Ultrastructural changes in the pars intermedia of the goldfish kept in calcium-free environments

The PAS-positive-calcium-sensitive (Ca-s) cells of the pars intermedia (PI) were studied in goldfish kept in fresh water (FW), deionized water (DW), 1/3 sea water (SW) and 1/3 Ca-free SW. Ultrastructural studies show that Ca-s cells of control goldfish kept in FW have a low activity with elongated or deeply indented nuclei. This activity is slightly reduced after 19 days in 1/3 SW. A considerable stimulation of most Ca-s cells is noted in goldfish kept in DW for 20 or 40 days. The stimulation is similar in 1/3 Ca-free SW, but it affects sometimes a smaller percentage of cells and may be less marked in peripheral areas of the PI. Exocytotic figures are more numerous in Ca-s cells of goldfish in 1/3 Ca-free SW than in DW. A basal lamina is rarely present and direct contacts between PI cells and nervous tissue are frequent, although a single synaptic contact with a type B fiber was observed. MSH cells are not affected in goldfish kept in DW. They are stimulated in 1/3 Ca-free SW: the physiological significance of this response remains unclear. Few agranular (Agr) cells are scattered in the PI. Evident changes are not observed in the different environments. The present ultrastructural data support the hypothesis that the Ca-s cells of the PI secrete a factor involved in calcium regulation in some teleosts.     

Ultrastructural changes in the calcium-sensitive (PAS-positive) cells of the pars intermedia of eels kept in deionized water and in normal and concentrated sea water

Summary The ultrastructure of the calcium-sensitive (Ca-s) (PAS-positive) cells of the pars intermedia was investigated in eels kept in hypo and hyperosmotic environments. Although the cells were moderately active in fresh water (FW), they were highly stimulated in deionized water (DW) and displayed an enlarged Golgi apparatus, a distinct rough endoplasmic reticulum, few secretory granules, some microtubules and an extended area of contact with the basal lamina that separates nervous and glandular tissues. Some mitosing cells were seen. A similar picture was observed in eels kept in sea water (SW) for 45 days, returned to FW and subsequently to DW for 21 days. In SW (30 and 33), and particularly in concentrated SW (50, 60 and 63), the Ca-s cells were inactive. Their granules were significantly smaller than in eels kept in FW, and the area of contact with the basal lamina was greatly reduced. However, signs of granule-release were seen in eels adapted to 50 and 60 SW. Nerve fibers rarely contacted the Ca-s cells and did not synapse with them. The ultrastructural data support the hypothesis that the Ca-s cells of Anguilla, like those of Carassius, are involved in ionic regulation. MSH cells were not greatly affected by the present experiments.     

Kinetics of the Response of Prolactin Cells to Environmental Changes in the Eel

The prolactin (PRL) cells of the pituitary are less active in seawater (SW)-adapted eels than in freshwater (FW) ones. The kinetics of their response during adaptation to SW or readaptation to FW was investigated. Morphometric studies show that transfer into SW induces a rapid nuclear atrophy, and a reduction of the cell height and of the amount of cytoplasmic granules. These parameters still continue to decrease slowly for one month, becoming then fairly stable. Readaptation to FW stimulates PRL cells after 2 to 10 days. After one or two months, the cells are similar to those of eels kept in FW. The responses of PRL cells appear to be slower in the eel than in Cyprinodonts, which need PRL to live in FW. A complete adaptation to both environments requires one month at least in Anguilla.     

Calcium-sensitive cells of the pars intermedia and osmotic balance in the eel

Summary The structure of the PAS-positive calcium-sensitive (Ca-s) cells of the pars intermedia was investigated in eels kept in deionized water (DW) or fresh water (FW) supplemented with Ca²⁺ or Mg²⁺. Ca²⁺ (2mM) reduces considerably the response to DW; plasma osmolarity, Na⁺ and Ca²⁺ levels are not significantly affected. In eels adapted to DW for 21 or 28 days, showing highly stimulated Ca-s cells, an addition of CaCl₂ for 2 days inhibits the release of granules, but does not immediately block their synthesis and the mitotic activity. The nuclear area is reduced, osmolarity and plasma sodium increase, but the rise in calcium is not always significant. Magnesium, at a 10-fold greater concentration than in FW (2 mM), slightly inhibits the release of secretory granules without reducing other indicators of stimulation. In Ca-enriched FW, the Ca-s cells appear inactive. These data show that the PAS-positive cells in the pars intermedia of the eel are calcium-sensitive, similar to those of the goldfish; their role in calcium regulation is briefly discussed.     

Calcium-sensitive cells of the pars intermedia and osmotic balance in the eel

Summary Freshwater eels were adapted to calcium-free sea water (SW) or 1/3 Ca-free SW. Survival was generally poor in Ca-free SW, although three eels were still in good condition after 19–30 days; survival in 1/3 Ca-free SW was excellent. Osmotic disturbances (increase of plasma osmolarity and sodium levels), which initially occur in Ca-free SW, were no longer detectable after 19–30 days, or in eels in 1/3 Ca-free SW after one month. Plasma calcium sharply decreases initially; it is less depressed after 19–30 days and in 1/3 Ca-free SW. Alterations in the mucus production may be involved in the osmotic changes. Under these conditions no clear stimulation of the calcium-sensitive (Ca-s) cells of the pars intermedia was registered, but in Ca-free SW (1/3 or full strength) the inhibitory effect normally observed in SW does not occur. In a hyperosmotic environment, other ion(s), possibly magnesium, may reduce the response of the Ca-s cells to a lack of environmental calcium.     

Response of prolactin cells to environmental calcium in the eel (Anguilla anguilla L.)

Prolactin (PRL) cell activity was investigated in eels kept in fresh water (FW), deionized water (DW) supplemented or not with Ca (2 mM), in Ca-enriched FW (10 mM), in normal (Ca 3.4 mM) or Ca-free 1/3 sea water (SW), and in SW (Ca 10.2 mM) or Ca-free SW (Ca 0.15 mM). Light-microscopic studies, including measurement of the nuclear area and cell height, showed that PRL cell activity, reduced in DW, is not affected by Ca supplementation. Activity is reduced in Ca-enriched FW, in 1/3 SW and in SW, conditions inducing an increase in the plasma sodium level. The lack of calcium in saline environments partly suppresses the nuclear atrophy occurring in SW. There is no significant correlation between external or total plasma calcium concentration and PRL cell activity. In artificial Ca-free SW, eels show a rapid increase in plasma osmolarity and sodium levels; there is a significant negative correlation between these two plasma values and the nuclear area or cell height of PRL cells. As in some other teleosts, plasma osmolarity and plasma sodium seem to play a more important role than external or internal calcium in controlling PRL secretion. This correlation is not apparent in eels kept in SW, having unstimulated PRL cells but active calcium-sensitive (Ca-s) cells in the pars intermedia.     

Response of calcium-sensitive cells in the pars intermedia of the goldfish adapted to diluted sea water with different calcium and magnesium contents

Summary Goldfish kept in diluted Ca-free sea water (SW) (23 or 30 %) or in Ca-Mg-deficient SW (23 %) have a limited survival, release large amounts of mucus, and show spasmodic seizures. Plasma calcium decreases. The PAS-positive calcium-sensitive (Ca-s) cells of the pars intermedia show a low activity in diluted SW and in 23 % Mg-free SW. In diluted Ca-free SW, Ca-s cells are stimulated, but cell hypertrophy is not uniform and often restricted to an area adjacent to the proximal pars distalis. Nuclear hypertrophy is significant in the reactive area, although less pronounced or even absent at the periphery of the lobe. Mitotic activity occurs in the Ca-s cells of goldfish gradually adapted to diluted Ca-free SW and Ca-Mg-deficient SW, and sacrificed after 19 and 28 days, respectively. A general stimulation of the Ca-s cells, which remains less intense than that in goldfish kept in deionized water (DW), appears unable to ensure the survival of the goldfish in an isosmotic Ca-free environment containing Mg²⁺ (0.1, 12 or 16.8 mM). These data are compared with those obtained in the eel kept in Ca-free SW.     

Specific effect of calcium ions on the calcium-sensitive cells of the pars intermedia in the goldfish

Summary Cytological changes in the calcium-sensitive (Ca-s) cells (formerly termed PAS-positive cells) of the pars intermedia were investigated in the goldfish after adaptation to deionized water (DW), with or without addition of sodium, potassium and magnesium. These ions were added as chloride salts at concentrations similar to those present in fresh water (FW). The marked stimulation of the Ca-s cells is not inhibited in DW supplemented with Na⁺ (0.35 mM/1), K⁺ (0.05 mM/1), and Mg²⁺ (0.2mM/1) for a period of 24 days. The inhibition of the response to DW with calcium chloride (2 mM/1) is reproduced with calcium formiate (2 mM/1). These data show that chloride ions are not responsible for the regression of the Ca-s cells observed in goldfish kept in DW supplemented with calcium chloride. The effect of calcium ions on the Ca-s cells appears to be specific. These results support the hypothesis that the Ca-s cells synthesize a factor (hypercalcin?) involved in calcium regulation, and that its release is influenced by the calcium content of the environment. The role of the pars intermedia in calcium metabolism is strengthened by the present results. Biochemical data suggest the presence of a hypercalcemic factor in the pituitary of fish (Parsons et al. 1978) and are in agreement with the present cytological findings.     

Effect of pimozide on the cytology of the eel pituitary

Pimozide, a specific blocker of dopaminergic receptors, was injected for 4 to 9 days in freshwater (FW) eels or eels acclimated to sea water (SW), for 10 to 30 days. The daily dose was 100 or 200 microgram/100 g. In FW, pimozide induces a nuclear hypertrophy in the prolactin (PRL) cells of eels; these elongated cells increase in height. The amount of erythrosinophilic granules in the cytoplasm, initially reduced, increases. Plasma electrolyte values are not modified: only the plasma sodium level slightly rises with the higher dose. In SW, PRL cells appear less active. After 10 days, this hypoactivity is not yet fully evident; pimozide stimulates PRL cells without affecting electrolyte values. After 1 month in SW, PRL cells are stimulated with pimozide and a slight regranulation may occasionally occur. The response in SW is never as marked as it is in FW; a high dose is not more effective than a low one. The higher dose significantly raises Na+, Ca2+ and Cl- plasma levels. These data suggest that prolactin synthesis and release increase with pimozide. They corroborate the hypothesis of a hypothalamic inhibitory control on PRL secretion mediated through dopaminergic fibers in the eel, but other factors may also be involved in this regulation in addition to the effect of salinity.     

Feeding habitat and silvering stage affect lipid content and fatty acid composition of European eel Anguilla anguilla tissues

Lipids, particularly fatty acids (FAs), are major sources of energy and nutrients in aquatic ecosystems and play key roles during vertebrate development. The European eel Anguilla anguilla goes through major biochemical and physiological changes throughout its lifecycle as it inhabits sea- (SW), and/or brackish- (BW) and/or freshwater (FW) habitats. With the ultimate goal being to understand the reasons for eels adopting a certain life history strategy (FW or SW residency vs. ‘habitat shifting’), we explored differences in lipid content and FA composition of muscle, liver and eyes from eels collected across Norwegian SW, BW and FW habitats, and at different lifecycle stages (yellow to silver). FW and SW eels had a higher lipid content overall compared to BW eels, reflecting differences in food availability and life history strategies. SW eels had higher proportions of certain monounsaturated FAs (MUFAs; 18:1n-9, 20:1n-9), and of the essential polyunsaturated FAs 20:5n-3 (eicosapentaenoic acid, EPA) and 22:6n-3 (docosahexaenoic acid) than FW eels, reflecting a marine-based diet. In contrast, the muscle of FW eels had higher proportions of 18:3n-3, 18:2n-6 and 20:4n-6 (arachidonic acid), as is typical of FW organisms. MUFA proportions increased in later stage eels, consistent with the hypothesis that the eels accumulate energy stores prior to migration. In addition, the decrease of EPA with advancing stage may be associated with the critical role that this FA plays in eel sexual development. Lipid and FA information provided further understanding of the habitat use and overall ecology of this critically endangered species.     

Effect of pimozide on the cytology of the eel pituitary

Summary Pimozide, a specifie blocker of dopaminergic receptors, was injected for 4 or 9 days in freshwater (FW) eels or eels acclimated to sea water (SW) for 10 or 30 days. The daily dose was 100 or 200 g/100g. Melanophore index values increase in FW and in 1 month-SW injected eels. All the treated fish react by a total or subtotal degranulation of the lead-hematoxylin positive cells in the pars intermedia. These cells were previously identified as -MSH-secreting cells. The MSH cell nuclear area is significantly increased, nucleoli are larger and the endoplasmic reticulum more developed. The intensity of the response is similar in FW and SW eels, but it does not increase with the higher dose. The rapid release of pituitary -MSH is also visualized by immunofluorescence and immunoenzymologic techniques. No effect on the second cell type of the pars intermedia (PAS-positive cell) is detected. The amount of neurosecretory material is often reduced in the neurohypophysis. These results suggest that the hypothalamic inhibitory control of MSH release and synthesis is mediated through dopaminergic fibers in the eel, but other factors cannot be ignored in this regulation.The author is grateful to Dr. P.A.J. Janssen for donating the pimozide used in this experiment and to Jacqueline Olivereau, from the C.N.R.S., for her excellent technical assistance. This work was supported by the Centre National de la Recherche Scientifique and a grant from the Délégation Générale à la Recherche Scientifique et Technique (n A 650 1588)     

Effect of environmental salinity change on osmotic permeability of the isolated gill of the eel, Anguilla anguilla L.

Net water fluxes in the isolated gills of Anguilla anguilla were studied during incubation in fresh water (FW) and in sea water (SW). When incubated in FW, water entry was greater in SW-adapted eels than in FW-adapted eels. In contrast, water loss in SW was less in SW-adapted eels than in FW-adapted eels. Rectification of osmotic water fluxes was observed for both FW and SW-adapted eels, net water fluxes in the mucosal-serosal (m-s) direction being greater than those in the opposite (s-m) direction. These results indicate that adaptation to a given external medium brings about a decrease in the osmotic permeability so that water gain in FW or water loss in SW is minimal.     

Osmoregulation during the development of glass eels and elvers

Drinking rates in glass eels and elvers of the European eel increased with environmental acclimation salinity from 0·07±0·02 (FW) to 0·70±0·09 μl g-¹ h-¹ (SW) at month 1 and from 1·12±0·42 (FW) to 12·85±1·05 ± l g-¹ h-¹ (SW) at month 5. Drinking rates increased with time in both FW and SW groups. FW acclimated eels when challenged acutely with SW increased drinking rate rapidly immediately upon transfer (0–15 min) and the magnitude of this response increased with developmental time from month 1 to month 5.     

Differential Effect of Sodium and Magnesium on the Pituitary of Goldfish Adapted to Calcium-Free Environments

Adaptation to deionized water (DW) affects several cell types in the goldfish. The pars intermedia PAS-positive cells are highly stimulated. Their low response or the absence of changes in goldfish kept in 1/3 Ca-free seawater (SW) and in Ca-free SW-adapted eels, respectively, suggest that sodium and/or magnesium are interfering. To test this hypothesis, young goldfish were adapted to DW supplemented or not with sodium (50 and 140 mM) for 8 and 16 days or with magnesium (16.5 and 50 mM) for 16 and 30 days. Cytological and morphometric studies of the pituitary showed that prolactin (PRL) cell activity was reduced by sodium. Thyrotropic (TSH) cells were stimulated. The activity of melanocyte-stimulating (MSH) cells increased in DW + Na+. Stimulation of the pars intermedia PAS+ cells in DW was partly inhibited by adding sodium; the cellular and nuclear areas increased only moderately, the endoplasmic reticulum (ER) was not conspicuous and mitotic activity disappeared. In DW + Mg²⁺ the activity of PRL, TSH and MSH cells tended to be lower after a long-term adaptation. The response of the PAS+ cells was as high as that noted in DW; complete degranulation, enlargement of the ER and important mitotic activity. Differential responses to Na+ and Mg²⁺ are not due to pH differences in the solutions. External sodium is able then to reduce the response of the PAS+ cells in a Ca-free environment, while magnesium is not inhibitory. Other cell types are also affected by high levels of Na+ and Mg²⁺.     

Two isoforms of the Na+/K+/2Cl- cotransporter are expressed in the European eel (Anguilla anguilla)

Two cDNA isoforms of the NKCC1 secretory cotransporter have been isolated from the European eel. The NKCC1a isoform exhibited mRNA expression in a wide range of tissues in a similar fashion to mammals, whereas NKCC1b was expressed primarily in the brain. The effect of freshwater (FW) to seawater (SW) transfer on NKCC1a expression was dependent on the developmental stage. In non-migratory yellow eels, NKCC1a mRNA expression in the gill was transiently up-regulated 4.3-fold after 2 days but also subsequently by 2.5-6-fold 3 weeks after SW transfer. Gill NKCC1a expression was localised mainly in branchial chloride cells of SW acclimated yellow eels. In contrast to yellow eels, NKCC1a mRNA abundance was not significantly different following SW acclimation in silver eel gill. NKCC1a mRNA abundance decreased in the kidney following SW acclimation and this may correlate with lower tubular ion/fluid secretion and urine flow rates in SW teleosts. Kidney NKCC1a mRNA expression in silver eels was also significantly lower than in yellow eels, suggesting some pre-acclimation of mRNA levels. NKCC1a mRNA was expressed at similar low levels in the middle intestine of FW- and SW-acclimated yellow or silver eels, suggesting the presence of an ion secretory mechanism in this gut segment.     

Stimulation of non-specific immune functions in seawater-acclimated rainbow trout, Oncorhynchus mykiss, with reference to the role of growth hormone

The influence of acclimation to seawater (SW) and growth hormone (GH) administration on immune functions was examined in the rainbow trout (Oncorhynchus mykiss). After 3 days acclimation to dilute SW (12 parts per thousand, ppt), an increase in plasma lysozyme activity was observed compared to the fish kept in fresh water (FW). No change was seen in plasma immunoglobulin M (IgM) levels. When they were transferred from dilute SW to full-strength SW (29 ppt) after a single intra-peritoneal injection of ovine or salmon GH, plasma sodium levels of GH-treated fish were significantly lower than those of the control fish injected with Ringer's solution 24 h after the transfer. The plasma level of IgM was not influenced by GH injection in the fish kept in FW nor in those transferred to SW. The administration of GH increased plasma lysozyme activity in the fish in FW, but no further increase was seen after SW transfer. The production of superoxide anions in peripheral blood leucocytes was stimulated by GH in both FW and SW. These results suggest that GH is involved in the stimulation of the non-specific immune functions in SW-acclimated salmonids.     

Antidiuretic Effect of Eel ANP Infused at Physiological Doses in Conscious, Seawater-Adapted Eels, Anguilla japonica

Atrial natriuretic peptide (ANP) is known as a potent natriuretic/diuretic hormone in vertebrates. However, eel ANP infused at doses that did not alter arterial blood pressure (0.3-3.0 pmol/kg/min) decreased urine volume and increased urinary Na concentration in seawater (SW)-adapted eels but not in freshwater (FW)-adapted eels. The renal effects were dose-dependent and disappeared after infusate was switched back to a vehicle (0.9% NaCl). Urinary Na excretion (volume x Na concentration) did not change during ANP infusion. ANP infusion increased plasma ANP concentration, but the increase at the highest dose was still within those observed endogenously after injection of hypertonic saline. Urinary Mg and Ca concentrations increased during ANP infusion in SW eels, but urinary Ca excretion decreased in FW eels. Plasma Na concentration profoundly decreased during ANP infusion only in SW eels, suggesting that ANP stimulates Na extrusion via non-renal routes. These results indicate that ANP is a hormone which specifically extrudes Na ions and thereby promotes SW adaptation in the eel. This is in sharp contrast with mammals where ANP is a volume regulating hormone that extrudes both Na and water.     

Cell proliferation and apoptosis in the anterior intestine of an amphibious, euryhaline mudskipper (Periophthalmus modestus)

In order to replace the diffusive loss of water to the surrounding environment, seawater (SW)-acclimated euryhaline fishes have gastrointestinal tracts with higher ion/water flux in concert with greater permeability, and contrast that to freshwater (FW)-acclimated fish. To understand the cellular basis for these differences, we examined cell proliferation and apoptosis in the anterior intestine of mudskipper transferred from one-third SW to FW or to SW for 1 and 7 days, and those kept out of water for 1 day. The intestinal apoptosis (indicated by DNA laddering) increased during seawater acclimation. TUNEL staining detected numerous apoptotic cells over the epithelium of SW-acclimated fish. Cell proliferation ([³H]thymidine incorporation) in the FW fish was greater than those in SW 7 days after transfer. Labeling with a Proliferating cell nuclear antigen (PCNA) antibody indicated that proliferating cells were greater in number and randomly distributed in the epithelium of FW fish, whereas in SW fish they were almost entirely in the troughs of the intestinal folds. There were no changes in cell turnover in fish kept out of water. During acclimation to different salinities, modification of the cell turnover and abundance may play an important role in regulating the permeability (and transport capacity) of the gastrointestinal tract of fish.     

Melanophore Responses and Intermediatelobe Activity in the Eel Anguilla anguilla after Injection of 6-OH-dopamine

When 6-OH dopamine (6-OHDA) was injected into the body cavity of eels (Anguilla anguilla L.), which had been kept on a light background with continuous artificial illumination or a natural day-night regime in May and June, evident but heterogeneous chromatic reactions were induced. After peripheral drug effects during the first 6 hours, the eels became darker for 2 or 3 days, whereupon the melanophore index (MI), in most cases, decreased. Darkening was accompanied by significant nuclear hypertrophy and moderate degranulation of the MSH (melanophore-stimulating hormone) cells. Probably only some of the adrenergic nerves in the neural lobe were affected. The blood supply to the brain was decreased for several days after each injection. The results support the assumption that in the eel catecholamines released from nerve endings in the neural lobe inhibit the release of MSH from intermedia cells by their own action as an inhibiting factor, or by affecting an MIF (MSH-release inhibiting factor) and/or an MRF (MSH-releasing factor).     

Effect of transfer to sea water and back to fresh water on the histological structure of the eel kidney

Summary A cytometrical study of the various segments of kidney tubules was performed on silver or silvering male eels during acclimation to sea water (SW) for 2 to 160 days and their return to fresh water (FW). Tubular epithelial cell height and nuclear area are markedly reduced during the first two days, and further reduced in the following period to reach a stable level around the 20th day. The glomerular size is slightly decreased. Phospholipids are less abundant and the brush borders become thinner. In a single eel kept for 9 months in pure SW slowly concentrated by evaporation (NaCl 45 g/l), cell and nuclear values were similar to those obtained in full strength SW after 160 days. Distal and collecting tubules exhibit maximal reactivity, that of the first proximal tubule being minimal.When eels kept for 20 days in SW are returned to FW, there is a rapid increase (48 h), sometimes with an overshoot, of all measured parameters, followed by a rapid decrease (5 days) and a normalization of the values in the distal and collecting tubules.The rapid response of eel kidney to salinity changes does not appear to be linked to cellular hydration as the various segments of the kidney tubules react differently. The data are discussed with respect to osmotic acclimation and in relation to variations of prolactin secretion. Prolactin (PRL) release during transfer to FW stimulates the renal tubules less strongly than mammalian PRL: while mitotic activity and differentiation of new nephrons are induced by ovine PRL treatment in intact or hypophysectomized FW eels (Olivereau and Lemoine, 1969b), no such events were detected during acclimation to this hypotonic medium, at least during the first ten days. This rather reflects insufficient PRL release than a different biological activity, despite immunological differences between fish and ovine prolactin.

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Résumé L'étude cytométrique (hauteur épithéliale et aire nucléaire) des divers segments du tube rénal, réalisée chez l'Anguille mâle argentée ou en cours d'argenture lors de l'adaptation à l'eau de mer (SW) montre une réduction marquée dès les premières 48 h en SW qui s'accuse légèrement pour atteindre un niveau stable vers le 20^e jour; la taille des glomérules est réduite. Les phospholipides sont moins abondants, la bordure en brosse est plus mince. Chez une Anguille conservée 9 mois en SW initialement normale et lentement concentrée par évaporation (NaCl 45 g/l), les valeurs obtenues sont peu différentes de celles après 160 jours en SW pure. La réactivité maximale s'observe au niveau du tube distal et du collecteur, celle du tube proximal l étant minimale.Le retour en eau douce (FW) provoque une rapide augmentation (2 jours), parfois excessive, de ces paramètres, suivie d'une baisse rapide (5 jours) et de la normalisation des valeurs du tube distal et collecteur (10 jours).Les réponses du rein aux changements de salinité, très rapides, ne paraissent pas liées à des processus de déshydratation ou hydratation cellulaire car elles affectent inégalement les divers segments du néphron. Elles sont discutées en fonction des variations des électrolytes plasmatiques et de la sécrétion hypophysaire de prolactine (PRL): sa décharge qui accompagne le retour en FW stimule moins intensément le tube rénal que l'injection de PRL ovine, elle ne provoque pas une intense activité mitotique ni une différenciation de nouveaux néphrons, au moins pendant les 10 premiers jours. Ce fait représente probablement plus une sécrétion insuffisante de PRL lors du retour en milieu hypotonique qu'une différence d'activité biologique, malgré des différences immunologiques entre prolactines ovine et de Poisson.