Resultados de investigación

1.Description of the methodology used to generate the dataset. The data were analysed using non-parametric statistical tests because they did not conform to a normal distribution. For this purpose, the Kolmogorov–Smirnov normality test was used. A bivariate correlation was performed using Spearman’s Rho test between the different constructs and factors that made up the SCQ-S tool in the sample under study. Likewise, using the chi-square test, we attempted to determine the relationship between the different nominal categorical variables added to the tool. Independent samples mean analysis was also performed using the Mann–Whitney U-test when the number of groups was 2 and the Kruskal–Wallis test when the number of groups was greater than 2. In addition, exploratory factor analysis was performed using principal axis factoring and Vari-max rotation based on a fixed number of 9 factors to be extracted, determined by a previous thorough literature review. The adequacy of the sample and the reliability of the factor models were assessed using Kaiser–Meyer–Olkin and Cronbach’s alpha. Descriptive data on means and standard deviations of the numerical variables included in the study were also obtained. 2. Software or tools needed to interpret the data. [Include the version of the software. If specific software with restricted access is required, explain how to obtain it. Assess whether it is possible to change the dataset to an open format (recommended)]. Data analysis was carried out with Statistical Package for Social Science® software, version 28 (SPSS®, Chicago, IL, USA). 3. Procedures followed for data quality assurance. The level of statistical significance was p < 0.05. For those cases where significance was obtained, effect size and statistical power were analysed using G*Power 3.1.9.7.

Datos de investigación relativos a un artículo de investigación: validación de un biomarcador, la proteína S100A12, de salud porcina, validación analítica y clínica de un ensayo para cuantificar las concentraciones del biomarcador en muestras de saliva porcina.

(Pilot experiment)-Serum levels of sST2 in XE animal model were evaluated increased in a time dependent manner after xenografting. *p<0.001 respect to control (t=0).

Cantharidin, a toxic monoterpene secreted by blister beetles, has long been used in traditional Chinese and modern medicine for its unique properties. However, despite its widespread use, its effects on fish have not been studied in depth. The aim of this study was to evaluate the potential therapeutic applications of cantharidin in fish by examining its antioxidant, hemoagglutinating, hemolytic and cytotoxic activities at different concentrations (0, 0.625, 1.25, 2.5, 5 and 10 μg mL-1) in three different cell lines. In addition, the study explored the bactericidal and bacteriostatic properties of cantharidin against various fish pathogenic bacteria. The results revealed that there were no significant differences in antioxidant, hemagglutinating or hemolytic activities between the different concentrations of cantharidin tested. However, the study found that cantharidin exhibited dose- and time-dependent cytotoxicity in sea bream (Sparus aurata) erythrocytes and in SAF-1, PLHC-1 and Hela cell lines, resulting in morphological changes indicative of apoptosis. Interestingly, the highest dose of cantharidin tested demonstrated potent bactericidal activity against four marine fish opportunistic bacteria, including Vibrio harveyi, V. anguillarum, Photobacterium damselae and Tenacibaculum maritimum, but no statistically significant changes in bacteriostatic activity were observed against any of the bacteria tested. Overall, these results provide valuable information on the potential therapeutic applications of cantharidin in fish aquaculture. Further research is needed to fully understand the mechanisms of action and to explore possible preventive uses of cantharidin in fish.

The role of hepcidins, antimicrobial peptides involved in iron metabolism, immunity, and inflammation is studied. First, gilthead seabream (Sparus aurata L.) head-kidney leucocytes (HKLs) were incubated with λ-carrageenin to study the expression of hepcidin and iron metabolism-related genes. The expression of most of the genes studied was up-regulated, whereas the ferroportin gene (slc40a) was down-regulated in HKLs incubated with λ-carrageenin. In the second part of the study, seabream specimens were injected with λ-carrageenin or buffer (control). The expression of the same genes was evaluated in the head kidney, liver, and skin at different time points after injection. The expression of Hamp1m, ferritin b and ferroportin genes (hamp1, fthb, and slc40a) was up-regulated in the head kidney of fish from the λ-carrageenin group, while the expression of Hamp2C and Hamp2E genes (hamp2.3 and hamp2.7) was down-regulated. In the liver, the expression of hamp1, ferritin a (ftha), slc40a, Hamp2J and Hamp2D (hamp2.5/6) genes was down-regulated in the λ-carrageenin group. In the skin, the expression of hamp1 and (Hamp2A Hamp2C) hamp2.1/3/4 genes was up-regulated in the λ-carrageenin group. A bioinformatic analysis was performed to predict the presence of transcription factor binding sites in the promoter region of hepcidins. Structural and physicochemical variations were found in the different mature hepcidin peptides. This study sheds light on the poorly understood roles of hepcidins in fish. The results provide insight into the regulatory mechanisms of inflammation in fish and could contribute to the development of new strategies for treat inflammation in farm animals.