Biochemical, endocrine, and histopathological profile of liver and kidneys of sheep with pregnancy toxemia / Perfil bioquímico, endócrino e histopatológico do fígado e rins de ovelhas com toxemia na prenhez

The objective of the present study was to characterize the biochemical, hormonal, and mineral profile, and histopathology of the liver and kidneys, related to the severity of natural cases of pregnancy toxemia (PT) in sheep. A total of 45 sheep with PT were analyzed at the "Clínica de Bovinos", Campus Garanhuns-UFRPE. The animals were submitted to clinical examination, followed by the collection of blood and urine. A necropsy was performed on thirteen animals that died and a histopathological examination was performed on samples of liver and kidneys. Increased creatinine, urea, glucose, fructosamine, non-esterified fatty acids, β-hydroxybutyrate, cortisol, chlorine, amylase, aspartate aminotransferase, gamma-glutamyltransferase, and folic acid were found, whereas insulin, potassium, and total and ionizable calcium presented low values for the species. Total protein, albumin, globulin, sodium, magnesium, and vitamin B12 remained within the normal range. In the macroscopic analysis of the liver, it was possible to observe an increase in organ and border size, yellowish coloration and parenchyma that varied from firm to friable. Vacuolation of the hepatocytes and renal tubular cells was observed. Metabolic disorders in sheep associated with hepatic and renal lesions are more apparent in overweight animals. With the greater impairment in hepatic and renal function, the clinical prognosis of animals with a high body score should be considered reserved.(AU)

Objetivou-se caracterizar o perfil bioquímico, hormonal, mineral e a histopatologia hepática e renal, relacionando com a severidade de casos naturais de toxemia da prenhez (TP) em ovelhas. Analisou-se 45 ovelhas na Clínica de Bovinos, Campus Garanhuns-UFRPE, com TP. Foram submetidas ao exame clínico, seguido de coleta de sangue e urina. Treze animais que vieram a óbito foram necropsiados, nas amostras de fígado e rins realizou-se exame histopatológico. Revelou-se elevação de creatinina, ureia, glicose, frutosamina, ácidos graxos não esterificados, β-hidroxibutirato, cortisol, cloro, amilase, aspartato aminotransferase, gama glutamiltransferase e ácido fólico, enquanto insulina, potássio, cálcio total e ionizável apresentaram valores abaixo para os da espécie. A proteína total, albumina, globulina, sódio, magnésio e vitamina B12 mantiveram-se dentro da normalidade. Na análise macroscópica do fígado, pôde-se observar aumento de tamanho do órgão e dos bordos, coloração amarelada e parênquima que variava de firme a friável. Observou-se vacuolização dos hepatócitos e das células tubulares renais. Os transtornos metabólicos nas ovelhas associados às lesões hepáticas e renais são mais aparentes nos animais com sobrepeso. Com o maior comprometimento da função hepática e renal, o prognóstico clínico dos animais com escore corporal elevado há de ser considerado reservado.(AU)

Estudio anatomopatológico de aislados de Leptospira spp., provenientes de Nicaragua en Mesocricetus auratus como biomodelo / Anatomopathologic study of Leptospira spp., isolated in Nicaragua in Mesocricetus auratus as biomodel

Objetivo. El objetivo de este trabajo fue caracterizar en el biomodelo Mesocricetus auratus la sintomatología y lesiones anatomopatológicas que provocan 5 aislados clínicos de Leptospira spp., provenientes de Nicaragua. Materiales y métodos. Con este fin se inocularon 50 hámster por vía i.p con 1mL del cultivo de cada una de las cepas en fase exponencial teniendo una concentración celular de 7.5 x 106 leptospira/mL (10 animales por cepa), evaluándose signos de la enfermedad, mortalidad durante 14 días, lesiones anatomopatológicas macroscópicas y microscópicas mediante tinción con hematoxilina-eosina y tinción de Warthyn Starryn. Resultados. Todas las cepas presentaron alta mortalidad, mostrando un cuadro tanto clínico, como lesional característico de la infección experimental. Además, causaron la muerte al 100% de los animales entre el tercer y décimo día postinfección. En el estudio anatomopatológico la cepa del serogrupo Ballum y la del serogrupo Pomona produjeron focos de hemorragias específicamente en el riñón y pulmones. De forma similar ocurrió una congestión hepática y renal, mientras que la hemorragia renal fue observada con mayor frecuencia en la cepa del serogrupo Pomona, diferenciándose del resto de las cepas que mostraron esta lesión con menos frecuencia. Conclusiones. Este trabajo permitió una mayor caracterización de estas cepas siendo utilizadas como futuras candidatas vacunales frente a una nueva epidemia de Leptospirosis en Nicaragua.

Objective. The aim of this study was to characterize the symptomatology and anatomopathological lesions caused by 5 clinical isolated Leptospira spp. from Nicaragua in a Mesocricetus auratus biomodel. Materials and methods. 50 hamsters were inoculated via i.p with 1mL of the culture of each strain in exponential phase having a cellular concentration of 7.5 x 106 leptospira/mL, (10 animals per strain). Signs of the disease, mortality during 14 days, and macroscopic and microscopic anatomopathological lesions by haematoxylin-eosin and Warthyn Starryn stain technique were evaluated. Results. All the strains presented high mortality, showing clinical lesions of the experimental infection. Death to 100% of the animals was caused between the third and tenth day post-infection. In the anatomopathologic study, the strains of the Ballum and Pomona serogroup produced haemorrhaging specifically in the kidney and lungs. The animals manifested hepatic and renal congestion, while the renal haemorrhage was observed with more frequency in the strain of the Pomona serogroup, differing from the other strains, which presented this lesion less frequently. Conclusions. This work allowed a better characterization of these strains in order to use them as future vaccine candidates for future Leptospirosis epidemics in Nicaragua.

Evaluación de los efectos tóxicos y concentración letal 50 del surfactante Cosmoflux® 411F sobre juveniles de cachama blanca (Piaractus brachypomus) / Assessment of toxic effects and lethal concentration 50 of surfactant Cosmoflux® 411F on juveniles of cachama blanca (Piaractus brachypomus)

En Colombia, el surfactante Cosmoflux® 411F es usado en fumigaciones de cultivos ilícitos para mejorar la efectividad del glifosato. El uso del Cosmoflux® 411F no está soportado por estudios toxicológicos. Los objetivos del presente trabajo fueron determinar las lesiones anatomopatológicas derivadas de la exposición al Cosmoflux® 411F y establecer la concentración letal 50 (CL50) a 96 horas en cachama blanca (Piaractus brachypomus). Se utilizaron juveniles de cachama blanca (40 g) en dos experimentos: 1) toxicidad subletal (n =126) y, 2) determinación de la CL50 (n =84). Las concentraciones del ensayo de toxicidad subletal fueron: 0 mg/l (Tratamiento 0), 0.17 mg/l (Tratamiento 1), 0.34 mg/l (Tratamiento 2), 0.68 mg/l (Tratamiento 3), 1.36 mg/l (Tratamiento 4), y 2.72 mg/l (Tratamiento 5), en sistema semiestático. Para determinar la CL50 las dosis fueron: 3000, 3450, 3900, 4350 y 4800 mg/l de Cosmoflux® 411F. La CL50 obtenida fue de 4417.99 mg/l. En los peces se evidenció leve disminución de la actividad de nado. A la necropsia se halló palidez del hígado y acumulación de material mucoso en las branquias. Por histopatología se halló: vacuolización de hepatocitos, hiperplasia de células epiteliales, de cloro y caliciformes branquiales, vacuolización de enterocitos, aumento de centros melanomacrófagos renales, gliosis, degeneración neuronal e infiltración de células granulares eosinofílicas/células mastocitos en telencéfalo. Los hallazgos concuerdan con lo reportado en peces expuestos a surfactantes, exceptuando las lesiones del sistema nervioso central que pueden tener consecuencias sobre interacciones sociales, de alimentación y reproducción de la especie; siendo necesario profundizar la investigación sobre dicho efecto. El hígado, branquias y piel constituyen órganos blanco de la acción tóxica. La CL50 hallada (4417.99 mg/l) es alta comparada con lo reportado en surfactantes no-iónicos.

In Colombia, surfactant Cosmoflux® 411F is used for the fumigation of illicit crops in order to improve the glyphosate herbicide activity. The use of Cosmoflux® 411F is not supported by toxicological surveys. The aims of this study were to determinate the anatomopathological lesions due to the exposure to Cosmoflux® 411F and to establish lethal concentration 50 (LC50) to 96 hours in cachama blanca (Piaractus brachypomus). Juveniles of cachama blanca (40 g) in two assays were used: 1) sublethal toxicity (n= 126) and 2) determination of LC50 (n=84). Sublethal toxicity assay concentrations were: 0 mg/l (Treatment 0) 0.17 mg/l (Treatment 1), 0.34 mg/l (Treatment 2), 0.68 mg/l (Treatment 3), 1.36 mg/l (Treatment 4), and 2.72 mg/l (Treatment 5); through semi-static system. For the determination of LC50 of Cosmoflux® 411F 3000, 3450, 3900, 4350 y 4800 mg/l concentrations were used. LC50 was 4417.99 mg/l. Animals showed slight decrease in swimming activity. At necropsy examination were found paleness in liver and whitish material accumulation in top of gill filament. Histopathologically, it was found fatty degeneration and hepatocyte vacuolization, epithelial cells, chloride cells and mucous cells hyperplasia, enterocyte vacuolization, increase in the expression of melanomacrophage centres in kidney, gliosis, neuronal degeneration and infiltration of eosinophilic granule cells/mast cells in telencephalon. With exception of central nervous system lesions, the findings are according to the reported in literature about surfactant exposure in fish. Central nervous system effects can have consequences on feeding, reproductive and social interactions, due to close telencephalon/olfactory system relationship, being necessary to deep in research to these processes. In same way, liver, gills and skin are target organs of toxic action of this xenobiotic. LC50 is high (4417.99 mg/l) compared with that reported for other nonionic surfactants.