Short communication: Acute toxicity of hydrogen peroxide in juvenile white shrimp Litopenaeus vannamei reared in biofloc technology systems

Biofloc technology (BFT) has been used to rear white shrimp, Litopenaeus vannamei. In this culturing system, the absence of aeration causes a rapid drop in dissolved oxygen levels, and hydrogen peroxide (H₂O₂) can be used as an emergency source of oxygen. This study aimed to determine the lethal concentration and safe level of H₂O₂ applied as a source of oxygen for juvenile white shrimp L. vannamei in a BFT system. Juveniles (1.39 ± 0.37 g) were exposed for 2 h to different concentrations of H₂O₂ [29 (100), 58 (200), 116 (400), 174 (600), 232 (800), 290 (1,000) and 348 (1,200) μL H₂O₂/L (ppm H₂O₂-29 %/L)] in addition to a control group without addition of H₂O₂, and the survival rates were monitored for 96 h. The LC₅₀ values and 95 % confidence intervals at 24, 48, 72 and 96 h were 235.5 (207–268), 199.1 (172–229), 171.1 (146–198) and 143.3 (120–170) μL H₂O₂/L, respectively. The safe level was 14.3 μL H₂O₂/L, and the highest concentration with survival rates similar to the control group (NOAEC) was 29 μL H₂O₂/L. In these concentrations, H₂O₂ can be used as a safe source of oxygen for L. vannamei reared in BFT systems.     

Survival of Diploid and Triploid Rhamdia quelen Juveniles Under Different Oxygen Concentrations

The objective of this study was to determinate the lethal concentration of dissolved oxygen (DO) over 96 hours of exposure (LC50–96h) for diploid and triploid jundia Rhamdia quelen juveniles. Diploid and triploid fish weighing approximately 4 g were subjected to DO concentrations varying between 0.4 and 1.3 mg O₂ L^?1; water temperature was maintained at 27?°C and pH at 6.3. The LC50–96h for diploids of Rhamdia quelen was 0.535 mg O₂ L^?1, while the value obtained for triploids was 6% greater. These results demonstrated that triploids of Rhamdia quelen juveniles have greater sensitivity to hypoxia compared to diploids.     

氧化应激对鲤抗氧化状态和免疫功能的影响

为探讨氧化应激对鲤抗氧化状态和免疫功能的影响,本实验以H_2O_2作为活性氧自由基(ROS),将鲤暴露于不同浓度的H_2O_2(0、0.25、0.50和1.00 mmol/L)中,诱导鲤产生氧化应激反应。连续暴露7 d后,采集鲤血液和肝组织,以检测相关生化指标以及基因表达量的变化。结果显示,与空白对照组(0 mmol/L)相比,随着H_2O_2浓度的升高,血清葡萄糖(GLU)、皮质醇(cortisol)和乳酸(LA)含量显著升高;而碱性磷酸酶(AKP)和酸性磷酸酶(ACP)活性仅在1.00 mmol/L H_2O_2处理组中显著高于其他实验组。氧化应激参数显示,与空白对照组(0 mmol/L)相比,0.50和1.00 mmol/L H2O2处理显著降低血清过氧化氢酶(CAT)活性,而提高还原型谷胱甘肽(GSH)、丙二醛(MDA)和总抗氧化能力(T-AOC)水平;在肝脏组织中,1.00 mmol/L H_2O_2处理显著降低了GSH含量,促进了MDA生成。基因表达结果显示,与空白对照组相比,1.00 mmol/L H2O2处理组显著上调了肝脏组织中cyp1a表达,而下调了cyp1b表达;同时0.50和1.00 mmol/L H2O2处理显著上调了hsp70、hsp90、c3、c-lyz和hep的表达。研究表明,氧化应激暴露可诱导鲤产生明显应激反应和脂质过氧化,降低机体抗氧化能力并激发免疫应答反应。     

Zebrafish fin‐derived fibroblast cell line: A model for in vitro wound healing

The goal of this study was to develop and characterize a cell line from the caudal fin tissue of zebrafish and also its application as an in vitro model to study the effect of H₂O₂ in wound healing. Fibroblastic cell line was developed using explant culture method from caudal fin tissue of zebrafish and characterized. This cell line was named as DrF cell line. The DrF cells treated with 0–10 µM/ml H₂O₂ were tested for viability, proliferation and motility by MTT assay, trypan blue assay and chemotaxis assay, respectively. Among the different concentrations of H₂O₂, 4 µM was found to be nontoxic to study cell migration in in vitro scratch wound assay. Furthermore, the expression of proliferating cell nuclear antigen (PCNA) and chemokine receptor (CXCR4) genes was carried by qPCR. The cell survival, proliferation and migration were extremely enriched at 4 µM level of H₂O₂. We observed accelerated wound closure in DrF cells treated with H₂O_2. The qPCR results indicated that H₂O₂ markedly up‐regulated mRNA expression of PCNA and CXCR4. The findings from our study suggest that H₂O₂ at low levels promotes cell survival, proliferation, migration and wound healing in DrF cells.     

Acute and Sublethal Effects of Ammonia on Striped Bass and Hybrid Striped Bass

Bioassays in static water (mean ± SD; temperature, 20–22 C; pH, 8.2–8.4; alkalinity, 205 ± 10 mg/L CaCO₃; total hardness, 220 ± 10 mg/L CaCO₃) were used to determine median lethal concentrations (LC₅₀) of un-ionized ammonia (NH₃-N) for striped bass Moronc saxatilis and hybrid striped bass M. saxatilis × M. chrysops. The 96 h LC₅₀ for striped bass was 1.01 ± 0.24 mg/L NH₃-N₃ and was significantly higher than the LC₅₀ for hybrid striped bass (0.64 ± 0.05 mg/L NH₃-N). The effects of sublethal ammonia were evaluated after fish were exposed for 96 h to 0.0, 0.25, or 0.5 mg/L NH₃-N or to additional exposure to oxygen depleted water (about 2.0 mg O₂/L). Plasma ammonia of striped hass did not change as sublethal ammonia increased, but exposure to oxygen depletion caused a decrease in plasma ammonia. In contrast, plasma ammonia of hybrid striped bass increased as environmental ammonia increased, and increased further after exposure to oxygen depletion. Plasma cortisol levels of striped bass were significantly higher and more variable than cortisol levels of hybrid striped bass; additional exposure to oxygen depletion increased this variability, but these responses may be due to the stress of handling and confinement. Mean differences also existed between species for hemoglobin and hematocrit, while differences in variability occurred for osmolality and oxygen depletion rates. Striped bass tolerated ammonia better than hybrid striped bass but were more susceptible than hybrid striped bass to the additional stress of oxygen depletion. Most changes in physiological characteristics were relatively independent of environmental ammonia, but they were affected by oxygen depletion challenge.     

Effects of Nitrite Exposure on Growth and Survival of Sea Bass,Lates calcarifer,Fingerlings in Various Salinities

Sea bass, Lates calcarifer, fingerlings were acclimated to 0. 15, and 32 ppt, and the toxic effects of nitrite exposure were assessed. The 96-hour median lethal concentrations (96-hour LC₅₀ for nitrite were estimated to be 14.5 mg/L at 0 ppt, 105 mg/L at 15 ppt and 93 mg/L at 32 ppt salinity. Chronic exposure to a nitrite concentration equivalent to 10% of the respective 96 hour LC₅₀ resulted in marked growth reduction: growth being reduced in the order of 0 ppt > 32 ppt > 15 ppt. In nitrite-free water, growth rate for fish raised at a salinity of 15 ppt was higher compared to fish raised at salinities of 0 ppt and 32 ppt, a phenomenon which probably reflected the advantage of a reduction in osmoregulatory work in an iso-osmotic environment.     

Toxicity of Peracetic Acid to Fish: Variation among Species and Impact of Water Chemistry

There has been strong interest in the use of peracetic acid (PAA) in aquaculture as it can be used to disinfect water and hard surfaces and thereby eliminate or lower the burden of fish pathogens. Unfortunately, there has been little research on the toxicity of PAA to fish. Twelve species of fingerling fish that are important to aquaculture were exposed to PAA for 24 h in static toxicity bioassays in well water. These fish were: fathead minnow, Pimephales promelas; black‐nose crappie, Pomoxis nigromaculatus; bluegill, Lepomis macrochirus; blue tilapia, Oreochromis aureus; channel catfish, Ictalurus punctatus; golden shiner, Notemigonus crysoleucas; goldfish, Carassius auratus; grass carp, Ctenopharyngodon idella; largemouth bass, Micropterus salmoides; rainbow trout, Oncorhynchus mykiss; sunshine bass, Morone chrysops × M. saxatilis; and walleye, Sander vitreus. Median lethal concentration (LC₅₀) values were estimated with the trimmed Spearman–Karber method using nominal PAA concentrations. The mean 24‐h LC₅₀ values ranged from 2.8 to 9.3 mg/L PAA. Fathead minnow were very sensitive and blue tilapia were very tolerant to PAA exposure; LC₅₀ values of other species tested were within the range of 4.1–6.2 mg/L PAA. More importantly, the 24‐h no‐observed‐effect concentration (NOEC) ranged from 1.9 to 5.8 mg/L PAA; the NOEC would be considered as the safe range for culturists to investigate the use of PAA. Decreased alkalinity/hardness increased the toxicity of PAA, while a small increase of dissolved organic content had no effect on PAA toxicity. Results of the present study are important information on the safe application of PAA for the aquaculture industry.     

急性氨氮暴露对大弹涂鱼炎性反应相关基因表达的影响

为研究急性氨氮胁迫对大弹涂鱼炎性反应相关基因表达的影响,实验挑选初始体质量为(15.14±0.05) g的健康大弹涂鱼幼鱼180尾,进行96 h的急性氨氮胁迫实验。结果显示,大弹涂鱼96 h氨氮半致死浓度为8.99 mg/L总氨氮(0.11 mg/L非离子氨,T-AN);氨氮胁迫后TNF基因的mRNA表达量分别于12和96 h时显著上调,96 h时表达量达到0 h时的2倍;IL-1基因的mRNA表达量12 h时显著上调,为0 h时表达量的6倍;氨氮胁迫后IL-6基因的mRNA表达量分别于12和96 h时显著上调,表达量达到0 h时的1.5倍;氨氮胁迫后IL-8基因的mRNA表达量在24 h时出现显著下调。研究表明,大弹涂鱼96 h氨氮半致死浓度为8.99 mg/L总氨氮;半致死浓度的氨氮胁迫48 h后,TNF、IL-1、IL-6和IL-8基因的mRNA表达量持续升高,推测过度炎性应激可能是导致鱼类氨中毒死亡的原因之一。     

Susceptibility of Caspian Roach (Rutilus rutilus caspicus) Fingerlings to Formalin

ABSTRACT

Caspian roach (Rutilus rutilus caspicus) were exposed to 0, 30, 40, 45, 50, 55, 60, 70, 100, 150 200, 250, 300, and 400 ppm formalin to determine LC₅₀. Respectively, 0.5 to 96 h LC₅₀ values were 252 to 49 ppm. The lowest observed effect concentrations (LOEC) and no observed effect concentrations (NOEC) varied between 40 to 150 and 30 to 100 ppm, respectively, across the tested time spectrum. Regression suggested that the concentrations of 88.4, 80.3, 51.2, and 40.1 ppm are maximum concentrations for 0.5, 1, 12, and 24 h bath treatment, respectively, which are not in the range suggested in the literature.     

Acute Toxicity and Sublethal Effects of Nitrite on Selected Hematological Parameters and Tissues in Dark-banded Rockfish, Sebastes inermis

Acute toxicity and sublethal effects of nitrite in dark‐banded rockfish, Sebastes inermis (83.3 ± 7.2 g), were studied under static conditions for a period of 96 h. The acute toxicity of nitrite evaluated for the 96‐h lethal concentration (LC₅₀) was 700 mg/L. The sublethal effects on selected hematological parameters of S. inermis, such as total erythrocyte count (TEC), hemoglobin, plasma glucose, and serum protein content, were measured after 0, 6, 12, 24, 48, 72, and 96 h of exposure to 0, 50, 100, 200, 400, and 700 mg/L of nitrite. Sublethal nitrite caused progressive reduction in the TEC, hemoglobin, and serum protein content in fish depending on the nitrite concentration and exposure period. The 96‐h exposure resulted in a 14–42% reduction in TEC and 25–33% reduction in hemoglobin content for 100–700 mg/L of nitrite compared to the control. A dose‐related reduction in plasma glucose (25.7–34.2%) was observed for concentrations of 200–700 mg/L of nitrite during 48 h of exposure, followed by an increase through 96 h. A significant reduction in serum protein (7.3–12.6%) was observed for 200–700 mg/L of nitrite after 96 h of exposure. Abnormal histological changes in skin, gill, liver, and kidney tissue were observed in fish exposed to 700 mg/L of nitrite after 96 h of exposure compared to the control. Although no mortality of S. inermis occurred at 500 mg/L of nitrite, all hematological parameters adversely responded to a nitrite dose of 200 mg/L for 96 h. These results showed that although acute toxicity concentration of nitrite in S. inermis is higher than 700 mg/L, sublethal concentrations of nitrite also negatively affect hematological parameters.     

Virucidal effects of common disinfectants against tilapia lake virus

Tilapia lake virus (TiLV) is an emerging virus associated with high fish mortality and economic losses. This study investigates the virucidal effects of the following disinfectants (active ingredients) on TiLV: 2.5 ppm iodine, 10 ppm sodium hypochlorite (NaOCl), 300 ppm hydrogen peroxide (H₂O₂), 80 ppm formalin and 5,000 ppm (0.5%) Virkon^®. Factors that affect the disinfectants’ efficacy, including temperature, contact time and soiling (organic matter) interference, were examined under conditions mimicking natural aquaculture practices. TiLV inactivation of higher than 5 log₁₀ TCID₅₀ ml^?1 was achieved after 10 min and at 28°C for all disinfectants except formalin; similar inactivation levels were reached by NaOCl and Virkon^® at 10 min and 4°C. Extended exposure to formalin from 10 to 60 min at 28°C rendered more than 5 log₁₀ inactivation. Increasing synthetic organic matter in the water to mimic soiling interference reduced the efficacy of NaOCl, iodine and H₂O₂ when tested at 10 min and 28°C; however, Virkon^® still achieved more than 5 log₁₀ inactivation. This study demonstrates that most common disinfectants effectively reduced viral loads to minimum levels. To limit the spread of TiLV in aquaculture farms and related facilities, the appropriate use of such disinfectants should therefore be promoted and implemented.     

Acute toxicity of alkylbenzene sulphonate (ABS) detergent to the toothed carp, Aphyosemion gairdneri (L.)

The acute toxicity of alkylbenzene sulphonate (ABS) detergent to the toothed carp, Aphyosemion gairdneri (L.), was investigated using static bioassays and continuous aeration over a period of 96 h. The 96-h LC₅₀, opercular ventilation rates per minute and behaviourial responses were evaluated. The 96-h LC was determined to be 25.11 ± 8.4 mg l^?1. The toxicant led to an initial increase in the opercular ventilation, which then decreased below the initial values by the 96th hour of exposure. Prior to death, erratic swimming, lost of balance and respiratory distress were observed. Skin lesions and haemorrhaging of the gill filaments were observed on dead fish.     

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 tolerance of juvenile Florida pompano, Trachinotus carolinus L., to ammonia and nitrite at various salinities

The acute tolerance of juvenile Florida pompano Trachinotus carolinus L. (mean weight±SE=8.1±0.5 g) to environmental unionized ammonia‐nitrogen (NH₃‐N) and nitrite‐nitrogen (NO₂‐N) at various salinities was determined via a series of static exposure trials. Median‐lethal concentrations (LC₅₀ values) of NH₃‐N and NO₂‐N at 24, 48, and 96 h of exposure were calculated at salinities of 6.3, 12.5 and 25.0 g L^?1 at 28 °C (pH=8.23–8.36). Tolerance of pompano to acute NH₃‐N exposure was not affected by salinity, with 24, 48 and 96 h LC₅₀ values ranging from 1.05 to 1.12, 1.00 to 1.08 and 0.95 to 1.01 mg NH₃‐N L^?1 respectively. Regarding NO₂‐N, tolerance of pompano to this environmental toxicant was compromised at reduced salinities. Median‐lethal concentrations of NO₂‐N to pompano at 24, 48 and 96 h of exposure ranged from 67.4 to 220.1, 56.9 to 140.7 and 16.7 to 34.2 mg NO₂‐N L^?1 respectively. The results of this study indicate that juvenile Florida pompano are relatively sensitive to acute NH₃‐N and NO₂‐N exposure, and in the case of the latter, especially at lower salinities.     

Acute toxicity of nitrite on white shrimp Litopenaeus vannamei (Boone) juveniles in low‐salinity water

The nitrite toxicity was estimated in juveniles of L. vannamei. The 24, 48, 72 and 96 h LC₅₀ of nitrite‐N on juveniles were 8.1, 7.9, 6.8 and 5.7 mg L^?1 at 0.6 g L^?1; 14.4, 9.6 8.3 and 7.0 mg L^?1 at 1.0 g L^?1; 19.4, 15.4, 13.4 and 12.4 mg L^?1 at 2.0 g L^?1 of salinity respectively. The tolerance of juveniles to nitrite decreased at 96 h of exposure by 18.6% and 54.0%, when salinity declined from 1.0 to 0.6 g L^?1 and from 2.0 to 0.6 g L^?1 respectively. The safe concentrations at salinities of 0.6, 1.0 and 2.0 g L^?1 were 0.28, 0.35 and 0.62 mg L^?1 nitrite‐N respectively. The relationship between LC₅₀ (mg L^?1), salinity (S) (g L^?1) and exposure time (T) (h) was LC₅₀ = 8.4688 + 5.6764S – 0.0762T for salinities from 0.6 to 2.0 g L^?1 and for exposure times from 24 to 96 h; the relationship between survival (%) and nitrite‐N concentration (C) for salinity of 0.6–2.0 g L^?1, nitrite‐N concentrations of 0–40 mg L^?1 and exposure times from 0 to 96 h was as follows: survival (%) = 0.8442 + 0.1909S – 0.0038T – 0.0277C + 0.0008ST + 0.0001CT–0.0029SC, and the tentative equation for predicting the 96‐h LC₅₀ to salinities from 0.6 to 35 g L^?1 in L. vannamei juveniles (3.9–4.4 g) was 96‐h LC₅₀ = 0.2127 S² + 1.558S + 5.9868. For nitrite toxicity, it is shown that a small change in salinity of waters from 2.0 to 0.6 g L^?1 is more critical for L. vannamei than when wider differences in salinity occur in brackish and marine waters (15–35 g L^?1).     

Thyroid Hormones and Their Influences on Larval Performance and Incidence of Cannibalism in Walleye Stizostedion vitreum1

Thyroid hormones, 3,5,3′,5′- tetraiodothyronine (T₄) and 3,5,3′- triiodothyronine (T₃) have been found in the eggs of several teleost species and are potential regulators of larval development, growth, and survival. The purpose of the present study was to determine whether natural variation of T₃ and T₄ in the eggs of six stocks of walleye, five wild stocks from Kansas, Iowa, Wisconsin, Minnesota, and North Dakota, and a semi-domesticated stock from an Ohio fish hatchery, have an effect on larval performance in mass culture. Immersion studies were conducted with samples of larvae from four of the same stocks at exposure concentrations of 0.01, 0.05, and 0.1 ppm of T₃ and T₄. Natural egg concentrations of T₃ (range from 0.70 to 1.5 ng/g wet weight of egg) were not significantly different among stocks. Although means of T₄ concentration among stocks were significantly different (range 0.53–9.27 ng/g), the difference was caused by the exceptionally high concentration for the Wisconsin stock (9.27 ng/g ± 2.20). Performance measures of the Wisconsin stock (Mississippi River), were not related to T₄ concentration in that stock. In spite of similarity in concentrations of T₄ and T₃ in the eggs, there were significant performance differences among the stocks (survival to 21 d, gas bladder inflation, viability, cannibalism, and growth). The immersion studies, however, revealed a significant difference in incidence of cannibalism and temperature units (TU) to 50% mortality (i.e., survival) between the control groups and treatment groups exposed to 0.01 to 0.1 ppm T₃ and T₄. Survival was extended more than 2-fold longer in larvae immersed in T₃ compared with T₄. The immersion study indicated that thyroid hormones are potentially regulators of walleye development, but further investigations are needed to determine reasons for differences in larval performance based on natural concentrations in the egg and artificial exposure (immersion).     

Preliminary success using hydrogen peroxide to treat Atlantic salmon,Salmo salar L., affected with experimentally induced amoebic gill disease (AGD)

Currently, the only effective and commercially used treatment for amoebic gill disease (AGD) in farmed Tasmanian Atlantic salmon is freshwater bathing. Hydrogen peroxide (H₂O₂), commonly used throughout the aquaculture industry for a range of topical skin and gill infections, was trialled in vitro and in vivo to ascertain its potential as an alternative treatment against AGD. Under in vitro conditions, trophozoites of Neoparamoeba perurans were exposed to three concentrations of H₂O₂ in sea water (500, 1000 and 1500 mg L^?1) over four durations (10, 20, 30 and 60 min) each at two temperatures (12 and 18 °C). Trophozoite viability was assessed immediately post‐exposure and after 24 h. A concentration/duration combination of 1000 mg L^?1 for >10 min demonstrated potent amoebicidal activity. Subsequently, Atlantic salmon mildly affected with experimentally induced AGD were treated with H₂O₂ at 12 and 18 °C for 15 min at 1250 mg L^?1 and their re‐infection rate was compared to freshwater‐treated fish over 21 days. Significant differences in the percentage of filaments affected with hyperplastic lesions (in association with amoebae) and plasma osmolality were noted between treatment groups immediately post‐bath. However, the results were largely equivocal in terms of disease resolution over a 3‐week period following treatment. These data suggest that H₂O₂ treatment in sea water successfully ameliorated a clinically light case of AGD under laboratory conditions.     

亚硝态氮胁迫下凡纳滨对虾体内亚硝态氮的积累与能量代谢响应

为探究亚硝态氮胁迫下凡纳滨对虾[体长为(6.8±0.3) cm,体质量为(4.0±0.6) g]体内亚硝态氮的时空分布与能量代谢相关酶活性的响应,实验设置0(对照组)、0.8、4.0和8.0 mmol/L 4个处理组,进行持续96 h的亚硝态氮胁迫实验和12 h的恢复实验。结果显示,凡纳滨对虾死亡率与胁迫浓度呈现显著的正相关性。胁迫6 h内,亚硝态氮在凡纳滨对虾鳃、血淋巴、肠道、肝胰腺和肌肉组织中明显积累,且积累量与胁迫浓度呈现正相关。相同胁迫浓度组,亚硝态氮在对虾鳃中积累最多,肌肉中最少,鳃中的积累量约为肌肉的3倍。Na~+-K~+-ATP酶活性在0.8和4.0 mmol/L组对虾肝胰腺和肌肉中显著升高,而在8.0 mmol/L组的肌肉中显著降低。胁迫各组对虾肝胰腺AMPK活性显著上升,且与胁迫浓度呈现正相关性。恢复期间,除血淋巴(8.0 mmol/L组)外,各组织中亚硝态氮1 h恢复效率均超过50%,且肝胰腺和鳃的恢复效率最高,达到74%以上。血淋巴、鳃、肠道中亚硝态氮恢复到对照组水平的时间最短,均在6 h以内,而水体中亚硝态氮含量显著升高。以上研究表明,胁迫下亚硝态氮会在对虾组织中迅速积累,并引起能量代谢进程的加快;胁迫解除后,积累在体内的亚硝态氮能够迅速排出体外,以减轻毒性影响。本研究结果将为缓解亚硝态氮对养殖对虾毒性效应的研究提供参考。     

Chemical Characterization,Temperature Stability,and Enzymatic Studies on Edible Marine Algae Kappaphycus alvarezii (Doty)

Antioxidant activity of the marine alga Kappaphycus alvarezii was investigated. Methanol, acetone, petroleum ether, aqueous methanol, ethyl acetate, and chloroform extracts (1 mg/mL) of K. alvarezii were tested for their 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity. The values were compared with those of Vitamin C and butylated hydroxytoluene (BHT). Extracts showing positive results, when tested for DPPH free radical scavenging, were examined for dose effect, in-vivo hydrogen peroxide (H₂O₂) and hydroxyl radical scavenging assays. All extracts showed dose-dependent DPPH scavenging and significant hydroxyl radical scavenging activities (> 82.6%). The acetone, aqueous methanol, and methanol extracts of K. alvarezii showed the highest scavenging activity. Ethyl acetate extract showed a moderate activity of 62.9%. In the DPPH method, petroleum ether and hexane extracts showed less activity with IC₅₀ values of 118.58 ± 8.94 and 116.25 ± 7.14 μg/mL, respectively. Acetone, methanol, and ethyl acetate extracts exhibited IC₅₀ values of 57.32 ± 1.07, 61.31 ± 0.67, and 79.50 ± 1.59 μg/mL, respectively. K. alvarezii showed higher antioxidant activity in both in vitro and in vivo studies. Proton NMR studies revealed signals in the region 0.5 to 2.0 ppm suggesting the presence of steroidal identity in the extracts.     

Evaluation of the immune response in rainbow trout fry,Oncorhynchus mykiss (Walbaum), after waterborne exposure to Flavobacterium psychrophilum and/or hydrogen peroxide

The immune response in rainbow trout fry against Flavobacterium psychrophilum was elucidated using an immersion‐based challenge with or without prior exposure to hydrogen peroxide (H₂O₂). Samples were taken from the head kidney 4, 48, 125 and 192 h after immersion, and the regulation of several genes was examined. Bacterial load was assessed based on the presence of 16S rRNA and correlated with gene expression, and the levels of specific antibodies in the blood were measured 50 days post‐infection. Separately, both H₂O₂ and F. psychrophilum influenced gene expression, and pre‐treatment with H₂O₂ influenced the response to infection with F. psychrophilum. Pre‐treatment with H₂O₂ also affected correlation between gene regulation and pathogen load for several genes. A delay in antibody production in H₂O₂‐treated fish in the early phase of infection was indicated, but H₂O₂ exposure did not affect antibody levels 50 days post‐infection. An increasing amount of F. psychrophilum 16S rRNA was found in the head kidneys of infected fish pre‐treated with H₂O₂ relative to the F. psychrophilum group. The results show that a single pre‐treatment with H₂O₂ impairs the response against F. psychrophilum and may intensify infection.