Hormone - Wikipedia Hormone From Wikipedia, the free encyclopedia Jump to navigation Jump to search Chemical released by a cell or a gland in one part of the body that sends out messages that affect cells in other parts of the organism For other uses, see Hormone (disambiguation). Different types of hormones are secreted in the body, with different biological roles and functions. A hormone (from the Greek participle ὁρμῶν, "setting in motion") is any member of a class of signaling molecules, produced by glands in multicellular organisms, that are transported by the circulatory system to target distant organs to regulate physiology and behavior.[1] Hormones have diverse chemical structures, mainly of three classes: eicosanoids steroids amino acid/protein derivatives (amines, peptides, and proteins) The glands that secrete hormones comprise the endocrine signaling system. The term "hormone" is sometimes extended to include chemicals produced by cells that affect the same cell (autocrine or intracrine signaling) or nearby cells (paracrine signalling). Hormones serve to communicate between organs and tissues for physiological regulation and behavioral activities such as digestion, metabolism, respiration, tissue function, sensory perception, sleep, excretion, lactation, stress induction, growth and development, movement, reproduction, and mood manipulation.[2][3] Hormones affect distant cells by binding to specific receptor proteins in the target cell, resulting in a change in cell function. When a hormone binds to the receptor, it results in the activation of a signal transduction pathway that typically activates gene transcription, resulting in increased expression of target proteins; non-genomic effects are more rapid, and can be synergistic with genomic effects.[4] Amino acid–based hormones (amines and peptide or protein hormones) are water-soluble and act on the surface of target cells via second messengers; steroid hormones, being lipid-soluble, move through the plasma membranes of target cells (both cytoplasmic and nuclear) to act within their nuclei. Hormone secretion may occur in many tissues. Endocrine glands provide the cardinal example, but specialized cells in various other organs also secrete hormones. Hormone secretion occurs in response to specific biochemical signals from a wide range of regulatory systems. For instance, serum calcium concentration affects parathyroid hormone synthesis; blood sugar (serum glucose concentration) affects insulin synthesis; and because the outputs of the stomach and exocrine pancreas (the amounts of gastric juice and pancreatic juice) become the input of the small intestine, the small intestine secretes hormones to stimulate or inhibit the stomach and pancreas based on how busy it is. Regulation of hormone synthesis of gonadal hormones, adrenocortical hormones, and thyroid hormones often depends on complex sets of direct-influence and feedback interactions involving the hypothalamic-pituitary-adrenal (HPA), -gonadal (HPG), and -thyroid (HPT) axes. Upon secretion, certain hormones, including protein hormones and catecholamines, are water-soluble and are thus readily transported through the circulatory system. Other hormones, including steroid and thyroid hormones, are lipid-soluble; to achieve widespread distribution, these hormones must bond to carrier plasma glycoproteins (e.g., thyroxine-binding globulin (TBG)) to form ligand-protein complexes. Some hormones are completely active[which?] when released into the bloodstream (as is the case for insulin and growth hormones), while others are prohormones that must be activated in specific cells through a series of activation steps that are commonly highly regulated. The endocrine system secretes hormones directly into the bloodstream, typically via fenestrated capillaries, whereas the exocrine system secretes its hormones indirectly using ducts. Hormones with paracrine function diffuse through the interstitial spaces to nearby target tissue. Contents 1 Introduction and overview 2 Discovery 2.1 Arnold Adolph Berthold (1849) 2.2 Bayliss and Starling (1902) 3 Types of signaling 4 Chemical classes 4.1 Vertebrates 4.2 Invertebrates 4.3 Plants 5 Receptors 6 Effects 7 Regulation 8 Therapeutic use 9 Hormone-behavior interactions 10 Comparison with neurotransmitters 11 Binding proteins 12 See also 13 References 14 External links Introduction and overview[edit] Further information: Signal transduction Hormonal signaling involves the following steps:[5] Biosynthesis of a particular hormone in a particular tissue Storage and secretion of the hormone Transport of the hormone to the target cell(s) Recognition of the hormone by an associated cell membrane or intracellular receptor protein Relay and amplification of the received hormonal signal via a signal transduction process: This then leads to a cellular response. The reaction of the target cells may then be recognized by the original hormone-producing cells, leading to a downregulation in hormone production. This is an example of a homeostatic negative feedback loop. Breakdown of the hormone. Hormone producing cells are typically of a specialized cell type, residing within a particular endocrine gland, such as the thyroid gland, ovaries, and testes. Hormones exit their cell of origin via exocytosis or another means of membrane transport. The hierarchical model is an oversimplification of the hormonal signaling process. Cellular recipients of a particular hormonal signal may be one of several cell types that reside within a number of different tissues, as is the case for insulin, which triggers a diverse range of systemic physiological effects. Different tissue types may also respond differently to the same hormonal signal. Discovery[edit] The discovery of hormones and endocrine signaling occurred during studies of how the digestive system regulates its activities, as explained at Secretin § Discovery. Arnold Adolph Berthold (1849)[edit] Arnold Adolph Berthold was a German physiologist and zoologist, who, in 1849, had a question about the function of the testes. He noticed that in castrated roosters that they did not have the same sexual behaviors as roosters with their testes intact. He decided to run an experiment on male roosters to examine this phenomenon. He kept a group of roosters with their testes intact, and saw that they had normal sized wattles and combs (secondary sexual organs), a normal crow, and normal sexual and aggressive behaviors. He also had a group with their testes surgically removed, and noticed that their secondary sexual organs were decreased in size, had a weak crow, did not have sexual attraction towards females, and were not aggressive. He realized that this organ was essential for these behaviors, but he did not know how. To test this further, he removed one testis and placed it in the abdominal cavity. The roosters acted and had normal physical anatomy. He was able to see that location of the testes do not matter. He then wanted to see if it was a genetic factor that was involved in the testes that provided these functions. He transplanted a testis from another rooster to a rooster with one testis removed, and saw that they had normal behavior and physical anatomy as well. Berthold determined that the location or genetic factors of the testes do not matter in relation to sexual organs and behaviors, but that some chemical in the testes being secreted is causing this phenomenon. It was later identified that this factor was the hormone testosterone.[6][7] Bayliss and Starling (1902)[edit] William Bayliss and Ernest Starling, a physiologist and biologist, respectively, wanted to see if the nervous system had an impact on the digestive system. They knew that the pancreas was involved in the secretion of digestive fluids after the passage of food from the stomach to the intestines, which they believed to be due to the nervous system. They cut the nerves to the pancreas in an animal model and discovered that it was not nerve impulses that controlled secretion from the pancreas. It was determined that a factor secreted from the intestines into the bloodstream was stimulating the pancreas to secrete digestive fluids. This factor was named secretin: a hormone, although the term hormone was not coined until 1905 by Starling.[8] Types of signaling[edit] Hormonal effects are dependent on where they are released, as they can be released in different manners.[9] Not all hormones are released from a cell and into the blood until it binds to a receptor on a target. The major types of hormone signaling are: Signaling Types - Hormones SN Types Description 1 Endocrine Acts on the target cells after being released into the bloodstream. 2 Paracrine Acts on the nearby cells and does not have to enter general circulation. 3 Autocrine Affects the cell types that secreted it and causes a biological effect. 4 Intracrine Acts intracellularly on the cells that synthesized it. Chemical classes[edit] As hormones are defined functionally, not structurally, they may have diverse chemical structures. Hormones occur in multicellular organisms (plants, animals, fungi, brown algae, and red algae). These compounds occur also in unicellular organisms, and may act as signaling molecules however there is no agreement that these molecules can be called hormones.[10][11] Vertebrates[edit] Further information: List of human hormones Hormone types in Vertebrates SN Types Description 1 Peptide Peptide hormones are made of a chain of amino acids that can range from just 3 to hundreds of amino acids. Examples include oxytocin and insulin.[6] Their sequences are encoded in DNA and can be modified by alternative splicing and/or post-translational modification.[9] They are packed in vesicles and are hydrophilic, meaning that they are soluble in water. Due to their hydrophilicity, they can only bind to receptors on the membrane, as travelling through the membrane is unlikely. However, some hormones can bind to intracellular receptors through an intracrine mechanism. 2 Amino acid Amino acid hormones are derived from amino acid, most commonly tyrosine. They are stored in vesicles. Examples include melatonin and thyroxine. 3 Steroid Steroid hormones are derived from cholesterol. Examples include the sex hormones estradiol and testosterone as well as the stress hormone cortisol.[12] Steroids contain four fused rings. They are lipophilic and hence can cross membranes to bind to intracellular nuclear receptors. 4 Eicosanoid Eicosanoids hormones are derived from lipids such as arachidonic acid, lipoxins and prostaglandins. Examples include prostaglandin and thromboxane. These hormones are produced by cyclooxygenases and lipoxygenases. They are hydrophobic and act on membrane receptors. Invertebrates[edit] Compared with vertebrates, insects and crustaceans possess a number of structurally unusual hormones such as the juvenile hormone, a sesquiterpenoid.[13] Plants[edit] Examples include abscisic acid, auxin, cytokinin, ethylene, and gibberellin.[14] Receptors[edit] The left diagram shows a steroid (lipid) hormone (1) entering a cell and (2) binding to a receptor protein in the nucleus, causing (3) mRNA synthesis which is the first step of protein synthesis. The right side shows protein hormones (1) binding with receptors which (2) begins a transduction pathway. The transduction pathway ends (3) with transcription factors being activated in the nucleus, and protein synthesis beginning. In both diagrams, a is the hormone, b is the cell membrane, c is the cytoplasm, and d is the nucleus. Most hormones initiate a cellular response by initially binding to either cell membrane associated or intracellular receptors. A cell may have several different receptor types that recognize the same hormone but activate different signal transduction pathways, or a cell may have several different receptors that recognize different hormones and activate the same biochemical pathway.[15] Receptors for most peptide as well as many eicosanoid hormones are embedded in the plasma membrane at the surface of the cell and the majority of these receptors belong to the G protein-coupled receptor (GPCR) class of seven alpha helix transmembrane proteins. The interaction of hormone and receptor typically triggers a cascade of secondary effects within the cytoplasm of the cell, described as signal transduction, often involving phosphorylation or dephosphorylation of various other cytoplasmic proteins, changes in ion channel permeability, or increased concentrations of intracellular molecules that may act as secondary messengers (e.g., cyclic AMP). Some protein hormones also interact with intracellular receptors located in the cytoplasm or nucleus by an intracrine mechanism.[16][17] For steroid or thyroid hormones, their receptors are located inside the cell within the cytoplasm of the target cell. These receptors belong to the nuclear receptor family of ligand-activated transcription factors. To bind their receptors, these hormones must first cross the cell membrane. They can do so because they are lipid-soluble. The combined hormone-receptor complex then moves across the nuclear membrane into the nucleus of the cell, where it binds to specific DNA sequences, regulating the expression of certain genes, and thereby increasing the levels of the proteins encoded by these genes.[18] However, it has been shown that not all steroid receptors are located inside the cell. Some are associated with the plasma membrane.[19] Effects[edit] Hormones have the following effects on the body:[20] stimulation or inhibition of growth wake-sleep cycle and other circadian rhythms mood swings induction or suppression of apoptosis (programmed cell death) activation or inhibition of the immune system regulation of metabolism preparation of the body for mating, fighting, fleeing, and other activity preparation of the body for a new phase of life, such as puberty, parenting, and menopause control of the reproductive cycle hunger cravings A hormone may also regulate the production and release of other hormones. Hormone signals control the internal environment of the body through homeostasis. Regulation[edit] The rate of hormone biosynthesis and secretion is often regulated by a homeostatic negative feedback control mechanism. Such a mechanism depends on factors that influence the metabolism and excretion of hormones. Thus, higher hormone concentration alone cannot trigger the negative feedback mechanism. Negative feedback must be triggered by overproduction of an "effect" of the hormone.[21][22] Hormone secretion can be stimulated and inhibited by: Other hormones (stimulating- or releasing -hormones) Plasma concentrations of ions or nutrients, as well as binding globulins Neurons and mental activity Environmental changes, e.g., of light or temperature One special group of hormones is the tropic hormones that stimulate the hormone production of other endocrine glands. For example, thyroid-stimulating hormone (TSH) causes growth and increased activity of another endocrine gland, the thyroid, which increases output of thyroid hormones.[23] To release active hormones quickly into the circulation, hormone biosynthetic cells may produce and store biologically inactive hormones in the form of pre- or prohormones. These can then be quickly converted into their active hormone form in response to a particular stimulus.[23] Eicosanoids are considered to act as local hormones. They are considered to be "local" because they possess specific effects on target cells close to their site of formation. They also have a rapid degradation cycle, making sure they do not reach distant sites within the body.[24] Hormones are also regulated by receptor agonists. Hormones are ligands, which are any kinds of molecules that produce a signal by binding to a receptor site on a protein. Hormone effects can be inhibited, thus regulated, by competing ligands that bind to the same target receptor as the hormone in question. When a competing ligand is bound to the receptor site, the hormone is unable to bind to that site and is unable to elicit a response from the target cell. These competing ligands are called antagonists of the hormone.[25] Therapeutic use[edit] Main article: Hormone therapy Many hormones and their structural and functional analogs are used as medication. The most commonly prescribed hormones are estrogens and progestogens (as methods of hormonal contraception and as HRT),[26] thyroxine (as levothyroxine, for hypothyroidism) and steroids (for autoimmune diseases and several respiratory disorders). Insulin is used by many diabetics. Local preparations for use in otolaryngology often contain pharmacologic equivalents of adrenaline, while steroid and vitamin D creams are used extensively in dermatological practice. A "pharmacologic dose" or "supraphysiological dose" of a hormone is a medical usage referring to an amount of a hormone far greater than naturally occurs in a healthy body. The effects of pharmacologic doses of hormones may be different from responses to naturally occurring amounts and may be therapeutically useful, though not without potentially adverse side effects. An example is the ability of pharmacologic doses of glucocorticoids to suppress inflammation. Hormone-behavior interactions[edit] This section does not cite any sources. Please help improve this section by adding citations to reliable sources. Unsourced material may be challenged and removed. (May 2014) (Learn how and when to remove this template message) At the neurological level, behavior can be inferred based on: hormone concentrations; hormone-release patterns; the numbers and locations of hormone receptors; and the efficiency of hormone receptors for those involved in gene transcription. Not only do hormones influence behavior, but also behavior and the environment influence hormones. Thus, a feedback loop is formed. For example, behavior can affect hormones, which in turn can affect behavior, which in turn can affect hormones, and so on.[27] Three broad stages of reasoning may be used when determining hormone-behavior interactions: The frequency of occurrence of a hormonally dependent behavior should correspond to that of its hormonal source A hormonally dependent behavior is not expected if the hormonal source (or its types of action) is non-existent The reintroduction of a missing behaviorally dependent hormonal source (or its types of action) is expected to bring back the absent behavior Comparison with neurotransmitters[edit] This section does not cite any sources. Please help improve this section by adding citations to reliable sources. Unsourced material may be challenged and removed. (May 2014) (Learn how and when to remove this template message) There are various clear distinctions between hormones and neurotransmitters:[28][29][25] A hormone can perform functions over a larger spatial and temporal scale than can a neurotransmitter. Hormonal signals can travel virtually anywhere in the circulatory system, whereas neural signals are restricted to pre-existing nerve tracts Assuming the travel distance is equivalent, neural signals can be transmitted much more quickly (in the range of milliseconds) than can hormonal signals (in the range of seconds, minutes, or hours). Neural signals can be sent at speeds up to 100 meters per second.[30] Neural signalling is an all-or-nothing (digital) action, whereas hormonal signalling is an action that can be continuously variable as dependent upon hormone concentration. Neurohormones are a type of hormone that are produced by endocrine cells that receive input from neurons, or neuroendocrine cells.[31] Both classic hormones and neurohormones are secreted by endocrine tissue; however, neurohormones are the result of a combination between endocrine reflexes and neural reflexes, creating a neuroendocrine pathway.[25] While endocrine pathways produce chemical signals in the form of hormones, the neuroendocrine pathway involves the electrical signals of neurons.[25] In this pathway, the result of the electrical signal produced by a neuron is the release of a chemical, which is the neurohormone.[25] Finally, like a classic hormone, the neurohormone is released into the bloodstream to reach its target.[25] Binding proteins[edit] Hormone transport and the involvement of binding proteins is an essential aspect when considering the function of hormones. There are several benefits with the formation of a complex with a binding protein: the effective half-life of the bound hormone is increased; a reservoir of bound hormones is created, which evens the variations in concentration of unbound hormones (bound hormones will replace the unbound hormones when these are eliminated).[32] See also[edit] Autocrine signaling Cytokine Endocrine disruptor Endocrine system Endocrinology Environmental hormones Growth factor Intracrine List of investigational hormonal agents Metabolomics Neuroendocrinology Paracrine signaling Plant hormones, a.k.a. plant growth regulators Semiochemical Sex-hormonal agent Sexual motivation and hormones Xenohormone References[edit] ^ Shuster, Michèle (2014-03-14). Biology for a changing world, with physiology (Second ed.). New York, NY. ISBN 9781464151132. OCLC 884499940. ^ Neave N (2008). Hormones and behaviour: a psychological approach. Cambridge: Cambridge Univ. Press. ISBN 978-0521692014. 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External links[edit] HMRbase: A database of hormones and their receptors Hormones at the US National Library of Medicine Medical Subject Headings (MeSH) v t e Hormones Endocrine glands Hypothalamic- pituitary Hypothalamus GnRH TRH Dopamine CRH GHRH Somatostatin (GHIH) MCH Posterior pituitary Oxytocin Vasopressin Anterior pituitary FSH LH TSH Prolactin POMC CLIP ACTH MSH Endorphins Lipotropin GH Adrenal axis Adrenal cortex Aldosterone Cortisol Cortisone DHEA DHEA-S Androstenedione Adrenal medulla Epinephrine Norepinephrine Thyroid Thyroid hormones T3 T4 Calcitonin Thyroid axis Parathyroid PTH Gonadal axis Testis Testosterone AMH Inhibin Ovary Estradiol Progesterone Activin Inhibin Relaxin GnSAF Placenta hCG HPL Estrogen Progesterone Pancreas Glucagon Insulin Amylin Somatostatin Pancreatic polypeptide Pineal gland Melatonin N,N-Dimethyltryptamine 5-Methoxy-N,N-dimethyltryptamine Other Thymus Thymosins Thymosin α1 Beta thymosins Thymopoietin Thymulin Digestive system Stomach Gastrin Ghrelin Duodenum CCK Incretins GIP GLP-1 Secretin Motilin VIP Ileum Enteroglucagon Peptide YY Liver/other Insulin-like growth factor IGF-1 IGF-2 Adipose tissue Leptin Adiponectin Resistin Skeleton Osteocalcin Kidney Renin EPO Calcitriol Prostaglandin Heart Natriuretic peptide ANP BNP v t e Cell signaling / Signal transduction Signaling pathways GPCR Wnt RTK TGF beta MAPK/ERK Notch JAK-STAT Akt/PKB Fas apoptosis Hippo PI3K/AKT/mTOR pathway Integrin receptors Agents Receptor ligands Hormones Neurotransmitters/Neuropeptides/Neurohormones Cytokines Growth factors Signaling molecules Receptors Cell surface Intracellular Co-receptor Second messenger cAMP-dependent pathway Ca2+ signaling Lipid signaling Assistants: Signal transducing adaptor protein Scaffold protein Transcription factors General Transcription preinitiation complex TFIID TFIIH By distance Juxtacrine Autocrine / Paracrine Endocrine Other concepts Intracrine action Neurocrine signaling Synaptic transmission Chemical synapse Neuroendocrine signaling Exocrine signalling Pheromones Mechanotransduction Phototransduction Ion channel gating Gap junction Authority control GND: 4025864-6 LCCN: sh85061980 NDL: 00563447 Retrieved from "https://en.wikipedia.org/w/index.php?title=Hormone&oldid=992580834" Categories: Hormones Physiology Endocrinology Cell signaling Signal transduction Human female endocrine system Hidden categories: CS1 maint: multiple names: authors list CS1 maint: others Articles with short description Articles with long short description Short description matches Wikidata Articles containing Ancient Greek (to 1453)-language text All articles with specifically marked weasel-worded phrases Articles with specifically marked weasel-worded phrases from July 2019 Articles needing additional references from May 2014 All articles needing additional references Wikipedia articles with GND identifiers Wikipedia articles with LCCN identifiers Wikipedia articles with NDL identifiers Navigation menu Personal tools Not logged in Talk Contributions Create account Log in Namespaces Article Talk Variants Views Read Edit View history More Search Navigation Main page Contents Current events Random article About Wikipedia Contact us Donate Contribute Help Learn to edit Community portal Recent changes Upload file Tools What links here Related changes Upload file Special pages Permanent link Page information Cite this page Wikidata item Print/export Download as PDF Printable version In other projects Wikimedia Commons Languages Afrikaans Alemannisch العربية Aragonés অসমীয়া Asturianu Azərbaycanca বাংলা Bân-lâm-gú Башҡортса Беларуская Беларуская (тарашкевіца)‎ Български Bosanski Català Čeština ChiShona Cymraeg Dansk Deutsch Eesti Ελληνικά Español Esperanto Euskara فارسی Fiji Hindi Français Gaeilge Galego 客家語/Hak-kâ-ngî 한국어 Հայերեն हिन्दी Hrvatski Ido Ilokano Bahasa Indonesia Interlingua Íslenska Italiano עברית Jawa ಕನ್ನಡ Kapampangan ქართული Қазақша Kiswahili Kreyòl ayisyen Kurdî Кыргызча ລາວ Latina Latviešu Lietuvių Lumbaart Magyar Македонски മലയാളം मराठी Bahasa Melayu မြန်မာဘာသာ Nederlands नेपाली नेपाल भाषा 日本語 Nordfriisk Norsk bokmål Norsk nynorsk Occitan Oʻzbekcha/ўзбекча ਪੰਜਾਬੀ پنجابی پښتو Polski Português Română Русиньскый Русский ᱥᱟᱱᱛᱟᱲᱤ Scots Shqip Sicilianu Simple English سنڌي Slovenčina Slovenščina کوردی Српски / srpski Srpskohrvatski / српскохрватски Sunda Suomi Svenska Tagalog தமிழ் ไทย Тоҷикӣ Türkçe Тыва дыл Українська اردو Vèneto Tiếng Việt Winaray 吴语 ייִדיש 粵語 中文 Edit links This page was last edited on 6 December 2020, at 01:05 (UTC). 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