Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P01178 (oxytocin)
 15,767 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Intraventricular injection of arginine-8-vasopressin and its analogues vasotocin and lysine-8-vasopressin into rat brain evoked a special rotational behavior resembling somatostatin-induced barrel rotation [1]. Oxytocin and oxypressin were less active while vasopressin fragments had no effect. Vasopressin-induced barrel rotation was accompanied by pathological symptoms indicating a disturbance of muscle tone regulation and is considered to be a non-specific and toxic effect. This rotational behavior was not prevented by atropine, propranolol, phentolamine, methylsergide or haloperidol but was reduced by chlorpromazine, probably due to the latter's muscle relaxing activity.
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PMID:Barrel rotation induced by vasopressin and related peptides in rats. 56 83

The administration of 5 I. U. oxytocin (by quick infusion) or of 5 I. U. vasopressin-lysine (intramuscularly) to healthy subjects was followed by a significant decrease in the plasma non-esterified fatty acid level. We regard this as evidence of inhibition of basal lipolysis in the adipose tissue. Vasopressin also completely blocked an increase induced in the plasma non-esterified fatty acid level by activating hormone-sensitive lipase in the adipose tissue by the infusion of 0.5 mg noradrenaline.
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PMID:Inhibition of lipolysis by oxytocin and vasopressin. 61 48

Low doses of arginine-vasotocin (AVT), isotocin and oxytocin (1 pg-1 ng/kg body weight) were antidiuretic in eels adapted to fresh water but not in those adapted to sea-water. High doses (more than 10 ng/kg) were always diuretic. No effects on tubular water reabsorption were observed and the glomerular filtration rate (GFR) was proportional to the maximum reabsorptive rate for glucose (Tm(glucose)) in eels adapted to sea-water. Increases in urinary flow appeared therefore to result from glomerular recruitment. Infusion of AVT or isotocin at low rates reduced the GFR and urinary flow of freshwater eels to the levels found in seawater eels. Vasopressin (lysine or arginine) had no direct effect on kidney function in freshwater eels but blocked both the diuretic and antidiuretic actions of the other hormones. When infused into seawater eels it was diuretic. This effect could have been due to blockade of the actions of endogenous AVT and/or isotocin.
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PMID:Neurohypophysial hormonal control of kidney function in the Furopean eel (Anguilla anguilla L.) adapted to sea-water or fresh water. 62 24

Vasopressin and oxytocin pathways were specifically localized in glutaraldehyde-paraformaldehyde fixed rat brains, with the use of the unlabelled antibody enzyme method and purification of the first antiserum. Vasopressin and oxytocin containing pathways were traced from the paraventricular nucleus towards the dorsal and ventral hippocampus, the nuclei of the amygdala, substantia nigra and substantia grisea, nucleus tractus solitarius, nucleus ambiguus and to the substantia gelatinosa of the spinal cord. In addition, a vasopressin containing pathway between the suprachiasmatic nucleus and the lateral habenular nucleus was demonstrated. The possible nature (axons or dendrites) and role of these extrahypothalamic fibres is discussed in relation to water balance, milk ejection and avoidance behaviour.
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PMID:Intra- and extrahypothalamic vasopressin and oxytocin pathways in the rat. Pathways to the limbic system, medulla oblongata and spinal cord. 69 26

1. In hepatocytes from starved rats, vasopressin, angiotensin (angiotensin II) and oxytocin stimulated gluconeogenesis from lactate by 25--50%; minimal effective concentrations were about 0.02pM, 1 nM and 0.2 nM respectively. 2. Vasopressin and angiotensin also stimulated gluconeogenesis from alanine, pyruvate, serine and glycerol. EGTA decreased gluconeogenesis from these substrates. 3. Hormonal stimulation of gluconeogenesis from lactate was abolished in the absence of extracellular Ca2+. 4. Insulin did not prevent stimulation of gluconeogenesis by vasopressin or angiotensin. 5. The potency of the stimulatory effects of vasopressin and angiotensin on hepatic gluconeogenesis suggests they are operative in vivo. Also, the data suggest that Ca2+ plays a role in the stimulation by these hormones.
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PMID:Stimulation by vasopressin, angiotensin and oxytocin of gluconeogenesis in hepatocyte suspensions. 74 59

Visualized by immunocytochemistry vasopression and neurophysin are observed in perikarya of the supraoptic and paraventricular nuclei and their fibers going to the neurohypophysis. In addition to these classical sites, vasopressin and neurophysin are located in perikarya of the organum vasculosum of the lamina terminalis and of the suprachiasmatic nuclei. Outside the hypothalamus, neurophysin-positive perikarya are found in the triangular nucleus of the septum which is a part of the limbic system. Vasopressin and neurophysin are contained in two types of extrahypothalamic fibers. Large caliber fibers are found in the amygdala, small caliber fibers in the septum and thalamus. The presence of neurosecretory perikarya and fibers outside the hypothalamus may be related to psychotropic effects of peptide hormones.
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PMID:Demonstration of extrahypothalamic peptide secreting neurons. A morphologic contribution to the investigation of psychotropic effects of neurohormones. 79 99

Vasopressin, other neurohpophyseal peptides and certain of their fragments can affect central nervous system function. Cyclo(Leu-Gly), formally derived from the C-terminal dipeptide of oxytocin, is also active in memory processes. This molecule, radioactively labeled for this study, was found to be resistant to enzymatic degradation both in vivo and in vitro. Furthermore, after its intravenous application in cat, it easily penetrated into cerebrospinal fluid. This indicates that cyclo(Leu-Gly) can readily pass from blood into the central nervous system to exert it's central pharmacological actions. Thus, labeled cyclo(Leu-Gly) is a valuable model for studying the distribution and localization of peptides which have activity in the central nervous system.
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PMID:An enzymatically stable peptide with activity in the central nervous system: its penetration through the blood-CSF barrier. 83 26

The effects of hormone binding on the reversible monomer in equilibrium dimer equilibrium of bovine neurophysins I or II in solution have been studied by sedimentation equilibrium measurements performed in conjunction with equilibrium dialysis experiments. Under normal solution conditions saturating amounts of oxytocin displace the neurophysin dimerization equilibrium toward the associated form of the protein to give a dimeric complex with two oxytocin molecules bound per dimer. Vasopressin exerts different influences on this oligomerization process. At low fractional saturation this ligand exhibits a behavior similar to oxytocin with a higher affinity for the neurophysin dimer than the monomer. But in contrast, at higher fractional saturation, vasopressin strongly displaces the aggregation equilibrium toward a monomeric complex bearing two vasopressin molecules. However, in the presence of a high concentration of LiCl two oxytocin molecules are bound per neurophysin protomer (10,000 daltons). These observations, together with earlier data for vasopressin binding, suggest that each neurophysin molecule possesses two structurally distinct hormone binding sites. These observations can be rationalized in a simple schematic model of hormone binding to neurophysin in which oxytocin favors a dimeric form with one hormone binding site available per 10,000 daltons while vasopressin favors the monomeric form with two hormone binding sites available per 10,000 daltons.
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PMID:Interactions of oxytocin and vasopressin with bovine neurophysins I and II. Effects of hormone binding on the protein quaternary structure: a simple model. 93 15

Vasopressin and oxytocin were measured by radioimmunoassay in rat posterior pituitary and microdissected hypothalamic areas after 3 and 10 days of oral 2 percent sodium chloride in place of drinking water. There was a significant decrease in concentration of both hormones in posterior pituitary and in specific areas of the hypothalamus. Supraoptic, paraventricular, and arcuate hypothalamic nuclei and the retrochiasmatic area had decreased concentration of one or both hormones following hypertonic saline, while hormone concentration in the suprachiasmatic nucleus and median eminence was unaffected.
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PMID:Vasopressin and oxytocin are depleted from rat hypothalamic nuclei after oral hypertonic saline. 93 63

Vasopressin (VP) can be shown to exert psychotropic effects independent of its antidiuretic activity, facilitating learning and consolidation of memory in rats. Immunoreactive VP and neurophysin (NP) are localized on serial section of Bouin fixed, paraffi embedded guinea pig, rat and hamster brains. Localization was not restricted to the classical sites of supraoptic and paraventricular nucleus, medianeminence and neurohypophysis...
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PMID:[Proceedings: Psychotropic effects of hypothalamic hormones: immunohistochemical indentification of extrahypophyseal connections of neuroendocrine neurons]. 98 14


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