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{{protein
{{subpages}}
| Name = arginine vasopressin (antidiuretic hormone)
 
| caption = [[Space-filling model]] of arginine vasopressin
{{Protein
| image = Arginine vasopressin3d.png
| Name = Arginine vasopressin (antidiuretic hormone) -human
| caption =  
| image =  
| width = 200
| width = 200
| HGNCid = 894
| HGNCid = 894
Line 18: Line 20:
| LocusSupplementaryData =  
| LocusSupplementaryData =  
}}
}}
{{Protein
 
  |Name=Arginine vasopressin receptor 1A
'''Arginine vasopressin''' ('''AVP'''), also known as '''vasopressin''', '''antidiuretic hormone''' ('''ADH''') or '''argipressin''', is a mammalian [[hormone]] that is mainly released when the body is low on [[water]]; it causes the [[kidney]]s to conserve water by concentrating the [[urine]] and reducing urine volume. It also causes vasoconstriction.<ref>{{MeSH|Vasopressins}}</ref>
  |Symbol=AVPR1A
  |AltSymbols=AVPR1
  |HGNCid=895
  |Chromosome=12
  |Arm=q
  |Band=14-15
  |LocusSupplementaryData=
  |ECnumber=
  |OMIM=600821
  |EntrezGene=552
  |RefSeq=NM_000706
  |UniProt=P37288
}}
{{Protein
  |Name=Arginine vasopressin receptor 1B
  |Symbol=AVPR1B
  |AltSymbols=
  |HGNCid=896
  |Chromosome=1
  |Arm=q
  |Band=32
  |LocusSupplementaryData=
  |ECnumber=
  |OMIM=600264
  |EntrezGene=553
  |RefSeq=NM_000707
  |UniProt=P47901
}}
{{Protein
  |Name=Arginine vasopressin receptor 2
  |Symbol=AVPR2
  |AltSymbols=
  |HGNCid=897
  |Chromosome=X
  |Arm=q
  |Band=28
  |LocusSupplementaryData=
  |ECnumber=
  |OMIM=304800
  |EntrezGene=554
  |RefSeq=NM_000054
  |UniProt=P30518
}}
'''Arginine vasopressin''' ('''AVP'''), also known as '''antidiuretic hormone''' ('''ADH''') or '''argipressin''', is a human [[hormone]] that is mainly released when the body is low on [[water]]; it causes the [[kidney]]s to conserve water by concentrating the [[urine]] and reducing urine volume. It also has various functions in the [[brain]] and [[blood vessel]]s.


A very similar substance, '''lysine vasopressin''' ('''LVP''') or '''lypressin''', has the same function in [[pig]]s and is often used in human therapy.
A very similar substance, '''lysine vasopressin''' ('''LVP''') or '''lypressin''', has the same function in [[pig]]s and is often used in human therapy.


These '''vasopressins''' are [[peptide hormone]]s produced in the [[hypothalamus]]. Most of the processed peptide is stored in the [[posterior pituitary|posterior part]] of the [[pituitary gland]] to be released into the blood stream; some of it is also released directly into the brain.
Vasopressin is a [[peptide hormone]] liberated from a preprohormone precursor, the bulk of which is synthesized by the magnocellular neurons of the [[paraventricular nucleus|paraventricular]] and [[supraoptic nucleus|supraoptic]] nuclei of the [[hypothalamus]], and transported to the [[posterior pituitary|posterior part]] of the [[pituitary gland]] from where it is secreted into the blood stream. Some of it is also released directly into the brain from the dendrites of the magnocellular neurons as well as from other brain neurons (see below).


==Physiology==
==Physiology==
===Control===  
===Control===  
AVP is secreted from the posterior pituitary gland in response to reductions in [[blood plasma|plasma]] volume and in response to increases in the plasma [[osmolality]]. Secretion in response to reduced plasma volume is activated by [[baroreceptor|pressure receptors]] in the [[vein]]s, [[atrium (anatomy)|atria]], and [[carotid]]s. Secretion in response to increases in plasma osmotic pressure is mediated by [[osmoreceptor]]s in the [[hypothalamus]]. The neurons that make AVP, in the [[supraoptic nucleus]] and [[paraventricular nucleus]], are themselves osmoreceptors, but they also receive synaptic input from other osmoreceptors located in regions adjacent to the anterior wall of the third ventricle. These regions include the [[organum vasculosum of the lamina terminalis]] and the [[subfornical organ]].
Vasopressin is secreted from the posterior pituitary gland in response to reductions in [[blood plasma|plasma]] volume and in response to increases in the plasma [[osmolality]]:
 
* Secretion ''in response to reduced plasma volume'' is activated by [[baroreceptor|pressure receptors]] in the [[vein]]s, [[atrium (anatomy)|atria]], and [[carotid]]s.  
* Secretion ''in response to increases in plasma osmotic pressure'' is mediated by [[osmoreceptor]]s in the [[hypothalamus]].  
 
The neurons that make vasopressin, in the [[supraoptic nucleus]] and [[paraventricular nucleus]], are themselves osmoreceptors, but they also receive synaptic input from other osmoreceptors located in regions adjacent to the anterior wall of the third ventricle. These regions include the [[organum vasculosum of the lamina terminalis]] and the [[subfornical organ]].


Many factors influence the secretion of AVP; for instance, [[ethanol]] and [[caffeine]] reduce AVP secretion. The resulting decrease in water reabsorption by the kidneys leads to a higher [[urine]] output.  [[Angiotensin]] II stimulates the secretion of AVP.<ref>Vander, A.J., Renal Physiology, McGraw-Hill, 1991.</ref>
Many factors influence the secretion of vasopressin:
* [[Ethanol]] and [[caffeine]] ''reduce'' vasopressin secretion. The resulting decrease in water reabsorption by the kidneys leads to a higher [[urine]] output.  [[Coffee]] is an example of a food product that suppresses the body's release of antidiuretic hormones, due to its level of caffeine. This intake of caffeine causes the body to lose more water and may lead to [[dehydration]] if consumed excessively.
* [[Angiotensin]] II ''stimulates'' the secretion of vasopressin.<ref>Vander AJ ''Renal Physiology'' McGraw-Hill, 1991</ref>


The AVP that is measured in peripheral blood is almost all derived from secretion from the posterior pituitary gland (except in cases of AVP-secreting tumours). However there are two other sources of AVP with important local effects:  
===Sources===
*AVP is secreted from parvocellular neurons of the [[paraventricular nucleus]] at the median eminence into the [[short portal vessels]] of the pituitary stalk. These vessels carry the peptide directly to the [[anterior pituitary]] gland, where it is an important releasing factor for [[ACTH]], acting in conjunction with [[Corticotropin-releasing hormone|CRH]].
The vasopressin that is measured in peripheral blood is almost all derived from secretion from the posterior pituitary gland (except in cases of vasopressin-secreting tumours). However there are two other sources of vasopressin with important local effects:  
* AVP is also released into the brain by several different populatons of neurons (see below).
*Vasopressin is secreted from parvocellular neurons of the [[paraventricular nucleus]] at the median eminence into the [[short portal vessels]] of the pituitary stalk. These vessels carry the peptide to the [[anterior pituitary]] gland, where it is an important releasing factor for [[ACTH]], acting in conjunction with [[Corticotropin-releasing hormone|CRH]].
* Vasopressin is also released into the brain by several different populations of neurons (see below).


===Peripheral actions===  
===Central actions===  
AVP acts on three different [[receptor (biochemistry)|receptor]]s, termed [[Arginine vasopressin receptor 1A|AVPR1a]], [[Arginine vasopressin receptor 1B|AVPR1b]] and [[Arginine vasopressin receptor 2|V2]]. The receptors are differently expressed in different tissues, and exert different actions:
* AVPR1a - [[vasoconstriction]], [[gluconeogenesis]] in the liver, [[platelet]] aggregation and release of [[factor VIII]] and [[von Willebrand factor]].
* AVPR1b - [[corticotropin]] secretion from the [[pituitary gland]].
* AVPR2 - control of free water reabsorption in the [[collecting duct]]s of the kidneys (especially the cortical and outer medullary collecting ducts). Activation of [[adenylate cyclase]] causes increase in [[cAMP]] which leads to the insertion of [[aquaporin]]-2 (AQP2) channels (water channels) into the apical membrane of the cells lining the collecting duct. This allows water to be reabsorbed down an osmotic gradient, and so the urine is more concentrated.


===Actions within the brain===
Vasopressin released within the brain has many actions:
Vasopressin released within the brain has many actions:
* It has been implicated in [[memory]] formation, including delayed reflexes, image, short- and long-term memory, though the mechanism remains unknown, and these findings are controversial.  However, the synthetic [[vasopressin analogue]] [[desmopressin]] has come to interest as a likely [[nootropic]].
* It has been implicated in [[memory]] formation, including delayed reflexes, image, short- and long-term memory, though the mechanism remains unknown, and these findings are controversial.  However, the synthetic [[vasopressin analogue]] [[desmopressin]] has come to interest as a likely [[nootropic]].


* AVP is released into the brain in a [[circadian rhythm]] by neurons of the [[Suprachiasmatic nucleus|suprachiasmatic nucleus of the hypothalamus]].  
* Vasopressin is released into the brain in a [[circadian rhythm]] by neurons of the [[Suprachiasmatic nucleus|suprachiasmatic nucleus of the hypothalamus]].  


* AVP released from centrally-projecting hypothalamic neurons is involved in aggression, blood pressure regulation and temperature regulation.
* Vasopressin released from centrally-projecting hypothalamic neurons is involved in aggression, blood pressure regulation and temperature regulation.


In recent years there has been particular interest in the role of AVP in social behavior. It is thought that AVP, released into the brain during sexual activity, initiates and sustains patterns of activity that support the pair-bond between the sexual partners; in particular, AVP seems to induce the male to become aggressive towards other males.
In recent years there has been particular interest in the role of vasopressin in social behavior. It is thought that vasopressin, released into the brain during sexual activity, initiates and sustains patterns of activity that support the pair-bond between the sexual partners; in particular, vasopressin seems to induce the male to become aggressive towards other males.
   
   
Evidence for this comes from experimental studies, in several species, which indicate that the precise distribution of AVP and AVP receptors in the brain is associated with species-typical patterns of social behavior. In particular, there are consistent differences between monogamous species and promiscuous species in the distribution of AVP receptors, and sometimes in the distribution of AVP-containing axons, even when closely-related species are compared. Moreover, studies involving either injecting AVP agonists into the brain, or blocking the actions of AVP, support the hypothesis that AVP is involved in aggression towards other males. There is also evidence that differences in the AVP receptor gene between individual members of a species might be predictive of differences in social behavior.
In several species, that the distribution of vasopressin and vasopressin receptors in the brain is associated with species-typical patterns of social behavior. In particular, there are differences between monogamous species and promiscuous species in the distribution of vasopressin receptors, and sometimes in the distribution of vasopressin-containing axons, even when closely-related species are compared. Moreover, studies involving either injecting vasopressin agonists into the brain, or blocking the actions of vasopressin, support the hypothesis that vasopressin is involved in aggression towards other males. There is also evidence that differences in the vasopressin receptor gene between individual members of a species might be predictive of differences in social behavior.
 
===Summary Table===
{{main|vasopressin receptor}}
This table summarizes some of the actions of AVP at its three [[cell surface receptor]]s which are differently expressed in different tissues and exerting different actions.
 
{| class="wikitable"
|+ Summary of vasopressin receptors
! Type!! [[Second messenger system]]!! Locations!! Actions
|-
| [[Arginine vasopressin receptor 1A|AVPR1A]] || [[phosphatidylinositol]]/[[calcium]] || [[liver]], [[kidney]], peripheral vasculature, [[brain]] ||  [[vasoconstriction]], [[gluconeogenesis]], [[platelet]] aggregation, and release of [[factor VIII]] and [[von Willebrand factor]]; social recognition<ref>Bielsky IF ''et al.'' (2004) Profound impairment in social recognition and reduction in anxiety-like behavior in vasopressin V1a receptor knockout mice ''Neuropsychopharmacology'' 29:483-93 PMID 14647484</ref>, circadian tau<ref>Wersinger SR ''et al.'' (2007) Vasopressin 1a receptor knockout mice have a subtle olfactory deficit but normal aggression ''Genes Brain Behav''PMID 17083331</ref>
|-
| [[Arginine vasopressin receptor 1B|AVPR1B]] || [[phosphatidylinositol]]/[[calcium]] || [[pituitary gland]], [[brain]] || [[adrenocorticotropic hormone]] secretion in response to stress<ref>Lolait SJ ''et al.'' (2007) The hypothalamic-pituitary-adrenal axis response to stress in mice lacking functional vasopressin V1b receptors ''Endocrinology'' 148:849-56 PMID 17122081</ref>; social interpretation to olfactory cues<ref>Wersinger SR''et al.'' (2004) Social motivation is reduced in vasopressin 1b receptor null mice despite normal performance in an olfactory discrimination task ''Horm Behav'' 46:638-45 PMID 15555506</ref>
|-
| [[Arginine vasopressin receptor 2|AVPR2]] || [[adenylate cyclase]]/[[cAMP]] || apical membrane of the cells lining the [[collecting duct]]s of the kidneys (especially the cortical and outer medullary collecting ducts) || insertion of [[aquaporin-2]] (AQP2) channels (water channels). This allows water to be reabsorbed down an osmotic gradient, and so the urine is more concentrated.
|}


==Structure and relation to oxytocin==
==Structure and relation to oxytocin==
Line 155: Line 131:
==Pharmacology==
==Pharmacology==
===Vasopressin analogues===
===Vasopressin analogues===
AVP agonists are used therapeutically in various conditions, and its long-acting synthetic analogue [[desmopressin]] is used in conditions featuring low AVP secretion, as well as for control of bleeding (in some forms of [[von Willebrand disease]]) and in extreme cases of bedwetting by children. [[Terlipressin]] and related analogues are used as [[vasocontrictor]]s in certain conditions. Use of AVP analogues for [[esophageal varices]] commenced in 1970.<ref>Baum S, Nusbaum M, Tumen HJ. The control of gastrointestinal hemorrhage by selective mesenteric infusion of pitressin. ''Gastroenterology'' 1970;58:926.<!--PMID not found--></ref>
Vasopressin agonists are used therapeutically in various conditions, and its long-acting synthetic analogue [[desmopressin]] is used in conditions featuring low vasopressin secretion, as well as for control of bleeding (in some forms of [[von Willebrand disease]]) and in extreme cases of bedwetting by children.


AVP infusion has been used as a second line of management in [[septic shock]] patients not responding to high dose of inotropes (e.g., [[dopamine]] or [[epinephrine]]). It had been shown to be more effective than epinephrine in [[asystole|asystolic]] [[cardiac arrest]]. <ref>Wenzel V, Krismer AC, Arntz HR, Sitter H, Stadlbauer KH, Lindner KH; European Resuscitation Council Vasopressor during Cardiopulmonary Resuscitation Study Group. A comparison of AVP and epinephrine for out-of-hospital cardiopulmonary resuscitation. ''N Engl J Med'' 2004;350:105-13.
[[Hepatorenal syndrome]] maybe be treated with [[terlipressin]] and related analogues which are splanchnic [[vasocontrictor]]s .<ref>Sanyal AJ ''et al.'' (2008) A randomized, prospective, double-blind, placebo-controlled trial of terlipressin for type 1 hepatorenal syndrome ''Gastroenterology'' 134:1360-8 PMID 18471513</ref><ref>Martín-Llahí M ''et al.'' (2008) Terlipressin and albumin vs albumin in patients with cirrhosis and hepatorenal syndrome: a randomized study ''Gastroenterology'' 134:1352-9 PMID 18471512</ref>
PMID 14711909.</ref> While not all studies are in agreement, a 2006 study of out-of hospital cardiac arrests has added to the evidence for the superiority of AVP in this situation. <ref>Grmec S, Mally S. Vasopressin improves outcome in out-of-hospital cardiopulmonary resuscitation of ventricular fibrillation and pulseless ventricular tachycardia: a observational cohort study. Crit Care. 2006 Feb;10(1):R13. PMID 16420660.</ref>


===Vasopressin receptor inhibition===
[[Esophageal varices]] may be treated with vasopressin analogues.<ref>Baum S ''et al.''  (1970) The control of gastrointestinal hemorrhage by selective mesenteric infusion of pitressin ''Gastroenterology'' 58:926</ref>
[[Demeclocycline]], a tetracycline antibiotic, is sometimes used to block the action of AVP in the kidney in hyponatremia due to inappropriately high secretion of AVP (SIADH, see above), when fluid restriction has failed. A [[as of 2004|new]] class of medication ([[conivaptan]], [[tolvaptan]], [[relcovaptan]], [[lixivaptan]]) acts by inhibiting the action of AVP on its [[receptor (biochemistry)|receptor]]s (V1 and V2), with tolvaptan acting on V1a and V2 and the remainder mainly on V1a receptors. The same class of drugs is also being studied in [[congestive heart failure]].


==References==
In [[septic shock]], vasopressin infusion has been used as a second line of management in patients not responding to high dose of inotropes (e.g., [[dopamine]] or [[epinephrine]]).
<div class="references-small"><references /></div>


:*Brenner & Rector's The Kidney, 7th ed., Saunders, 2004. [http://home.mdconsult.com/das/search/openres/56203699-5?searchId=460046813 Full Text with MDConsult subscription]
In [[asystole|asystolic]] [[cardiac arrest]], vasopressin may be more effective than epinephrine according to a randomized controlled trial<ref>Wenzel V ''et al.'' (2004) European Resuscitation Council Vasopressor during Cardiopulmonary Resuscitation Study Group. A comparison of AVP and epinephrine for out-of-hospital cardiopulmonary resuscitation ''N Engl J Med'' 350:105-13 PMID 14711909.</ref> and a [[cohort study]]. <ref>Grmec S, Mally S (2006) Vasopressin improves outcome in out-of-hospital cardiopulmonary resuscitation of ventricular fibrillation and pulseless ventricular tachycardia: an observational cohort study ''Crit Care'' 10:R13 PMID 16420660</ref> Vasopressin may be combined with a [[corticosteroid]].<ref>{{Cite journal
| doi = 10.1001/archinternmed.2008.509
| volume = 169
| pages = 15-24
| last = Mentzelopoulos
| first = SD
| coauthors = ''et al.'' | title = Vasopressin, Epinephrine, and Corticosteroids for In-Hospital Cardiac Arrest
| journal = Arch Intern Med
| accessdate = 2009-01-13
| date = 2009-01-12
}}</ref>


:*Caldwell, H.K. and Young, W.S., III. Oxytocin and Vasopressin: Genetics and Behavioral Implications in Lim, R. (ed.) Handbook of Neurochemistry and Molecular Neurobiology, 3rd edition, Springer, New York, pp. 573-607, 2006. [http://refworks.springer.com/mrw/fileadmin/pdf/Neurochemistry/0387303480C25.PDF 320kb PDF]
===Vasopressin receptor inhibition===
==External Links==
In [[hyponatremia]], [[demeclocycline]], a tetracycline antibiotic, is sometimes used to block the action of vasopressin in the kidney when there is inappropriately high secretion of vasopressin (SIADH, see above) and fluid restriction has not corrected the hyponatremia.


In [[heart failure]], tolvaptan, a vasopressin antagonist, may be beneficial according to a [[randomized controlled trial]].<ref>Gheorghiade M ''et al.'' (2007) Short-term clinical effects of tolvaptan, an oral vasopressin antagonist, in patients hospitalized for heart failure: the EVEREST Clinical Status Trials ''JAMA'' 297:1332-43 PMID 17384438</ref><ref>Konstam MA ''et al.'' (2007) Effects of oral tolvaptan in patients hospitalized for worsening heart failure: the EVEREST Outcome Trial. ''JAMA'' 297:1319-31 PMID 17384437</ref>  Tolvaptan is a selective [[cell surface receptor]]s V2 antagonist in the distal nephron which causes loss of free water.<ref>Goldsmith SR, Gheorghiade M (2005) Vasopressin antagonism in heart failure ''J Am Coll Cardiol'' 46:1785-91 PMID 16286160</ref> Other [[vasopressin]] antagonists  ([[conivaptan]], [[tolvaptan]], [[relcovaptan]], [[lixivaptan]]) act mainly on V1a [[cell surface receptor]]s.


{{Hormones}}
[[Tolvaptan]] can be used for [[hyponatremia]].<ref>(2009) [http://www.medicalletter.org/restricted/articles/w1326c.html Tolvaptan (Samsca) for Hyponatremia] The Medical Letter</ref>


{{kidney}}
==References==
<div class="references-small"><references /></div>


[[Category:Neuropeptides]]
[[Category:Suggestion Bot Tag]]
[[Category:Posterior pituitary hormones]]
[[Category:Neuroendocrinology]]

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Arginine vasopressin (antidiuretic hormone) -human
Identifiers
Symbol(s) AVP VP, ADH
Entrez 551
OMIM 192340
RefSeq NM_000490
UniProt P01185
Other data
Locus Chr. 20 p13


Arginine vasopressin (AVP), also known as vasopressin, antidiuretic hormone (ADH) or argipressin, is a mammalian hormone that is mainly released when the body is low on water; it causes the kidneys to conserve water by concentrating the urine and reducing urine volume. It also causes vasoconstriction.[1]

A very similar substance, lysine vasopressin (LVP) or lypressin, has the same function in pigs and is often used in human therapy.

Vasopressin is a peptide hormone liberated from a preprohormone precursor, the bulk of which is synthesized by the magnocellular neurons of the paraventricular and supraoptic nuclei of the hypothalamus, and transported to the posterior part of the pituitary gland from where it is secreted into the blood stream. Some of it is also released directly into the brain from the dendrites of the magnocellular neurons as well as from other brain neurons (see below).

Physiology

Control

Vasopressin is secreted from the posterior pituitary gland in response to reductions in plasma volume and in response to increases in the plasma osmolality:

The neurons that make vasopressin, in the supraoptic nucleus and paraventricular nucleus, are themselves osmoreceptors, but they also receive synaptic input from other osmoreceptors located in regions adjacent to the anterior wall of the third ventricle. These regions include the organum vasculosum of the lamina terminalis and the subfornical organ.

Many factors influence the secretion of vasopressin:

  • Ethanol and caffeine reduce vasopressin secretion. The resulting decrease in water reabsorption by the kidneys leads to a higher urine output. Coffee is an example of a food product that suppresses the body's release of antidiuretic hormones, due to its level of caffeine. This intake of caffeine causes the body to lose more water and may lead to dehydration if consumed excessively.
  • Angiotensin II stimulates the secretion of vasopressin.[2]

Sources

The vasopressin that is measured in peripheral blood is almost all derived from secretion from the posterior pituitary gland (except in cases of vasopressin-secreting tumours). However there are two other sources of vasopressin with important local effects:

  • Vasopressin is secreted from parvocellular neurons of the paraventricular nucleus at the median eminence into the short portal vessels of the pituitary stalk. These vessels carry the peptide to the anterior pituitary gland, where it is an important releasing factor for ACTH, acting in conjunction with CRH.
  • Vasopressin is also released into the brain by several different populations of neurons (see below).

Central actions

Vasopressin released within the brain has many actions:

  • It has been implicated in memory formation, including delayed reflexes, image, short- and long-term memory, though the mechanism remains unknown, and these findings are controversial. However, the synthetic vasopressin analogue desmopressin has come to interest as a likely nootropic.
  • Vasopressin released from centrally-projecting hypothalamic neurons is involved in aggression, blood pressure regulation and temperature regulation.

In recent years there has been particular interest in the role of vasopressin in social behavior. It is thought that vasopressin, released into the brain during sexual activity, initiates and sustains patterns of activity that support the pair-bond between the sexual partners; in particular, vasopressin seems to induce the male to become aggressive towards other males.

In several species, that the distribution of vasopressin and vasopressin receptors in the brain is associated with species-typical patterns of social behavior. In particular, there are differences between monogamous species and promiscuous species in the distribution of vasopressin receptors, and sometimes in the distribution of vasopressin-containing axons, even when closely-related species are compared. Moreover, studies involving either injecting vasopressin agonists into the brain, or blocking the actions of vasopressin, support the hypothesis that vasopressin is involved in aggression towards other males. There is also evidence that differences in the vasopressin receptor gene between individual members of a species might be predictive of differences in social behavior.

Summary Table

For more information, see: vasopressin receptor.

This table summarizes some of the actions of AVP at its three cell surface receptors which are differently expressed in different tissues and exerting different actions.

Summary of vasopressin receptors
Type Second messenger system Locations Actions
AVPR1A phosphatidylinositol/calcium liver, kidney, peripheral vasculature, brain vasoconstriction, gluconeogenesis, platelet aggregation, and release of factor VIII and von Willebrand factor; social recognition[3], circadian tau[4]
AVPR1B phosphatidylinositol/calcium pituitary gland, brain adrenocorticotropic hormone secretion in response to stress[5]; social interpretation to olfactory cues[6]
AVPR2 adenylate cyclase/cAMP apical membrane of the cells lining the collecting ducts of the kidneys (especially the cortical and outer medullary collecting ducts) insertion of aquaporin-2 (AQP2) channels (water channels). This allows water to be reabsorbed down an osmotic gradient, and so the urine is more concentrated.

Structure and relation to oxytocin

The vasopressins are peptides consisting of nine amino acids (nonapeptides). (NB: the value in the table above of 164 amino acids is that obtained before the hormone is activated by cleavage). The amino acid sequence of AVP is Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly, with the cysteine residues form a sulfur bridge. Lysine vasopressin has a lysine in place of the arginine.

The structure of oxytocin is very similar to that of the vasopressins: it is also a nonapeptide with a sulfur bridge and its amino acid sequence differs at only two positions (see table below). These two neuropeptides are encoded by genes that arose through duplication approximately 400 million years ago. The two genes are located on the same chromosome separated by a relatively small distance of less than 15,000 bases in various species. The magnocellular neurons that make AVP are adjacent to magnocellular neurons that make oxytocin, and are similar in many respects. The similarity of the two peptides can cause some cross-reactions: oxytocin has a slight antidiuretic function, and high levels of AVP can cause uterine contractions.

Here is a table showing the superfamily of vasopressin and oxytocin neuropeptides:

Vertebrate Vasopressin Family
Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 Argipressin (AVP, ADH) Most mammals
Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Lys-Gly-NH2 Lypressin (LVP) Pigs, hippos, warthogs, some marsupials
Cys-Phe-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 Phenypressin Some marsupials
Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Arg-Gly-NH2 Vasotocin† Non-mammals
Vertebrate Oxytocin Family
Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 Oxytocin (OXT) Most mammals, ratfish
Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Ile-Gly-NH2 Mesotocin Most marsupials, all birds, reptiles, amphibians, lungfishes
Cys-Tyr-Ile-Ser-Asn-Cys-Pro-Ile-Gly-NH2 Isotocin Bony fishes
Cys-Tyr-Ile-Asn/Gln-Asn-Cys-Pro-Leu/Val-Gly-NH2 Various tocins Sharks
Invertebrate VP/OT Superfamily
Cys-Leu-Ile-Thr-Asn-Cys-Pro-Arg-Gly-NH2 Diuretic Hormone Locust
Cys-Phe-Val-Arg-Asn-Cys-Pro-Thr-Gly-NH2 Annetocin Earthworm
Cys-Phe-Ile-Arg-Asn-Cys-Pro-Lys-Gly-NH2 Lys-Connopressin Geography & imperial cone snail, pond snail, sea hare, leech
Cys-Ile-Ile-Arg-Asn-Cys-Pro-Arg-Gly-NH2 Arg-Connopressin Striped cone snail
Cys-Tyr-Phe-Arg-Asn-Cys-Pro-Ile-Gly-NH2 Cephalotocin Octopus
Cys-Phe-Trp-Thr-Ser-Cys-Pro-Ile-Gly-NH2 Octopressin Octopus
†Vasotocin is the evolutionary progenitor of all the vertebrate neurohypophysial hormones. Only vasotocin found in hagfish & lampreys (Agnatha appeared 500 million years ago)

Role in disease

Decreased AVP release or decreased renal sensitivity to AVP leads to diabetes insipidus, a condition featuring hypernatremia (increased blood sodium content), polyuria (excess urine production), and polydipsia (thirst).

High levels of AVP secretion (syndrome of inappropriate antidiuretic hormone, SIADH) and resultant hyponatremia (low blood sodium levels) occurs in brain diseases and conditions of the lungs. In the perioperative period, the effects of surgical stress and some commonly used medications (e.g., opiates, syntocinon, anti-emetics) lead to a similar state of excess AVP secretion. This may cause mild hyponatraemia for several days.

Pharmacology

Vasopressin analogues

Vasopressin agonists are used therapeutically in various conditions, and its long-acting synthetic analogue desmopressin is used in conditions featuring low vasopressin secretion, as well as for control of bleeding (in some forms of von Willebrand disease) and in extreme cases of bedwetting by children.

Hepatorenal syndrome maybe be treated with terlipressin and related analogues which are splanchnic vasocontrictors .[7][8]

Esophageal varices may be treated with vasopressin analogues.[9]

In septic shock, vasopressin infusion has been used as a second line of management in patients not responding to high dose of inotropes (e.g., dopamine or epinephrine).

In asystolic cardiac arrest, vasopressin may be more effective than epinephrine according to a randomized controlled trial[10] and a cohort study. [11] Vasopressin may be combined with a corticosteroid.[12]

Vasopressin receptor inhibition

In hyponatremia, demeclocycline, a tetracycline antibiotic, is sometimes used to block the action of vasopressin in the kidney when there is inappropriately high secretion of vasopressin (SIADH, see above) and fluid restriction has not corrected the hyponatremia.

In heart failure, tolvaptan, a vasopressin antagonist, may be beneficial according to a randomized controlled trial.[13][14] Tolvaptan is a selective cell surface receptors V2 antagonist in the distal nephron which causes loss of free water.[15] Other vasopressin antagonists (conivaptan, tolvaptan, relcovaptan, lixivaptan) act mainly on V1a cell surface receptors.

Tolvaptan can be used for hyponatremia.[16]

References

  1. ↑ Anonymous (2024), Vasopressins (English). Medical Subject Headings. U.S. National Library of Medicine.
  2. ↑ Vander AJ Renal Physiology McGraw-Hill, 1991
  3. ↑ Bielsky IF et al. (2004) Profound impairment in social recognition and reduction in anxiety-like behavior in vasopressin V1a receptor knockout mice Neuropsychopharmacology 29:483-93 PMID 14647484
  4. ↑ Wersinger SR et al. (2007) Vasopressin 1a receptor knockout mice have a subtle olfactory deficit but normal aggression Genes Brain BehavPMID 17083331
  5. ↑ Lolait SJ et al. (2007) The hypothalamic-pituitary-adrenal axis response to stress in mice lacking functional vasopressin V1b receptors Endocrinology 148:849-56 PMID 17122081
  6. ↑ Wersinger SRet al. (2004) Social motivation is reduced in vasopressin 1b receptor null mice despite normal performance in an olfactory discrimination task Horm Behav 46:638-45 PMID 15555506
  7. ↑ Sanyal AJ et al. (2008) A randomized, prospective, double-blind, placebo-controlled trial of terlipressin for type 1 hepatorenal syndrome Gastroenterology 134:1360-8 PMID 18471513
  8. ↑ Martín-Llahí M et al. (2008) Terlipressin and albumin vs albumin in patients with cirrhosis and hepatorenal syndrome: a randomized study Gastroenterology 134:1352-9 PMID 18471512
  9. ↑ Baum S et al. (1970) The control of gastrointestinal hemorrhage by selective mesenteric infusion of pitressin Gastroenterology 58:926
  10. ↑ Wenzel V et al. (2004) European Resuscitation Council Vasopressor during Cardiopulmonary Resuscitation Study Group. A comparison of AVP and epinephrine for out-of-hospital cardiopulmonary resuscitation N Engl J Med 350:105-13 PMID 14711909.
  11. ↑ Grmec S, Mally S (2006) Vasopressin improves outcome in out-of-hospital cardiopulmonary resuscitation of ventricular fibrillation and pulseless ventricular tachycardia: an observational cohort study Crit Care 10:R13 PMID 16420660
  12. ↑ Mentzelopoulos, SD; et al. (2009-01-12). "Vasopressin, Epinephrine, and Corticosteroids for In-Hospital Cardiac Arrest". Arch Intern Med 169: 15-24. DOI:10.1001/archinternmed.2008.509. Retrieved on 2009-01-13. Research Blogging.
  13. ↑ Gheorghiade M et al. (2007) Short-term clinical effects of tolvaptan, an oral vasopressin antagonist, in patients hospitalized for heart failure: the EVEREST Clinical Status Trials JAMA 297:1332-43 PMID 17384438
  14. ↑ Konstam MA et al. (2007) Effects of oral tolvaptan in patients hospitalized for worsening heart failure: the EVEREST Outcome Trial. JAMA 297:1319-31 PMID 17384437
  15. ↑ Goldsmith SR, Gheorghiade M (2005) Vasopressin antagonism in heart failure J Am Coll Cardiol 46:1785-91 PMID 16286160
  16. ↑ (2009) Tolvaptan (Samsca) for Hyponatremia The Medical Letter
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