Eye and Pineal Gland Connection Shannon B. Jackson Follow this and additional works at: https://dsc.duq.edu/duquark Recommended Citation Jackson, S. B. (2020). Rolling My Third Eye: The Third Eye and Pineal Gland Connection. D.U.Quark, 5 (1). Retrieved from https://dsc.duq.edu/duquark/vol5/iss1/2 This Staff Piece is brought to you for free and open access by Duquesne Scholarship Collection. It has been accepted for inclusion in D.U.Quark by an authorized editor of Duquesne Scholarship Collection. Rolling My Third Eye: The Third Eye and Pineal Gland Connection By Shannon Bow Jackson D.U.Quark 2020. Volume 5 (Issue 1) pgs. 6-13 Published December 27, 2020 Staff Article Chances are the optometrist only checks that two of your eyes are functioning. But what about your third eye; who checks on that? A neurologist? Spiritual Healer? Yoga Instructor? Yourself? The answer might vary, given that this third eye is believed to reside within the pineal gland inside of the brain. The name “third eye” comes from the pineal gland’s primary function of ‘letting in light and darkness’, just as our two eyes do. This gland is the melatonin-secreting neuroendocrine organ containing light-sensitive cells that control the circadian rhythm (1). The diagram shows that nerve cells in the retinas of our eyes allow for light to be sensed. When there is light, the nerve cells in the retina then signal to the suprachiasmatic nucleus (SCN) in the hypothalamus. -
The Fine Structure of the Parathyroid Gland*
The Fine Structure of the Parathyroid Gland* BY JERRY STEVEN TRIER, M.D. (From the Department of Anatomy, University of Washington School of Medicine, Seattle) PLATES 3 TO 10 (Received for publication, July 29, 1957) ABSTRACT The fine structure of the parathyroid of the macaque is described, and is cor- related with classical parathyroid cytology as seen in the light microscope. The two parenchymal cell types, the chief cells and the oxyphil cells, have been recognized in electron mierographs. The chief cells contain within their cyto- plasm mitochondria, endoplasmic reticulum, and Golgi bodies similar to those found in other endocrine tissues as well as frequent PAS-positive granules. The juxtanuclear body of the light microscopists is identified with stacks of parallel lamellar elements of the endoplasmic rcticulum of the ergastoplasmic or granular type. Oxyphll cells are characterized by juxtanuclear bodies and by numerous mito- chondria found throughout their cytoplasm. Puzzling lamellar whorls are described in the cytoplasm of some oxyphil cells. The endothelium of parathyroid capillaries is extremely thin in some areas and contains numerous fenestrations as well as an extensive system of vesicles. The possible significance of these structures is discussed. The connective tissue elements found in the perivascular spaces of macaque parathyroid are described. INTRODUCTION Other contributions to the present concepts con cerning the human parathyroid can be found in the It is the purpose of the present paper to report some observations on the fine structure of the reports of Bergstrand (7), Morgan (34), Pappen- parathyroid gland employing the electron micro- heimer and Wilens (45), Castleman and Mallory (10), and Gilmour (20). -
The Digestive System
69 chapter four THE DIGESTIVE SYSTEM THE DIGESTIVE SYSTEM The digestive system is structurally divided into two main parts: a long, winding tube that carries food through its length, and a series of supportive organs outside of the tube. The long tube is called the gastrointestinal (GI) tract. The GI tract extends from the mouth to the anus, and consists of the mouth, or oral cavity, the pharynx, the esophagus, the stomach, the small intestine, and the large intes- tine. It is here that the functions of mechanical digestion, chemical digestion, absorption of nutrients and water, and release of solid waste material take place. The supportive organs that lie outside the GI tract are known as accessory organs, and include the teeth, salivary glands, liver, gallbladder, and pancreas. Because most organs of the digestive system lie within body cavities, you will perform a dissection procedure that exposes the cavities before you begin identifying individual organs. You will also observe the cavities and their associated membranes before proceeding with your study of the digestive system. EXPOSING THE BODY CAVITIES should feel like the wall of a stretched balloon. With your skinned cat on its dorsal side, examine the cutting lines shown in Figure 4.1 and plan 2. Extend the cut laterally in both direc- out your dissection. Note that the numbers tions, roughly 4 inches, still working with indicate the sequence of the cutting procedure. your scissors. Cut in a curved pattern as Palpate the long, bony sternum and the softer, shown in Figure 4.1, which follows the cartilaginous xiphoid process to find the ventral contour of the diaphragm. -
Biology F – Lesson 4 – Endocrine & Reproductive Systems
Unit: Biology F – Endocrine & Reproduction LESSON 4.1 - AN INTRODUCTION TO THE ENDOCRINE SYSTEM Overview: Students research the location and function of the major endocrine glands and consider some endocrine system disorders. Suggested Timeline: 1 hour Materials: • An Introduction to the Endocrine System (Student Handout) • QUIZ – The Endocrine System (Student Handout) • student access to computers with the internet Method: 1. Allow students to use computers with internet access and other resources from the library to complete their questions on the endocrine system. 2. Students write quiz on the endocrine system. Assessment and Evaluation: • Affective assessment of student understanding of parts of the endocrine system • Student grade on quiz Extension: Assign a student or group of students to ‘be’ a specific endocrine gland. Have them role play for the class to get the idea of the function of the gland across to their classmates. Science 21 Bio F – Endocrine B152 Unit: Biology F – Endocrine & Reproduction Student Handout Name: ______________ Partner(s): _________________________ Date: ____________ Period: _____ An Introduction to the Endocrine System Go to the following website: http://health.howstuffworks.com/adam-200091.htm Watch the video to complete the following questions. 1. The endocrine system is composed primarily of _________________ that produce chemical messengers called __________________. 2. List the names of glands of the endocrine system, as mentioned in the video. Hint: There are 8 in total. 3. The endocrine and ________________ systems work closely together. The brain sends info to the endocrine glands and the endocrine glands send feedback to the brain. 4. The part of the brain that is known as the ‘master switchboard’ and controls the endocrine system is called the _____________________. -
Pineal Calcification, Melatonin Production, Aging, Associated
molecules Review Pineal Calcification, Melatonin Production, Aging, Associated Health Consequences and Rejuvenation of the Pineal Gland Dun Xian Tan *, Bing Xu, Xinjia Zhou and Russel J. Reiter * Department of Cell Systems & Anatomy, UT Health San Antonio, San Antonio, TX 78229, USA; [email protected] (B.X.); [email protected] (X.Z.) * Correspondence: [email protected] (D.X.T.); [email protected] (R.J.R.); Tel.: +210-567-2550 (D.X.T.); +210-567-3859 (R.J.R.) Received: 13 January 2018; Accepted: 26 January 2018; Published: 31 January 2018 Abstract: The pineal gland is a unique organ that synthesizes melatonin as the signaling molecule of natural photoperiodic environment and as a potent neuronal protective antioxidant. An intact and functional pineal gland is necessary for preserving optimal human health. Unfortunately, this gland has the highest calcification rate among all organs and tissues of the human body. Pineal calcification jeopardizes melatonin’s synthetic capacity and is associated with a variety of neuronal diseases. In the current review, we summarized the potential mechanisms of how this process may occur under pathological conditions or during aging. We hypothesized that pineal calcification is an active process and resembles in some respects of bone formation. The mesenchymal stem cells and melatonin participate in this process. Finally, we suggest that preservation of pineal health can be achieved by retarding its premature calcification or even rejuvenating the calcified gland. Keywords: pineal gland; calcification; melatonin; aging; neurodegenerative diseases; rejuvenation 1. Introduction Pineal gland is a unique organ which is localized in the geometric center of the human brain. Its size is individually variable and the average weight of pineal gland in human is around 150 mg [1], the size of a soybean. -
Chapter 20: Endocrine System
EndocrineEndocrine SystemSystem Modified by M. Myers 1 TheThe EndocrineEndocrine SystemSystem 2 EndocrineEndocrine GlandsGlands z The endocrine system is made of glands & tissues that secrete hormones. z Hormones are chemicals messengers influencing a. metabolism of cells b. growth and development c. reproduction, d. homeostasis. 3 HormonesHormones Hormones (chemical messengers) secreted into the bloodstream and transported by blood to specific cells (target cells) Hormones are classified as 1. proteins (peptides) 2. Steroids 4 HormoneHormone ClassificationClassification z Steroid Hormones: – Lipid soluble – Diffuse through cell membranes – Endocrine organs z Adrenal cortex z Ovaries z Testes z placenta 5 HormoneHormone ClassificationClassification z Nonsteroid Hormones: – Not lipid soluble – Received by receptors external to the cell membrane – Endocrine organs z Thyroid gland z Parathyroid gland z Adrenal medulla z Pituitary gland z pancreas 6 HormoneHormone ActionsActions z “Lock and Key” approach: describes the interaction between the hormone and its specific receptor. – Receptors for nonsteroid hormones are located on the cell membrane – Receptors for steroid hormones are found in the cell’s cytoplasm or in its nucleus 7 http://www.wisc- online.com/objects/index_tj.asp?objID=AP13704 8 EndocrineEndocrine SystemSystem z There is a close assoc. b/w the endocrine & nervous systems. z Hormone secretion is usually controlled by either negative feedback or antagonistic hormones that oppose each other’s actions 9 HypothalamusHypothalamus 1. regulates the internal environment through the autonomic system 2. controls the secretions of the pituitary gland. 10 HypothalamusHypothalamus && PituitaryPituitary GlandGland posteriorposterior pituitary/pituitary/ anterioranterior pituitarypituitary 11 PosteriorPosterior PituitaryPituitary The posterior pituitary secretes zantidiuretic hormone (ADH) zoxytocin 12 13 14 AnteriorAnterior pituitarypituitary glandgland 1. -
Thyroid & Parathyroid Glands
THYROID & PARATHYROID GLANDS Objectives: ◧ Editing file • Describe the histological structure of ◧ thyroid & parathyroid glands. Important • Identify and correlate between the different ◧ Doctor notes / Extra endocrine cells in thyroid gland and their functions. • Describe the functional structure of the parathyroid cells. 438 Histology Team Endocrine Block THYROID GLAND STROMA 1- Capsule: dense irregular collagenous C.T. 2- Septa (Interlobular septa) 3- Reticular fibers: Thin C.T. composed mostly of reticular fibers with rich capillary plexus surrounds each thyroid follicle. PARENCHYMA Are the structural and functional units of the thyroid gland. 1- Simple cuboidal epithelium: 2- Colloid: central colloid-filled lumen. a- Follicular (principal) cells b- Parafollicular cells (C cells) (Clear cells) - Pale-stained cells (Clear Cells). (Polygonal/pyramidal cells) N.B. Each follicle is - Simple cuboidal cells. - Found singly or in clusters in between the follicular cells. - Round nucleus with prominent nucleoli. surrounded by thin - Their apices do not reach the lumen of the follicle. L/M: - Basophilic cytoplasm. basal lamina. - Are larger than follicular cells (2-3 times).(larger but less in number) - Apical surface reaches the lumen of the (Acidophilic) - Only 0.1% of the epithelial cells. thyroid follicle. - Have round nucleus - Mitochondria. - RER. (synthesis of thyroglobulin) - Supranuclear Golgi Complex. - Mitochondria. E/M: - Numerous apically-located lysosomes. - RER (moderate). - Numerous dispersed small vesicles - Well-developed Golgi. - The vesicles contain newly formed thyroglobulin. - Numerous apical short microvilli. Function: Synthesis of thyroid hormones (T4 & T3). Secrete calcitonin. 438 Histology Team - Endocrine Block 2 PARATHYROID GLAND They are 4 glands on the posterior of thyroid gland. STROMA 1- Capsule: Each gland has its Thin capsule.