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Physiological control of melatonin synthesis and secretion: mechanisms, generating rhythms in melatonin, methoxytryptophol, and arginine vasotocin levels and effects on the pineal of endogenous catecholamines, the estrous cycle, and environmental lighting.

Daily rhythms in pineal methoxyindole metabolism have been described in rodents and humans: serotonin levels in rat pineals are highest during the daylight hours and fall markedly soon after the onset of darkness, coincident with increases in the levels of pineal melatonin and 5-methoxy-tryptophol and the activities of pineal serotonin-N--acetyltransferase (SNAT) and hydroxyindole-O-methyltransferase (HIOMT). The fact that the levels of melatonin and 5-methoxytryptophol vary in parallel suggests that the major factor generating the methoxyindole rhythms is not SNAT activity, as has been suggested, but a proximal step, perhaps a change in the availability (for metabolism) of "stored" serotonin. Melatonin levels in human serum and urine exhibit rhythms similar to those observed in rats, i.e., they rise sharply during the daily dark period. When the onset of darkness is delayed by 12 hours, human melatonin rhythms usually require 3 or 4 days to adjust to the new lighting regimen. Environmental factors, other than light, that activate the sympathetic nervous system or cause epinephrine to be secreted from the adrenal medulla (e.g., the stress of immobilization; insulin-induced hypoglycemia) can override the inhibitory effects of light and accelerate melatonin synthesis. Melatonin levels in rat blood and urine are lowest during the proestrous and estrous phases of the estrous cycle. Although this effect of the ovarian steroid hormones is accompanied by a reduction in urinary norepinephrine levels, it is not caused simply by a decrease in the quantity of norepinephrine acting on the pineal but also involves a direct action of the hormones. Ovariectomy increases serum melatonin levels, whereas the administration of estradiol plus progesterone (to ovariectomized animals) lowers melatonin levels. The spectral and intensity-response characteristics of the photic inhibition of melatonin synthesis have been established for the rat. Rhythms in melatonin synthesis apparently persist among animals placed in environments of continuous darkness; the source of the cyclic signal (mediated by the pineal sympathetic nerves) has not yet been identified. Preliminary evidence suggests that levels of a peptide hormone, arginine vasotocin, in rat pineals and sera also exhibit daily rhythms and are increased by norepinephrine.

Animals↗

[Phylogeny of neurohypophyseal hormones in birds: microidentification of mesotocin and vasotocin in the ostrich (Struthio camelus)].

Ostrich (Struthio camelus) neurohypophysial hormones have been isolated from 5 freeze-dried posterior pituitary glands. Purification has involved three steps: a first molecular sieving on Sephadex G-75 for eliminating proteins, a second molecular sieving on Bio-Gel P4 for separating the two active principles and a high pressure reverse-phase liquid chromatography (HPLC) on Nova-Pak C 18 with an 10 mM acetate-acetonitrile gradient for isolating each hormone. The active peptides have been identified by their retention time in HPLC and their amino acid composition. Mesotocin and vasotocin have thus been characterized. Although the phylogeny of Ratites is disputed, in particular their possible common origin with Carinates, which include most of the living birds, species of the first sub-class seem to have the same neurohypophysial hormones as those of the second.

Animals↗

Tentative identification of arginine vasotocin in the bovine pineal extract prepared by in the bovine pineal extract prepared by the Milcu-Nanu method.

The bovine pineal extract prepared by the Milcu-Nanu method (BPE-MN) has frog bladder, rat antidiuretic and rat uterine activities susceptible to tryptic digestion. The ratios of these activities are characteristic of arginine vasotocin (AVT). Desalting on Amberlite CG25 and partial purification of BPE-MN by free-flow continuous electrophoresis (FFCE) allow the separation of some fractions with AVT-like biological activities and with a carrier-free electrophoretic mobility similar to the synthetic AVT. The results strongly suggest the presence of AVT in the bovine pineal extract prepared by the Milcu-Nanu method.

Animals↗

Vasotocin release from the pineal gland of newborn mammals: the involvement of GABA mechanisms.

The arginine vasotocin (AVT) levels were bioassayed in the pineal extracts from 20-day-old kittens and from 10-day-old rat pups and in the cerebrospinal (CSF) samples taken from 20-day-old kittens. The animals received daily (between the postnatal day 2 and the day of sacrifice) the selective GABA receptor antagonist picrotoxin (5 X 10(-7) mg) or the specific GABA agonist valproic acid (10(-5) mg). Picrotoxin was found to produce a decrease of the pineal AVT levels in newborn kittens and rats, and an increase of the AVT amount of the CSF samples from kittens. Valproic acid had opposite effects, producing an increase of pineal AVT in both species and a decrease of AVT levels in the kittens CSF samples below the sensitivity limit of the bioassay method. The result suggests that not only in adult, but also in newborn mammals, the inhibitory feed-back loop between the brain and the pineal gland is GABA-mediated and that the GABA-ergic mechanisms are involved in regulating the release of AVT from the pineal gland.

Animals↗

Extrahypothalamic distribution of vasotocin-immunoreactive fibers and perikarya in the avian central nervous system.

Immunohistochemical analysis of the extrahypothalamic distribution of vasotocin-like immunoreactive elements within the central nervous system of the domestic fowl and Japanese quail, revealed several mesencephalic, pontine and bulbar target areas topographically identifiable. Extrahypothalamic immunopositive perikarya were observed in diencephalic and mesencephalic locations after glutaraldehyde fixation.

Animals↗

Immunohistochemical study of the distribution of vasotocin reacting neurons in avian diencephalon.

Vasotocin (VT)- and neurophysin (NPH)-containing neurons were immunocytochemically demonstrated in the diencephalon of the Japanese quail (Coturnix coturnix japonica), domestic fowl (Gallus gallus), and Pekin duck (Anas platyrhynchos). In these three avian species, the immunoreactive cells are similarly distributed into three different diencephalic regions: lateral (L), periventricular (P), and dorsal diencephalic (DD). A different number of cell clusters can be easily identified in each region according to its topographical location. Interspecific differences depend on the total number of immunoreactive cells, the cell sizes and the density in each cell cluster. Present results show that the nomenclature of the VT-system originally proposed for the pigeon can be easily applied to all the avian species so far topographically studied. The group nomenclature based only upon the location of immunoreactive elements may avoid potentially inaccurate mammalian homologies, and makes easier the comparison between studies performed in different birds.

Animals↗

REM sleep rebound after its suppression by vasotocin in cats.

Extremely small amounts (10(-4) pg) of synthetic arginine vasotocin (AVT) injected into the pineal recess of unanesthetized cats induced a continuous NREM sleep for about 60 minute and completely suppressed REM sleep for about 5 hours. The reappearance of the REM sleep following AVT administration occurred with a marked rebound, lasting for more than one hour. Since neither vasopressin nor oxytocin, at the same doses, were able to affect significantly the REM sleep, it is concluded that AVT is specifically involved in the modulation and/or circadian organization of the REM sleep.

Animals↗

Vasotocin involvement in the maturation of the rat brain.

In order to investigate the effects of arginine vasotocin (AVT), (a pineal nonapeptide hormone) on the brain maturation, the sleep-wake cycle, the day of eyelids opening and the total brain lipids level were followed up in new-born rats receiving daily (between day 2 and 8 of life) 100 ng of synthetic AVT, arginine-vasopressin (AVP), oxytocin (OT) or 0.1 ml saline solution. While AVP and OT had no effect, AVT induced: 1) an increase in the amount of active sleep (AS); 2) a decrease in the brain weight and the total brain lipids, and 3) a delay in the eyelids opening. These findings demonstrate that chronic administration of AVT induces a delay in the brain maturation of the new-born rats. Association of low brain lipids with a high percentage of AS is a very useful index of brain maturation. It is suggested that the drop in the endogenous brain levels of AVT below a critical threshold might represent a hormonal signal for triggering the beginning of brain maturation in mammals.

Age Factors↗

[Immunocytochemical characterization of neurosecretory systems producing mesotocin and vasotocin in the brain of several Lacertidae].

Using immunofluorescent techniques vasotocin (VT) and mesotocin (MT) neurosecretory systems were identified in the brain of Lacertidae: one european species and of two south-algerian species. In the 3 species MT and VT was shown to be synthetized in specific neurons located in the anterior preoptic area (POA), the supraoptic (SON) and in the paraventricular (PVN) nuclei. The axons originating in SON and PVN were ending either in the external zone of the rostral median eminence (ME) near to the adenohypophysial portal vessels, or in the neural lobe. In Lacerta muralis the neurosecretory axons of the POA terminated in the vicinity of the vascular organ of the lamina terminalis (OVLT), while in the two desertic species several additional fibers extended more rostrally toward the olfactory peduncle (PO). A short exposure to cold (+ 4 degrees C) of some specimens of Lacerta muralis induced a differential response in the dorsal and ventral parts of the NPV, respectively. Whereas the dorsal part remained unchanged, the ventral part, instead appeared then of essentially composed of small neurons void of secretory granules. Cold exposure also led to a marked accumulation of both MT and VT in the internal zone of the ME, and of VT only, in the external ME zone. On the other hand, a conspicuous amount of MT appeared in adenohypophysial cells.

Animals↗

[Effect of lysyl vasopressin and vasotocin on a disorder of the conditioned avoidance reaction by a serotonin receptor blockader].

A study was made of the effect of systemic injection of lys8-vasopressin (LVP) and Arg8-vasotocin (AVT) on avoidance reaction in male rats. Both the compounds had no appreciable effect on the rate of the formation. However, in the presence of learning disorders induced by cyproheptadine. LVP completely and AVT partially recovered the normal time course of learning.

Acoustic Stimulation↗

Effect of delta sleep inducing peptide (DSIP) and arginine vasotocin (AVT) on sleep and motor activity in the rat.

The effect of Delta Sleep Inducing Peptide (DSIP) and arginine vasotocin (AVT) on motor activity and sleep was investigated in the rat. Motor activity was not significantly reduced during the 24 h following systemic DSIP administration (40-160 nmol/kg i.p.), nor were sleep and the power of the EEG delta-band significantly increased in the 2 hours following injection or infusion of DSIP into the lateral or third ventricle (7-24 nmol). Injection or infusion of AVT into the lateral or third ventricle (10(-15)-10(-19) mol) did not enhance sleep and the power of the EEG delta-band. Nevertheless, the following significant effects indicate an unspecified biological action of the peptides: Dark-time motor activity was reduced 1 and 2 days after DSIP administration (160 nmol/kg), and the activity in the first 4 h after injection (80 nmol/kg) was increased. In addition, the power in the delta-band was reduced after administration of DISP (7 nmol) and AVT (10(-17) mol) into the third ventricle. Thus exceedingly small doses of AVT seem to exert not only endocrine, but also electrophysiological effects. It is concluded that neither DSIP nor AVT qualify as a specific sleep-promoting substance.

Animals↗

Vasotocin effects in depressive patients with eating disorders.

Since arginine vasotocin (AVT) effects are mediated by serotonin, which was involved in the production of eating disorders, disorders which show many common mechanisms with the depressive disorders, and since AVT was used as treatment of depressive disorders, we investigated the AVT effects in a double-blind study with patients with eating disorders. We compared AVT effects on 15 patients with eating disorders to 18 patients with eating disorders which received tricyclic antidepressants or cognitive-behavioral psychotherapy. The severity of depression was assessed by means of the Hamilton Depression Scale and of Beck's Depression Inventory, before and after three months therapy. Data showed a significant improvement of depressive symptomatology after AVT treatment. Comparison of AVT effects on depression of eating disorders subgroups versus tricyclic antidepressant or psychotherapy treatment are discussed.

Adolescent↗

Evidence for inhibition of steroid hormone secretion by arginine vasotocin (AVT) in tissue culture of isolated ovarian follicular cells.

Two follicular compartments, granulosa (G) and theca interna (T) cells isolated from porcine ovaries were cultured alone or in co-culture (GT). Cells were grown as monolayers in a control medium without hormone and in a media supplemented with arginine-vasotocin (AVT) at a concentration of either 10(-7)M or 2 x 10(-7)M. Progesterone (P4), estrogen (E2) and androgen (A) concentrations in the culture media were taken as measures of the effect of AVT on the function of follicular cells. Steroids were analysed by radioimmunoassay. AVT action in this culture system was expressed as a decrease in progesterone secretion by cultures of granulosa cells alone, and especially as a change in the pattern of estradiol and androgen secretion by co-cultures. Control T and G cells cultured alone secreted small amounts of A (238.0pg/10(5) cells, 27.3pg/10(5) cells, respectively), and E2 (272.5pg/10(5) cells, 10.6pg/10(5) cells, respectively) while in co-culture these two cell types interacted and the result of this positive interaction was a significant increase in secretion of these two steroids (941.0pg/10(5) cells androgen secretion and 854.1pg/10(5) cells estradiol secretion). This phenomenon is similar to that observed in the intact follicle in vivo. AVT introduced to the culture medium impaired the effect of this positive interaction of mixed G and T cells on the production of high levels of E2 and A by untreated co-cultures.

Androgens↗

Atrial natriuretic peptide inhibited the natriferic and hydrosmotic effects of arginine vasotocin on toad skin.

The effect of rat atrial natriuretic peptide (rANP) on hormonal stimulated osmotic water permeability (Jw, hydrosmotic effect) and net ion transport (short-circuit current, SCC, natriferic effect) was studied on toad skin, a tissue with functional similarities to the mammalian distal nephron, in order to assess actions on transport mechanisms. Rat atrial natriuretic peptide, rANP-99-126 (rANP) inhibited stimulated SCC and Jw to submaximal concentrations of arginine vasotocin (AVT) at a site before cyclic AMP generation. The angiotensin-converting enzyme inhibitor (ACEI) MK-422 did not modify the inhibitory effect of ANP in the stimulated Jw.

Animals↗

The effect of adrenergic blocking and stimulating agents on arginine vasotocin release in birds.

The effect of adrenergic blocking and stimulating agents on arginine vasotocin (AVT) release from the neurohpophysis following osmotic stimuli was studied in hens. It was found that alpha - adrenergic blocking drug - regitine inhibits the release of AVT after the intravenous injection of hypertonic solution of NaCl. The alpha - adrenergic stimulating drug - vasoxine as well as beta - adrenergic blocking drug - propranolol and beta - stimulating drug isoprenalinsulphate had no effect on the release of AVT.

Adrenergic alpha-Agonists↗

Lung liquid production by in vitro lungs from fetal guinea pigs: effects of arginine vasopressin and arginine vasotocin.

Lungs from near-term fetal guinea pigs were supported in vitro for 3 h; lung liquid production rates were measured by a dye dilution technique. Seventy preparations were used to study the effects of arginine vasopressin (AVP) placed in the outer saline for the middle hour, at concentrations reported at birth [fetuses 61 +/- 2 days of gestation; 94.7 +/- 16.2 g (SD) body weight]. At 1200 microU/ml, AVP arrested fluid production (rates, successive hours, 3.03 +/- 0.60, 0.50 +/- 0.14 and 0.02 +/- 0.08 ml/kg body weight per h; falls significant, P < 0.01-0.0005). At 600, 300 and 100 microU/ml there were significant but smaller reductions. Reabsorptions were seen in 8 preparations given 600-1200 microU/ml, AVP. Preparations given 10 microU/ml AVP, AVP carrier or control saline showed no significant change. The responses (% reductions during treatment), were linearly related to the log concentration of AVP (r = 0.99); theoretical threshold, 8 microU/ml). Increasing treatment to 2h did not increase final responses. Preparations from 5 fetuses > 120 g body weight showed significantly greater responses (P < 0.025) [fetuses 64 +/- 2 days of gestation; 135.1 +/- 18.6 g (SD) body weight]. 10(-6) M amiloride abolished responses to AVP [fetuses 62 +/- 1 days of gestation; 93.4 +/- 18.5 g (SD) body weight, n = 30; rates, succeeding hours; AVP alone, 1.78 +/- 0.22, 0.48 +/- 0.09, 0.16 +/- 0.99 (P < 0.01-0.0005); AVP with amiloride, 1.15 +/- 0.07, 0.93 +/- 0.10, 0.86 +/- 0.08 (no significant fall) ml/kg body weight per h]. Thirty-six preparations treated with arginine vasotocin (AVT, 10-600 microU/ml) showed closely similar responses to those from AVP. These studies extend results to fetal guinea pigs, and show that AVP, at concentrations reported at delivery, can slow lung liquid production or cause reabsorption by a direct action on the lung. The effect increases close to term, and is due to activation of amiloride-sensitive Na+ channels.

Amiloride↗

Vasotocin fibers and neurons in the brain of the domestic fowl (Gallus gallus domesticus).

Vasotocin fibers (VIFs) and neurons (VINs) in the brain stem of the domestic fowl (Gallus gallus domesticus) were described using an immunohistochemical technique. Attention was especially focused on the VIF network. VIFs were seen in the preoptic area around the septomesecephalic tract, periventricular nuclei of the hypothalamus, the lateral geniculate nucleus, the superficial synencephalic nucleus, the triangular nucleus, the ovoidal nucleus, the ectomammillary nucleus, the superficial layer (IIa-d) of the tectum, the locus ceruleus, the caudal lineal nucleus, the descending nucleus of the trigeminal nerve and the nucleus of raphe. VIFs in the retinorecipient nuclei such as the lateral geniculate nucleus and tectum indicated the possibility of interplay between the visual and the vasotocinergic nervous systems. Moreover, VIFs in the non-retinorecipient nuclei mentioned above suggested that the vasotocinergic nervous system was related not only to the visual but also to other functions, such as the autonomic and sensory nervous systems. VINs were found in the preoptic area, the lateral and the medial hypothalamus, including the nucleus periventricularis magnocelullaris, and the dorsolateral thalamus. The dorsolateral thalamic VINs were found lateral and dorsal to the lateral forebrain bundle, lateral to the nucleus periventricularis magnocellullaris, and around the nucleus rotundus.

Animals↗