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PubMed1993

At low dose, arginine vasotocin has vasopressor rather than vasodepressor effect in chickens.

It is widely accepted that both arginine vasopressin (AVP), and its avian analogue, arginine vasotocin (AVT) are vasopressor (VP) in mammals, but vasodepressor (VDP) in birds. The rat VP and chicken VDP assays were used to characterize neurohypophysial peptides and their analogues. However, these assays use pharmacological doses. Like AVP in mammals, AVT is secreted in birds during dehydration, when peripheral vasoconstriction rather than vasodilatation is needed. Mature White Leghorn cockerels with permanent cannulas in brachial artery and vein were put restrained in a sling. Mean arterial pressure (MAP); heart rate; and rectal, shank, skin, and comb temperatures were continuously recorded. The i.v. infusion regimen was: 1 hr of 0.05 ml/kg*min of saline followed by an hour of tested drug and another hour of saline. The drugs were: AVT, V1-agonist ([Phe2 Orn8]VT), and V2-agonist (DDAVP), in dosage of 50 pmol/kg*min each. AVT and to a lesser extent the V1-agonist increased MAP, caused bradycardia, and reduced thermal conductivity between core and skin or comb. The V2-agonist had no significant effect. Thus, at a low dosage AVT has a VP rather than a VDP effect. Bolus i.v. injection of 2 nmol AVT/kg caused an immediate and large drop in MAP accompanied by tachycardia which subsided within 20-30 sec. This was followed by a small rise in MAP and significant bradycardia. Bolus injection of 2 nmol/kg of either agonist had no hypotensive effect and only the V1-agonist caused the second-phase bradycardia.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1994

Atrial natriuretic peptide suppresses osmotically stimulated plasma arginine vasotocin levels in the Pekin duck.

Plasma arginine vasotocin (AVT) concentrations were measured at 15-min intervals in conscious Pekin ducks intravenously infused with 1 M saline at a rate of 0.5 ml/min for 1 hr. The responses were compared in eight birds, each given in random order a polyclonal antiserum against atrial natriuretic peptide (anti-ANP) or normal rabbit serum (control). The elevations in plasma osmolalities and sodium concentrations and the reductions in hematocrit values caused by the hypertonic saline were similar in both conditions. Plasma ANP in the control animals was elevated threefold during the saline infusion (from 66.8 +/- 8.8 pg/ml to a peak of 193.3 pg/ml), whereas in the same birds treated with specific antiserum, circulating ANP concentrations fell to less than 10 pg/ml and remained at this level for the duration of the experiment. Plasma AVT concentrations rose steadily and significantly from basal levels of 5.8 +/- 0.5 and 5.8 +/- 0.8 pg/ml in the control and anti-ANP groups, respectively; however, the concentrations measured in the birds with low plasma ANP were consistently higher (P < 0.02) than those under the control condition. Furthermore, the sensitivity of AVT release for the control birds (0.35 pg/ml per mOsm/kg) was significantly lower (P < 0.001) than that in the anti-ANP animals (0.86 pg/ml per mOsm/kg). Elevated plasma ANP may suppress osmotically stimulated AVT release during states of vascular volume expansion.

Animals↗

PubMed1994

Sites of action of arginine vasotocin in the nephron of the bullfrog kidney.

The nature and location of arginine vasotocin (AVT) V2-type receptors in the bullfrog kidney with respect to cellular 3',5'-cyclic monophosphate (cAMP) production in response to AVT were studied in microdissected segments of the nephron and urinary bladder. The basal levels of cAMP were similar in renal corpuscles, proximal, distal convoluted, and connecting tubules, and urinary bladder of normal bullfrogs. A marked dose-dependent increase in cAMP production by AVT occurred in preparations from both the connecting tubule and the urinary bladder. The minimum effective and half-maximal concentrations of AVT on the connecting tubule were about 100 nM and 2 microM, respectively. No activation by AVT was observed in renal corpuscles and proximal tubules. These results suggest that V2-type AVT receptors exist in the connecting tubule of the nephron and the urinary bladder. The lack of hormonal activation of cAMP production observed in some tissues may reflect either the total absence or the presence of minor amounts of hormonal receptors associated with the cAMP-generating system in bullfrog nephron segments.

Adenylyl Cyclases↗

PubMed1994

A radioimmunoassay for the determination of arginine vasotocin (AVT): plasma and pituitary concentrations in fresh- and seawater fish.

A specific radioimmunoassay was developed and characterized for the measurement of arginine vasotocin (AVT) in teleost fish. Specificity of the antibody for AVT was demonstrated by parallelism of a series of AVT standards with serially diluted pituitary and plasma extracts. Crossreactivity of the antibody with the other teleost neurohypophysial peptide, isotocin, was less than 1% and the sensitivity of the assay was 0.24 fmol/assay tube. AVT was extracted from plasma by reverse-phase liquid chromatography [efficiency of 87.6 +/- 9.3% (n = 5)] and demonstrated as an effective procedure for plasma volumes ranging from 0.4 to 1.2 ml. Plasma AVT concentrations measured in a range of euryhaline and stenohaline teleost fish were between 10(-12) and 2 x 10(-11) M (1-20 pg/ml). There were no consistent differences between plasma AVT levels in euryhaline fish (flounder, trout, and eel) adapted to fresh water (FW) and sea water (SW). In flounder, pituitary AVT levels in FW- and SW-adapted fish were also similar.

Adaptation, Physiological↗

PubMed1995

Urinary clearance of arginine vasotocin in Pekin ducks.

To quantify the renal excretion of arginine vasotocin (AVT) in birds, synthetic AVT was infused into conscious Pekin ducks at rates of 0.03, 0.10, and 0.30 ng/kg/min for 30 min and the relationships between plasma and urine AVT concentrations were monitored by radioimmunoassay. As plasma AVT concentrations increased (from a basal value of 7.8 +/- 1.1 pg/ml to levels of 11.5 +/- 1.9, 17.6 +/- 2.2, and 24.2 +/- 2.5 pg/ml, respectively) the urinary concentrations and excretion rates increased linearly from basal levels of 26.0 +/- 3.1 pg/ml and 14.9 +/- 1.8 pg/min to 215.6 +/- 36.6 pg/ml and 39.2 +/- 3.7 pg/min, respectively. The metabolic clearance rate of AVT (approximately 23 ml/min/kg) and urinary clearance (approximately 0.91 ml/min/kg) remained constant at each infusion dose and were therefore independent of plasma AVT levels. Over the range of plasma AVT concentrations tested, a constant fraction of about 5% of the AVT cleared from the blood was excreted intact in the urine.

Animals↗

PubMed1996

Changes in poly(A) tail length of arginine vasotocin messenger ribonucleic acid in the hypothalamus of water-deprived chickens.

The effects of water deprivation on the secretion of vasotocin (AVT) and expression of the AVT gene were studied in White Leghorn cockerels. Animals deprived of water for 4 days were compared with normally hydrated controls. Blood samples were obtained for measurements of plasma osmolality and AVT levels, and the hypothalamus was collected for extraction of total cellular RNA. A 519-bp AVT cDNA was prepared by reverse transcriptase-polymerase chain reaction and a 209-bp PstI/EcoRI restriction fragment from the 3' region of the fowl AVT cDNA was used as a probe for Northern blot analysis. Plasma osmolality and AVT levels in dehydrated birds were about 30 and 350% greater, respectively, than those in normally hydrated controls. The quantity of hypothalamic AVT mRNA was 2. 3-fold greater in water-deprived birds compared to controls. The size of the hypothalamic AVT transcript was about 100-bp longer in the water-deprived birds. As determined by RNase H treatment in the presence and absence of oligo(dT)12-18, the increase in mean size of the AVT mRNA in dehydrated animals was due to a longer poly(A) tract. Our results indicate that osmotic stress up-regulates expression of the AVT gene and increases the accumulation of AVT mRNA in the hypothalamus. This accumulation may, in part, be due to lengthening of the AVT mRNA poly(A) tail which is a general mechanism associated with stabilization of vertebrate mRNAs.

Animals↗

PubMed1996

Arginine vasotocin relaxation of gar (Lepisosteous spp.) hepatic vein in vitro.

The effects of arginine vasotocin (AVT) were examined in isolated gar arteries (afferent branchial, ABA; conus arteriosus, CA; ventral aorta, VA) and veins (hepatic, HV; intestinal; ovarian). AVT (10(-11) - 10(-7) M) had no effect in CA, produced contraction in ABA and VA and stimulated relaxation in veins. In precontracted HV, AVT relaxation was dose-dependent, long-lived (> 30 min) and reduced total tension by 49.0 +/- 10.7%. EC50s for AVT, arginine vasopressin, oxytocin, desmopressin, and isotocin in gar HV were 1.4 +/- 0.3, 3.6 +/- 0.2, 5.3 +/- 1.7, 11.0 +/- 6.5, and 19.0 +/- 0.4 nM, respectively. AVT was more potent compared with isotocin. Strength of relaxation (percentage decrease in total tension) of AVT and structural analogs was similar (range = 32.5 to 55%). Endothelium removal did not alter percentage relaxation or sensitivity to AVT in HV. AVT relaxation was not inhibited by nitric oxide synthase inhibitors or propranolol or reversed by addition of methylene blue but it was significantly enhanced by indomethacin (10(-5) M). Arginine vasopressin-receptor antagonists (V1- or V2-type selectivity; 10(-6) M) were equally effective inhibitors, each blocked 99% of AVT relaxation. Forskolin (10(-6) M) and papaverine (10(-4) M) relaxed precontracted gar arteries and veins. The adenylyl cyclase inhibitors SQ 22536 and MDL 12,330A (10(-5) M) produced transient contraction and stable relaxation, respectively, but did not inhibit AVT-induced relaxation in HV. Atrial natriuretic peptide (3 x 10(-8) M) and sodium nitroprusside (10(-4) M) had no effect in precontracted HV. AVT acts directly on gar venous smooth muscle cells via a nonclassical AVP receptor, possibly by increasing [cAMP]. AVT is a potent vasoconstrictor in vertebrate vasculature but produces a novel relaxation in gar veins.

Adrenergic beta-Antagonists↗

PubMed1996

Diurnal changes in plasma arginine vasotocin and isotocin in rainbow trout adapted to fresh water and brackish Baltic water.

The plasma levels of arginine vasotocin (AVT) and isotocin (IT) in rainbow trout (Oncorhynchus mykiss) were studied to assess possible diurnal variations in neurohypophysial nonapeptides. Fish were kept under natural photoperiod and adapted to fresh and brackish Baltic water. Blood was sampled at 5:00, 11:00, 16:00, 22:30, and again at 5:00. Hormones were determined by gradient high-performance liquid chromatography preceded by solid-phase extraction. The marked diurnal changes of AVT were detected in plasma of fish adapted to both fresh and brackish waters. AVT levels (fmol/ml) were maximal at 16:00 and minimal at 5:00 (253.4 +/- 35.7 and 45.5 +/- 17.3, respectively). Unlike AVT, isotocin levels displayed no diurnal changes. AVT concentrations at 11:00, 16:00, and 22:30 were significantly higher than IT values measured throughout the day. Plasma AVT concentrations determined in brackish water-adapted fish at 16:00 were significantly lower than those of freshwater-adapted fish at the same time. These data suggest that synthesis and/or release of AVT and IT are controlled independently, so that these nonapeptides have different physiological roles in teleost fish. AVT might participate in circadian time-keeping system in fish.

Adaptation, Physiological↗

PubMed1997

Changes in plasma arginine vasotocin (AVT) concentration and dorsal aortic blood pressure following AVT injection in the teleost Platichthys flesus.

Dorsal aortic blood pressure and plasma arginine vasotocin (AVT) concentrations have been assessed in free swimming, chronically cannulated flounder following AVT injection. Intraarterial AVT at doses of 4.76 x 10(-12) mol.kg-1 and greater caused a biphasic change in blood pressure (an initial fall followed by a sustained pressor response). Doses above 4.76 x 10(-12) mol.kg-1 were associated with plasma AVT concentrations (20 min after injection) 2-3 orders of magnitude greater than the physiological range and must be considered pharmacological. Injection of the lowest pressor AVT dose (4.76 x 10(-12) mol.kg-1), 20 min after injection, increased plasma AVT concentrations to 23.4 +/- 6.1 fmol x ml-1. This increase is close to plasma AVT concentrations recently reported in untreated fish; however, in the initial period after injection plasma levels were calculated to be considerably higher than the physiological range. These results confirm that AVT is pressor in flounder but suggest that the pressor response may occur only at circulating AVT levels above the normal physiological range. The biphasic response to AVT and the differing responses to mammalian V1 and V2 type receptor agonists in the current work suggests that AVT may contribute to regional blood flow distribution in teleosts rather than blood pressure regulation.

Animals↗

PubMed1997

Arginine vasotocin gene expression and secretion during osmotic stimulation and hemorrhagic hypotension in hens.

In chickens, hyperosmolality stimulates the secretion of vasotocin (AVT) and up-regulates hypothalamic AVT gene expression. Hemorrhage, on the other hand, has not been considered an effective stimulus for AVT release in this species. The effects of acute osmotic stress and prolonged hemorrhagic hypotension on AVT gene expression and secretion were studied in White Leghorn hens. Conscious hens were osmotically stimulated by administering a single ip injection of 3 M NaCl (5 ml/kg). Urethane-anesthetized hens were bled to a mean arterial pressure of 80-90 mm Hg and the pressure was maintained within this range by additional bleeding. A total of about 30% of the estimated blood volume was removed. Both experiments were terminated after 1 hr of stimulation. Plasma AVT levels in the hyperosmotic and hypovolemic hens were 4- and 2-fold higher, respectively, compared to controls. Hypothalamic AVT mRNA levels, detected by Northern blot analysis, were 2.5- and 2-fold higher in the osmotically stimulated and hypotensive groups, respectively, compared to control groups. As determined by in situ hybridization, both osmotic stimulation and hypovolemia resulted in an increase in the number of AVT mRNA-containing neurons in the supra-optic and paraventricular nuclei. Our results indicate that, under the conditions used, hypotension and hyperosmolality are equally effective in stimulating AVT gene expression and secretion of AVT.

Animals↗

PubMed1998

Vasotocin and vasoactive intestinal polypeptide modulate aggression in a territorial songbird, the violet-eared waxbill (Estrildidae: Uraeginthus granatina).

Previous research demonstrates that intraseptal administrations of arginine vasotocin (AVT) inhibit male aggression in the territorial field sparrow (Emberizidae: Spizella pusilla) but facilitate aggression in the colonial zebra finch (Estrildidae: Taeniopygia guttata). In order to determine whether this difference may be related to the territorial and colonial social organizations of these two species, the effect of AVT infusions was examined in a territorial Estrildid species, the violet-eared waxbill (Uraeginthus granatina). This species is more closely related to the zebra finch than to the field sparrow and shares most critical features of breeding ecology in common with zebra finches, but differs in social organization. AVT infusions administered via chronic guide cannulae directed at the septum significantly inhibited aggressive behavior, consistent with results in the territorial field sparrow, supporting the hypothesis that social organization is correlated with AVT function. Similar experiments with mesotocin and substance P produced no effects on any of the behaviors measured, but infusions of vasoactive intestinal polypeptide (VIP) significantly facilitated aggression. This result contrasts with the inhibitory effect of septal VIP obtained in the colonial zebra finch, suggesting that VIP function may be correlated with social organization as well.

Aggression↗

PubMed1999

Pharmacological characterization of arginine vasotocin vascular smooth muscle receptors in the trout (Oncorhynchus mykiss) in vitro.

Arginine vasotocin (AVT) is present in the neurohypophysis of all nonmammalian vertebrates and it appears to be the antecedent of the neurohypophysial nonapeptide hormones. Relatively little is known about AVT receptors in lower vertebrates, especially fish, and the present study was designed to examine AVT receptor interactions in trout vascular and nonvascular smooth muscle in vitro. AVT produced dose-dependent contraction of isolated rings from celiacomesenteric, coronary, and efferent branchial arteries, ventral aorta, anterior cardinal vein, and strips of ductus Cuvier. The greatest efficacy (magnitude of contraction per unit tissue weight) and sensitivity (effective concentration for half-maximal response, EC50) to AVT was found in the efferent bronchial artery (EBA) and its receptors were characterized further. Other neurohypophysial peptides, including arginine vasopressin (AVP), lysine vasopressin (LVP), isotocin (IST), and oxytocin (OXY), contracted EBA with an efficacy order of (most to least) AVT = AVP = OXY > LVP > IST and a sensitivity order of AVT > OXY >/= AVP > IST > LVP. Neither Desmopressin, an AVP V2-receptor agonist, nor the AVP ring fragment, AVP4-9, contracted EBA nor did they inhibit AVT contraction. Pretreatment of EBA rings with the selective AVP V1-receptor antagonists (deamino-Pen1, O-Me-Tyr2, Arg8-vasopressin and deamino-Pen1, Val4, Arg8-vasopressin), the selective V2-receptor antagonist (adamantaneacetyl1, O-Et-D-Tyr0, Val4, aminobutyryl6, Arg8,9-vasopressin), or the combined V1-oxytocin receptor antagonist (d(CH2)5[Tyr(Me)2, Orn8-AVT]) competitively inhibited AVT contractions without affecting AVT efficacy. Receptor affinity constants (pA2) determined by Schild analysis were in the range of 6.8-7.3, with slightly higher constants for the AVP V1-/oxytocin receptor antagonists than for the selective V2-receptor antagonist. Endothelium removal had no effect on EBA sensitivity to AVT. EBA rings were an order of magnitude more sensitive to AVT than nonvascular gastrointestinal and urinary bladder smooth muscle rings or strips. However, AVT (10(-7) M) was as efficacious as acetylcholine (10(-5) M) in gastrointestinal, gallbladder, and urinary bladder smooth muscle. It is concluded that trout EBA possess an AVT smooth muscle receptor that shares a similar pharmacological profile with the mammalian vascular AVP V1a-receptor and the OXY-receptor, but it is distinct from the previously reported gill epithelial cell receptor.

Acetylcholine↗

PubMed2000

A sexual dimorphism in hypothalamic arginine vasotocin (AVT) gene expression and AVT plasma levels in the Japanese quail (Coturnix coturnix japonica) in response to water deprivation.

To examine a possible sexual dimorphism in the osmotic control of arginine vasotocin (AVT) release in birds, age-matched male and female Japanese quail were subjected to water deprivation. The observed increased plasma osmolalities were accompanied by increased plasma AVT levels. Plasma mesotocin levels did not change with water deprivation. The sensitivity of the osmotic control of AVT release as determined by the slope of the relationship between plasma AVT levels and plasma osmolalities was significantly (P < 0.05) higher in males than in females. By Northern blot analysis, levels of hypothalamic AVT gene transcripts were increased 2.3 +/- 0.14- and 3.5 +/- 0.13-fold in water-deprived male and female Japanese quail, respectively, compared to normally hydrated birds. Our data suggest gender-related differences in the osmotic control of AVT release and in hypothalamic AVT gene expression in the Japanese quail.

Animals↗

PubMed2000

Sexual dimorphism in numbers of vasotocin-immunoreactive neurons in brain areas associated with reproductive behaviors in the roughskin newt.

Vasotocin (VT) and vasopressin control many endocrine and neuroendocrine functions, including the regulation of reproductive behaviors. In the roughskin newt (Taricha granulosa), VT administration can enhance courtship behaviors in males and egg-laying behaviors in females. This study used immunohistochemistry to investigate whether there are sex differences in VT in specific brain areas, and whether these differences persist in nonbreeding animals. Numbers of VT immunoreactive (ir) cell bodies were counted in males and females collected in February, April, June, and August. Radioimmunoassay of plasma samples confirmed that testosterone and 5alpha-dihydrotestosterone concentrations were higher in males than females, and that 17beta-estradiol concentrations were higher in females than males. In 11 brain areas, no sexual or seasonal differences in the number of VTir cells were found. But in 3 brain regions-the bed nucleus of the stria terminalis (BNST), the nucleus amygdalae dorsolateralis (AMYG), and the anterior preoptic area (aPOA)-there were significantly greater numbers of VTir cells in males than in females, and these differences did not change seasonally. In the aPOA, an area important to male sex behaviors, the sexual dimorphism in VTir was particularly pronounced. In four brain regions, there were significantly greater numbers of VTir cells in females than males, but only in specific seasons. In April-collected (breeding) animals, more VTir cells were found in females than in males in the populations of VT cells within the pars dorsalis hypothalami and ventromedial hypothalamus, brain regions frequently associated with stress responses and female mating behaviors. In August-collected (nonbreeding) animals, more VTir cells were found in females than in males, in the region of the bed nucleus of the decussation of the fasciculus lateralis telencephali and in the nucleus visceralis superior, nucleus isthmi region. Significantly greater numbers of VTir cells were observed in the magnocellular preoptic area of males and females collected in February. These results indicate that the functional interactions between gonadal steroid hormones and VT are complex and appear to involve site-, sex-, and season-specific regulatory mechanisms. Furthermore, it seems likely that populations of VT neurons in the BNST, AMYG, and aPOA are involved in regulating male-specific behaviors, and that the VT neurons in the pars dorsalis hypothalami/ventromedial hypothalamus may be involved in female-specific behaviors.

Animals↗

PubMed2000

The effects of highly selective opioid receptor antagonists on the release of arginine vasotocin induced by hyperosmotic stimulation and angiotensin II injection.

The effects of highly selective antagonists to mu-, delta-, and kappa-opioid receptor subtypes on hyperosmotic- or angiotensin II (AII)-induced arginine vasotocin (AVT) release were investigated in chicks. Plasma levels of AVT increased about 1.5-fold after the administration of 1.5 M NaCl (200 microl, ip) or 100 ng AII (5 microl, icv). The administration of the mu-antagonist naloxonazine and the kappa-antagonist nor-Binaltorphimine further elevated plasma levels of AVT stimulated by hypertonic NaCl or AII. These effects of mu- and kappa-opioid receptor antagonists on AVT release were dose dependent. Nor-Binaltorphimine enhanced hyperosmotically stimulated plasma levels of AVT at a lower dose than that of naloxonazine. Conversely, the delta-selective antagonist naltrindole did not significantly affect AVT secretion. None of the opioid receptor antagonists influenced basal plasma levels of AVT. Therefore, these results suggest that mu- and kappa-opioid receptors are involved in hyperosmotic- and AII-induced AVT release, and the effect of the kappa-opioid receptor antagonist in the AVT release stimulated by hyperosmolality is strong compared to that of the mu-opioid receptor antagonist.

Angiotensin II↗

PubMed2001

Behavioral and hormonal effects of exogenous vasotocin and corticosterone in the green treefrog.

Vasotocin (AVT) promotes courtship in a wide range of vertebrates. However, this effect is not independent of steroid hormones. For example, androgens may work in concert with AVT and corticosterone (CORT) may work to oppose AVT action. In frogs, AVT promotes calling, and in some species, CORT inhibits calling. In addition, androgens are known to modulate AVT in the brain, and CORT may depress androgen secretion. Previous work in amphibians has suggested that AVT promotes courtship by overcoming a CORT-mediated stress response. Possible behavioral and hormonal interactions among AVT, CORT, and androgens were investigated in wild, free-living green treefrogs (Hyla cinerea). Saline, AVT, CORT, or a combination of AVT and CORT were administered to calling males, and several measures of spontaneous calling were evaluated for 1.5 h following injection. Plasma testosterone, dihydrotestosterone, and CORT were also measured. Saline-injected males had low CORT levels, and AVT and CORT injection elevated plasma CORT levels. AVT increased the likelihood of calling, but, in males who did call, AVT did not influence latency to call or how often they were observed calling. Very few saline-injected males resumed calling after injection, and therefore a CORT effect was only detectable in AVT-injected males. CORT inhibited calling in AVT-injected males only at the highest dose of CORT (40 microg); lower levels of CORT were unsuccessful at inhibiting AVT-induced calling. AVT appeared to have a specific effect on calling motivation. Further, the data suggest that disinhibition of a CORT response is not the primary mechanism by which AVT increases calling. In addition, CORT injection reduced endogenous androgen levels. Finally, endogenous androgens were negatively correlated with latency to begin calling, suggesting that they may have a positive effect on calling. These data indicate that AVT has positive effects on calling but provide only weak evidence that CORT inhibits courtship in this species.

Animals↗

PubMed2001

Cloning and characterization of an arginine vasotocin receptor from the euryhaline flounder Platichthys flesus.

A sequence coding for an arginine vasotocin (AVT) receptor has been identified by the screening of a hepatic cDNA library from the teleost Platichthys flesus. The 2701-bp receptor sequence is predicted to yield a 384-amino acid peptide, analysis of which indicates a seven-transmembrane spanning sequence typical of G-protein-coupled receptors with the N terminus on the outer surface of the cell membrane. Sequence analysis showed this sequence to have a high homology with the Catostomus commersoni AVT receptor (76%) and mammalian vasopressin V(1)-type receptor (62%), but only 55% homology with the C. commersoni isotocin receptor. A two-electrode voltage clamp was used to characterize the receptor expressed in Xenopus laevis oocytes. AVT induced an inward current which was dose dependent over the range 16.7 fmol to 5 pmol; isotocin was without effect over the same dose range. The mammalian vasopressin V(1)-type receptor agonist ([Phe(2), Orn(8)] oxytocin)() induced an inward current but was less potent than AVT, whereas the mammalian vasopressin V(2)-type receptor agonist ([Deamino(1), Val(4), D-Arg(8)] AVP) was without effect. Injection of oocytes with heparin or BAPTA suppressed the response to AVT, indicating receptor linkage to the phospholipase C-phosphatidylinositol pathway. Northern analysis demonstrated the presence of this AVT receptor mRNA in the brain, kidney, and gill of flounder.

Amino Acid Sequence↗

PubMed2002

Plasma concentrations of arginine vasotocin and urotensin II are reduced following transfer of the euryhaline flounder (Platichthys flesus) from seawater to fresh water.

Plasma concentrations and stored levels of the neuroendocrine peptides arginine vasotocin (AVT) and urotensin II (UII) were measured in the euryhaline flounder (Platichthys flesus) following the acute hypo-osmotic challenge of direct seawater (SW) to fresh water (FW) transfer. Hormone measures, plasma osmolality, and ion concentrations and tissue water content were determined 1, 4, 8, 24, 72, and 144 h after transfer. Plasma AVT concentration fell initially following FW transfer but then returned toward pretransfer levels by day 6. Plasma UII concentration decreased while urophysial UII content was increased following hypo-osmotic challenge relative to SW time-matched controls, suggesting down regulation of the UII system during the initial stages after FW transfer. These changes in neuroendocrine activity were associated with a significant fall in plasma osmolality and major plasma ions. Positive correlations were observed between plasma AVT and osmolality and Cl- and Mg2+ concentrations, suggesting functional association of these plasma parameters with AVT action and/or control of AVT secretion. The initial response to hypotonic challenge involves reduced plasma AVT and UII levels consistent with the proposed role for these hormones, supporting flounder osmoregulation in hypertonic media.

Animals↗