![]() | This ![]() It is of interest to the following WikiProjects: | |||||||||||||||||||||||
|
I feel like this article should be moved to Vasopressin. First of all, it would allow us to quickly get out of the way the issue of arginine vasopressin vs. lysine vasopressin. More importantly, the actions of vasopressin go way beyond water retention, etc.. ADH is a pretty outdated name. AVP has a lot of important neuralpeptide actions, as a social recognition signal in the forebrain. Hard to get into this in the current article structure and with the current title. -- Chinasaur 19:14, 28 Jan 2005 (UTC)
Just a note from a google searcher... Both articles (ADH and Vasopressin) are practically the same, and neither mentions VP's effect on urea reabsorption, which is a fairly important effect.
I was recently taught that ADH is the better name, and that vasopressin is outdated - higher quantities are needed for ADH to act as vasopressin, and its primary function is as an anti-diuretic hormone - ie, it stops diuresis. Also, there is still no mention of urea in the article - I don't feel qualified to put this in, but it does seem like rather a large omission. 131.111.8.104 11:19, 16 May 2007 (UTC)
There is an error in the second infobox, but I haven't a clue how to fix those prot box things. Fuzzform 20:08, 11 February 2006 (UTC)
Some references to all the various effects of vasopressin would be nice...
Should "parvocellular" be linked to parvocellular part or is this a different use of the term? AxelBoldt 15:27, 6 April 2006 (UTC)
DDAVP induced VWF release goes through the vasopressin-2 receptor. This is a cAMP-mediated process.
Prayingmantis78
18:58, 4 June 2007 (UTC)
I would like to see the vasopressin dosages typically used in asystolic arrest posted. 75.19.187.142 18:40, 1 April 2007 (UTC)Yaek
Caffeine is certainly a diuretic and natriuretic, but I can't find any original research article saying caffeine decreases vasopressin release. I found one saying it may be having its effect via adenosine receptors. Timo Rieg, Hannah Steigele, Jurgen Schnermann, Kerstin Richter, Hartmut Osswald, and Volker Vallon. Requirement of intact adenosine A1 receptors for the diuretic and natriuretic action of the methylxanthines theophylline and caffeine. J Pharmacol Exp Ther. 2005 Apr;313(1):403-9. Epub 2004 Dec 8. Misskidney 19:49, 16 April 2007 (UTC)
The name vasopressin is indeed outdated, all newer textbooks I've seen use ADH. Vasoconstriction is only a tertiary fuction of this hormone expressed in the extreme case of hemorrage. Its main function is homeostasis as antidiuretic hormone therefore ADH is definitely a more appropriate name. EerieNight 11:02, 25 August 2007 (UTC)
I concur that arginine vasopressin (AVP) is the more appropriate name to use. And just the opposite, the use of ADH is antiquated. A simple pubmed search will reveal that the vast majority of research articles refer to this hormone as arginine vasopressin (AVP). In addition, the gene name is arginine vasopressin (NM_000490.4) and the names of the receptor are arginine vasopressin receptors, i.e., AVPR1a, AVPR1b, and AVPR2. — Preceding unsigned comment added by 71.185.67.31 ( talk) 21:54, 25 November 2013 (UTC)
This article was automatically assessed because at least one WikiProject had rated the article as start, and the rating on other projects was brought up to start class. BetacommandBot 16:32, 10 November 2007 (UTC)
Anyone know why this is? 72.161.203.107 ( talk) 02:15, 19 November 2007 (UTC)
Apparently vasopressin is linked with agressive behaviour in males and anti-agressive behaviour in females http://www.standaard.be/cnt/dmf20180706_03601976 — Preceding unsigned comment added by Patrick3004 ( talk • contribs) 10:20, 7 July 2018 (UTC)
Under the Kidney Action section. I think the discussion of the G protein-coupled receptor, and cAMP second messenger systems are inappropriate. A description of the V2 receptor as a G protein-coupled receptor acting by a cAMP second messenger system would be a sufficient description. For the interim I have left the section unchanged except for a link to the appropriate article. —Preceding unsigned comment added by Backwardtoes ( talk • contribs) 10:14, 15 December 2007 (UTC)
The section describing the interaction of vasopressin and behavior is, like too much scientific and medical writing, a maddening exercise in circumlocution. For Pete's sake, state what the hormone does or doesn't do and let the article be revised by someone else in the future rather than write an article for the ages so open-ended that it ought not to have been written at all because it says absolutely NOTHING.
The description of G protein signaling by G alpha s within the "Kidney" chapter is a crap.
G protein alpha subunit does exchange GDP by GTP for activation and not - as described here - vice versa.
The cyclisation of ATP to cAMP does not provide 2 anorganic phosphates. Indeed, one molecule of pyrophosphate is produced.
cAMP may regulate the gene repressor of PKA. However, this cellular response would be far to slow. For fast response reactions the interaction of cAMP to regulatory subunits of PKA is important, resulating in the release of PKAs catalytic subunits. —Preceding unsigned comment added by 85.179.128.249 ( talk) 15:25, 10 March 2008 (UTC)
To explain a small (but important) edit I made...
Previously, the article stated that ADH retains water, but not salt. This is not entirely true.
ADH's primary function is indeed to increase water permeability in the collecting system. However, ADH also stimulates Na/K/Cl cotransport (in the thick asc. limb of loop of Henle), and stimulates apical Na channels in collecting tubules. Source: Boron & Boulpaep, Medical Physiology, Updated Ed., p. 787.
I have changed the page (removing the words "but not salt").
Enclosed please find a helpful reference for sodium reabsorption by - acute - admionitration of AVP, with serveral further referecnes, which one might use as citation within the article. Chronic administartion of AVP has not been studies so far. AVP has an intrinsic activity on the amiloride-sensitive sodium channel ENaC of the collecting duct of the kidney, and the epithelium of the colon (Bücker 2018), with increased reabsortion of Na. however Na absortion might require highter concentrations of AVP than water reabsorption.
Am Soc Nephrol
• • • . 2005 Jul;16(7):1920-8.
doi: 10.1681/ASN.2004121079. Epub 2005 May 11.
Vasopressin-V2 receptor stimulation reduces sodium excretion in healthy humans Lise Bankir 1, Sandrine Fernandes, Pascale Bardoux, Nadine Bouby, Daniel G Bichet Affiliations expand • PMID: 15888562
• DOI: 10.1681/ASN.2004121079Mucosal Immunol . 2018 Mar;11(2):474-485. doi: 10.1038/mi.2017.66. Epub 2017 Aug 2. Campylobacter jejuni impairs sodium transport and epithelial barrier function via cytokine release in human colon R Bücker 1, S M Krug 1, V Moos 2, C Bojarski 2, M R Schweiger 3, M Kerick 3, A Fromm 1, S Janßen 2, M Fromm 1, N A Hering 4, B Siegmund 2, T Schneider 2, C Barmeyer 2, J D Schulzke 1 Affiliations expand PMID: 28766554 DOI: 10.1038/mi.2017.66 Robertley1 ( talk) 10:44, 24 August 2020 (UTC)
--
-bob (
talk)
18:26, 21 March 2008 (UTC)
I have also added the word "main" in the paragraph describing vasopressin's effects in the kidney to clarify that it does play other roles (ie. increase of Na-K-Cl2 channels in the TAL)
-- User:Soroboto ( talk) 18:13, 18 October 2013 (UTC)
Do Camels have any sort of increased retention of ADH and that is how they save so much water? 76.14.97.253 ( talk) 17:47, 4 April 2008 (UTC)
Vassopressin has been shown to be ineffective in septic shock when added to Norepinephirine , no mortality benefit at 28 days and at 90 days. —Preceding unsigned comment added by Alshamsi2000 ( talk • contribs) 02:58, 14 July 2008 (UTC)
This article never actually mentions which preprohormone or whatever you call it vasopressin comes from. It comes from preprooxyphysin, as does Neurophysin I apparently. Same problem with the oxytocin article. —Preceding unsigned comment added by Pelirojopajaro ( talk • contribs) 13:52, 9 March 2009 (UTC)
The result of the move request was no consensus for move. Arbitrarily0 ( talk) 22:52, 24 November 2009 (UTC)
Vasopressin → arginine vasopressin — As the preceding explanation by AlbertHall indicates, the official name is arginine vasopressin. I suggest renaming this article as arginine vasopressin and redirecting vasopressin here -- Chibibrain ( talk) 04:15, 16 November 2009 (UTC)
In light of the naming convention, I now believe it is better to leave the article name unchanged. Perhaps it is best to just provide a statement near the beginning that there are homologous peptides for other species. In any case, this name change proposal should be rejected due to a lack of consensus.-- Chibibrain ( talk) 11:11, 17 November 2009 (UTC)
I realize such assertions seem unwelcome sometimes, but I wish to call attention to a specific lack of rigor with regard to (1) the use of the term peripheral resistance, and (2) the belief that the mammalian arterial pressure is regulated via any mechanism involving the direct control of generalized peripheral resistance. This latter concept reached its heyday forty years ago when Frank Netter illustrated ads for Ciba-Geigy's Apresoline. The simple fact is that the net venous return is a real measurable phenomenon, and peripheral resistance is an artificial concept defined by a word experiment. The net venous return at the heart is the sum of all the local blood flows. Each local blood flow is determined by local arteriolar diameters, which in turn relate to specific local mechanisms — from oxygen tension in many cells to carbon dioxide in others. Also, when autonomic neurohormonal factors override local mechanisms, the various results can include death from shock. Remember, we are talking about Homeostasis, not the Ischemic Reflex. Local arterioles MUST respond to changes in BP in order to provide the correct local flow. Not the other way around. Every physiologist knows this. Since Harvey.
Most engineers would understand how these circulatory systems are easily described as elastic reservoir trees interconnected with programmable peripheral current sources, and a variable transconductance amplifier heart. However, a simple experiment can show it far more easily. My father did this at Emory University School of Medicine in 1945. Some number of subjects are tested on a ballistocardiogram (which estimates cardiac output). Their pressures are measured before and after by cuff. Between measurements, you release a previously attached tourniquet from one or both legs, and the blood rushes in due to reactive hyperemia. This shows a 2X to 5X increase in total blood flow. Yet blood pressures are still well regulated here, showing both small increases and decreases, presumably related to discomfort or fear in the procedure.
Based on my studies at my father knee, and extensive simulations in the Pennsylvania State University Hybrid Computer Lab and the Penn State mainframe (1976), the sensitivities of the mammalian circulation to small changes in "Total Blood Flow" (a proxy for "PR") would never keep pace with the big blood flow changes that are otherwise normal among organs doing their normal jobs. Simulations suggest that short term regulation seems reasonably likely by modifying the heart function (increased contractility and hear rate) and long term arterial blood pressure control is synonomous with body fluid level control, especially the total blood volume. Other mechanisms (rather than direct control of PR) seem likely as well. Arthur Guyton tried to bring this out, but he lacked credibility as a theorist later in his career. Vasodilators, obviously, can have a big impact on blood volume if they act on the kidneys. In this way, I would expect them to work, but _not_ because they overperfuse tissues or cause a cardiac output that would kill you.
Therefore, I hereby dispute the statement "It also increases peripheral vascular resistance, which in turn increases arterial blood pressure." I challenge anyone to produce scientific evidence to support it. It is _not_ common knowledge; it is a common misconception. If you remove that ONE sentence, the remaining paragraph actually describes well enough (for me) how Vasopressin controls [arterial] blood pressure by helping to manage water, salt, and kidney functions.
Please remove that ONE sentence. It is a small (even if some might feel outrageous) request on behalf of scientific rigor and the facts. Having stated a bias here, I should not do it myself. Should I?
-- JimRodgers ( talk) 03:24, 13 February 2011 (UTC)
I think that the Vasopressin receptor antagonist page should be merged with the full article on AVP. As it stands, the AVP page already includes a section on AVP pharmacology, and the receptor antagonist page is basically a stub article with links to more detailed descriptions of the relevant drugs. If we can reach some kind of consensus, I'd like to carry out the merge in one week's time. Techfiend ( talk) 06:10, 2 May 2011 (UTC)
For some strange reason, when an IP user sees the 3 options at the top right (next to the search bar) they have to click "View Sources" to edit, because there is no "edit" button. I have confirmed this and took a screenshot: [2] 67.77.174.6 ( talk) 07:59, 31 August 2011 (UTC)
The name VACM-1, for Vasopressin-Activated Calcium Mobilizing receptor, comes from its first discovery as a protein with a vasopressin-response activity. But it has been revealed as Cullin 5, a scaffold protein for ubiquitin ligase E3. That is not a receptor, even though it may well be a protein necessary for vasopressin response in endothelial cells. It should be removed from the vasopressin receptors table. — Preceding unsigned comment added by Takiar ( talk • contribs) 22:22, 9 January 2014 (UTC)
I have tagged as 'dubious' the first para of 'Central nervous system' because it makes a significant assertion that is not supported by any citations - and then tries to hide by saying that it is 'controversial'. This smells of original research?. Whoever put it in needs to fix it or I will delete it by end May. -- 88.97.11.54 ( talk) 12:34, 14 May 2014 (UTC)
The subsections numbered 4.2.1 "Vasopressin vs. epinephrine" and 4.2.2 "Vasopressin and epinephrine vs. epinephrine alone", including Table 1 and Table 2, are much too technical and esoteric. They show raw data from clinical trials with various clinical endpoints. It looks like something that was meant for a review article in "Critical Care Medicine". Additionally, the general message is inconclusive on vasopressin's role in this situation. I think the entire paragraphs should be deleted or perhaps summarized in one or two sentences. mattelfesso ( talk) 08:11, 3 December 2014 (UTC)
The content and referencing of this article is notable and admirable. I will be editing for brevity and to simply the contents for readers that may not have the vocabulary of those who contributed to this article. If I have edited incorrectly or have removed some vital piece of information that inadvertently changes the meaning of the content, please revert such edits and let me know so that I don't do it again.
Howdy,
I'm a bit concerned that this page has a lot of copyvio material. A large fraction of the text reads identically to http://reliawire.com/vasopressin/ - this may be them copying wikipedia, but they attribute "Anderson DA (2012) Dorland’s Illustrated Medical Dictionary (32nd ed.) Elsevier. ISBN 978-1-4160-6257-8"
Can someone with access to Dorland's help determine the direction of the copying?
Second, in the section relating to Kidney effects, quite a bit of the wording is identical to several pages in Hayes' Principles and Methods of Toxicology.
Google books link: https://books.google.com/books?id=FChZBAAAQBAJ&lpg=PA1762&ots=ZUWJ3GUYS2&pg=PA1762#v=onepage&f=false
Citation of work: Title Hayes' Principles and Methods of Toxicology, Sixth Edition Editors A. Wallace Hayes, Claire L. Kruger:: Edition 6, illustrated, revised Publisher CRC Press, 2014 ISBN 1842145363, 9781842145364 Page 1762
Example sentence which is nearly identical: "Vasopressin also increases the concentration of calcium in the collecting duct cells, by episodic release from intracellular stores"
I wanted to document a couple of the sources, and solicit feedback about how to proceed - it seems a shame to delete much of the page for copyvio, but I don't have access to the original sources, and do not have the time on hand to rewrite. talk ( talk) 00:20, 14 June 2017 (UTC)
I have spotted a problem with the Receptors section: all references in the section, references 21 - 26 are original research, most are animal studies. I'm not enough of an expert to do this, but IMO this section needs to be converted into a narrative text, with appropriate references from review articles and/or text books. Are all the receptors equally important? IiKkEe ( talk) 17:46, 13 September 2017 (UTC)
The role and precise mecanism of vasopressin in aggression and hypothalamic-related dysfunctions should be clarified. See: https://jamanetwork.com/journals/jamapsychiatry/fullarticle/204124 Tkadm30 ( talk) 12:55, 3 March 2018 (UTC)
Added this section previously. Updated citations today. A previously inserted image, based on published research, was removed, stating "we don't need figures from research papers". I strongly disagree, the image helps the reader to understand how vasopressin and blood pressure change in parallel during surgery. Please note: self-citation. Link: https://commons.wikimedia.org/wiki/File:Blood_pressure_and_Vasopressin_at_removal_of_ovaries,_Z-scores.jpg Odd Höglund (SLU) ( talk) 13:28, 3 February 2019 (UTC)
Please kindly check the references for circuitries between AVP and temperature control, and fit it into the article, if appreciated.
The temperature centre at the median preoptic nucleus of the anterior hypothalamus (MnPO) is in overlapping, i.e. close proximity of he osmocentre of he OVLT and der circumventricular organs of 3. Ventricle (Romanowsky 2003, Nakamura2011) , both areas have interleukin-6 receptors (Swart 2011), are stimulated by non-osmotic stimuli, i.e. IL-6, In other words: fever due to IL-6 released from monocytes, PMN, or further to that from central cells inside oft he blood-brain-barrier, such pituicytes will release AVP thru activation of osmocentre from the pituitary, causing hyponatremia due to water reabsorption at the kidney,i.e. dilutuion of plasma, similar to SIADH (Mastorakos 1994), which is different from salt wasting. Acute – not chronic - fever as a course of AVP release is now a well now fact in clinical settings, such as bacterial tuberculosis, or viral SARS, Dengue etc.
INFLAMMATION, CYTOKINES, AND TEMPERATURE REGULATION
The organum vasculosum laminae terminalis in immune-to-brain febrigenic signaling: a reappraisal of lesion experiments
Andrej A. Romanovsky
,
Naotoshi Sugimoto
,
Christopher T. Simons
, and
William S. Hunter
01 AUG 2003https://doi.org/10.1152/ajpregu.00757.2002
EXPERIMENTAL BIOLOGY 2010 | New Investigator Award of the Neural Control and Autonomic Regulation (NCAR) Section, 2010New Investigator Award of the Neural Control and Autonomic Regulation (NCAR) Section, 2010
Central circuitries for body temperature regulation and fever
Kazuhiro Nakamura
01 NOV 2011https://doi.org/10.1152/ajpregu.00109.2011
Nephron Physiol • • • . 2011;118(2):45-51.
doi: 10.1159/000322238. Epub 2010 Dec 22.
Hyponatremia and inflammation: the emerging role of interleukin-6 in osmoregulation Reinout M Swart 1, Ewout J Hoorn, Michiel G Betjes, Robert Zietse Affiliations expand • PMID: 21196778
• DOI: 10.1159/000322238
J Clin Endocrinol Metab • • • . 1994 Oct;79(4):934-9.
doi: 10.1210/jcem.79.4.7962300.
Hypothalamic-pituitary-adrenal axis activation and stimulation of systemic vasopressin secretion by recombinant interleukin-6 in humans: potential implications for the syndrome of inappropriate vasopressin secretion G Mastorakos 1, J S Weber, M A Magiakou, H Gunn, G P Chrousos Affiliations expand • PMID: 7962300
• DOI: 10.1210/jcem.79.4.7962300 Robertley1 ( talk) 10:22, 24 August 2020 (UTC)
please correct the article, the diuretic statement is wrong
The statement within the article on diuresis is wrong.
Carbamezepin, chlorpropamide are anitidiurectic, releasing ADH from pitiuitary
Acta Endocrinol (Copenh)
• . 1981 Feb;96(2):145-53.
doi: 10.1530/acta.0.0960145.
Essential hypernatraemia, antidiuretic hormone and neurophysin secretion: response to chlorpropamide T W AvRuskin, S C Tang, C Juan • PMID: 7468100
• DOI: 10.1530/acta.0.0960145
Case Reports
Tohoku J Exp Med • • • . 1979 Feb;127(2):101-11.
doi: 10.1620/tjem.127.101.
Hypothalamic hypernatremia due to volume--dependent ADH release, and its treatment with carbamazepine and clofibrate T Kimura, K Matsui, K Ota, K Yoshinaga • PMID: 760257
• DOI: 10.1620/tjem.127.101 Robertley1 ( talk) 11:55, 24 August 2020 (UTC)
They contain 10 amino acids and not only 9, as written several times in the text. 141.63.224.168 ( talk) 15:53, 16 August 2023 (UTC)