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Science Review: Vasopressin and the cardiovascular system part 1 – receptor physiology
Critical Care volume 7, Article number: 427 (2003)
Vasopressin is emerging as a rational therapy for vasodilatory shock states. Unlike other vasoconstrictor agents, vasopressin also has vasodilatory properties. The goal of the present review is to explore the vascular actions of vasopressin. In part 1 of the review we discuss structure, signaling pathways, and tissue distributions of the classic vasopressin receptors, namely V1 vascular, V2 renal, V3 pituitary and oxytocin receptors, and the P2 class of purinoreceptors. Knowledge of the function and distribution of vasopressin receptors is key to understanding the seemingly contradictory actions of vasopressin on the vascular system. In part 2 of the review we discuss the effects of vasopressin on vascular smooth muscle and the heart, and we summarize clinical studies of vasopressin in shock states.
Arginine vasopressin (hereafter referred to as vasopressin), also known as antidiuretic hormone, is essential for survival, as attested by its teleologic persistence. Oxytocin- and vasopressin-like peptides have been isolated from four invertebrate phyla and the seven major vertebrate families, representing more than 120 species . Therefore, the ancestral gene encoding the precursor protein appears to antedate the divergence of the vertebrate and invertebrate families, about 700 million years ago . Virtually all vertebrate species possess an oxytocin-like and a vasopressin-like peptide, and so two evolutionary lineages can be traced. The presence of a single peptide, vasotocin ([Ile3]-vasopressin or [Arg8]-oxytocin), in the most primitive cyclostomata supports the notion that primordial gene duplication with subsequent mutations gave rise to the two lineages .
Vasopressin is essential for cardiovascular homeostasis. The vasopressor effect of pituitary extract, first observed in 1895, was attributed to the posterior lobe of this gland . It was not until 18 years later that the antidiuretic effect of neurohypophyseal extract was demonstrated [4, 5]. After isolation and synthesis of vasopressin in the 1950s, it was proven that the same hormone in the posterior pituitary possessed both antidiuretic and vasopressor effects [6, 7]. The importance of vasopressin in osmotic defense is fundamental. Indeed, the antidiuretic effect of vasopressin has been exploited clinically for over half a century to treat diabetes insipidus. Only recently has vasopressin emerged as a therapy for shock states, renewing interest in the cardiovascular effects of vasopressin.
Shock states induce an increase in vasopressin levels from 20- to 200-fold [8–12]. These supraphysiologic levels cause profound vasoconstriction and help to maintain end-organ perfusion [13, 14]. Prolonged shock is associated with a fall in vasopressin levels [15–18], probably due to depletion of vasopressin stores [19, 20], and may contribute to the refractory hypotension that is seen in advanced shock states. Paradoxically, vasopressin has also been demonstrated to cause vasodilation in some vascular beds [21–28], distinguishing this hormone from other vasoconstrictor agents.
The present review explores the vascular actions of vasopressin. First, a discussion of the signaling pathways and distribution of vasopressin receptors is necessary to gain an understanding of the seemingly paradoxic vasodilatory and vasoconstrictor actions of vasopressin. We discuss the structural elements responsible for the functional diversity found within the vasopressin receptor family. In part 2 of our review, we explore the mechanisms of vasoconstriction and vasodilation of the vascular smooth muscle, with an emphasis on vasopressin interaction in these pathways. We review the seemingly contradictory studies and some new information regarding the actions of vasopressin on the heart. Finally, we summarize the clinical trials of vasopressin in vasodilatory shock states and comment on areas for future research.
Overview of vasopressin
Structure of the hormone and the genes
Vasopressin is a nonapeptide with a disulfide bridge between two cysteine amino acids  and is synthesized by the magnocellular neurons of the hypothalamus  (Fig. 1). Although oxytocin differs from vasopressin by only one amino acid (80% homology), they have clearly divergent physiologic activity. Vasopressin is involved in osmotic and cardiovascular homeostasis, whereas oxytocin is important in parturition, lactation, and sexual behavior.
Oxytocin and vasopressin are encoded by separate genes but they lie on the same chromosome, at 20p , separated by a segment of DNA only 12 kilobases long . The similarities in structure as well as the close apposition are suggestive of recent gene duplication . Despite ample documentation of cell-specific expression and physiologic regulation of the vasopressin gene, there is striking lack of progress in identifying transcription factors that act on the vasopressin promoter .
Structure of the receptor
The actions of vasopressin are mediated by stimulation of tissue-specific G-protein-coupled receptors (GPCRs), which are currently classified into V1 vascular (V1R), V2 renal (V2R), V3 pituitary (V3R) and oxytocin (OTR) subtypes  and P2 purinergic receptors (P2R) . The GPCRs are comprised of seven hydrophobic transmembrane α-helices joined by alternating intracellular and extracellular loops, an extracellular amino-terminal domain, and a cytoplasmic carboxyl-terminal domain (Fig. 2) . The actions of vasopressin are signaled through pathways that are similar to extracellular agents such as hormones (glucagon, luteinizing hormone, and epinephrine [adrenaline]), neurotransmitters (acetylcholine, dopamine, and serotonin) and chemokines (interleukin-8). Local mediators signal to the four main G protein families to regulate cellular machinery such as metabolic enzymes, ion channels, and transcriptional regulators . The extracellular signals are routed to specific G proteins through distinct types of receptors. For example, epinephrine's signal is transmitted through the β-adrenergic receptor coupled to Gi, and the α1-adrenergic receptor coupled to Gq and G11. Many important hormones, including epinephrine, acetylcholine, dopamine, and serotonin, interact with the Gi pathway, which is characterized by inhibition of adenylyl cyclase .
Agonist stimulation of vasopressin receptors leads to receptor subtype-specific interactions with G-protein-coupled receptor kinases (GRKs) and protein kinase C (PKC) through specific motifs that are present in the carboxyl termini of the receptors . Guanine nucleotide-binding proteins (G-proteins) are signal transducers, attached to the cell surface membrane, that connect receptors to effectors and thus to intracellular signaling pathways . Functional characterization of the G-proteins, including Gs, Gi/o, Gq/11, and G12/13 , indicates that a single receptor can activate multiple second messenger pathways through interaction with one or more G-proteins [40–42].
Vasopressin's signal is transmitted through both Gs and Gq/11 subtypes . The Gs pathway is characterized by inhibition of adenylyl cyclase, leading to increased levels of cAMP that in turn connects to multiple cellular machines, including ion channels, transcription factors, and metabolic enzymes. Both β-adrenergic receptors and vasopressin receptors regulate Gs protein signaling. The Gq/11 pathway is the classical pathway that is activated by calcium-mobilizing hormones and stimulates phospholipase-β to produce the intracellular messengers inositol trisphosphate and diacylglycerol (DAG) . Inositol trisphosphate triggers the release of calcium from intracellular stores and DAG recruits PKC to the membrane and activates it. The α-subunit of Gq also activates the transcription factor nuclear factor-κB .
The V1 receptor
The V1R gene is located on chromosome 12 and maps to region 12q14-15 . Functionally, the V1R activates G-proteins of the Gq/11 family. The α-subunits regulate the activity of the β-isoforms of phospholipase C . A variety of signaling pathways is associated with the V1R, and these pathways include activation of calcium influx, phospholipase A2, phospholipase C, and phospholipase D .
V1Rs are found in high density on vascular smooth muscle and cause vasoconstriction by an increase in intracellular calcium via the phosphatidyl–inositol-bisphosphonate cascade. Cardiac myocytes also possess the V1R and are discussed in part 2 of the review. Additionally, V1Rs are located in brain, testis, superior cervical ganglion, liver, blood vessels, and renal medulla . The exact physiologic role of vasopressin in many of these diverse tissues remains unknown.
Platelets express the V1R, which upon stimulation induces an increase in intracellular calcium, facilitating thrombosis . However, there appears to be tremendous variability in the aggregation response of normal human platelets to vasopressin . Based on kinetic studies and the effects of PKC inhibition on the aggregation response to vasopressin, significant heterogeneity in the aggregation response of normal human platelets to vasopressin has been demonstrated, which is probably related to a polymorphism of the platelet V1R .
V1Rs are found in the kidney, where they occur in high density on medullary interstitial cells, vasa recta, and epi thelial cells of the collecting duct. Vasopressin acts on medullary vasculature through the V1R to reduce blood flow to inner medulla without affecting blood flow to outer medulla . V1Rs on the luminal membrane of the collecting duct probably exerted through V1a receptors located on luminal membrane limit the antidiuretic effects of vasopressin . Interestingly, cyclosporine A induces upregulation of V1R mRNA in vascular smooth muscle , increasing the number of V1Rs by twofold , which could be a key mechanism by which cyclosporine A causes both hypertension and reduced glomerular filtration. Additionally, vasopressin selectively contracts efferent arterioles , probably through the V1R, but not the afferent arteriole. This selectivity, which is not shared by catecholamine vasopressors, would tend to increase glomerular filtration, probably accounting for the paradoxic increase in urine output observed when this antidiuretic hormone is administered to patients in vasodilatory shock [54, 55].
There is considerable interspecies variation in the V1R. For instance, although rat and human vasopressin are identical, the human V1R is only 80% homologous with the rat V1R . This must be kept in mind when interpreting animal studies aimed at interpreting receptor subtypes based on the use of specific receptor inhibitors.
The V2 receptor
The V2 R differs from the V1R primarily in the number of sites susceptible to N-linked glycosylation; the V1R has sites at both the amino-terminus and at the extracellular loop, whereas the V2R has a single site at the extracellular amino-terminus . Despite structural similarities, the V2R differs functionally from the V1R. Mutagenesis experiments involving the V1R and V2R have confirmed that the short sequence at the amino-terminus of the cytoplasmic tail confers V2 receptor–Gs coupling selectivity. The efficiency of V2R–Gs coupling can be modulated by the length of the central portion of the third intracellular loop , whereas the second intracellular loop of the V1R is critically involved in selective activation of Gq/11 .
The well known antidiuretic effect of vasopressin occurs via activation of the V2R. Vasopressin regulates water excretion from the kidney by increasing the osmotic water permeability of the renal collecting duct – an effect that is explained by coupling of the V2R with the Gs signaling pathway, which activates cAMP . The increased intracellular cAMP in the kidney [60, 61] in turn triggers fusion of aquaporin-2-bearing vesicles with the apical plasma membrane of the collecting duct principal cells, increasing water reabsorption . Vasopressin regulates water homeostasis in two ways: regulation of the fast shuttling of aquaporin 2 to the cell surface and stimulation of the synthesis of mRNA encoding aquaporin 2 . Most cases of diabetes insipidus can be explained by mutations in the V2R gene, which is located on chromosome region 10q28 . For example, an Arg137→His mutation in the V2R abolishes coupling to the Gs protein, causing a complete phenotype of nephrogenic diabetes insipidus .
It has been postulated that the V2R is also expressed in endothelium because the potent V2R agonist 1-deamino-8-D-arginine vasopressin (DDAVP) causes both release of von Willebrand factor and vasodilation . Previous studies of the localization and distribution of different vasopressin receptors have been hampered by the use of nonselective radioligands such as [3H]arginine vasopressin, which binds to all types of V1R and V2R, certain OTRs, and neurophysins. When selective V1R and V2R radioligands with in vitro auto-radiography were used to study V1R and V2R binding sites, no binding was demonstrated on endothelium or liver, where DDAVP might influence clotting factor release, or in the brain, spinal cord, sympathetic ganglia, heart or vascular smooth muscle – regions where DDAVP might cause vasodilation . Specific binding was only identified in the kidney, which is consistent with the known distribution of antidiuretic V2Rs on renal collecting tubules.
The V3 receptor
The human V3R (previously known as V1bR) is a G-protein-coupled pituitary receptor that, because of its scarcity, was only recently characterized. The V3R gene maps to chromosome region 1q32 . The 424-amino-acid sequence of the V3R has homologies of 45%, 39%, and 45% with the V1R, V2R, and OTR, respectively . However, the V3R has a pharmacologic profile that distinguishes it from the human V1R and activates several signaling pathways via different G-proteins, depending on the level of receptor expression . Interestingly the V3R is also is over-expressed in adrenocorticotropic hormone (ACTH)-hypersecreting tumors.
More than one G-protein appears to participate in signal transduction pathways linked to V3Rs, depending on the level of receptor expression and the concentration of vasopressin . For instance, vasopressin causes secretion of ACTH from the anterior pituitary cells in a dose-dependent manner through activation of PKC  via the Gq/11 class . Other cellular responses, including increased synthesis of DNA and cAMP, which are important in the induction and phenotype maintenance of ACTH-secreting tumors, are mediated through recruitment of several pathways, including Gs, Gi, and Gq/11 . The V3R has been inferred to exist in the pancreas  on the basis of antagonist studies; however, this conclusion may be suspect because significant homology exists between the V3R and the V1R .
The oxytocin receptor
The OTR can be considered a 'nonselective' vasopressin receptor. The OTR has equal affinity for vasopressin and oxytocin, whereas the V1R has a 30-fold higher affinity for vasopressin than for oxytocin . OTRs are functionally coupled to Gq/11 class binding proteins, which stimulate the activity of phospholipase C . This leads to the generation of inositol trisphosphate and 1,2-DAG. Inositol trisphosphate triggers calcium release from intracellular stores, whereas DAG stimulates PKC, which phosphorylates unidentified target proteins . A variety of cellular events are initiated in response to an increase in intracellular calcium. For example, the forming calcium–calmodulin complexes trigger activation of neuronal and endothelial isoforms of nitric oxide synthase. Nitric oxide in turn stimulates the soluble guanylate cyclase to produce cGMP, leading to vasodilation. In smooth muscle cells, the calcium–calmodulin system triggers the activation of myosin light chain kinase activity, which initiates smooth muscle contraction (e.g. in myometrial or mammary myoepithelial cells) . In neurosecretory cells, rising calcium levels control cellular excitability, modulate their firing patterns, and lead to transmitter release. Further calcium-promoted processes include gene transcription and protein synthesis.
OTRs have been localized to a variety of reproductive and nonreproductive tissues . Importantly, OTRs exist in high density on vascular endothelium, mediating nitric oxide dependent vasodilation . Recently, the oxytocin/OTR system has been discovered in the heart. Activation of cardiac OTR stimulates the release of atrial natriuretic peptide, which is involved in natriuresis, regulation of blood pressure, and cell growth . Embryonic stem cells exposed to oxytocin exhibit increased atrial natriuretic peptide mRNA and abundant mitochondria, and express sarcomeric myosin heavy chain, which is consistent with promotion of cardiomyocyte differentiation .
Recently, vasopressin was demonstrated to act on the P2 class of purinoreceptors (P2Rs) . P2Rs also belong to the seven-transmembrane-domain GPCR superfamily. ATP released from platelets and damaged cells bind endothelial P2Rs . ATP can act on either of the two subclasses of purinoceptors, namely P2γ and P2ν. In both cases, activation of phospholipase C leads to mobilization of intracellular calcium stores. This binding stimulates phospholipase A2 and nitric oxide synthase, resulting in increased synthesis and release of prostacyclin and nitric oxide, respectively, and causing vascular smooth muscle vasodilation .
Purinoreceptors may also have an important role in cardiac contractility. ATP released by platelets, endothelial cells, and damaged myocardium activates the P2R, causing a large increase in cytosolic calcium and myocyte contractile amplitude . ATP is also released as a cotransmitter with norepinephrine from sympathetic nerve endings and acts in a synergistic manner with β-adrenergic agents, increasing myocardial contractility . In contrast to β-adrenergic agents, inotropy is not accompanied by a positive chronotropic effect. It is speculated that P2R agonist-stimulated increase in contractility could occur without the expense of a rate-related increase in myocardial oxygen demand .
Recently, vasopressin was shown to exert cardiac effects through activation of P2Rs expressed on cardiac endothelium. Intracoronary infusion of vasopressin-dextran (confines vasopressin to the intravascular space) and vasopressin at maximal concentration in isolated perfused guinea pig hearts caused coronary vasoconstriction and negative inotropy-effects that were blocked with vasopressin antagonists and P2R antagonist . Caution must be exercised in interpreting this study because activation of P2Rs and increased levels of ATP normally increase inotropy. Furthermore, the same experiments performed in isolated perfused rat hearts demonstrated positive inotropy – an effect that was blocked by P2R antagonists . Further study is necessary to ascertain the significance of vasopressin P2R activation in the human heart, but the discovery that vasopressin acts on P2Rs is intriguing.
A number of pharmacologic observations have suggested the existence of vasopressin receptor/OTR subtypes beyond the five described above . These include receptors for the metabolites of vasopressin and oxytocin (VP4-9 R and OT4-9 R) , and a cAMP-coupled vasopressin receptor with a V1-like pharmacologic profile termed V2b . A novel 'vasotocin-like' receptor subtype has also been proposed .
Vasopressin/oxytocin receptor downregulation
Upon ligand binding, GPCRs undergo activation followed by a decrease in receptor responsiveness (desensitization). Agonist-dependent desensitization of these receptors can reduce their signaling responsiveness to maximum stimulation by up to 70–80% . Receptor desensitization occurs when activated receptors become phosphorylated and bind to β-arrestin proteins, inhibiting further interaction with G-proteins [84, 85]. Receptor responsiveness is also limited by the degradation of cAMP by phosphodiesterases. β-Arrestins coordinate both phosphorylation of receptors and the rate of cAMP degradation by phosphodiesterases .
Exposure to vasopressin leads to desensitization of the V1R, which occurs quickly and is accompanied by sequestration of receptors inside the cell . The V1R can also be desensitized by angiotensin II . Compared with V1Rs and β2-adrenergic receptors, which are known to recycle and resensitize rapidly, the V2R recycles and resensitizes slowly . Mutagenesis experiments demonstrate that the interaction of β-arrestin with a specific motif in the GPCR carboxyl-terminal tail dictates the rate of receptor dephosphorylation, recycling, and resensitization [87, 88]. The clinical importance of vasopressin desensitization of the vasopressin receptor/ OTR family in human disease states is currently unknown.
Despite the clinical importance of the vasopressin receptors and OTRs, little is known about the mechanisms by which they undergo internalization and desensitization. Agonist activation of all vasopressin receptor/OTR subtypes leads to a specific physical association of the receptors with GRKs and/or PKC, following different time courses that are specific to the receptor subtype . The pattern of interaction with GRKs and PKC is also unique to each vasopressin receptor subtype and occurs at the level of their carboxyl-termini .
Vasopressin is known to modulate the effect of other vasoactive agents [89, 90] – an interaction that may be explained by arrestin trafficking. Isoproterenol-dependent internalization of β2-adrenergic receptors is specifically blocked (>65% inhibition) by vasopressin-induced activation of V2Rs coexpressed at similar levels . β2-Adrenergic receptors caused no detectable effect on V2R internalization in the same cells. There is evidence to suggest that this nonreciprocal inhibition of endocytosis is mediated by receptor-specific intracellular trafficking of β-arrestins . Interestingly, interaction of vasopressin with arrestins and resistance of vasopressin receptors to downregulation may explain the reported ability of vasopressin to bypass desensitized myocardial adrenergic receptors in an experimental model of congestive heart failure . The clinical importance of vasopressin upregulation of adrenergic receptors in critically ill humans is an important area for further study.
During the past 10 years, considerable progress has been made in our understanding of vasopressin receptor structure and function. The physiologic significance of the various receptors has been elucidated by the development of specific agonists and antagonists, particularly by Dr Maurice Manning's group [92–94]. An understanding of the molecular basis of receptor function will greatly aid in the development of new molecules with high selectivity for the different subtypes of receptors, and will have potential therapeutic significance, not only for conditions as diverse as hypertension, diabetes insipidus and premature labor, but also in vasodilatory shock with organ dysfunction. In part 2 of the review, we discuss the interaction of vasopressin with its various receptors in vascular smooth muscle and the heart, and its potential utility in vasodilatory shock states.
ACTH = adrenocorticotropic hormone
DAG = diacylglycerol
DDAVP = 1-deamino-8-D-arginine vasopressin
GPCR = G-protein-coupled receptor
GRK = G protein-coupled receptor kinase
OTR = oxytocin receptor
PKC = protein kinase C
P2R = P2 purinergic receptors
V1R = V1 vascular receptor
V2R = V2 renal receptor
V3R = V3 pituitary receptor.
Hoyle CH: Neuropeptide families and their receptors: evolutionary perspectives. Brain Res 1999, 848: 1-25. 10.1016/S0006-8993(99)01975-7
Acher R, Chauvet J, Chauvet MT: Man and the chimaera. Selective versus neutral oxytocin evolution. Adv Exp Med Biol 1995, 395: 615-627.
Oliver H, Schaefer EA: On the physiological action of extracts of the pituitary body and certain other glandular organs. J Physiol (Lond) 1895, 18: 277-279.
von den Velden R: The renal effects of hypophyseal extract in humans [in German]. Berl Klin Wochenscgr 1913, 50: 2083-2086.
Verney EB: The antidiuretic hormone and the factor which determines its release. Proc R Soc Lond (Biol) 1947, 135: 25-106.
Turner RA, Pierce JG, Du Vigneaud V: The purification and the amino acid content of vasopressin preparation. J Biol Chem 1951, 191: 21.
Du Vigneaud V, Gash DT, Katsoyannis PG: A synthetic preparation possessing biological properties associated with argininevasopressin. J Am Chem Soc 1954, 76: 4751-4752.
Arnauld E, Czernichow P, Fumoux F, Vincent JD: The effects of hypotension and hypovolaemia on the liberation of vasopressin during haemorrhage in the unanaesthetized monkey ( Macaca mulatta ). Pflugers Arch Eur J Physiol 1977, 371: 193-200.
Cowley AW Jr, Switzer SJ, Guinn MM: Evidence and quantification of the vasopressin arterial pressure control system in the dog. Circ Res 1980, 46: 58-67.
Wilson MF, Brackett DJ, Hinshaw LB, Tompkins P, Archer LT, Benjamin BA: Vasopressin release during sepsis and septic shock in baboons and dogs. Surg Gynecol Obstet 1981, 153: 869-872.
Wilson MF, Brackett DJ: Release of vasoactive hormones and circulatory changes in shock. Circ Shock 1983, 11: 225-234.
Wang BC, Flora-Ginter G, Leadley RJ Jr, Goetz KL: Ventricular receptors stimulate vasopressin release during hemorrhage. Am J Physiol 1988, 254: R204-R211.
Schwartz J, Reid IA: Effect of vasopressin blockade on blood pressure regulation during hemorrhage in conscious dogs. Endocrinology 1981, 109: 1778-1780.
Abboud FM, Floras JS, Aylward PE, Guo GB, Gupta BN, Schmid PG: Role of vasopressin in cardiovascular and blood pressure regulation. Blood Vessels 1990, 27: 106-115.
Errington ML, Rocha e Silva M Jr: The secretion and clearance of vasopressin during the development of irreversible haemorrhagic shock. J Physiol (Lond) 1971, 217: 43P-45P.
Landry DW, Levin HR, Gallant EM, Seo S, D'Alessandro D, Oz MC, Oliver JA: Vasopressin pressor hypersensitivity in vasodilatory septic shock. Crit Care Med 1997, 25: 1279-1282. 10.1097/00003246-199708000-00012
Landry DW, Levin HR, Gallant EM, Ashton RC Jr, Seo S, D'A-lessandro D, Oz MC, Oliver JA: Vasopressin deficiency contributes to the vasodilation of septic shock. Circulation 1997, 95: 1122-1125.
Morales D, Madigan J, Cullinane S, Chen J, Heath M, Oz M, Oliver JA, Landry DW: Reversal by vasopressin of intractable hypotension in the late phase of hemorrhagic shock. Circulation 1999, 100: 226-229.
Landry DW, Oliver JA: The pathogenesis of vasodilatory shock. N Engl J Med 2001, 345: 588-595. 10.1056/NEJMra002709
Sharshar T, Carlier R, Blanchard A, Feydy A, Gray F, Paillard M, Raphael JC, Gajdos P, Annane D: Depletion of neurohypophyseal content of vasopressin in septic shock. Crit Care Med 2002, 30: 497-500. 10.1097/00003246-200203000-00001
Bichet DG, Razi M, Lonergan M, Arthus MF, Papukna V, Kortas C, Barjon JN: Hemodynamic and coagulation responses to 1-desamino[8-D-arginine] vasopressin in patients with congenital nephrogenic diabetes insipidus. N Engl J Med 1988, 318: 881-887.
Walker BR, Haynes J Jr, Wang HL, Voelkel NF: Vasopressin-induced pulmonary vasodilation in rats. Am J Physiol 1989, 257: H415-H422.
Evora PR, Pearson PJ, Schaff HV: Arginine vasopressin induces endothelium-dependent vasodilatation of the pulmonary artery. V1-receptor-mediated production of nitric oxide. Chest 1993, 103: 1241-1245.
Suzuki Y, Satoh S, Oyama H, Takayasu M, Shibuya M: Regional differences in the vasodilator response to vasopressin in canine cerebral arteries in vivo. Stroke 1993, 24: 1049-1053.
Rudichenko VM, Beierwaltes WH: Arginine vasopressin-induced renal vasodilation mediated by nitric oxide. J Vasc Res 1995, 32: 100-105.
Tamaki T, Kiyomoto K, He H, Tomohiro A, Nishiyama A, Aki Y, Kimura S, Abe Y: Vasodilation induced by vasopressin V2 receptor stimulation in afferent arterioles. Kidney Int 1996, 49: 722-729.
Okamura T, Toda M, Ayajiki K, Toda N: Receptor subtypes involved in relaxation and contraction by arginine vasopressin in canine isolated short posterior ciliary arteries. J Vasc Res 1997, 34: 464-472.
Okamura T, Ayajiki K, Fujioka H, Toda N: Mechanisms underlying arginine vasopressin-induced relaxation in monkey isolated coronary arteries. J Hypertens 1999, 17: 673-678. 10.1097/00004872-199917050-00011
Barberis C, Mouillac B, Durroux T: Structural bases of vasopressin/oxytocin receptor function. J Endocrinol 1998, 156: 223-229.
Swaab DF, Nijveldt F, Pool CW: Distribution of oxytocin and vasopressin in the rat supraoptic and paraventricular nucleus. J Endocrinol 1975, 67: 461-462.
Riddell DC, Mallonee R, Phillips JA, Parks JS, Sexton LA, Hamerton JL: Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor. Somat Cell Mol Genet 1985, 11: 189-195.
Summar ML, Phillips JA III, Battey J, Castiglione CM, Kidd KK, Maness KJ, Weiffenbach B, Gravius TC: Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20. Mol Endocrinol 1990, 4: 947-950.
Ruppert S, Scherer G, Schutz G: Recent gene conversion involving bovine vasopressin and oxytocin precursor genes suggested by nucleotide sequence. Nature 1984, 308: 554-557.
Burbach J: Regulation of gene promoters of hypothalamic peptides. Front Neuroendocrinol 2002, 23: 342-369. 10.1016/S0091-3022(02)00005-5
Thibonnier M, Conarty DM, Preston JA, Wilkins PL, Berti-Mattera LN, Mattera R: Molecular pharmacology of human vasopressin receptors. Adv Exp Med Biol 1998, 449: 251-276.
Zenteno-Savin T, Sada-Ovalle I, Ceballos G, Rubio R: Effects of arginine vasopressin in the heart are mediated by specific intravascular endothelial receptors. Eur J Pharmacol 2000, 410: 15-23. 10.1016/S0014-2999(00)00853-0
Neves SR, Ram PT, Iyengar R: G protein pathways. Science 2002, 296: 1636-1639. 10.1126/science.1071550
Berrada K, Plesnicher CL, Luo X, Thibonnier M: Dynamic interaction of human vasopressin/oxytocin receptor subtypes with g protein-coupled receptor kinases and protein kinase c after agonist stimulation. J Biol Chem 2000, 275: 27229-27237.
Ross EM, Gilman AG: Biochemical properties of hormone-sensitive adenylate cyclase. Annu Rev Biochem 1980, 49: 533-564. 10.1146/annurev.bi.49.070180.002533
Birnbaumer M: Mutations and diseases of G protein coupled receptors. J Recept Signal Transduct Res 1995, 15: 131-160.
Zhu X, Gilbert S, Birnbaumer M, Birnbaumer L: Dual signaling potential is common among Gs-coupled receptors and dependent on receptor density. Mol Pharmacol 1994, 46: 460-469.
Klein U, Muller C, Chu P, Birnbaumer M, von Zastrow M: Heterologous inhibition of G protein-coupled receptor endocytosis mediated by receptor-specific trafficking of beta-arrestins. J Biol Chem 2001, 276: 17442-17447. 10.1074/jbc.M009214200
Shi CS, Kehrl JH: PYK2 links G(q)alpha and G(13)alpha signaling to NF-kappa B activation. J Biol Chem 2001, 276: 31845-31850. 10.1074/jbc.M101043200
Thibonnier M, Graves MK, Wagner MS, Auzan C, Clauser E, Willard HF: Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene. Genomics 1996, 31: 327-334. 10.1006/geno.1996.0055
Briley EM, Lolait SJ, Axelrod J, Felder CC: The cloned vasopressin V1a receptor stimulates phospholipase A2, phospholipase C, and phospholipase D through activation of receptor-operated calcium channels. Neuropeptides 1994, 27: 63-74.
Phillips PA, Abrahams JM, Kelly JM, Mooser V, Trinder D, Johnston CI: Localization of vasopressin binding sites in rat tissues using specific V1 and V2 selective ligands. Endocrinology 1990, 126: 1478-1484.
Filep J, Rosenkranz B: Mechanism of vasopressin-induced platelet aggregation. Thromb Res 1987, 45: 7-15.
Vittet D, Launay JM, Chevillard C: Homologous regulation of human platelet vasopressin receptors does not occur in vivo. Am J Physiol 1989, 257: R1400-R1405.
Lachant NA, Smith MR, Xie ZJ, Romani WR: Heterogeneity of the aggregation response of human platelets to arginine vasopressin. Am J Hematol 1995, 49: 56-66.
Bankir L: Antidiuretic action of vasopressin: quantitative aspects and interaction between V1a and V2 receptor-mediated effects. Cardiovasc Res 2001, 51: 372-390. 10.1016/S0008-6363(01)00328-5
Cottet-Maire F, Avdonin PV, Roulet E, Buetler TM, Mermod N, Ruegg UT: Upregulation of vasopressin V1A receptor mRNA and protein in vascular smooth muscle cells following cyclosporin A treatment. Br J Pharmacol 2001, 132: 909-917.
Lo Russo A, Passaquin AC, Ruegg UT: Mechanism of enhanced vasoconstrictor hormone action in vascular smooth muscle cells by cyclosporin A. Br J Pharmacol 1997, 121: 248-252.
Edwards RM, Trizna W, Kinter LB: Renal microvascular effects of vasopressin and vasopressin antagonists. Am J Physiol 1989, 256: F274-F278.
Holmes CL, Walley KR, Chittock DR, Lehman T, Russell JA: The effects of vasopressin on hemodynamics and renal function in severe septic shock: a case series. Intensive Care Med 2001, 27: 1416-1421. 10.1007/s001340101014
Patel B, Chittock D, Walley K: Vasopressin infusion in SIRS and septic shock: a randomized controlled trial. Am J Respir Crit Care Med 1999, 159: A608.
Innamorati G, Sadeghi H, Birnbaumer M: A fully active nonglycosylated V2 vasopressin receptor. Mol Pharmacol 1996, 50: 467-473.
Erlenbach I, Wess J: Molecular basis of V2 vasopressin receptor/Gs coupling selectivity. J Biol Chem 1998, 273: 26549-26558. 10.1074/jbc.273.41.26549
Liu J, Wess J: Different single receptor domains determine the distinct G protein coupling profiles of members of the vasopressin receptor family. J Biol Chem 1996, 271: 8772-8778. 10.1074/jbc.271.15.8772
Birnbaumer M: Vasopressin receptors. Trends Endocrinol Metab 2000, 11: 406-410. 10.1016/S1043-2760(00)00304-0
Orloff J, Handler J: The role of adenosine 3',5'-phosphate in the action of antidiuretic hormone. Am J Med 1967, 42: 757-768.
Dousa TP, Walter R, Schwartz IL, Sands H, Hechter O: Role of cyclic AMP in the action of neurohypophyseal hormones on kidney. Adv Cyclic Nucleotide Res 1972, 1: 121-135.
Harris HW Jr, Zeidel ML, Jo I, Hammond TG: Characterization of purified endosomes containing the antidiuretic hormone-sensitive water channel from rat renal papilla. J Biol Chem 1994, 269: 11993-12000.
Knepper MA, Inoue T: Regulation of aquaporin-2 water channel trafficking by vasopressin. Curr Opin Cell Biol 1997, 9: 560-564. 10.1016/S0955-0674(97)80034-8
Kambouris M, Dlouhy SR, Trofatter JA, Conneally PM, Hodes ME: Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28. Am J Med Genet 1988, 29: 239-246.
Rosenthal W, Antaramian A, Gilbert S, Birnbaumer M: Nephrogenic diabetes insipidus. A V2 vasopressin receptor unable to stimulate adenylyl cyclase. J Biol Chem 1993, 268: 13030-13033.
Rousseau-Merck MF, Rene P, Derre J, Bienvenu T, Berger R, de Keyzer Y: Chromosomal localization of the human V3 pituitary vasopressin receptor gene (AVPR3) to 1q32. Genomics 1995, 30: 405-406.
Sugimoto T, Saito M, Mochizuki S, Watanabe Y, Hashimoto S, Kawashima H: Molecular cloning and functional expression of a cDNA encoding the human V1b vasopressin receptor. J Biol Chem 1994, 269: 27088-27092.
Thibonnier M, Preston JA, Dulin N, Wilkins PL, Berti-Mattera LN, Mattera R: The human V3 pituitary vasopressin receptor: ligand binding profile and density-dependent signaling pathways. Endocrinology 1997, 138: 4109-4122.
Thibonnier M, Berti-Mattera LN, Dulin N, Conarty DM, Mattera R: Signal transduction pathways of the human V1-vascular, V2-renal, V3-pituitary vasopressin and oxytocin receptors. Prog Brain Res 1998, 119: 147-161.
Liu JP, Engler D, Funder JW, Robinson PJ: Arginine vasopressin (AVP) causes the reversible phosphorylation of the myristoylated alanine-rich C kinase substrate (MARCKS) protein in the ovine anterior pituitary: evidence that MARCKS phosphorylation is associated with adrenocorticotropin (ACTH) secretion. Mol Cell Endocrinol 1994, 101: 247-256. 10.1016/0303-7207(94)90241-0
Lee B, Yang C, Chen TH, al-Azawi N, Hsu WH: Effect of AVP and oxytocin on insulin release: involvement of V1b receptors. Am J Physiol 1995, 269: E1095-E1100.
Peter J, Burbach H, Adan RA, Lolait SJ, van Leeuwen FW, Mezey E, Palkovits M, Barberis C: Molecular neurobiology and pharmacology of the vasopressin/oxytocin receptor family. Cell Mol Neurobiol 1995, 15: 573-595.
Gimpl G, Fahrenholz F: The oxytocin receptor system: structure, function, and regulation. Physiol Rev 2001, 81: 629-683.
Sanborn BM, Dodge K, Monga M, Qian A, Wang W, Yue C: Molecular mechanisms regulating the effects of oxytocin on myometrial intracellular calcium. Adv Exp Med Biol 1998, 449: 277-286.
Thibonnier M, Conarty DM, Preston JA, Plesnicher CL, Dweik RA, Erzurum SC: Human vascular endothelial cells express oxytocin receptors. Endocrinology 1999, 140: 1301-1309.
Gutkowska J, Jankowski M, Lambert C, Mukaddam-Daher S, Zingg HH, McCann SM: Oxytocin releases atrial natriuretic peptide by combining with oxytocin receptors in the heart. Proc Natl Acad Sci USA 1997, 94: 11704-11709. 10.1073/pnas.94.21.11704
Paquin J, Danalache BA, Jankowski M, McCann SM, Gutkowska J: Oxytocin induces differentiation of P19 embryonic stem cells to cardiomyocytes. Proc Natl Acad Sci USA 2002, 99: 9550-9555. 10.1073/pnas.152302499
Boarder MR, Weisman GA, Turner JT, Wilkinson GF: G protein-coupled P2 purinoceptors: from molecular biology to functional responses. Trends Pharmacol Sci 1995, 16: 133-139. 10.1016/S0165-6147(00)89001-X
Mei Q, Liang BT: P2 purinergic receptor activation enhances cardiac contractility in isolated rat and mouse hearts. Am J Physiol Heart Circ Physiol 2001, 281: H334-H341.
Zheng JS, Christie A, De Young MB, Levy MN, Scarpa A: Synergism between cAMP and ATP in signal transduction in cardiac myocytes. Am J Physiol 1992, 262: C128-C135.
Diaz Brinton R, Brownson EA: Vasopressin-induction of cyclic AMP in cultured hippocampal neurons. Brain Res Dev Brain Res 1993, 71: 101-105.
de Wied D, Elands J, Kovacs G: Interactive effects of neurohypophyseal neuropeptides with receptor antagonists on passive avoidance behavior: mediation by a cerebral neurohypophyseal hormone receptor? Proc Natl Acad Sci USA 1991, 88: 1494-1498.
Freedman NJ, Lefkowitz RJ: Desensitization of G protein-coupled receptors. Recent Prog Horm Res 1996, 51: 319-351.
Chuang TT, Iacovelli L, Sallese M, De Blasi A: G protein-coupled receptors: heterologous regulation of homologous desensitization and its implications. Trends Pharmacol Sci 1996, 17: 416-421. 10.1016/S0165-6147(96)10048-1
Perry SJ, Baillie GS, Kohout TA, McPhee I, Magiera MM, Ang KL, Miller WE, McLean AJ, Conti M, Houslay MD, Lefkowitz RJ: Targeting of cyclic AMP degradation to beta 2-adrenergic receptors by beta-arrestins. Science 2002, 298: 834-836. 10.1126/science.1074683
Zhang M, Turnbaugh D, Cofie D, Dogan S, Koshida H, Fugate R, Kem DC: Protein kinase C modulation of cardiomyocyte angiotensin II and vasopressin receptor desensitization. Hypertension 1996, 27: 269-275.
Oakley RH, Laporte SA, Holt JA, Barak LS, Caron MG: Association of beta-arrestin with G protein-coupled receptors during clathrin-mediated endocytosis dictates the profile of receptor resensitization. J Biol Chem 1999, 274: 32248-32257. 10.1074/jbc.274.45.32248
Innamorati G, Sadeghi H, Birnbaumer M: Phosphorylation and recycling kinetics of G protein-coupled receptors. J Recept Signal Transduct Res 1999, 19: 315-326.
Karmazyn M, Manku MS, Horrobin DF: Changes of vascular reactivity induced by low vasopressin concentrations: interactions with cortisol and lithium and possible involvement of prostaglandins. Endocrinology 1978, 102: 1230-1236.
Noguera I, Medina P, Segarra G, Martinez MC, Aldasoro M, Vila JM, Lluch S: Potentiation by vasopressin of adrenergic vasoconstriction in the rat isolated mesenteric artery. Br J Pharmacol 1997, 122: 431-438.
Laugwitz KL, Ungerer M, Schoneberg T, Weig HJ, Kronsbein K, Moretti A, Hoffmann K, Seyfarth M, Schultz G, Schomig A: Adenoviral gene transfer of the human V2 vasopressin receptor improves contractile force of rat cardiomyocytes. Circulation 1999, 99: 925-933.
Hibert M, Hoflack J, Trumpp-Kallmeyer S, Mouillac B, Chini B, Mahe E, Cotte N, Jard S, Manning M, Barberis C: Functional architecture of vasopressin/oxytocin receptors. J Recept Signal Transduct Res 1999, 19: 589-596.
Bankowski K, Manning M, Haldar J, Sawyer WH: Design of potent antagonists of the vasopressor response to argininevasopressin. J Med Chem 1978, 21: 850-853.
Manning MSWH: Discovery, development, and some uses of vasopressin and oxytocin antagonists. J Lab Clin Med 1989, 114: 617-632.
Holmes CL, Patel BM, Russell JA, Walley KR: Physiology of vasopressin relevant to management of septic shock. Chest 2001, 120: 989-1002. 10.1378/chest.120.3.989
Thibonnier M, Coles P, Thibonnier A, Shoham M: Molecular pharmacology and modeling of vasopressin receptors. Prog Brain Res 2002, 139: 179-196.
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Holmes, C.L., Landry, D.W. & Granton, J.T. Science Review: Vasopressin and the cardiovascular system part 1 – receptor physiology. Crit Care 7, 427 (2003). https://doi.org/10.1186/cc2337
- adrenergic agents
- antidiurectic hormone
- cardiac inotropy
- nitric oxide
- potassium channels
- septic shock
- smooth muscle