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PL
W pracy oceniono za pomocą systemu QIM wyróżniki sensoryczne 30 pstrągów tęczowych w czasie przechowywania chłodniczego przez 48 godz. Ponadto dokonano instrumentalnych pomiarów właściwości fizykochemicznych tkanki mięśniowej: pH, przewodności elektrycznej właściwej i barwy skóry (wg CIE L*a*b*). Indeks (QI) po uśmierceniu ryb oceniono na 0 pkt, po 24 godz. – 3 pkt, a po 48 godz. – 9 pkt. W tkance mięśniowej ryb stwierdzono istotny spadek pH (z 6,93 do 6,54) i wzrost przewodności elektrycznej właściwej (z 4,14 do 7,95 mS cmˉ¹). Instrumentalne pomiary właściwości fizykochemicznych potwierdziły zmianę świeżości określone indeksem (QIM), co wskazuje na praktyczne wykorzystanie tego wskaźnika dla ryb przechowywanych w warunkach chłodniczych w ocenianym okresie.
EN
The sensory characteristics of 30 rainbow trout during chilling storage for 48 hours using QIM system were evaluated. In addition, instrumental measurements of muscle intrinsic properties, i.e. value of pH and electrical conductivity, and color of skin (according to CIE L*a*b*) were determined. Quality Index (QI) after fish killing amounted 0 pts., after 24 h 3 pts., and after 48 h 9 pts. The significant pH decrease (from 6.93 to 6.54), and an electrical conductivity increase (from 4.14 to 7.95 mS cmˉ¹) in fish muscle tissue were found. Instrumental measurements of intrinsic properties which confirmed the change of freshness specified by QIM method, indicate the practical use of this index for fish stored in chilling conditions during evaluated period.
EN
Multiplex PCR is a useful technique for estimating genetic diversity. This paper presents 3 new sets of primer pairs for effectively amplifying 10 microsatellite DNA loci from rainbow trout (Oncorhynchus mykiss). Unlike other sets of primer pairs that have been developed for amplifying rainbow trout microsatellite loci, ours do not require the hot-start PCR technique. In the paper, we describe the steps taken to choose the loci for each multiplex assay and to verify the genotyping results. We provide the compositions of the PCR mixture and the characteristics of the PCR thermal profile recommended for amplification.
EN
Although p53, a protein of important tumor suppressive function, has been extensively studied in mammals, relatively little is known about the p53 pathways in lower vertebrates. Particularly, limited information exists on possible influences of environmental contaminants on the expression of the p53 gene in fish. In the current study, we assessed the effects of benzo[a]pyrene (B[a]P; potent tumor promoter) and cyclopenta[c]phenanthrene (CP[c]Ph; clastogenic agent) exposure on a 24h profile of p53 gene expression in head kidney of juvenile rainbow trout (Oncorhynchus mykiss). To analyze the p53 transcription rate, we developed protocol for the examination of both mRNA and heterogeneous nuclear (hn) RNA of the gene, using Real-Time RTPCR approach. The results show that both compounds are capable of suppressing p53 transcriptional activity within 12h of the treatment. Our finding supports the idea that structurally different PAHs may influence cell physiologic functions controlled by p53 in fish, in part, by down-regulating its RNA expression levels.
EN
The aim of the study was to evaluate and compare changes in the selected haematological parameters of rainbow trout after long-term (14 days) exposure to sublethal concentrations of two kinds of contaminants: 1) highway traffic emission pollutants (model mixture of heavy metals) and 2) road maintenance salt. Four groups of fish exposed to sublethal concentrations of model mixture metal solutions demonstrated an increased frequency of abnormal erythrocytes and elevated percentage of neutrophiles. The percentage of juvenile and abnormal erythrocytes was significantly increased in the blood of fish exposed to sublethal concentrations of road maintenance salt solutions. Our data confirm that even low amounts of metals found in soil near roadsides and road maintenance salt can induce adverse effects on fish. Morphological analysis of erythrocytes seems to be a reliable tool for detection of toxic effects upon fish.
EN
Proximate to the environment, adipose fin of fish may be considered as a lipid storing tissue, and thus can be a target for either waterborne or dietary polycyclic aromatic compounds (PACs). We determined the effects of benzo[a]pyrene (B[a]P), a model PAC member, on CYP1A gene expression in adipose fin and compared that with the effects in gill of juvenile rainbow trout (Oncorhynchus mykiss Walbaum) using the quantitative reverse transcription polymerase chain reaction (Q-RT-PCR). The results of the study demonstrated that constitutive CYP1A mRNA was present in adipose fin of rainbow trout, but the transcripts were far less abundant than those in gill tissue. We confirmed high CYP1A gene induction potential of the gills in rainbow trout injected with benzo[a]pyrene, but also showed moderately and transiently induced CYP1A mRNA in adipose fin. The modest and transitory gene expression may preclude rainbow trout adipose fin CYP1A mRNA levels from using it as an indicator of sustained exposure of fish to the polycyclic aromatic compounds.
EN
We assessed the effects of cyclopenta[c]phenanthrene (CP[c]Ph) and benzo[a]pyrene (B[a]P; positive control) on CYP1A gene expression in brain of juvenile rainbow trout (Oncorhynchus mykiss) using the quantitative reverse transcription polymerase chain reaction (Q-RT-PCR). A group of hatchery raised rainbow trout, with an average body mass of 49.4 g and total length of 15.5 cm were given an intraperitoneal injection (10 mg*kg-1) of either CP[c]Ph or B[a]P in corn oil (2 mg*mi-1 corn oil) or corn oil alone (control). After 24 and 48 h, trout brains were collected for mRNA isolation and analysis. After 24 hours of the exposure, only B[a]P-treated rainbow trout had 10-fold higher number of CYP1A transcripts (mean = 3.63*106 transcripts*µg-1 total RNA) than control fish (3.24*105 transcripts*µg-1 total RNA; Tukey test, P<0.05). After 48 hrs, significantly higher levels of CYP1A expression (Tukey test, P<0.001) were found in either CP[c]Ph- or B[a]P- induced group (1.45*106 and 6.92*106 transcriptsźµg-1 total RNA, respectively) over a control group (mean=1.41*105 transcripts*µg-1 total RNA). The finding that CYP1A in brain tissue was inducible by CP[c]Ph, a polycyclic aromatic hydrocarbon (PAH) of different than B[a]P planar characteristics, may further validate the use of rainbow trout brain CYP1A mRNA levels as a biomarker of PAH exposure.
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