Myeloid differentiation factor-88/interleukin-1 signaling controls cardiac fibrosis and heart failure progression in inflammatory dilated cardiomyopathy.

RATIONALE: The myeloid differentiation factor (MyD)88/interleukin (IL)-1 axis activates self-antigen-presenting cells and promotes autoreactive CD4(+) T-cell expansion in experimental autoimmune myocarditis, a mouse model of inflammatory heart disease. OBJECTIVE: The aim of this study was to determine the role of MyD88 and IL-1 in the progression of acute myocarditis to an end-stage heart failure. METHODS AND RESULTS: Using alpha-myosin heavy chain peptide (MyHC-alpha)-loaded, activated dendritic cells, we induced myocarditis in wild-type and MyD88(-/-) mice with similar distributions of heart-infiltrating cell subsets and comparable CD4(+) T-cell responses. Injection of complete Freund's adjuvant (CFA) or MyHC-alpha/CFA into diseased mice promoted cardiac fibrosis, induced ventricular dilation, and impaired heart function in wild-type but not in MyD88(-/-) mice. Experiments with chimeric mice confirmed the bone marrow origin of the fibroblasts replacing inflammatory infiltrates and showed that MyD88 and IL-1 receptor type I signaling on bone marrow-derived cells was critical for development of cardiac fibrosis during progression to heart failure. CONCLUSIONS: Our findings indicate a critical role of MyD88/IL-1 signaling in the bone marrow compartment in postinflammatory cardiac fibrosis and heart failure and point to novel therapeutic strategies against inflammatory cardiomyopathy.

Animal Industry News, February 2001, Vol. 2, no. 1

Newsletter produced by Department of Agriculture and Land Stewardship about the animal industry in Iowa.

Animal Industry News, April 2002, Vol. 3, no. 1

Newsletter produced by Department of Agriculture and Land Stewardship about the animal industry in Iowa.

Animal Industry News, February 2005, Vol. 6, no. 1

Newsletter produced by Department of Agriculture and Land Stewardship about the animal industry in Iowa.

Animal Industry News, April 2006, Vol. 7, no. 1

Newsletter produced by Department of Agriculture and Land Stewardship about the animal industry in Iowa.

Transglutaminase 1-deficient recessive lamellar ichthyosis associated with a LINE-1 insertion in Jack Russell terrier dogs.

BACKGROUND: Congenital, nonepidermolytic cornification disorders phenotypically resembling human autosomal recessive ichthyosis have been described in purebred dog breeds, including Jack Russell terrier (JRT) dogs. One cause of gene mutation important to humans and dogs is transposon insertions. OBJECTIVES: To describe an autosomal recessive, severe nonepidermolytic ichthyosis resembling lamellar ichthyosis (LI) in JRT dogs due to insertion of a long interspersed nucleotide element (LINE-1) in the transglutaminase 1 (TGM1) gene. METHODS: Dogs were evaluated clinically, and skin samples were examined by light and electron microscopy. Phenotypic information and genotyping with a canine microsatellite marker suggested TGM1 to be a candidate gene. Genomic DNA samples and cDNA generated from epidermal RNA were examined. Consequences of the mutation were evaluated by Western blotting, quantitative reverse transcription-polymerase chain reaction (RT-PCR) and enzyme activity from cultured keratinocytes. RESULTS: Affected dogs had generalized severe hyperkeratosis. Histological examination defined laminated to compact hyperkeratosis without epidermolysis; ultrastructurally, cornified envelopes were thin. Affected dogs were homozygous for a 1980-bp insertion within intron 9 of TGM1. The sequence of the insertion was that of a canine LINE-1 element. Quantitative RT-PCR indicated a significant decrease in TGM1 mRNA in affected dogs compared with wild-type. TGM1 protein was markedly decreased on immunoblotting, and membrane-associated enzyme activity was diminished in affected dogs. CONCLUSIONS: Based on morphological and molecular features, this disease is homologous with TGM1-deficient LI in humans, clinically models LI better than the genetically modified mouse and represents its first spontaneous animal model. This is the first reported form of LI due to transposon insertion.

Perdas de solo e água em plantio de Acacia mangium wild e savana em Roraima, norte da Amazônia

Plantios florestais de Acacia mangium constituem uma alternativa cada vez mais adotada em áreas de savanas do norte da Amazônia (Roraima) e podem causar alterações significativas de características do solo. Neste sentido, o objetivo deste estudo foi determinar perdas de solo e de água por erosão, que ocorrem em escoamento superficial (run off) em savana nativa e plantios de acácia na região Amazônica. Para isso, foram instaladas em duas fazendas, Santa Rita e Araçá, localizadas no município de Bonfim, na região da Serra da Lua, calhas coletoras de sedimentos, acopladas a caixas d'água, em Argissolo Vermelho-Amarelo. Foram determinadas a granulometria, a densidade aparente (Dap), a resistência à penetração (RP) e a velocidade de infiltração (VIB), bem como parâmetros físicos relacionados a perdas de solo. O delineamento experimental utilizado foi o de blocos ao acaso, com três tratamentos: cobertura natural de savana (SV), plantio de Acacia mangium com um ano de idade (P1) e plantio de Acacia mangium com quatro anos de idade (P4), em três repetições. O experimento teve a duração de 12 meses (setembro de 2006 a agosto de 2007). Os resultados indicaram maiores perdas de solo e de água no plantio mais recente de acácia (P1), de savana nativa e do plantio com 4 anos (P4). Os resultados foram atribuídos à exposição do solo no período inicial de desenvolvimento da planta, ao selamento superficial e à coesão do solo. O pico de perdas de solo ocorreu nos meses de abril a agosto, sendo o tipo de cobertura vegetal o fator determinante para redução das perdas de solo e de água por erosão, sendo que as práticas de plantio no sentido do declive provavelmente agravaram as perdas de solo nos plantios de Acácia. Neste trabalho, a densidade do solo e o teor de matéria orgânica não representaram bons indicadores do tipo de manejo adotado na área.

Eläinaiheiset luonnonkasvien nimet kansankielessä

Summary: Animal themes in vernacular names of wild-growing plants

The effect of genotype on anther culture response of cultivated and wild oats

Selostus: Genotyypin vaikutus kauran, kuorettoman kauran ja villikauran ponsiviljelyvasteeseen

Comportamento e impacto ambiental de antibióticos usados na produção animal brasileira

Antibióticos têm sido utilizados em grandes quantidades nas criações animais. Muitas dessas moléculas não são totalmente metabolizadas no organismo animal e seus resíduos têm sido detectados em amostras de solo, água superficial e subterrânea. A ocorrência desses resíduos no ambiente pode favorecer a resistência de microrganismos aos agentes antibióticos, além de causar problemas de ordem toxicológica a determinados organismos vivos. Os antibióticos de uso veterinário são, no geral, representados por moléculas anfóteras, com vários grupos funcionais ionizáveis (diferentes valores de pKa), massas molares bastante variáveis (172 a 916 g mol-1) e baixos potenciais de volatilização (pressão de vapor < 1,1 x 10-11 mm Hg). Em relação aos pesticidas, esses compostos apresentam maiores valores de solubilidade em água e menores valores de coeficiente de partição n-octanol-água (log Kow), provavelmente devido à presença de muitos grupos funcionais ionizáveis, o que sugere menor potencial de bioacumulação e maior mobilidade no solo. No presente trabalho avaliam-se o uso de antibióticos e a importância da produção animal no Brasil, aspectos do seu comportamento ambiental em condições de clima temperado e, por fim, enfatiza-se a necessidade de conduzir investigações sobre sua ocorrência e comportamento em solos muito intemperizados, predominantes nos ambientes tropicais.

Drug-eluting beads loaded with antiangiogenic agents for chemoembolization: in vitro sunitinib loading and release and in vivo pharmacokinetics in an animal model.

PURPOSE: The combination of embolic beads with a multitargeted tyrosine kinase inhibitor that inhibits tumor vessel growth is suggested as an alternative and improvement to the current standard doxorubicin-eluting beads for use in transarterial chemoembolization. This study demonstrates the in vitro loading and release kinetics of sunitinib using commercially available embolization microspheres and evaluates the in vitro biologic efficacy on cell cultures and the resulting in vivo pharmacokinetics profiles in an animal model. MATERIALS AND METHODS: DC Bead microspheres, 70-150 µm and 100-300 µm (Biocompatibles Ltd., Farnham, United Kingdom), were loaded by immersion in sunitinib solution. Drug release was measured in saline in a USP-approved flow-through apparatus and quantified by spectrophotometry. Activity after release was confirmed in cell culture. For pharmacokinetics and in vivo toxicity evaluation, New Zealand white rabbits received sunitinib either by intraarterial injection of 100-300 µm sized beads or per os. Plasma and liver tissue drug concentrations were assessed by liquid chromatography-tandem mass spectroscopy. RESULTS: Sunitinib loading on beads was close to complete and homogeneous. A total release of 80% in saline was measured, with similar fast-release profiles for both sphere sizes. After embolization, drug plasma levels remained below the therapeutic threshold (< 50 ng/mL), but high concentrations at 6 hours (14.9 µg/g) and 24 hours (3.4 µg/g) were found in the liver tissue. CONCLUSIONS: DC Bead microspheres of two sizes were efficiently loaded with sunitinib and displayed a fast and almost complete release in saline. High liver drug concentrations and low systemic levels indicated the potential of sunitinib-eluting beads for use in embolization.

Morphostructural characterization of soil conventionally tilled with mechanized and animal traction with and without cover crop

The structural stability and restructuring ability of a soil are related to the methods of crop management and soil preparation. A recommended strategy to reduce the effects of soil preparation is to use crop rotation and cover crops that help conserve and restore the soil structure. The aim of this study was to evaluate and quantify the homogeneous morphological units in soil under conventional mechanized tillage and animal traction, as well as to assess the effect on the soil structure of intercropping with jack bean (Canavalia ensiformis L.). Profiles were analyzed in April of 2006, in five counties in the Southern-Central region of Paraná State (Brazil), on family farms producing maize (Zea mays L.), sometimes intercropped with jack bean. The current structures in the crop profile were analyzed using Geographic Information Systems (GIS) and subsequently principal component analysis (PCA) to generate statistics. Morphostructural soil analysis showed a predominance of compact units in areas of high-intensity cultivation under mechanized traction. The cover crop did not improve the structure of the soil with low porosity and compact units that hamper the root system growth. In areas exposed to animal traction, a predominance of cracked units was observed, where roots grew around the clods and along the gaps between them.

Sequence analysis and expression of the attachment and fusion proteins of canine distemper virus wild-type strain A75/17.

The biological properties of wild-type A75/17 and cell culture-adapted Onderstepoort canine distemper virus differ markedly. To learn more about the molecular basis for these differences, we have isolated and sequenced the protein-coding regions of the attachment and fusion proteins of wild-type canine distemper virus strain A75/17. In the attachment protein, a total of 57 amino acid differences were observed between the Onderstepoort strain and strain A75/17, and these were distributed evenly over the entire protein. Interestingly, the attachment protein of strain A75/17 contained an extension of three amino acids at the C terminus. Expression studies showed that the attachment protein of strain A75/17 had a higher apparent molecular mass than the attachment protein of the Onderstepoort strain, in both the presence and absence of tunicamycin. In the fusion protein, 60 amino acid differences were observed between the two strains, of which 44 were clustered in the much smaller F2 portion of the molecule. Significantly, the AUG that has been proposed as a translation initiation codon in the Onderstepoort strain is an AUA codon in strain A75/17. Detailed mutation analyses showed that both the first and second AUGs of strain A75/17 are the major translation initiation sites of the fusion protein. Similar analyses demonstrated that, also in the Onderstepoort strain, the first two AUGs are the translation initiation codons which contribute most to the generation of precursor molecules yielding the mature form of the fusion protein.