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1.
The branchial Ca2+ uptake by teleost fish is under inhibitory control by the hormone stanniocalcin (STC) which is generated by the corpuscles of Stannius (CS). Removal of the CS in North American eel, Anguilla rostrata LeSueur, induced a rapid rise in blood calcium levels. Branchial Ca2+ influx following the extirpation of the CS (stanniectomy, STX) increased during the first four days and stayed elevated thereafter (in agreement with previous studies). The transepithelial potential (TEP) across the gills did not change after STX and this means that the electrochemical gradient for Ca2+ is less favourable for passive influx of Ca2+ in STX eel. Therefore, the Ca2+ influx in STX eels is a transcellular flux, with Ca2+ crossing the apical and basolateral membrane barrier. The kinetics of ATP-driven Ca2+-transport across basolateral plasma membranes from eel gills did not change after STX. Thus, the increased Ca2+-influx after STX is not correlated with changes in ATP-dependent Ca2+-extrusion across the basolateral membrane, suggesting a regulation at the apical membrane. Moreover, STC did not affect ATP-driven Ca2+-transport in isolated basolateral membranes (in vitro). STC (0.1 nM) reduced cAMP levels in dispersed eel gill cells. It had no significant effect on the IP3 levels in these cells. We postulate that STC controls the permeability to Ca2+ of the apical membranes of the Ca2+ transporting cells of fish gills by controlling second messenger operated Ca2+ channels in the apical membrane.
Résumé L'entrée de calcium au niveau des branchies est sous le controle inhibiteur de la stanniocalcine (STC) qui est synthétisée au niveau des corpuscules de Stannius (CS). L'ablation des CS chez l'anguille d'Amérique du Nord, Anguilla rostrata LeSueur, induit une augmentation rapide des niveaux de calcium dans le sang. Le flux entrant branchial de calcium consécutif à l'ablation des CS (stanniectomie, STX) augmente pendant les 4 premiers jours et reste élevé au-delà (en accord avec des études antérieures). Le potentiel transépithélial (TEP) à travers les branchies ne change pas après STX, ceci indiquant que le gradient électrochimique du Ca2+ est moins favorable pour le flux entrant passif du Ca2+ chez l'anguille STX. En conséquence, le flux entrant de Ca2+ chez l'anguille STX est un flux transcellulaire, avec le Ca2+ traversant la barrière membranaire apicale et basolatérale. La cinétique du transport de Ca2+ conduit par l'ATP à travers les membranes plasmatiques basolatérales de branches d'anguille n'est pas modifiée après STX. Ainsi, l'augmentation du flux entrant de Ca2+ après STX n'est pas corrlée avec des modifications de l'excrétion de Ca2+ conduit par l'ATP à travers la membrane basolatérale, suggérant donc une régulation au niveau de la membrane apicale. De plus, la STC ne modifie pas le transport de Ca2+ conduit par l'ATP dans des membranes basolatérales isolées (in vitro). La STC (0.1 nM) réduit les niveaux d'AMPc dans des cellules dispersées de branchies d'anguille. Cette hormone n'a pas d'effet significatif sur les niveaux d'IP3 dans ces cellules. Nous suggérons que la STC régule la perméabilité au Ca2+ des membranes apicales des cellules branchiales transporteuses de Ca2+ en controlant un second messager agissant sur les canaux calciques de la membrane apicale.
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2.
Biochemical procedures developed to isolate plasma membranes from the branchial epithelium of rainbow trout (Oncorhynchus mykiss) yield membrane fractions that are specifically enriched in the plasma membrane marker enzyme Na+/K+-ATPase. As the bulk of the branchial Na+/K+-ATPase is assumed to be confined to the mitochondria-rich chloride cells, such membrane preparations must contain the essence of the enzymatic machinery of the chloride cells. Basal Na+ activity in branchial (chloride) cells is around 10 millimolar and, accordingly, we find a Km for Na+ of the Na+/K+-ATPase of 13 millimolar, indicating that the enzyme may be regulated by changes in cytosolic sodium. The Na+-gradient across the serosal plasma membrane created by this pump provides energy for 3Na+/Ca2+-exchange and bumetanide-sensitive Na+/K+/2Cl--cotransport. Here we further postulate the presence of a Na+/Cl--cotransporter, indicated by thiazide-sensitive, bumetanide-insensitive transport of Na+ and Cl-; this cotransporter activity awaits the characterization of its kinetics. The Na+/Ca2+-exchanger has kinetic characteristics compatible with a regulatory role of cytosolic Na+ in the activity of this carrier. Both Na+/Ca2+-exchange and Ca2+-ATPase activity may contribute to transport of Ca2+, the former having lower affinity for calcium but a higher capacity than the latter carrier. The Na+/K+/2Cl--cotransporter has kinetics that favor a regulatory role for plasma K+ in the activity of this carrier. Seawater adaptation leads to increased activity of cotransporter molecules in the plasma membrane fractions (the activity increases relative to that of the Na+/K+-ATPase) and this may reflect a function in Cl--extrusion performed by the chloride cells in a seawater environment. A function for the cotransporter in the gills of freshwater fish may be the regulation of cell volume.  相似文献   

3.
The role of environmental ion composition and osmolality in Ca2+ signaled activation was assessed in spermatozoa of brook trout Salvelinus fontinalis. Milt from ten mature males was obtained by abdominal massage. Spermatozoa motility was evaluated in 0, 100, and 300 mOsm/kg NaCl or sucrose solutions, buffered by 10 mM Tris–HCl pH 8.5. For investigation of spermatozoa reaction to external Ca2+ concentration, 2 mM ethylene glycol tetraacetic acid (EGTA) was added to the activation media as a calcium ions chelator. For investigation of the effect of external Na+ concentration in conditions of low external Ca2+, 100 µM amiloride was added to the EGTA-containing solutions as a Na+ transport blocker. Low motility was observed in sucrose (Na+ free) solutions containing 2 mM EGTA but not in Na+ solutions containing 2 mM EGTA. Addition of amiloride led to significantly increased motility (P < 0.05) compared with sucrose (Na+ free) solutions containing 2 mM EGTA. We conclude that Na+ transport in Ca2+-free solutions plays a regulatory role in brook trout spermatozoa activation. The influence of competitive Na+ and Ca2+ transport on the control of spermatozoa activation requires further study with respect to its application for improvement of artificial activation and storage media.  相似文献   

4.
The effects of the Na+/K+ and Mg2+/Ca2+ ratios in saline groundwaters on Na+-K+-ATPase activity, survival and growth of Marsupenaeus japonicus postlarvae were investigated. The results indicate that the Na+-K+-ATPase activity, survival rate and weight gain of postlarvae were significantly affected by the Na+/K+ and Mg2+/Ca2+ ratios (P < 0.05). The Na+-K+-ATPase activity of postlarvae, in every treatment, changed corresponding to Na+/K+ and Mg2+/Ca2+ ratios, and came to a stable level after 24 h. There was a negative relation between Na+-K+-ATPase activity and Na+/K+ ratio, while there was a positive relation between Na+-K+-ATPase activity and Mg2+/Ca2+ ratio. Compared with seawater (the Na+/K+ and Mg2+/Ca2+ ratios are 27.8 and 4.64 respectively), the Na+-K+-ATPase activity of the Na+/K+ ratio 30 treatment showed no significant difference, while the Mg2+/Ca2+ ratio 4.5 treatment showed distinct difference. The survival rates and weight gain of postlarvae increased markedly when the suitable amount of K+ and Ca2+ was added to test water, and arrived at their maximum in the Na+/K+ ratio 20-30 or Mg2+/Ca2+ ratio 4.5 treatment, having no significant difference compared with normal seawater. Therefore, considering the Na+/K+, Mg2+/Ca2+ ratios and the absolute concentration of Mg2+, Ca2+ in the experimental saline groundwaters applied to Marsupenaeus japonicus farming, it should be modulated to around 30, 4.5 and 1312 mg/l, 291 mg/l, respectively.  相似文献   

5.
The sperm duct epithelium of brook trout (Salvelinus fontinalis), mountedin vitro in Ussing-style epithelial chambers actively absorbs Na+ (measured as the short-circuit current, Isc) and secretes K+ (measured using86Rb+ as tracer). Dibutyryl-cyclic-adenosine monophosphate (db-cAMP) and 3-isobutyl-1-methylxanthine (IMX) produce a rapid, sustained stimulation of both ion transport processes, but the hormone connected to the response is unknown. Purified sockeye salmon CON A2 gonadotropin (GtH) produces a dose-dependent, rapid and sustained rise in Na+ uptake and K+ secretion. The time course, electrophysiological and transport characteristics are similar to those evoked by IMX. Carbohydrate-poor (chum salmon CON A1) GtH is ineffective. Pretreatment of fish with 17α,20β-dihydroxy-4-pregnen-3-one (17α,20β-P) significantly increases milt volume but is without effect on resting or stimulated (IMX + db-cAMP) levels of sperm duct ion transport. This is the first indication of a direct, rapid action of GtH on ion transport by the vertebrate blood-testis barrier. The results suggest direct involvement of GtH in control of later stages of sperm maturation.  相似文献   

6.
Branchial activities of Na+,K+-ATPase (ouabain sensitive), Mg2+ ATPase (ouabain insensitive) and kinetic analysis of high and low affinity Ca2+ ATPase were measured inAnguilla anguilla that had been acclimated to demineralized water (DW, Ca < 10 M), freshwater (FW, Ca = 2 mM), and Low calcium freshwater (L-Ca, Ca = 0.9 mM). Na+,K+-ATPase activity decreased while ouabain insensitive activity increased when ambient Ca2+ decreased. Two kinetic forms of Ca2+ ATPase could be resolved in each environmental condition. The stimulation coefficients of both sites or enzymes were not affected by ambient Ca2+ concentrations. The maximal velocity of both the high and the low affinity Ca2+ ATPase was increased when external Ca2+ was decreased during acclimation. The low affinity Ca2+ ATPase and the Mg2+ stimulated enzyme could be a non specific enzyme accepting either Ca2+ or Mg2+. Results are compared with previous results in the literature and in relation to the branchial morphology and ionic exchanges in fish.  相似文献   

7.
The fluid uptake rate of the posterior intestine of salmonids increases during the parr-smolt transformation. Intestinal fluid uptake in post-smolt Atlantic salmon was investigated after treatment with cortisol and growth hormone (GH), alone or together. Two replicate experiments were conducted in August 1991 and August 1992. Cortisol was emulsified in vegetable shortening and vegetable oil (1:1) and implanted into the peritoneal cavity. GH was administered as intraperitoneal injections in a saline vehicle on days 0 and 2. On days 5 and 6, plasma cortisol levels, gill Na+,K+-ATPase activity, andin vitro measurements of fluid transport rate (Jv) across the posterior intestine were measured. Implants of cortisol elevated the plasma cortisol levels within a physiological range, and resulted in elevated gill Na+,K+-ATPase activity, as expected. The fluid uptake rate across the posterior intestine was roughly doubled by cortisol treatment. GH treatment did not affect intestinal fluid transport, gill Na+,K+-ATPase activity, or plasma cortisol concentrations. The seawater-adapting increase in the rate of fluid uptake by the posterior intestine of smolting salmon is probably stimulated by elevated plasma cortisol concentrations.  相似文献   

8.
Metamorphic responses of pediveliger larvae of Mytilus galloprovincialis to different ions were investigated through a series of bioassays. Effects of tetraethylammonium chloride (TEA) on inductive effects of these above ions were also investigated. Excess ions including Li+, Cs+, Rb+ and Ca2+ induced larval metamorphosis at 10?3 M to 5 × 10?2 M in 24‐h exposure assays. In continuous exposure assays, only excess Ca2+ showed inductive activity and induced 25% metamorphosis at 5 × 10?2 M. Larval responses to Li+ and Rb+were inhibited by TEA, while induction of metamorphosis by Cs+and Ca2+ was independent of the presence of TEA. Thus, these ions used can be useful inducers of larval metamorphosis for application in the aquaculture industry. The finding provides new insights on the biochemical mechanism controlling larval metamorphosis in this species.  相似文献   

9.
The purpose of this study was to examine regulatory volume decrease (RVD) in Atlantic salmon red blood cells (RBCs). Osmotic fragility was determined optically, mean cell volume was measured electronically, and changes in intracellular Ca2+ concentration were visualized using fluorescence microscopy and fluo-4-AM. Cells displayed an increase in osmotic fragility and an inhibition of volume recovery following hypotonic shock when they were exposed to a high taurine Ringer or when placed in a high K+ medium. Interestingly, RVD in cells from fish collected during the summer depended more on taurine efflux, whereas fall cells relied more on the loss of K+. In addition, RVD in fall cells was prevented with the K+ channel inhibitor quinine, whereas the ionophore gramicidin decreased osmotic fragility and potentiated volume recovery. Further, hypotonic shock (0.5X Ringer) for both summer and fall cells caused an increase in cytosolic Ca2+, which resulted from influx of this ion because it was not observed when extracellular Ca2+ was chelated with EGTA (10 nM free Ca2+). Cells exposed to a low Ca2+ hypotonic Ringer also had a greater osmotic fragility and failed to recover from hypotonic swelling. Finally, inhibition of phospholipase A2 with ONO-RS-082 blocked volume recovery. In conclusion, Atlantic salmon RBCs displayed volume decrease in response to hypotonic shock, which depended on a swelling-induced influx of Ca2+ and an increase in the efflux of K+ and taurine.  相似文献   

10.
Whole-body influx and efflux of K+ were determined for 25-day-old striped bass,Morone saxatilis, in conditions that simulated harvesting fish from ponds. During the first 5h in fresh water with combined high NaCl (80 mM) and low Ca2+ (0.12 mM) concentrations, a combination that is acutely lethal to this age of striped bass, K+ influx for fish in 0.07 mM K+ was 21±1.7 (SEM) compared to 3.4±0.33 nmol g–1 h–1 for fish in water with low Na+ (0.25 mM) or high Ca2+ (2.5 mM) concentrations. Influx of K+ was inhibited during the first few hours after fish were placed in flux chambers. Potassium efflux as percentage of42K lost per hour was two-fold higher from fish in the high Na-low Ca treatment compared to fish in low concentrations of Na+ or high concentrations of Ca2+. Potassium efflux was probably much greater than influx, but exact values for efflux could not be calculated from the data available. Survival of fish in water with high Na-low Ca was not increased by addition of KCl to the water, indicating that the net loss of K+ was probably not the cause of death.  相似文献   

11.
Two approaches (i.e. water and dry or semi‐dry transport) have been developed for the transport of swimming crabs Portunus trituberculatus in recent years. To evaluate their differential effects on physiological responses of crabs, we measured haemolymph components (metabolic substrates, metabolites and ions) and hepatopancreas glycogen level at different time intervals after exposure of crabs to thermal stresses in water and air. The immersed crabs exhibited no significant change in all metabolic substrates except the glucose level in the hypothermal stressed treatment (> 0.05), whereas there was a great variation in haemolymph glucose and lipid level of air exposed crabs under both thermal stresses (< 0.05). With respect to metabolites in immersed crabs, only urea concentration in hypothermal stressed crabs and lactate concentration in hyperthermal stressed crabs changed significantly during the experiment; by contrast, the air exposed crabs responded significantly in all metabolites to thermal stresses (< 0.05). The immersed crabs decreased the concentration of Na+ and Mg2+, but increased the concentration of K+ and Ca2+. The change in Na+ and Ca2+ were not significant in the hyperthermal stressed crabs (> 0.05). Nevertheless, all ions except K+ accumulated significantly in the air exposed crabs after thermal stresses (< 0.05). Crabs in the two different media responded similar to thermal stresses in metabolism but differed greatly in ions regulation. The effects of thermal stresses on crabs could be magnified by exposure to air, leading to animals relying more on anaerobic metabolism and therefore limiting the usage of dry or semi‐dry transport approach especially at high temperature.  相似文献   

12.
The suitability of inland saline water (ISW) from the Lahli‐Baniyani Fish Farm, Rohtak was investigated for the larval rearing of giant freshwater prawn (GFP), Macrobrachium rosenbergii. Six experiments were conducted. In Experiment‐I, 54% of the larvae metamorphosed to postlarvae (PL) in constituted seawater (CSW) whereas total mortality occurred at larval stages (LS)‐II and LS‐III in ISW with salinity of 12 g L?1. Larvae survived to LS‐IV in Experiment‐II, when ISW was supplemented with K+~ SW. In Experiment‐III, total hardness in ISW was reduced serially, but K+ ~ SW was supplemented. The larvae did not survive beyond LS‐V. In Experiment‐IV, ISW was amended with different ratios of Mg2+/Ca2+ and K+ ~ SW. The larvae successfully metamorphosed to postlarvae with highest survival of 51.6% in Mg2+/Ca2+ ratio of 2.5. In Experiment‐V, eight larval cycles were run with water quality used in Experiment V, where all the cycles produced PL's with a survival rate of 20–67%. In Experiment VI, the larvae were reared in Mg2+/Ca2+ ratio of 2.5 and different levels of K+ to optimize its requirement. The ISW amended with K+ 80% ~ SW and Mg2+/Ca2+ ratio of 2.5 was found to be commercially suitable for the seed production of GFP.  相似文献   

13.
The motility and fertilizing ability of the Persian sturgeon, Acipenser persicus, spermatozoa were investigated. Optimum ionic content (Na+, K+, Ca2+ and Mg2+) and pH of activation solution as well as the optimum dilution rate were determined. The results show optimum motility characteristics of spermatozoa in buffered solutions containing 25, 0.2, 3 and 10 mM L?1 Na+, K+, Ca2+ and Mg2+, respectively, at dilution rate 1:50 and pH 8.0. To test the fertilizing ability of sperm, two buffered saline solutions were used as activation solution of sperm motility. The present study indicated (1) spermatozoa motility is one of key factors that influence on fertilizing ability of sperm, (2) a high fertilizing ability of sperm is obtained after dilution in saline solutions rather than in freshwater and (3) a maximum fertilization rate occurs in buffered saline solution containing 0.2 mM L?1 K+. There is also a good correlation between biochemical characteristics of seminal plasma and fertilizing ability of sperm.  相似文献   

14.
The chorions of rainbow trout were investigated to measure their ion-exchange characteristics. These characteristics have been incorporated into a model, based on ion-exchange theory, which attempts to describe interactions between chorions and a range of water qualities, in terms of the distribution of K+. The model was tested by comparing predicted K+ accumulation by chorions with that actually measured in experimental conditions. The model successfully predicted the influence of combinations of K+ and Ca2+ on K+ accumulation, and was able to predict the direction of changes in K+ accumulation in the presence of aluminium and low pH.  相似文献   

15.
Changes in Ca2+ content and flux, and the development of skin chloride cells in embryos and larvae of tilapia, Oreochromis mossambicus, were studied. Tilapia embryos hatched within 96h at an ambient temperature of 26–28°C. Total body Ca2+ content was maintained at a constant level, about 4–8 nmol per individual, during embryonic development. However, a rapid increase in body Ca2+ level was observed after hatching, 12.8 to 575.3 nmol per individual from day 1 to day 10 after hatching. A significant influx and efflux of Ca2+ occurred during development, with the average influx rate for Ca2+ increasing from 5.9 pmol mg−1 h−1 at 48h postfertilization to 47.8 pmol mg−1 h−1 at 1 day posthatching. The skin was proposed as the main site for Ca2+ influx before the development of gills, and the increased Ca2+ influx may be ascribed to gradual differentiation of skin surface and chloride cells during embryonic development. Ca2+ efflux was 16–56 pmol mg−1 h−1 in 1-day-old larvae. The resulting net influx of Ca2+, 10–12 pmol mg−1 h−1, accounted for the increased Ca2+ content after hatching. When comparing the measured and estimated ratios of efflux and influx, active transport was suggested to be involved in the uptake of Ca2+. Chloride cells, which may be responsible for the active uptake of Ca2+, started to differentiate in the skin of embryos 48h after fertilization, and the density of chloride cells increased following the development. A possibility of active transport for Ca2+ in early developmental stages of tilapia is suggested.  相似文献   

16.
During capture and storage of tuna, a small but significant number of fish display a characteristic muscle degeneration termed tuna burn. Based on detailed amino acid analyses and on previous studies of metabolite changes during online swimming of tuna, a new model of the etiology of burnt muscle is developed. According to this model oxygen-lack to white muscle (developing initially during capture) leads to a metabolic collapse, to a drop in ATP concentration, to a consequent opening of ATP-dependent K+ channels, with an efflux of K+, and thus to a collapse of membrane potential. When the membrane potential falls far enough to open voltage-dependent Ca++ channels, Ca++ influx occurs leading to elevated Ca++ concentrations in the cytosol. This process is augmented by simultaneous movement of Ca++ from sarcoplasmic reticulum (SR) and from mitochondria into the cytosol. At high intracellular concentrations Ca++ can be devastating. One of its more notable effects involves the activation of Ca++-dependent proteases, which preferentially target key components of the contractile machinery (troponins, tropomyosin, C-protein, M-protein, Z-discs, -actinin) and thus cause disassembly of myofilaments prior to any significant hydrolysis of myosin or actin. This process is autocatalytic in the sense that Ca++-activated proteases may act upon SR, thus increasing Na+ /Ca++ exchange, and ultimately adding more Ca++ to the cytosolic pool. According to this model, the difference between burnt and unburnt regions of the myotome is simply due to how far each region has moved along this self-destructive, autocatalytic pathway. The model is helpful in explaining previously perplexing data and in making useful (i.e. measurable) predictions for further studies of this important problem.  相似文献   

17.
An increase in salinity of freshwater can affect the physiology and metal uptake in fish. In the present study, Nile tilapia Oreochromis niloticus were exposed to copper (1.0 mg/l) in increased salinities (2, 4, and 8 ppt) for 0, 1, 3, 7, and 14 days. Following the exposures, the activities of Na+/K+-ATPase, Mg2+-ATPase, and Ca2+-ATPase were measured in the gill, kidney, and intestine to evaluate the changes in osmoregulation of fish. Results showed that increases in salinity and Cu exposure of fish significantly altered the ATPase activities depending on the tissue type, salinity increase, and exposure durations. Salinity-alone exposures increased Na+/K+-ATPase activity and decreased Ca2+-ATPase activity. Na+/K+-ATPase activity decreased following Cu exposure in 2 and 4 ppt salinities, though the activity increased in 8 ppt salinity. Ca2+-ATPase activity decreased in the gill and intestine in all salinities, while the activity mostly increased in the kidney. However, there were great variations in Mg2+-ATPase activity following exposure to salinity alone and salinity+Cu combination. Cu accumulated in the gill and intestine following 14 days exposure and accumulation was negatively correlated with salinity increase. Data indicated that ATPases were highly sensitive to increases in salinity and Cu and might be a useful biomarker in ecotoxicological studies. However, data from salinity increased freshwaters should carefully be handled to see a clear picture on the effects of metals, as salinity affects both metal speciation and fish osmoregulation.  相似文献   

18.
Catfish, Ictalurus melas, were pre-adapted to artificial tap water with 1.2 mM Ca2+ for two weeks, and subsequently transferred to artificial tap water with 0.6, 1.2, or 2.2 mM Ca2+ for one week in order to investigate the effect of the environmental Ca2+-concentration on stimulus encoding and the frequency characteristics in ampullary electroreceptor organs. Within 30 minutes after transfer, the spontaneous activity of the primary afferents, as well as gain and phase of the stimulus induced responses changed transiently corresponding to the Ca2+-concentration. One day after transfer the Ca2+-induced changes of the spontaneous activity had disappeared as well as the differences between the sensitivities at frequencies of 2, 8, 12, 16 and 20 Hz in 0.6 and 1.2 mM Ca2+, whereas at 16 and 20 Hz in 2.2 mM Ca2+ the sensitivity was still elevated. The Ca2+-induced phase shift was strongly frequency dependent. At 2 Hz no Ca2+ effect on the phase was observed, whereas at 12, 16 and 20 Hz significant effects could be demonstrated up till three days after transfer. The latency was not affected by the transfer.The Ca2+-induced effects on the primary afferent spontaneous activity are probably related to a Na+/Ca2+-exchanger at the basal faces of the receptor cells. The frequency dependent effects on gain and phase are concluded to relate to properties of the apical membrane, most likely to Ca-dependent K-channels. These findings further support the concept that ampullary electroreceptor might serve as chemoreceptor organs.  相似文献   

19.
The purpose of this work was to determine the tissue accumulation of lead (Pb) and its effects on osmoregulatory processes of the freshwater fish Prochilodus lineatus. Juvenile fish were exposed to Pb (from 1.7 to 0.7 mg of dissolved Pb L?1) for 6, 24 and 96 h and Pb accumulation was analyzed in the gills, liver, kidneys, blood cells and muscle. The following parameters were also analyzed: hematologic (hemoglobin content, hematocrit and number of red blood cells), metabolic (blood glucose), endocrine (blood cortisol), osmo ionic (plasma osmolality and Na+, K+, Cl? and Ca+2 concentrations), gill enzymes (Na+/K+-ATPase and carbonic anhydrase), chloride cell (CC) density and CC location in the gills. Pb accumulated in all the analyzed tissues, with the kidneys showing the highest concentration, followed by the gills and liver. The lowest Pb concentrations were found in blood cells and muscle. Pb promoted an increase in blood glucose after 6 and 24 h exposure. Gill Na+/K+-ATPase was inhibited after 24 h of exposure, but its activity was restored at 96 h, probably due to the increase in CC in gill lamellae. Plasma Na+ was reduced after 6 and 96 h, while K+ concentrations increased at all the experimental times. Fish exposed to Pb showed reduced plasma Ca+2 at all experimental periods. Hematologic parameters remained unchanged. Overall, this study demonstrated that Pb interferes in osmoregulatory processes of P. lineatus and the proliferation of CC in the gills is a response in order to reestablish adequate ion concentrations.  相似文献   

20.
This study investigated the effect of 0.25–5 mM K+, Ca2+, and Mg2+ on sperm motility in the perch, Perca fluviatilis. In 75 mM NaCl, the used motility-activating solution, motility rate, and swimming velocity decreased within the first 4 min after activation, and the rate of locally motile sperm increased. Thereafter, the motility parameters remained constant for periods >20 min. Based on the decrease in sperm motility, two types of semen samples could be distinguished. Semen samples of type I retained a high motility rate of >65 % after 20 min, and the rate of locally motile sperm was <20 %. In semen samples of type II, the motility rate decreased to values <30 % after 20 min, and the rate of locally motile sperm exceeded >50 %. Ca2+ and Mg2+ concentrations of 0.25–0.5 mM had no effect on the sperm motility parameters 10 s after activation, while 0.25 mM K+ increased the swimming velocity. K+, Ca2+, and Mg2+ concentrations ≥1.5 mM had suppressive effects on the sperm motility 10 s after activation. No differences were found between the two semen types. Twenty minutes after activation, type I semen was not affected by the tested cations. On the contrary, 0.25–2.5 mM K+, 0.25 mM Mg2+, and 0.25–2.5 mM Ca2+ significantly increased the sperm motility rate and/or sperm velocity of type II semen. Therefore, supplementation of saline solution with cations might stabilize the motility of perch sperm, which can be a benefit for experimental purposes and for specific handling procedures in aquaculture.  相似文献   

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