Oxidative stress and antioxidant responses in juvenile Brazilian flounder <Emphasis Type="Italic">Paralichthys orbignyanus</Emphasis> exposed to sublethal levels of nitrite

This study evaluated the effects of short-term exposure to sublethal levels of nitrite on oxidative stress parameters and histology of juvenile Brazilian flounder Paralichthys orbignyanus. An assessment of fish recovery was also performed. Fish were exposed to 0.08 (control), 5.72, 10.43, and 15.27 NO₂-N mg L^?1 for 10 days followed by the same recovery time. Gill, liver, and muscle samples were collected after 1, 5, and 10 days of exposure and after recovery for the measurement of antioxidant capacity against peroxyl radicals (ACAP), glutathione-S-transferase (GST) activity, content of non-protein (NPSH) and protein thiols (PSH), and lipid peroxidation levels by thiobarbituric acid-reactive substances (TBARS) content. Nitrite exposure induced alterations which compromised the overall antioxidant system (reduced ACAP and GST activity) and enhanced oxidative damage in lipids and proteins. Increases in GST activity and NPSH and PSH contents were also demonstrated. The recovery period allowed for resumption of basal levels for all (treatment 5.72 NO₂-N mg L^?1) or some of the evaluated parameters (other treatments). In conclusion, exposure to nitrite concentrations from 5.72 to 15.27 NO₂-N mg L^?1 induced oxidative stress and antioxidant responses in juvenile Brazilian flounder. The 10-day recovery period was sufficient for a complete resumption of basal physiological condition of fish exposed to concentrations of up to 5.72 NO₂-N mg L^?1.     

Effect of dietary vitamin E and selenium supplementation on growth, body composition, and antioxidant defense mechanism in juvenile largemouth bass (Micropterus salmoide) fed oxidized fish oil

Six oxidized fish oil contained diets were formulated to investigate the effect of graded levels of vitamin E (V_E) (α-tocopherol acetate: 160, 280, and 400 mg kg^?1) associated with either 1.2 or 1.8 mg kg^?1 selenium (Se) on growth, body composition, and antioxidant defense mechanism of juvenile largemouth bass. Another control diet containing fresh fish oil with 160 mg kg^?1 V_E and 1.2 mg kg^?1 Se was also prepared. Over a 12-week feeding trial, about 5 % of Micropterus salmoide fed diet OxSe1.2/V_E160 showed inflammation and hemorrhage symptoms at the base of dorsal, pectoral, and tail fin. Fish in all treatments survived well (above 90 %). Feed intakes (88.42?89.58 g fish^?1) of all treatments were comparable. Growth performances (weight gain and specific growth rate) and feed utilization (feed and protein efficiency ratio) were significantly impaired by dietary oil oxidation, and they did not benefit from neither V_E nor Se supplementation. Regardless of dietary V_E and Se supplementation, oxidized oil ingestion resulted in markedly decreased hepatosomatic index and intraperitoneal fat ratio. Oxidized oil ingestion also induced markedly lower liver and muscle lipid contents, and these effects could be alleviated by dietary Se supplementation. Dietary oil oxidation stimulated hepatic catalase activities relative to the control, and supplementation of V_E abrogated this effect. Hepatic reduced glutathione content in the control was markedly higher than that of treatment OxSe1.2/V_E160, without any significant differences comparing with the other oxidized oil receiving groups. Hepatic glutathione peroxidase activity and liver Se concentration reflected dietary Se profile, whereas liver V_E level reflected dietary V_E profile. Compared with the control, fish fed diet OxSe1.2/V_E160 obtained markedly higher serum, liver and muscle malondialdehyde contents, which droppe significantly with increasing either V_E or Se supplementation. In conclusion, the overall results in this study suggested that both V_E and Se inclusion could protect largemouth bass from the oxidative damage challenged by dietary oil oxidation.     

Ammonia and nitrite toxicity to false clownfish <Emphasis Type="Italic">Amphiprion ocellaris</Emphasis>

False clownfish, Amphiprion ocellaris, is one of the most commercialized fish species in the world, highly produced to supply the aquarium market. The high stocking densities used to maximize fish production can increase ammonia and nitrite to toxic levels. In this study, A. ocellaris juveniles (1.20 ± 0.34 g) were exposed to six concentrations of ammonia ranged from 0.23 to 1.63 mg/L NH₃-N and eight concentrations of nitrite (26.3–202.2 mg/L NO₂ ^?-N). The LC₅₀- 24, LC₅₀-48, LC₅₀-72 and LC₅₀-96 h were estimated to be 1.06, 0.83, 0.75 and 0.75 mg/L for NH₃-N and 188.3, 151.01, 124.1 and 108.8 mg/L for NO₂ ^?-N. Analysis of gill lesions caused by sublethal concentrations of these nitrogenous compounds showed that both nitrogenous compounds induced tissue lesions such as hyperplasia of epithelium cells, hypertrophy of chloride cells and lamellar lifting to all concentrations tested. However, histopathological alterations were more conspicuous accordingly the increase of ammonia or nitrite in fish exposed to 0.57 mg/L NH₃-N or 100 mg/L NO₂ ^?-N. Based on our results, we recommend to avoid concentrations higher than 0.57 mg/L of NH₃-N and 25 mg/L of NO₂-N in water.     

Acclimation to a low oxygen environment alters the hematology of largemouth bass (Micropterus salmoides)

One of the most severe impacts of urbanization on aquatic systems is the increasing presence of low oxygen environments caused by anthropogenic sources of pollution. As urbanization increases nationally and globally, it is becoming exceedingly important to understand how hypoxia affects aquatic fauna, especially fish species. In an effort to better understand the impacts of prolonged hypoxia on fishes, largemouth bass were held at 3.0 and 9.0 mg L^?1 for 50 days, which has previously shown to be temporally sufficient to impart plastic phenotypic changes. Following the holding period, fish from each group were subjected to a low dissolved oxygen (DO) challenge of 2.0 mg L^?1 for 6 h, and their physiological and hematological parameters were compared with control fish held for 6 h with no change in DO. There were no differences in the physiological stress responses between the two holding groups; however, the low oxygen holding group had increased hemoglobin and hematocrit levels following the 6-h low oxygen challenge compared with the high oxygen group. These results suggest largemouth bass exposed to chronic low oxygen conditions, either naturally or anthropogenically, may possess a beneficial advantage of increased oxygen uptake capacity during periods of low oxygen.     

The energy requirements of Eurasian perch (Perca fluviatilis L.) in intensive culture

Fish feed constitutes one of the largest costs in aquaculture, therefore inefficient feed management will have a negative impact on fish farm economics. Eurasian perch (Perca fluviatilis L.) is a relatively new candidate for freshwater aquaculture, however little is known about the energy requirements of this species. The aim of this study was to develop an energy requirement model for intensive culture of Eurasian perch reared at rational temperatures. Data on growth (the thermal unit growth coefficient, TGC, ³√g · (°C · days)^?1) and digestible energy need (DEN, kJ DE · g^?1) of Eurasian perch at a size range of 20–180 g and at temperatures of 17–23 °C were used. Regression analysis revealed that both TGC and DEN were affected significantly by fish size (P < 0.001) but not by temperature (P > 0.05). Two models including body size of the fish were developed: (i) an inverse TGC model for evaluation of the daily theoretical weight increment (TWi, g · day^?1) and (ii) a linear DEN model. The TGC model was validated by comparing theoretical data with data obtained from a commercial growth trial. By combining the TWi and the DEN, a model describing the daily theoretical energy requirement (TER, kJ · day^?1) at different temperatures and for Eurasian perch of different sizes was successfully developed.     

Water quality and growth of Pacific white shrimp Litopenaeus vannamei (Boone) in co-culture with green seaweed Ulva lactuca (Linaeus) in intensive system

An indoor trial was conducted for 28 days to evaluate the effects and interactions of biofloc and seaweed Ulva lactuca in water quality and growth of Pacific white shrimp Litopenaeus vannamei in intensive system. L. vannamei (4.54 ± 0.09 g) were stocked in experimental tanks at a density 132 shrimp m^?2 (566 shrimp m^?3) and the U. lactuca was stocked at a density 0.46 kg m^?2 (2.0 kg m^?3). Biofloc with seaweed (BF-S) significantly reduced (P < 0.05) total ammonia nitrogen (TAN) by 25.9 %, nitrite–nitrogen (NO₂–N) by 72.8 %, phosphate (PO ₄ ³ -P) by 24.6 %, and total suspended solids by 12.9 % in the water and significantly increased (P < 0.05) settleable solids by 34.2 % and final weight of shrimp by 6.9 % as compared to biofloc without seaweed. The BF-S can contribute by reducing nitrogen compounds (TAN and NO₂–N), phosphate (PO ₄ ³ -P), and total suspended solids in water and increased final weight of shrimp.     

Nitrite Toxicity and Methemoglobin Changes in Southern Flounder,Paralichthys lethostigma,in Brackish Water

This study was performed to estimate the nitrite toxicity to southern flounder, Paralichthys lethostigma, in brackish water (7.5 ppt of salinity). For a LC₅₀ test, 20 fingerlings (5.7 ± 0.4 cm) in each aquarium (15 L) were exposed to the concentrations of 0, 1, 5, 10, 15, 30, 60, 120, and 240 mg NO₂^?‐N/L in duplication for 10 d. Median lethal concentration at 96 h (96‐h LC₅₀) was calculated as 81.6 mg NO₂^?‐N/L. For a verification test, young flounder (164.2 ± 9.1 g) were exposed to a simulated culture condition in recirculating systems (1000 L). Sodium nitrite was not added to control system, whereas it was added to Treatment system 1 (TS 1) and Treatment system 2 (TS 2) to maintain nitrite concentrations of 20 and 30 mg NO₂^?‐N/L, respectively. The plasma nitrite concentrations of the young flounder in TS 1 and TS 2 were 4.5 and 6.6 mg NO₂^?‐N/L, respectively, after 2 wk. At this time, the methemoglobin percentages in TS 1 and TS 2 reached 85.8 and 89.7%, and survival rates were 37.5 and 25.0%, respectively. The results of these tests indicate that southern flounder do not concentrate nitrite in blood from the environment, but they seem to be more sensitive to nitrite compared with other species that do not concentrate nitrite.     

Acute ammonia toxicity during early ontogeny of ide Leuciscus idus (Cyprinidae)

Acute ammonia toxicity was investigated in four developmental stages of the juvenile ide, Leuciscus idus: 1, 10, 20 and 30 days after the first feeding. Mean (±SD) total length of the larvae was 8.5 ± 0.3, 15.7 ± 0.7, 23.0 ± 2.0 and 29.7 ± 2.0 mm, and standard weight was 1.6 ± 0.3, 9.2 ± 5.5, 94.9 ± 31.0 and 196.0 ± 31.7 mg, respectively. The larvae used for toxicity tests were reared in the experimental, closed recirculating system. Groups of fishes (n from 7 to 10; in respect of fish size) were exposed to the ammonium chloride solutions in 1-L glass units. Water temperature was 25 ± 0.1 °C for both the rearing and the toxicity tests. pH was not adjusted and ranged between 8.4 and 8.7. The ammonium chloride solutions were renewed every 12 h. At the same time, dead larvae were counted and removed, and the pH and temperature measurements were taken. Each acute toxicity test duration was 96 h, and lethal concentration LC₁, LC₅₀ and LC₉₉ values were calculated for 24, 48, 72 and 96 h. The susceptibility of the ide larvae to ammonia decreased linearly with age up to 20th day and surprisingly increased during the next 10 days. The LC₅₀ (48 h) values ranged from 0.27 mg L^?1 of unionized ammonia nitrogen for 1 day after the first feeding (AFF) larvae to 1.42 mg L^?1 at day 20 after first feeding. The LC₅₀ (48 h) for 30 days AFF was as high as 0.67 mg L^?1. The critical level of the unionized ammonia nitrogen for ide larvae was suggested as 0.21 mg L^?1.     

Respiratory response of grass carp <Emphasis Type="Italic">Ctenopharyngodon idellus</Emphasis> to dissolved oxygen changes at three acclimation temperatures

Respiratory parameters of grass carp were studied during dissolved oxygen (DO) changes from normal DO to hypoxia, then return to normal DO at 15, 25, and 30 °C acclimation, respectively. The results showed that with increases of acclimation temperature at normoxia the respiratory frequency (f_R), oxygen consumption rate (VO₂), respiratory stroke volume (V_S.R), gill ventilation (V_G), and V_G/VO₂ of grass carp increased significantly, but the oxygen extraction efficiency (EO₂) of fish decreased significantly (P < 0.05). With declines of DO levels, the f_R, V_S.R, V_G, and V_G/VO₂ of fish increased significantly at different acclimation temperatures (P < 0.05). A slight increase was found in VO₂, and the EO₂ of fish remained almost constant above DO levels of 3.09, 2.91, and 2.54 mg l^?1 at 15, 25, and 30 °C, while the VO₂ and EO₂ began to decrease significantly with further reductions in DO levels (P < 0.05). After 0.5 h of recovery to normoxia from hypoxia at three acclimation, the f_R, V_S.R, V_G, and V_G/VO₂ of the fish decreased sharply; meanwhile, the VO₂ and EO₂ increased sharply (P < 0.05). The respiratory parameters of fish gradually approached initial values with prolonged recovery time to normoxia, and reached their initial values in 2.5 h at 25 and 30 °C acclimation. The critical oxygen concentrations (C_c) of fish for VO₂ were 2.42 mg l^?1 at 15 °C, 2.02 mg l^?1 at 25 °C, and 1.84 mg l^?1 at 30 °C, respectively. The results suggest that grass carp are highly adapted to varied DO and short-term hypoxia environments.     

No reason for keeping 0+ perch (Perca fluviatilis L.) with the prey fish

Growth and survival of 0+ perch were studied in 4 ponds with the topmouth gudgeon (Pseudorasbora parva) and without it. In the end of April, all ponds were stocked by free-swimming perch larvae (120,000 ind ha^?1). In June, topmouth gudgeon was introduced as forage fish (40 kg ha^?1) into two of the experimental ponds. Topmouth gudgeon significantly influenced neither the total abundance of zooplankton nor the abundance of its groups (Rotifera, Cladocera, Copepoda). The most important food item for perch (TL > 29 mm) was macroinvertebrates (especially Chironomidae). In the ponds with topmouth gudgeon, copepods and cladocerans were more important than in ponds without it. Specific growth rate of perch was 0.01 mm day^?1 in all ponds. Final mean total length (TL ± SD) of perch was 73 ± 13 and 70 ± 6 mm in the ponds with topmouth gudgeon and without it, respectively. Only 1 % of the perch reached higher TL than that recorded in the ponds without the topmouth gudgeon. Survival rate of perch varied from 12 to 36 % depending on ponds. Piscivory was recorded in all ponds from the age of 57 days (post-stocking); however, perch siblings were preferred to topmouth gudgeon. The highest asymptotic growth (L∞ = 88 mm) was calculated in the pond stocked with topmouth gudgeon. This corresponded with the highest cannibalism and lowest survival rate (12 %). Perch growth rate increased till 42–53 days of perch age and then started to decrease. There was no significant influence of potential prey fish (topmouth gudgeon) on the growth of 0+ perch; however, two size cohorts were found in the ponds with the topmouth gudgeon. Presence or absence of littoral macrophytes seems to be more substantial for rearing perch in ponds than stocking with the prey fish.     

Physiological responses of largemouth bass to acute temperature and oxygen stressors

Abstract Temperature and oxygen gradients exist in nearly every water body, but anthropogenic activities can subject fish to rapid changes in these important environmental variables. These rapid changes in temperature and oxygen (generally referred to as temperature or oxygen shock) may have sub‐lethal consequences depending upon the magnitude and the fish species. This study quantified physiological changes in largemouth bass, Micropterus salmoides (Lacepède), exposed to two levels of heat and cold shocks and to two levels of hypoxic and hyperoxic shocks. Following a cold shock from 20 °C to 8 °C, plasma cortisol and glucose increased after 1 h and lactate dehydrogenase activity increased after 6 h. Plasma glucose and K⁺ concentrations increased 1 h after a heat shock from 20 °C to 32 °C but not after 6 h. Bass subjected to a hypoxic shock from 8 to 2 mg O₂ L^?1 showed decreased plasma K⁺ and increased plasma glucose and white muscle lactate. No changes in physiological parameters were observed in bass subjected up to 18 mg O₂ L^?1 hyperoxia. Results from this study suggest that largemouth bass can tolerate a wide range of temperature and oxygen shocks, but temperature decreases of 20 to 8 °C and hypoxia as low as 4 mg O₂ L^?1 should be avoided to minimise physiological perturbations.     

Nitrogenous and phosphorus excretions in juvenile silver catfish (Rhamdia quelen) exposed to different water hardness, humic acid, and pH levels

This study examined ammonia, urea, creatinine, protein, nitrite, nitrate, and phosphorus (P) excretion at different water hardness, humic acid, or pH levels in silver catfish (Rhamdia quelen) juveniles. The fish were exposed to different levels of water hardness (4, 24, 50, or 100 mg L^?1 CaCO₃), humic acid (0, 2.5, or 5.0 mg L^?1), or pH (5.0, 6.0, 7.0, 8.0, or 9.0) for 10 days. The overall measured nitrogen excretions were 88.1 % (244–423 μmol kg^?1 h^?1) for ammonia, 10.9 % (30–52 μmol kg^?1 h^?1) for creatinine, 0.02 % (0.05–0.08 μmol kg^?1 h^?1) for protein, 0.001 % (0.002–0.004 μmol kg^?1 h^?1) for urea, 0.5 % (0.64–3.6 μmol kg^?1 h^?1) for nitrite, and 0.5 % (0.0–6.9 μmol kg^?1 h^?1) for nitrate, and these proportions were not affected by water hardness or humic acid levels. The overall P excretion in R. quelen was 0.14–2.97 μmol kg^?1 h^?1. Ammonia excretion in R. quelen usually was significantly higher in the first 12 h after feeding, and no clear effect of water hardness, humic acid levels, and pH on this daily pattern of ammonia excretion could be observed. Water hardness only affected the ammonia and P excretion of R. quelen juveniles in the initial and fifth days after transfer, respectively. The exposure of this species to humic acid increased ammonia excretion after 10 days of exposure but did not affect P excretion. An increase in pH decreased ammonia and increased creatinine excretion but did not change P excretion in R. quelen. Therefore, when there is any change on humic acid levels or pH in the culture of this species, nitrogenous compounds must be monitored because their excretion rates are variable. On the other hand, P excretion rates determined in the present study are applicable to a wide range of fish culture conditions.     

Involvement of sex steroids in final stages of oogenesis in Eurasian perch, Perca fluviatilis

Significant plasma 17,20β-dihydroxy-4-pregnen-3-one peaks were measured for the first time in female Eurasian perch, Perca fluviatilis, during the pre-ovulatory period, reaching 3.5 ng ml^?1, but was not synchronized with final maturation and ovulation stages.     

Dietary ascorbic acid influences the intestinal morphology and hematology of hybrid sorubim catfish (<Emphasis Type="Italic">Pseudoplatystoma reticulatum</Emphasis> × <Emphasis Type="Italic">P. corruscans</Emphasis>)

This study evaluated the effect of graded levels of dietary ascorbic acid (AA) (12.47, 20.27, 115.44, 475.50, 737.72, and 850.70 mg kg^?1) on growth, hematology, intestinal morphometry, and phagocyte activity of hybrid sorubim Pseudoplatystoma reticulatum × Pseudoplatystoma corruscans. Fish (n = 420, 14.57 ± 2.71 g, 15.11 ± 0.90 cm) were distributed in 30 polyethylene tanks (80 l) (5 replicates per treatment with 14 fish per tank) and fed for 45 days. Dietary treatment did not have a significant effect on growth metrics (P > 0.05). Fish fed 737.72 mg AA kg^?1 had a higher villi height (289.80 ± 19.96 μm) (P < 0.05) than fish fed 850.70 mg AA kg^?1 (245.4 ± 18.25 μm). Hemoglobin in fish fed 850.70 mg AA kg^?1 (5.34 ± 0.96 g dl^?1) was higher (P < 0.05) than fish fed 12.47 mg AA kg^?1 (3.42 ± 0.55 g dl^?1) and 20.27 mg AA kg^?1 (3.06 ± 1.26 g dl^?1). The erythrocyte number of hybrid sorubim fed 115.40 mg AA kg^?1 (1.73 ± 0.27 × 10⁶ μl^?1) and 475.50 mg AA kg^?1 (1.70 ± 0.28 × 10⁶ μl^?1) were higher (P < 0.05) than in those fed diets containing 20.27 mg AA kg^?1 (1.11 ± 0.34 × 10⁶ μl^?1). There was no significant effect (P > 0.05) of dietary AA on leukocyte and thrombocyte and on phagocyte activity and phagocyte index. Inclusion of AA in feed seems to increase the integrity of the intestinal mucosa and stimulate erythropoiesis in hybrid sorubim catfish.     

Experimental oral transmission of largemouth bass virus

Largemouth bass virus (LMBV) is a recently discovered iridovirus that causes a fatal disease of largemouth bass, Micropterus salmoides (Lacepède). Fish can become infected by waterborne LMBV, but oral transmission of this virus has not been demonstrated previously. Largemouth bass were gavaged with guppies, Poecilia reticulata Peters, which had been injected with LMBV, and then sampled periodically during a 7‐week observation period. The dose of LMBV averaged 10^5.6 tissue culture infectious doses – 50% cytopathic endpoint (TCID₅₀) per largemouth bass. Five of 24 largemouth bass exposed to LMBV became infected with the virus, but none of the fish had clinical signs typical of LMBV disease. Virus titres in largemouth bass were highest in swim bladder (10^5.5–9.5 TCID₅₀ g^?1) and were 10^5.2 TCID₅₀ g^?1 or lower in cutaneous mucus, head kidney, trunk kidney, spleen, gonad and intestine. These results indicate that LMBV can be transmitted orally to largemouth bass, but further study is needed to determine the factors affecting pathogenicity of the virus.     

A survey on the environmental impact of pond aquaculture in Hungary

The aim of the study was to survey the nutrient loads of receiving waters and evaluate the nitrogen, phosphorus and organic matter budget of the conventional fishponds in Hungary. The average nitrogen (N), phosphorus (P) and organic matter (OM) concentrations in the filling-up water of the fishponds were 2.51 ± 1.25, 0.57 ± 0.57 and 23.8 ± 13.4 mg l^?1, respectively. Contrarily, the N, P and OM concentrations in the effluents of fishponds were 1.64 ± 2.19, 0.37 ± 0.51 and 30.2 ± 20.5 mg l^?1, respectively. The sediment nutrient content in the fishponds during the operation was 5.77 ± 4.42 mg g dry sediment^?1 for N, 1.25 ± 0.75 for P and 30.5 ± 43.3 for total organic carbon. The retained nutrients represented on average 53 % (84 kg ha^?1 year^?1) of N, 74 % (21 kg ha^?1 year^?1) of P and 74 % (2400 kg ha^?1 year^?1) of OM, introduced into the fishponds. In the fishponds, the ratio of input N, P and OM accumulated in fish biomass was 18.4 ± 6.7, 10.4 ± 4.4 and 6.8 ± 2.1 %, respectively. The investigated fishponds discharged 48 % less N and 62 % less P into the recipient waters than received with the intake water. However, 78 % more OM was discharged with the effluent from the fishponds than received with the inlet and supplement water.     

The use of formaldehyde for the disinfection of maternally incubated eggs of noble crayfish (<Emphasis Type="Italic">Astacus astacus</Emphasis>)

The high mortality of maternally incubated eggs represents a serious problem that prevents the development of noble crayfish (Astacus astacus) farming in Italy. In this experiment, formaldehyde bath technique has been tested with maternally incubating females. The survival rate of maternally incubated eggs, exposed to progressively reduced concentrations of formaldehyde (4000, 3000, 2000, 1000, 1500 and 500 mg l^?1), has been compared with that of untreated controls for two consecutive years (2010 and 2011). The formaldehyde treatments were administered as disinfection baths, for a period of 15 min, twice a week. A concentration of formaldehyde of 500 mg 1^?1, or greater, was found to be effective in controlling egg mortality, without apparent harming the female broods.     

Immunomodulatory effect of cimetidine in common carp (Cyprinus carpio L.)

The main indication of cimetidine is being H₂-receptor antagonist, but studies suggest that cimetidine may also act as a non-specific stimulant of cell-mediated immunity and immunomodulator. In order to determine the immunomodulatory effect of dietary intake of cimetidine in the common carp (100 ± 10 g), subjects were fed diets containing 0 (control), 50, 100 and 200 mg cimetidine kg^?1 of dry diet for a period of 6 weeks. TLC and NBT assays were significantly (P < 0.05) stimulated in cimetidine-supplemented groups displaying the highest value in 200 mg kg^?1 group. A decrease (P < 0.05) in cortisol and ACH50 value was recorded in fish treated with cimetidine. Serum protein, albumin and serum globulin levels were not significantly changed. The findings of the present investigation suggest that the incorporation of cimetidine in the diet of common carp enhances the non-specific immunity.     

Effect of nitrite exposure on oxygen-carrying capacity and gene expression of <Emphasis Type="Italic">NF-κB</Emphasis>/<Emphasis Type="Italic">HIF-1α</Emphasis> pathway in gill of bighead carp (<Emphasis Type="Italic">Aristichthys nobilis</Emphasis>)

Nitrite (NO₂^?) contamination of water can severely impact the health of aquatic life and is a major concern for commercial aquaculture. In order to study the effect of nitrite on Aristichthys nobilis, we investigated the oxygen-carrying capacity, NF-κB/HIF-1α pathway, and the gill tissue structure under nitrite stress. In the current study, bighead carp (initial weight 180.05?±?0.092 g) were exposed to nitrite (48.634 mg/L) for 96 h and then for 96 h recovery test. After nitrite exposure for 6 h, hypoxia-inducible factor-1α (HIF-1α) and nuclear factor-κB (NF-κB) mRNA expression increased significantly in the gill of bighead carp (P?<?0.05). After nitrite exposure for 12 h, hemoglobin (Hb) and methemoglobin reductase (MHBR) content in blood decreased significantly (P?<?0.05); TLR4 mRNA expression increased significantly (P?<?0.05). After nitrite exposure for 24 h, methemoglobin (MetHb) content increased significantly (P?<?0.05). After recovery test, all the indicators except TLR4 mRNA expression level recovered to initial level. In conclusion, nitrite exposure can affect hemoglobin dynamics, as oxidization of nitrite by hemoglobin results in the reduction of Hb to MetHb leading to hypoxia and nitrite exposure can also result into gill tissue damage. In the face of nitrite exposure, NF-κB and HIF-1α mRNA expression level increased immediately to protect the body from oxidative damage and eased hypoxic condition caused by nitrite. It was also observed that nitrite damage is recoverable in Aristichthys nobilis, but it may be need more than 96 h.     

Effects of dietary selenium on the pathological changes and oxidative stress in loach (Paramisgurnus dabryanus)

In this study, loach (Paramisgurnus dabryanus) were fed artificial diets containing 0.31 (control), 0.39, 0.48, 0.50 and 0.62 mg kg^?1 of selenium (Se) for 60 days, respectively. Liver histopathology, hepatocyte ultrastructure, blood indices, biochemical parameters of liver functions and oxidative stress in the Se-treated loach were then assayed. The results showed the following: histopathological and ultrastructural lesions in liver were only observed in loach fed the 0.62 mg Se kg^?1 diet; Haemoglobin and total protein were significantly increased in the 0.50 mg Se kg^?1 group; albumin and high-density lipoprotein were increased significantly in the 0.48–0.50 mg Se kg^?1 groups. However, white blood cell count was significantly decreased in the 0.48 mg Se kg^?1 group; alanine aminotransferase, aspartate aminotransferase and lactate dehydrogenase were decreased in the 0.39–0.50 mg Se kg^?1 groups. In liver tissue, the content of hydrogen peroxide was lower than that of controls in the 0.48–0.50 mg Se kg^?1 groups, and the malondialdehyde level was lowest in the 0.48 mg Se kg^?1 group. The activities of superoxide dismutase and glutathione peroxidase were significantly increased in the 0.50 mg Se kg^?1 group; catalase and total antioxidant capacity were markedly increased in the 0.48–0.50 mg Se kg^?1 group. These present results indicated that the dietary Se requirement for loach is 0.48–0.50 mg Se kg^?1 diet.