Prolactin cell activity and ion regulation in tilapia, Oreochromis mossambicus (Peters): effects of a low magnesium diet

Freshwater tilapia feeding on a diet containing 1 mmol kg⁻¹ magnesium (control diet: 30 mmol kg⁻¹) grow although at a decreased rate. The diet does not noticeably affect the blood ionic composition. Prolactin cell activity increases in these fish as judged from the enhanced rate of synthesis of ³H-leucine labelled prolactins in vitro and the ultrastructure of the cells. Na⁺ intake and Na⁺ loss decreases, and chloride cell density increases, phenomena typical for enhanced prolactin cell activity in tilapia. We conclude that tilapia manage to cope with a dietary magnesium insufficiency and suggest that prolactin is involved in the acclimation to this diet.     

The interhepatocytic macrophages and pale-grey cells in brown trout liver ontogenesis

Pale-grey cells appeared in the livers of healthy and non-stressed brown trout Salmo trutta 3 weeks post-hatching whereas interhepatocytic macrophages appeared at 5 months. Cells with intermediate morphological characteristics between those of pale-grey cells and macrophages were identified in all ages studies. Cell ultrastructure supported the idea that pale-grey cells probably belonged to the macrophage lineage, being eventual precursors of the active phagocytes residing amongst hepatocytes.     

Demersal fish biomass declines with temperature across productive shelf seas

Aim

Theory predicts fish community biomass to decline with increasing temperature due to higher metabolic losses resulting in less efficient energy transfer in warm-water food webs. However, whether these metabolic predictions explain observed macroecological patterns in fish community biomass is virtually unknown. Here, we test these predictions by examining the variation in demersal fish biomass across productive shelf regions.

Location

Twenty one continental shelf regions in the North Atlantic and Northeast Pacific.

Time Period

1980–2015.

Major Taxa Studied

Marine teleost fish and elasmobranchs.

Methods

We compiled high-resolution bottom trawl survey data of fish biomass containing 166,000 unique tows and corrected biomass for differences in sampling area and trawl gear catchability. We examined whether relationships between net primary production and demersal fish community biomass are mediated by temperature, food-web structure and the level of fishing exploitation, as well as the choice of spatial scale of the analysis. Subsequently, we examined if temperature explains regional changes in fish biomass over time under recent warming.

Results

We find that biomass per km² varies 40-fold across regions and is highest in cold waters and areas with low fishing exploitation. We find no evidence that temperature change has impacted biomass within marine regions over the time period considered. The biomass variation is best explained by an elementary trophodynamic model that accounts for temperature-dependent trophic efficiency.

Main Conclusions

Our study supports the hypothesis that temperature is a main driver of large-scale cross-regional variation in fish community biomass. The cross-regional pattern suggests that long-term impacts of warming will be negative on biomass. These results provide an empirical basis for predicting future changes in fish community biomass and its associated services for human wellbeing that is food provisioning, under global climate change.     

Effects of development and altered gravity conditions on cytochrome oxidase activity in a vestibular nucleus of the larval teleost brain: A quantitative electronmicroscopical study

The mitochondrial enzyme, cytochrome oxidase, was localized cytochemically in the nucleus magnocellularis, a primary relay nucleus of vestibular information within the area octavolateralis in the fish brain. Larvae of the cichlid fish Oreochromis mossambicus were analyzed at different developmental stages (4, 10, and 35 days posthatching) and after long-term exposure (8 days) to increased gravity (2–4 g). Quantification of highly reactive, moderately reactive, and nonreactive mitochondria reveals differences in the cytochrome oxidase activity of various cellular structures, for example, perikarya of neurons, presynaptic terminals, and myelinated and nonmyelinated cell profiles. Cytochrome oxidase activity in the mitochondria of neuronal perikarya increases during development which parallels the differentiation of the area octavolateralis. This possibly reflects the increasing energy demand during maturation and innervation of the magnocellular nucleus. Hyper-g-exposure of the larvae for 8 days (centrifuge) caused a further augmentation of cytochrome oxidase activity in the perikarya within the nucleus magnocellularis. This may reflect an increased oxidative metabolism resulting from the need for compensation of altered inputs from gravity-sensitive epithelia in the inner ear. Another possibility is that acceleration within a centrifuge causes physiological stress for the animals and, therefore, influences the cytochrome oxidase activity in neurons. © 1993 John Wiley & Sons, Inc.     

Ipsilateral retinopetal projection of the nucleus olfactoretinalis (NOR) during development and regeneration: A dil study in a cichlid fish

The development and regeneration of the ipsilateral retinopetal projection of the nucleus olfactoretinalis (NOR) in the cichlid fish Haplochromis burtoni was studied with 1,1′-dioctadecyl-3,3,3′,3′-tetramethyl indocarbocyanine perchlorate (DiI) in fixed tissue. Through out development most NOR cells projected to the contralateral retina. Only an insignificant, transient elevation of a projection to the ipsilateral retinawas found in a few animals; however, after severing the contralateral processes of NOR cells by either enucleation or nerve crush, many animals had significantly more NOR cells with a regenerated process to the ipsilateral retina. Nevertheless, within a few weeks of surgery, the number of animals with ipsilaterally projecting cells were reduced to control values. The transiently enhanced ipsilateral projections to the retina imply changes in the guiding mechanism after these operations and the existence of control mechanisms against unusual connections to the retina in this bony fish. © 1993 John Wiley & Sons, Inc.     

Ca2+ Uptake Through Voltage-gated L-type Ca2+ Channels by Polarized Enterocytes from Atlantic Cod Gadus morhua

The presence and localization of voltage-gated Ca²⁺ channels of L-type were investigated in intestinal cells of the Atlantic cod. Enterocytes were loaded with the fluorescent Ca²⁺ probe, fure-2/AM and changes in intracellular Ca²⁺ concentrations ([Ca²⁺] _i ) were measured, in cell suspensions, in the presence of high potassium levels (100 mm), BAY K-8644 (5 μm), nifedipine (5 μm) or ω-conotoxin (1 μm). L-type Ca²⁺ channels were visualized on intestinal sections using the fluorescent dihydropyridine (-)-STBodipy. Depolarization of the plasma membrane produced a rapid (within 5 sec) and transient (at basal levels after 21 sec) increase in [Ca²⁺] _i . BAY K-8644 increased the [Ca²⁺] _i by 7.2%. Cells in a Ca²⁺-free buffer increased [Ca²⁺] _i after addition of 10 mm Ca²⁺, and this increase was abolished by nifedipine in both depolarizing and normal medium but not by ω-conotoxin. Single cell experiments using video microscopy revealed that enterocytes remained polarized several hours after preparation and that the Ca²⁺ entry and extrusion occurred at specific and different regions of the enterocyte outer membrane. Fluorescent staining of L-type Ca²⁺ channels in the intestinal mucosa showed the most intense staining at the brushborder membrane. These results demonstrate the presence of voltage gated L-type Ca²⁺ channels in enterocytes from the Atlantic cod. The channels are mainly located at the apical side of the cells, and there is a polarized uptake of Ca²⁺ into the enterocytes. This suggests that the L-type Ca²⁺ channels are involved in the transcellular Ca²⁺ entry into the enterocytes. Received: 21 August 1997/Revised: 15 April 1998     

Primary and secondary stress responses to line capture in the blue mao mao

Primary and secondary stress responses were measured in wild Scorpis violaceus subjected to burst swimming from angling. Fish were blood sampled from 20 s to 30 min after hooking. Consequent rises in plasma adrenaline (14–316 nmol l⁻¹), noradrenaline (25–345 nmol l⁻¹), and cortisol (0.4–197 ng ml⁻¹) correlated with time since capture, and plasma lactate (0.1–12.2 mmol l⁻¹) reflected work done during intense exercise. Haemoglobin concentration and haematocrit also increased with exercise, and erythrocyte swelling occurred. Wild S. violaceus demonstrated a spontaneity and intensity of exercise not seen in fish acclimatized to aquarium conditions. By contrast, the stress responses of fish in captivity, despite careful husbandry, differed qualitatively and quantitatively from those in the wild. Cannulated fish had higher resting plasma cortisol concentrations (61.9±9.5 ng ml⁻¹) than did rapidly caught wild fish (<5 ng ml⁻¹) and these values were not significantly changed with burst swimming. Catecholamine secretion, possibly suppressed by cortisol, was insufficient to cause erythrocyte swelling. Erythrocyte nucleotides do not play a role in exercise, but are elevated in captive fish. It is hypothesized that primary endocrine responses are triggered by higher cortical processing of sensory information which is fundamentally different in the natural environment.     

Respiratory responses and tolerance to hypoxia in two marine teleosts,Epinephelus akaara (Temminck & Schlegel) and Mylio macrocephalus (Basilewsky)

The respiratory responses and tolerance of hypoxia were studied in two marine teleosts, the red grouper (Epinephelus akaara, a sluggish species) and the black sea bream (Mylio macrocephalus, an active species). Neither species showed abnormal behaviour or mortality when exposed to 2 mg O₂ l^–1 for 7 h. The black sea bream was, however, comparatively more tolerant when exposed to 1 mg O₂ l^–1, but tolerance of both species became similar under extremely hypoxic conditions (i.e. 0.5 mg O₂ l^–1). In contrast to most other teleosts, both species showed a reduction in opercular beating rate during hypoxia, and oxygen conformity was found in the range of 0.5 to 7.0 mg O₂l ^–1. O₂ dissociation curves were constructed, and the P₅₀ value of the black sea breams (27 ± 5.6 mm Hg) was found to be much lower than that of the red groupers (50 ± 2.5 mm Hg). For both species, the general levels of venous PO₂ showed a direct relationship to ambient PO₂, and were markedly reduced after 1 h exposure to various levels of hypoxia. Compared with the red groupers, the black sea breams appeared to be more able to maintain its venous PO₂ levels during prolonged hypoxic exposure.     

Serine proteinase inhibitors of seminal plasma of teleost fish: distribution of activity, electrophoretic profiles and relation to proteinase inhibitors of blood

Anti-proteinase activity has been found in seminal plasma of eight teleost fish species: brown trout, rainbow trout, brook trout, lake whitefish, bream, northern pike, Danube salmon and burbot. This activity correlated with seminal plasma protein and sperm concentrations. Using a mammalian (bovine) trypsin for detecting proteinase inhibitors it was found for the first time that there are species-specific electrophoretic profiles of anti-proteinase activity. One to three bands could be identified by this method. However, additional proteinase inhibitors could be identified by using fish (cod) trypsin. These inhibitors were detected in seminal plasma of salmonids and coregonids and have a slow migration rate. Fast-migrating proteinase inhibitors were present in rainbow, brown and brook trout, northern pike, whitefish and burbot. These inhibitors could be detected in brook and brown trout by using either trypsins. However, they were detected only with bovine trypsin in rainbow trout, northern pike, whitefish and burbot. These results suggest that multiple forms of serine proteinase inhibitors exist in seminal plasma of teleost fish and they differ in their affinity toward serine proteinases. Seminal plasma serine proteinase inhibitors of rainbow trout migrated during electrophoresis similarly to blood plasma proteinase inhibitors, and suggests that the two inhibitors may be similar or the same. Anti-proteinase specific activity was similar in blood and seminal plasma. Proteinase inhibitors of fish seminal plasma seem to be an important part of sperm physiology, possibly related to protection of spermatozoa. Staining for detection of serine proteinase inhibitors also allowed detection of presence of nonspecific esterase in seminal plasma of most species.     

Actions of cadmium on basolateral plasma membrane proteins involved in calcium uptake by fish intestine

Summary The inhibition of Ca^2–-ATPase, (Na⁺+K⁺)-ATPase and Na⁺/Ca²⁺ exchange by Cd²⁺ was studied in fish intestinal basolateral plasma membrane preparations. ATP driven ⁴⁵Ca²⁺ uptake into inside-out membrane vesicles displayed a K _m for Ca²⁺ of 88±17 nm, and was extremely sensitive to Cd²⁺ with an IC₅₀ of 8.2±3.0 pM Cd²⁺, indicating an inhibition via the Ca²⁺ site. (Na⁺+K⁺)-ATPase activity was half-maximally inhibited by micromolar amounts of Cd²⁺, displaying an IC₅₀ of 2.6±0.6 m Cd²⁺. Cd²⁺ ions apparently compete for the Mg²⁺ site of the (Na^– +K⁺)-ATPase. The Na⁺/Ca²⁺ exchanger was inhibited by Cd²⁺ with an IC₅₀ of 73±11 nm. Cd²⁺ is a competitive inhibitor of the exchanger via an interaction with the Ca²⁺ site (K _i = 11 nm). Bepridil, a Na⁺ site specific inhibitor of Na⁺/Ca²⁺ exchange, induced an additional inhibition, but did not change the K _i of Cd²⁺. Also, Cd²⁺ is exchanged against Ca²⁺, albeit to a lesser extent than Ca²⁺. The exchanger is only partly blocked by the binding of Cd²⁺. In vivo cadmium that has entered the enterocyte may be shuttled across the basolateral plasma membrane by the Na⁺/Ca²⁺ exchanger. We conclude that intracellular Cd²⁺ ions will inhibit plasma membrane proteins predominantly via a specific interaction with divalent metal ion sites.We would like to thank Dr. D. Fackre (University of Alberta, Canada) for stimulating discussions and Mr. F.A.T. Spanings (University of Nijmegen, The Netherlands) for excellent fish husbandry. The fura-2 measurements of intracellular Ca²⁺ concentrations in tilapia enterocytes were carried out in the Department of Physiology, School of Medicine, University of Alberta, Edmonton, Alberta T6G 2H7, Canada. Th.J.M. Schoenmakers and G. Flik were supported by travel grants from the Foundation for Fundamental Biological Research (BION) and the Netherlands Organization for Scientific Research (NWO).