Changes in the cerebral phosphotransfer network impair energetic homeostasis in an aflatoxin B<Subscript>1</Subscript>-contaminated diet

The phosphotransfer network system, through the enzymes creatine kinase (CK), adenylate kinase (AK), and pyruvate kinase (PK), contributes to efficient intracellular energetic communication between cellular adenosine triphosphate (ATP) consumption and production in tissues with high energetic demand, such as cerebral tissue. Thus, the aim of this study was to evaluate whether aflatoxin B₁ (AFB₁) intoxication in diet negatively affects the cerebral phosphotransfer network related to impairment of cerebral ATP levels in silver catfish (Rhamdia quelen). Brain cytosolic CK activity decreased in animals fed with a diet contaminated with AFB₁ on days 14 and 21 post-feeding, while mitochondrial CK activity increased, when compared to the control group (basal diet). Also, cerebral AK and PK activity decreased in animals fed with a diet contaminated with AFB₁ on days 14 and 21 post-feeding, similarly to the results observed for cerebral ATP levels. Based on this evidence, inhibition of cerebral cytosolic CK activity is compensated by stimulation of mitochondrial CK activity in an attempt to prevent impairment of communication between sites of ATP generation and ATP utilization. The inhibition of cerebral AK and PK activity leads to impairment of cerebral energy homeostasis, decreasing the brain’s ATP availability. Moreover, the absence of a reciprocal compensatory mechanism between these enzymes contributes to cerebral energetic imbalance, which may contribute to disease pathophysiology.     

Purinergic signalling displays an anti‐inflammatory profile in the spleen of fish experimentally infected with Aeromonas caviae: Modulation of the immune response

Extracellular adenosine triphosphate (ATP) and its metabolite adenosine (Ado) are recognized as key mediators of immune and inflammatory responses. Depending on its concentration, ATP may act as an immunostimulant or immunodepressant, while Ado levels display an anti‐inflammatory profile. The aim of this study was to evaluate whether splenic purinergic signalling is capable of modulating immune and inflammatory responses in fish experimentally infected with Aeromonas caviae. Triphosphate diphosphohydrolase (NTPDase) and 5′‐nucleotidase activities increased in the spleen of silver catfish (Rhamdia quelen) experimentally infected with A. caviae compared with the uninfected control group. Moreover, splenic Ado levels increased in the infected animals relative to the uninfected control group. Based on these lines of evidence, our findings revealed that adenine nucleotide hydrolysis is modified in the spleen of fish infected with A. caviae attempting to restrict the inflammatory process through the upregulation of NTPDase and 5′‐nucleotidase activities, which occurs in an attempt to hydrolyse the excessive ATP in the extracellular environment and rapidly hydrolyse AMP to form Ado. In summary, purinergic signalling can modulate immune and inflammatory responses during A. caviae infection.     

Characterization of mevalonate metabolism in the sea bass (Dicentrarchus labrax L) liver

The activities of mevalonate kinase, mevalonate 5-phosphate kinase and mevalonate 5-pyrophosphate decarboxylase, were examined in sea bass (Dicentrarchus labrax L) liver. The activities of the three enzymes were studiedin vitro in relation to the influence of protein content, time of incubation, pH, temperature, mevalonate, ATP and Mg⁺⁺ concentration. Protein content in the assay medium affected the three enzymes differently. Mevalonate kinase, mevalonate 5-phosphate kinase, and mevalonate 5-pyrophosphate decarboxylase activities were linear up to 0.2, 0.4 and 0.8 mg protein, respectively. With respect to the time course studies, the enzymes also behaved differently. Mevalonate kinase activity increased over forty minutes, reaching a plateau thereafter, while mevalonate 5-phosphate kinase and decarboxylase increased over the entire assay period. All the three enzymes showed a maximum in activity at pH 7.5. The effect of reaction temperature showed that phosphorylation increased to maximum around 35°C for mevalonate kinase and 30°C for mevalonate 5-phosphate kinase while decarboxylation rates remained constant well until 30°C temperature decreasing afterwards. The enzymes behaved differently as a function of mevalonate concentration. Mevalonate 5-phosphate formed was maximal when the initial mevalonate concentration was 272 M, whereas mevalonate 5-pyrophosphate and CO₂ were formed maximally at mevalonate concentrations of 136 M and 68M, respectively. Optimal ATP concentration in the medium was 3 mM for decarboxylase and 6 mM for kinases, and Mg⁺⁺ requirements varied from 4 mM for decarboxylase to 6 mM for kinases.     

Involvement of cholinergic and adenosinergic systems on the branchial immune response of experimentally infected silver catfish with Streptococcus agalactiae

It has been recognized that the cholinergic and adenosinergic systems have an essential role in immune and inflammatory responses during bacterial fish pathogens, such as the enzymes acetylcholinesterase (AChE) and adenosine deaminase (ADA), which are responsible for catalysis of the anti‐inflammatory molecules acetylcholine (ACh) and adenosine (Ado) respectively. Thus, the aim of this study was to investigate the involvement of the cholinergic and adenosinergic systems on the immune response and inflammatory process in gills of experimentally infected Rhamdia quelen with Streptococcus agalactiae. Acetylcholinesterase activity decreased, while ACh levels increased in gills of infected animals compared to uninfected animals. On the other hand, a significant increase in ADA activity with a concomitant decrease in Ado levels was observed in infected animals compared to uninfected animals. Based on this evidence, we concluded that infection by S. agalactiae in silver catfish alters the cholinergic and adenosinergic systems, suggesting the involvement of AChE and ADA activities on immune and inflammatory responses, regulating the ACh and Ado levels. In summary, the downregulation of AChE activity exerts an anti‐inflammatory profile in an attempt to reduce or prevent the tissue damage, while the upregulation of ADA activity exerts a pro‐inflammatory profile, contributing to disease pathophysiology.     

Motility of spermatozoa ofAlburnus alburnus (Cyprinidae) and its relationship to seminal plasma composition and sperm metabolism

The composition of seminal plasma and metabolism of sperm of the cyprinid fishAlburnus alburnus were investigated. Statistically significant correlations were found between motility parameters and seminal fluid osmolality, pH, Na⁺, K⁺ and protein levels (negative correlations: % immotile spermatozoa-Na⁺, K⁺; positive correlations: % motile spermatozoa-osmolality, pH, Na⁺, K⁺, protein; % linear motile spermatozoa-pH protein; swimming velocity of spermatozoa-pH, Na⁺, protein). Spermatozoan motility and ATP metabolism and glycolysis were correlated as indicated by measurement of ATPase, pyruvate kinase, adenylate kinase and lactate dehydrogenase activity. The physiological meanings of these correlations and their possible significance for quality control of semen are discussed.Abbreviations used ACP acid phosphatase - ADP adenosine diphosphate - AK adenylate kinase - ALP alkaline phosphatase - ASPAT aspartate aminotransferase - ATP adenosine triphosphate - ATPase magnesium dependent adenosine triphosphatase - CRPO creatine phosphate - -GLU \-D-glucuronidase - ICDH isocitrate dehydrogenase - LDH lactate dehydrogenase - PK pyruvate kinase     

Effects of lead nitrate on the activity of metabolic enzymes during early developmental stages of the African catfish, <Emphasis Type="Italic">Clarias gariepinus</Emphasis> (Burchell, 1822)

Glucose-6-phosphate dehydrogenase (G6PDH), lactate dehydrogenase (LDH) and pyruvate kinase (PK) are key metabolic enzymes. G6PDH has been used as a biomarker of pollution-induced carcinogenesis in fish. LDH has been used as marker of lesions in toxicology and clinical chemistry, and PK catalyses the conversion of phosphoenol pyruvate to pyruvate, with regeneration of ATP. The effect of different concentrations of lead nitrate on the activity of these enzymes in two different early ontogenetic stages (embryonic and free embryonic stage) of the African catfish Clarias gariepinus was investigated. Embryo homogenates were used for measurements of G6PDH, LDH and PK activity spectrophotometrically at 340 nm and 25°C. The ontogenetic variations of the three enzymes during early ontogeny, from the 30 h to the 168 h post-fertilisation stage (PFS) (beginning of exogenous feeding), were studied. There was a significant decrease in activities of all three enzymes from 30 h-PFS to 96 h-PFS, followed by a significant increase in G6PDH and LDH. PK showed insignificant fluctuations in activity. Different patterns of enzyme activities were recorded due to exposure to different lead nitrate concentrations (100 μg/l, 300 μg/l and 500 μg/l). In the pre-hatching stage (30 h-PFS) the activity of the three enzymes increased at exposure to 100 μg/l lead nitrate and then decreased with increasing dose. In the post-hatching stages (48 h-PFS–168 h-PFS) G6PDH activity increased and LDH activity decreased with increasing lead concentrations. Unlike G6PDH and LDH, the PK enzyme fluctuated during the post-hatching stages and did not reveal a specific trend of response (increase or decrease) with increasing lead concentrations. Therefore, the measurement of G6PDH and LDH activities, but not PK activity, could be useful biomarkers of intoxication to reveal the embryotoxic potential of lead nitrate in fish embryos. The post-hatching stages of the African catfish are more sensitive than the pre-hatching stage (30 h-PFS) is, probably due to the protective capacity provided by the hardened chorion. The interaction and the main effects of age and lead doses were found to be highly significant, referring to the great impact of lead on these enzyme systems with increasing early development.     

感染溶藻弧菌对日本蟳肝胰腺免疫功能的影响

摘 要：为探讨日本蟳感染溶藻弧菌的致病机理,采用溶藻弧菌人工感染健康日本蟳,分析了感染前后日本蟳肝胰腺 PO、SOD和LSZ活性变化及注射免疫多糖后的免疫保护率,并研究了细胞超微结构的病理组织学。结果表明：日本蟳感染溶藻弧菌后,肝胰腺中PO、SOD和 LSZ的活性均受到不同程度的影响,感染6~12 h,3种酶的活性均有一个上升的过程,但之后随时间的延长呈现下降趋势;免疫感染组因感染弧菌前注射了免疫多糖,日本蟳肝胰腺中PO、SOD和LSZ酶活性均显著高于感染组的酶活性,感染7 d后的免疫保护率高达72.73％,表明免疫多糖可提高酶的活性,使机体的抗病菌能力增强。超微结构显示：对照组日本蟳肝胰腺细胞结构形态正常,上皮细胞表面的微绒毛排列整齐,各细胞器结构完整;免疫组内质网、糖原颗粒和线粒体丰富,微绒毛排列致密;感染组肝胰腺组织受到明显的损伤,细胞和部分微绒毛脱落、受损;线粒体和粗面内质网变形、水肿或仅剩一空泡;核高度异染色质化,核膜破裂。与感染组相比,免疫后感染组具有形态结构较正常的细胞核、整齐致密的微绒毛和丰富的溶酶体,但依然可见水肿的内质网和狭长畸变的线粒体。     

凡纳滨对虾精氨酸激酶的多克隆抗体制备及组织特异性表达分析

精氨酸激酶（arginine kinase,AK）在调节无脊椎动物磷酸精氨酸与ATP之间能量平衡的过程中具有重要作用。在前期工作基础上,设计特异引物,以凡纳滨对虾肌肉组织cDNA为模版,克隆得到了1 071 bp的凡纳滨对虾精氨酸激酶的完整开放阅读框;将它克隆到原核表达载体pGEX-4T-2上,转化BL21 (DE3) 菌株,经诱导后表达出GST-AK融合蛋白。以纯化的融合蛋白作为抗原免疫小鼠,制备多克隆抗血清,经检测该抗原与抗体识别良好。利用得到的抗体对凡纳滨对虾AK在蛋白质水平上的特异性表达进行分析发现,精氨酸激酶在对虾的肌肉、心脏、神经、血细胞和胃组织中具有高的表达量,而在眼柄、肝胰腺、鳃和皮肤组织中表达量较低。为进一步研究精氨酸激酶在对虾体内的功能奠定了基础。     

饥饿及再投喂处理对草鱼生长、葡萄糖代谢和转运蛋白1表达的影响

设置持续投喂组(C,持续投喂8周)、饥饿再投喂组(R,饥饿4周+再投喂4周)和持续饥饿组(S,饥饿8周)3个处理组,研究3种不同饥饿处理对草鱼(Ctenopharyngodon idellus)血清生化指标、糖原和糖代谢相关酶和葡萄糖转运蛋白1(GLUT1)的影响,同时在此实验基础上研究草鱼在急性高糖负荷胁迫下的糖耐受能力、糖代谢相关酶和GLUT1的变化规律,旨在阐明草鱼在饥饿及再投喂处理条件下的糖代谢特征。选取初重为(125.35±0.54)g的草鱼,饲养8周后以30 mg/100 g体重的剂量腹腔注射葡萄糖研究其糖耐受能力。结果显示,S组肝糖原和血清的血糖、甘油三酯含量均最低。饥饿处理对草鱼糖耐受能力影响显著,S组血糖含量在各时间点上显著低于其余两组(P0.05),肝糖原在6 h达到峰值;饥饿处理对草鱼肝脏糖代谢关键酶影响显著,饥饿处理(S组)诱使磷酸烯醇式丙酮酸激酶(PEPCK)活性上升但抑制丙酮酸激酶(PK)和果糖-6-磷酸激酶(PFK)的活性(P0.05),而饥饿再投喂(R组)后PEPCK、PK和PFK酶活性恢复到持续投喂(C组)处理水平。注射葡萄糖后S组肝脏GK酶活性增幅最大,PK酶活性呈上升趋势,而R组则呈先下降后上升的趋势;饥饿处理对草鱼肝脏和肌肉GLUT1表达影响显著,注射葡萄糖后,除R组肝脏组织外,其余各组草鱼肝脏和肌肉组织GLUT1表达量均呈先上升后下降的趋势,且S组肌肉GLUT1表达量在各个时间点上均高于其余两组(P0.05)。研究结果表明,在不同饥饿处理下,草鱼可通过消耗肝糖原和甘油三酯及降低肝脏糖酵解相关酶(PK和PFK)活性和促进糖异生PEPCK酶活性来应对饥饿胁迫,而饥饿处理可诱使GK和PK酶活性上升、促进糖原合成和激活GLUT1基因的表达和转运来缓解草鱼急性高糖负荷,从而提高其糖耐受能力。     

The parasite Ichthyophonus sp. in Pacific herring from the coastal NE Pacific

The protistan parasite Ichthyophonus occurred in populations of Pacific herring Clupea pallasii Valenciennes throughout coastal areas of the NE Pacific, ranging from Puget Sound, WA north to the Gulf of Alaska, AK. Infection prevalence in local Pacific herring stocks varied seasonally and annually, and a general pattern of increasing prevalence with host size and/or age persisted throughout the NE Pacific. An exception to this zoographic pattern occurred among a group of juvenile, age 1+ year Pacific herring from Cordova Harbor, AK in June 2010, which demonstrated an unusually high infection prevalence of 35%. Reasons for this anomaly were hypothesized to involve anthropogenic influences that resulted in locally elevated infection pressures. Interannual declines in infection prevalence from some populations (e.g. Lower Cook Inlet, AK; from 20–32% in 2007 to 0–3% during 2009–13) or from the largest size cohorts of other populations (e.g. Sitka Sound, AK; from 62.5% in 2007 to 19.6% in 2013) were likely a reflection of selective mortality among the infected cohorts. All available information for Ichthyophonus in the NE Pacific, including broad geographic range, low host specificity and presence in archived Pacific herring tissue samples dating to the 1980s, indicate a long‐standing host–pathogen relationship.     

Effects of acute hyperglycaemia stress on indices of glucose metabolism and glucose transporter genes expression in cobia (Rachycentron canadum)

The objective of the present study is to preliminarily clarify the mechanism of carbohydrates metabolism in cobia (Rachycentron canadum) (85 ± 3 g) receiving injection of glucose solution. We examined plasma glucose (GLU), total protein (TP), triglyceride (TG), cholesterol (CHOL), insulin, liver glycogen and muscle glycogen, activities of hepatic hexokinase (HK), phosphofructokinase (PFK) and pyruvate kinase (PK), as well as relative expressions of glucose transporter 1 (GLUT1), GLUT2, GLUT3, GLUT4, GLUT5 and GLUT9 in hemocyte, liver and muscle of R. canadum when fish were injected with 200 μl of glucose solution (255 mg/ml) after 0, 1, 2, 4, 8, 12, 24 and 48 hr. Fish received injection of 0.68% saline served as control. Results indicated that the plasma GLU, TG and CHOL increased and reached peak at 1, 8 and 48 hr postinjection (hpi) respectively. The hepatic glycogen increased from 1 hpi, and reached peak at 8 hpi, plasma insulin increased at 1 hpi, and reached peak at 2 hpi, and activity of hepatic PK peaked at 8 hpi. Furthermore, the relative expressions of GLUT1, GLUT2, GLUT3, GLUT4 and GLUT5 in hemocytes reached peak at 1,4, 8, 4 and 8 hpi, respectively, relative expressions of GLUT2, GLUT3, GLUT5 and GLUT9 in liver reached peak at 24, 24, 12 and 24 hpi, respectively, and relative expressions of GLUT1 and GLUT3 in muscle were significantly higher at 2 and 2–4 hpi, respectively compared with those in controls. In conclusion, low ability of utilizing glucose in R. canadum may be attributed to insufficient insulin secretion, low activities of key glycolytic enzymes (HK, PFK and PK) regulated by glucose injection and slow increase of GLUTs.     

A comparative study on protein‐sparing effects among juvenile Erythroculter ilishaeformis line,Ancherythroculter nigrocauda line and their hybrid F1 fed diets with different protein to carbohydrate ratios

To investigate the mechanism underlying the difference of dietary protein requirements among Erythroculter ilishaeformis line, Ancherythroculter nigrocauda line and their hybrid F₁ (E. ilishaeformis♀×A. nigrocauda ♂), juvenile fish of these three species with initial body weight (5.86 ± 0.10 g) were fed the six isoenergy diets with different dietary protein/carbohydrate ratios (P/C ratios were 0.56, 0.78, 1.11, 1.61, 2.52 and 4.43, respectively) for 8 weeks. The results showed that the hybrid culter had the higher weight gain rate (WGR), protein efficiency ratio and protein deposition ratio compared with its parents lines; using WGR as a response criteria, the dietary carbohydrate tolerant level of juvenile E. ilishaeformis line, A. nigrocauda line and their hybrid was 24.3%, 28.5% and 29.7%, respectively, and the optimal P/C ratio was 1.69, 1.35, 1.22 and respectively. Dietary carbohydrate activated hepatic protein kinase B (Akt), dietary protein activated hepatic target of rapamycin (TOR) and the induction of mRNA expression of hepatic phosphoenolpyruvate carboxykinase and pyruvate kinase showed a similar change in hybrid F₁ and its parents. A. nigrocauda had the highest enzymes activities in intestinal protease and amylase, and hybrid culter had the highest intestinal lipase activities. Our results demonstrated that the hybrid culter has the better protein‐sparing effects by increasing carbohydrate metabolism than its parent lines.     

Metabolic enzyme activities in larvae of the African catfish,Clarias gariepinus: changes in relation to age and nutrition

The influence of ontogeny and nutrition on metabolic enzyme activities in larvae of the African catfish, Clarias gariepinus, was studied. After start of exogenous feeding, the larvae were reared for 10 days under three different nutritional conditions: Artemia nauplii, a dry starter diet, and starvation. The live feed gave the best growth (96 mg within 10 days) whereas the dry diet resulted in low growth (33 mg). This growth difference was reflected in larval RNA and DNA concentrations, but not in the levels of soluble protein. Enzymes representing the following aspects of metabolism have been analysed: NADPH generation (G6PDH, ME), glycolysis (PFK, PK), gluconeogenesis (FDPase), amino acid catabolism (GOT, GPT) and oxidative catabolism (CS). All enzymes were present from the start of exogenous feeding onwards, but their maximum specific activities displayed different developmental patterns. In catfish larvae fed on Artemia, G6PDH and ME activities steadily increased with age and weight of the larvae. CS levels remained, after an immediate enhancement upon onset of exogenous feeding, on a rather stable plateau. The amino acid-degrading enzymes GOT and GPT showed maximum levels at days 3–5 of feeding or at a body weight of 10–20 mg, but decreased thereafter. Activities of PFK, PK and FDPase showed low initial levels, and increased significantly with age and size. Based on the ontogenetic patterns of metabolic enzymes, in C. gariepinus larvae an early and a late developmental phase can be distinguished. During the early phase, the glycolytic and gluconeogenetic capacities are low, whereas they are enforced during the later phase. The oxidative capacity is high both during the early and the late phase. The metabolic changes in catfish development coincide with other major ontogenetic events, e.g., alterations of muscle organization, gill morphology, respiration and stomach structure and function. Rearing catfish larvae on a dry diet instead of Artemia partly altered the developmental pattern described: The ontogenetic elevation of CS, PFK and FDPase was delayed and the early peak in GOT and GPT activities was not realized. Particularly during the early developmental phase, the enzyme behaviour of the larvae fed on dry food was similar to that of starved larvae.Abbreviations CS citrate synthase - FDPase fructose-1,6-diphosphatase - GOT glutamate oxaloacetate transaminase - GPT glutamate pyruvate transaminase - G6PDH glucose-6-phosphate dehydrogenase - ME malic enzyme - PFK phosphofructokinase - PK pyruvate kinase     

Effect of dietary carbohydrate-to-lipid ratios on growth, lipid deposition and metabolic hepatic enzymes in juvenile Senegalese sole (Solea senegalensis, Kaup)

A study was undertaken to determine the effect of various dietary carbohydrate‐to‐lipid ratios on growth performance, whole‐body composition and tissue lipid content in Senegalese sole (Solea senegalensis) juveniles. Data on the dietary regulation of key hepatic enzymes of the lipogenic and glycolytic pathways (glucose‐6‐phosphate dehydrogenase, G6PD; malic enzyme, ME; fatty acid synthetase, FAS; pyruvate kinase, PK and glucokinase, GK) were also generated. Four isonitrogenous (crude protein: 52% dry matter (DM)) diets were formulated to contain one of two lipid levels (11% and 21% DM). Within each dietary lipid level, the nature of the carbohydrate fraction (raw or extruded peas) was varied. Triplicate groups of 54 sole (initial body weight: 23.6±1.2 g) were grown in recirculated seawater over 67 days. Fish were fed using automated feeders. At the end of the study, whole‐body, liver, viscera and muscle samples were withdrawn for analyses. During the experimental period, the mean fish weight about doubled in all treatments. No significant differences were found in growth performance (ranging from 1.1% to 1.4% body weight day^?1) among dietary treatments. High‐fat diets increased whole‐body fat content. Similarly, daily fat gain ranged from 0.54 to 0.78 g kg^?1 day^?1 and highest values were found in fish fed high‐lipid diets. Dietary treatments also affected tissue lipid content (liver, viscera and muscle), with highest values in fish fed high‐fat diets. The nature of dietary carbohydrates had little influence on performance criteria, but affected tissue lipid deposition. The activities of G6PD, ME and FAS were depressed by elevated levels of dietary lipid, confirming the inhibitory effect of dietary fats on lipid biosynthesis. At both dietary lipid levels, ME and FAS activities were little affected by dietary carbohydrate. Activities of PK and GK were not affected by the starch level of the diets. In Senegalese sole juveniles, the lipogenic pathway is more susceptible to modulation by dietary means (particularly through lipid intake) than the glycolytic pathway.     

五氯酚钠对梨形环棱螺毒理效应的研究

采用在体暴露试验的方法,研究了不同浓度五氯酚钠(Na-PCP)在不同暴露时间(24、48、72和96 h)下对梨形环棱螺的急性毒性,以及Na-PCP对肝脏、鳃和腹足中精氨酸激酶(AK)活性的影响.结果显示,Na-PCP对梨形环棱螺的半致死浓度为0.411 mg/L,安全浓度为0.0411 mg/L;在Na-PCP暴露下,梨形环棱螺肝脏中单位蛋白AK活性在低浓度下被诱导增长,在高浓度下则出现被抑制的现象,鳃和腹足中单位蛋白AK活性伴随Na-PCP浓度的增加而下降,表现出时间剂量效应,且腹足中下降幅度相对鳃中较大.试验结果表明AK活性可以作为指示五氯酚钠对梨形环棱螺毒理效应的生物标志物.     

亚硒酸钠对刺参免疫反应中体腔液酶活力的影响

为了合理评价硒对水产养殖刺参的作用,实验检测和观察了室内模拟亚硒酸钠处理及病菌感染条件下刺参体腔液免疫酶的变化、组织病理变化和相对保护率。结果表明,随着亚硒酸钠处理强度的增加,刺参体腔液中超氧物岐化酶(SOD)、谷胱甘肽过氧化物酶(GP-X)、溶菌酶(LYZ)、酚氧化酶(PO)及碱性磷酸酶(ALP)活性升高;在同时感染病菌的情况下,SOD、GP-X及LYZ活性表现为先升高后下降的趋势,PO和ALP活性则持续上升,但随亚硒酸钠浓度升高,ALP活性增加的幅度减少,而较高亚硒酸钠浓度时累计发病率上升,相对保护率下降。研究结果表明,适宜浓度的亚硒酸钠可增强刺参对病菌感染的免疫力,而病菌感染可以加剧亚硒酸钠胁迫对刺参造成的免疫功能损伤,所以适度利用硒可减轻刺参养殖病害的发生。     

溶氧变化模式对菲律宾蛤仔鳃组织和血淋巴液氧化应激及生理代谢的影响

为了探究菲律宾蛤仔(Ruditapesphilippinarum)鳃组织和血淋巴液响应溶氧变化的氧化应激反应和生理代谢情况,并筛选出蛤仔响应溶氧变化的标志性物质,设置3种溶氧变化模式,分别为一直维持正常溶氧(C)处理、正常溶氧-急性低氧-急性复氧(AHR)处理、正常溶氧-慢性低氧-慢性复氧(CHR)处理。用酶标仪微板法96样检测3种溶氧变化模式下血淋巴液和鳃组织的超氧化物歧化酶(SOD)活性、过氧化氢酶(CAT)活性、谷胱甘肽过氧化物酶(GSH-px)活性、丙二醛(MDA)含量、丙酮酸激酶(PK)活性、己糖激酶(HK)活性、乳酸脱氢酶(LDH)活性、ATP酶(ATPase)活性、脯氨酸羟基化酶(PHD)活性和脂质过氧化物(LPO)含量。结果发现菲律宾蛤仔最先响应溶氧变化的是鳃组织,其氧化-抗氧化酶体系、代谢相关酶活性和相关产物的含量及变化幅度均明显高于血淋巴液;鳃组织和血淋巴液中氧化-抗氧化酶体系变化趋势一致, SOD和CAT作为最重要的抗氧化酶能在一定程度上缓解溶氧变化对蛤仔机体的损伤;氧化应激和能量利用体系在鳃和血淋巴液中的变化趋势也一致,其中PK和HK随溶氧变化调节糖酵解代谢效率...     

Study of the distribution of active caspase‐3‐positive cells in turbot,Scophthalmus maximus (L.), enteromyxosis

Enteromyxosis caused by Enteromyxum scophthalmi is one of the parasitizations with a higher economic impact on turbot, Scophthalmus maximus (L.), aquaculture. This myxosporean produces severe catarrhal enteritis with abundant inflammatory infiltrates in the lamina propria‐submucosa (LP), epithelial detachment and leucocyte depletion of the lymphohaematopoietic organs. Some advances made on the pathogenesis pointed to a role of apoptosis in the enteromyxosis. Therefore, the main aim of this work was to employ the TUNEL assay and the anti‐(active caspase‐3) immunohistochemical assay to detect apoptotic cells in both healthy and E. scophthalmi‐infected turbot in order to establish the presence and distribution of apoptotic cells during development of the disease. More apoptotic cells located within the gastrointestinal epithelium were observed in the initial stages of the infection in E. scophthalmi‐infected turbot compared with non‐infected turbot. As the infection progressed, a higher degree of apoptosis occurred in the epithelium of folds heavily parasitized. In the severely infected turbot, apoptosis was also found among the leucocytes of the intestinal inflammatory infiltrates. Moreover, the number of active caspase‐3‐positive cells in the lymphohaematopoietic organs tended to increase with disease severity. In view of the results, increased apoptosis in the epithelium may favour the scaling that occurs during enteromyxosis and cell death of leucocytes in the intestinal LP, contributing to leucocyte depletion in severe cases.