Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
Comp Hepatol ; 8: 3, 2009 Jul 08.
Artigo em Inglês | MEDLINE | ID: mdl-19586524

RESUMO

BACKGROUND: To minimize the necessary number of biopsies for molecular and histological research we evaluated different sampling techniques, fixation methods, and storage procedures for canine liver tissue. For addressing the aim, three biopsy techniques (wedge biopsy, Menghini, True-cut), four storage methods for retrieval of RNA (snap freezing, RNAlater, Boonfix, RLT-buffer), two RNA isolation procedures (Trizol and RNAeasy), and three different fixation protocols for histological studies (10% buffered formalin, RNAlater, Boonfix) were compared. Histological evaluation was based on hematoxylin-eosin (HE) and reticulin (fibrogenesis) staining, and rubeanic acid and rhodanine stains for copper. Immunohistochemical evaluation was performed for cytokeratin-7 (K-7), multidrug resistance binding protein-2 (MRP-2) and Hepar-1. RESULTS: RNA quality was best guaranteed by the combination of a Menghini biopsy with NaCl, followed by RNAlater preservation and RNAeasy mini kit extraction. These results were confirmed by quantitative RT-PCR testing. Reliable histological assessment for copper proved only possible in formalin fixed liver tissue. Short formalin fixation (1-4 hrs) improved immunohistochemical reactivity and preservation of good morphology in small liver biopsies. CONCLUSION: At least two biopsies (RNAlater and formalin) are needed. Since human and canine liver diseases are highly comparable, it is conceivable that the protocols described here can be easily translated into the human biomedical field.

2.
Anal Bioanal Chem ; 390(6): 1653-8, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18264701

RESUMO

The heritability of chronic hepatitis in the Labrador Retriever is studied with the aim of identifying the related gene mutation. Identification of cases and controls is largely based on instrumental neutron activation analysis (INAA) Cu determination in liver biopsies. The burden for these companion animals may be reduced if nail clippings and hair (fur) could serve as a noninvasive indicator for the hepatic Cu concentrations. No correlation was found between hepatic Cu concentrations and Cu concentrations in hair and nail samples. However, hair and nail samples were also analyzed by X-ray tube excitation, taking advantage of the X-ray Compton, Rayleigh, and Raman scattering which reflects the organic components such as the type of melanin. Principal component analysis provided first indications that some differentiation between healthy and sick dogs could indeed be obtained from hair and nail analysis.


Assuntos
Cobre/análise , Cães/metabolismo , Cabelo/química , Casco e Garras/química , Fígado/química , Nêutrons , Análise Espectral Raman/métodos , Animais , Biópsia , Cor , Cobre/química , Feminino , Genótipo , Masculino , Melaninas/química , Estrutura Molecular , Raios X
3.
Vet J ; 178(1): 70-7, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18314358

RESUMO

Hepatocyte growth factor (HGF) is crucial for the development and regeneration of the liver and offers a possible new therapeutic strategy for the treatment of canine liver disease. In this study, the in vitro and in vivo bioactivity of recombinant canine HGF (rcHGF) produced with a baculoviral expression system in insect cells was measured. In vitro rcHGF induced mitogenesis, motogenesis, and phosphorylated the HGF receptor c-MET and its downstream mediators PKB and ERK1/2 in two canine epithelial cell lines. After a partial hepatectomy (phx) in dogs, rcHGF increased phosphorylation of c-MET, PKB and ERK1/2. A moderate increase was seen with the cell cycle protein PCNA in rcHGF treated livers, but no HGF-induced increase in liver weight was seen 7 days after phx. Furthermore, rcHGF treated livers showed lower levels of the key mediator of apoptosis, caspase-3, at 7days after phx. It is concluded that rcHGF is a biologically active protein in vitro and in vivo and the baculoviral expression system supplies sufficient amounts of rcHGF for future clinical studies in dogs.


Assuntos
Fator de Crescimento de Hepatócito/metabolismo , Hepatócitos/efeitos dos fármacos , Regeneração Hepática/efeitos dos fármacos , Animais , Linhagem Celular , Cães , MAP Quinases Reguladas por Sinal Extracelular/genética , MAP Quinases Reguladas por Sinal Extracelular/metabolismo , Feminino , Regulação da Expressão Gênica/efeitos dos fármacos , Hepatectomia , Fator de Crescimento de Hepatócito/genética , Fígado/efeitos dos fármacos , Fígado/fisiologia , Tamanho do Órgão , Proteínas Proto-Oncogênicas c-akt/genética , Proteínas Proto-Oncogênicas c-akt/metabolismo , Proteínas Proto-Oncogênicas c-met/genética , Proteínas Proto-Oncogênicas c-met/metabolismo , Proteínas Recombinantes
4.
Comp Hepatol ; 4(1): 3, 2005 Mar 24.
Artigo em Inglês | MEDLINE | ID: mdl-15790412

RESUMO

BACKGROUND: The role of copper accumulation in the onset of hepatitis is still unclear. Therefore, we investigated a spontaneous disease model of primary copper-toxicosis in Doberman pinschers so to gain insights into the pathophysiology of copper toxicosis, namely on genes involved in copper metabolism and reactive oxygen species (ROS) defences. RESULTS: We used quantitative real-time PCR to determine differentially expressed genes within a target panel, investigating different groups ranging from copper-associated subclinical hepatitis (CASH) to a clinical chronic hepatitis with high hepatic copper concentrations (Doberman hepatitis, DH). Furthermore, a non-copper associated subclinical hepatitis group (N-CASH) with normal hepatic copper concentrations was added as a control. Most mRNA levels of proteins involved in copper binding, transport, and excretion were around control values in the N-CASH and CASH group. In contrast, many of these (including ATP7A, ATP7B, ceruloplasmin, and metallothionein) were significantly reduced in the DH group. Measurements on defences against oxidative stress showed a decrease in gene-expression of superoxide dismutase 1 and catalase in both groups with high copper. Moreover, the anti-oxidative glutathione molecule was clearly reduced in the DH group. CONCLUSION: In the DH group the expression of gene products involved in copper efflux was significantly reduced, which might explain the high hepatic copper levels in this disease. ROS defences were most likely impaired in the CASH and DH group. Overall, this study describes a new variant of primary copper toxicosis and could provide a molecular basis for equating future treatments in dog and in man.

5.
FEMS Immunol Med Microbiol ; 42(3): 307-11, 2004 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-15477044

RESUMO

Lymphocytic cholangitis (LC) in cats is a biliary disease of unknown etiology. Helicobacter spp. were recently implicated in human primary sclerosing cholangitis (PSC) and primary biliary cirrhosis (PBC). Because of the similarities between PSC/PBC with LC, we hypothesized that Helicobacter spp. are involved in feline LC. A PCR with Helicobacter genus-specific 16S rRNA primers was performed on DNA isolated from feline bile samples. Four of the 15 (26%) LC samples were positive, whereas only 8/51 (16%) of non-LC samples were PCR positive (p=0.44). Sequence analysis of the amplicons revealed a 100% identity with the Helicobacter pylori specific DNA fragments. Our data suggest an etiological role of H. pylori in feline LC and that cats are a potential zoonotic reservoir.


Assuntos
Bile/microbiologia , Doenças do Gato/microbiologia , Colangite/veterinária , Infecções por Helicobacter/veterinária , Helicobacter pylori/isolamento & purificação , Animais , Gatos , Colangite/microbiologia , DNA Bacteriano/química , DNA Bacteriano/genética , DNA Bacteriano/isolamento & purificação , Genes de RNAr , Infecções por Helicobacter/microbiologia , Helicobacter pylori/genética , Reação em Cadeia da Polimerase , RNA Bacteriano/genética , RNA Ribossômico 16S/genética , Análise de Sequência de DNA
6.
Vet Clin North Am Small Anim Pract ; 39(3): 489-511, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19524791

RESUMO

The liver is essential for copper metabolism. Copper metabolism is highly conserved between different species. This article provides the reader with an overview of copper storage disorders in humans and animals. Diagnosis and treatment of copper-associated hepatitis are described, and breed-specific characteristics of the disease are explained. A literature review references publications about the disease in companion animals.


Assuntos
Cobre/efeitos adversos , Cobre/metabolismo , Doenças do Cão/induzido quimicamente , Hepatopatias/veterinária , Erros Inatos do Metabolismo dos Metais/veterinária , Animais , Doença Hepática Induzida por Substâncias e Drogas/patologia , Doença Hepática Induzida por Substâncias e Drogas/terapia , Doença Hepática Induzida por Substâncias e Drogas/veterinária , Colestase/complicações , Colestase/veterinária , Modelos Animais de Doenças , Doenças do Cão/patologia , Doenças do Cão/terapia , Cães , Humanos , Hepatopatias/etiologia , Hepatopatias/patologia , Hepatopatias/terapia , Erros Inatos do Metabolismo dos Metais/complicações , Camundongos , Ratos , Ovinos
7.
Trop Med Int Health ; 8(2): 129-32, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12581437

RESUMO

Point mutations in the dihydrofolate reductase (DHFR) and dihydropteroate synthase (DHPS) genes of Plasmodium falciparum can lead to an increasing resistance of P. falciparum to pyrimethamine/sulphadoxine. We examined the prevalence of these mutations in 36 samples from Colombia. Analysed by polymerase chain reaction (PCR) for infection with P. falciparum, 25 (69%) tested positive. These positive isolates were tested further for point mutations in the genes of DHFR (codons 16, 51, 59, 108 and 164) and DHPS (codons 436, 437, 540, 581 and 613) by nested PCR and following mutation-specific restriction enzyme digestion. Gene mutations occurred in both the DHFR and DHPS gene of the Colombian isolates, suggesting that resistance to antifolate drugs exists or may develop soon in Colombia.


Assuntos
Di-Hidropteroato Sintase/genética , Resistência a Medicamentos/genética , Plasmodium falciparum/genética , Mutação Puntual/genética , Tetra-Hidrofolato Desidrogenase/genética , Adulto , Idoso , Animais , Antimaláricos/uso terapêutico , Colômbia , Combinação de Medicamentos , Genes de Protozoários/genética , Humanos , Malária Falciparum/tratamento farmacológico , Malária Falciparum/genética , Pessoa de Meia-Idade , Plasmodium falciparum/enzimologia , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Pirimetamina/uso terapêutico , Sulfadoxina/uso terapêutico
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa