RESUMO
The finding of acquired chromosomal translocations that are consistently associated with specific tumour types supports the premise of lineage-specific mechanisms of tumorigenesis. We review the evidence indicating that the specificity of these translocations and the corresponding gene fusions is related to biological constraints at the level of recombination, expression, and protein function. A dynamic relationship between the gene fusion and the cellular environment is proposed in which the environment influences the selection of oncogenic fusions and the oncogenic fusion in turn influences the cellular environment.
Assuntos
Neoplasias/genética , Translocação Genética , Animais , Modelos Animais de Doenças , Regulação Neoplásica da Expressão Gênica , Rearranjo Gênico , Genes Supressores de Tumor , Humanos , Neoplasias Experimentais/genéticaRESUMO
We have determined that PAX3 (found previously to be mutated in Waardenburg syndrome) is the chromosome 2 locus rearranged by the t(2;13)(q35;q14) translocation of the paediatric solid tumour alveolar rhabdomyosarcoma. The rearrangement breakpoints occur within an intron downstream of the paired box and homeodomain-encoding regions. Upstream PAX3 sequences hybridize to a novel transcript in t(2;13)-containing lines. Cloning and characterization of this novel transcript indicate that the translocation juxtaposes the PAX3 DNA binding elements with chromosome 13 sequences, suggesting formation of a hybrid transcription factor. Therefore, PAX3 gene alterations are associated with two completely unrelated human diseases.
Assuntos
Rearranjo Gênico , Genes Homeobox , Rabdomiossarcoma/genética , Sequência de Bases , Criança , Quimera , Mapeamento Cromossômico , Cromossomos Humanos Par 13 , Cromossomos Humanos Par 2 , Clonagem Molecular , DNA de Neoplasias/genética , Humanos , Dados de Sequência Molecular , Transcrição Gênica , Translocação Genética , Células Tumorais CultivadasRESUMO
We have examined the structure and expression of the products associated with the t(2;13)(q35;q14) translocation associated with alveolar rhabdomyosarcoma. The chromosome 13 gene (FKHR) is identified as a member of the fork head domain family of transcription factors characterized by a conserved DNA binding motif. Polymerase chain reaction analysis demonstrates that a 5'PAX3-3' FKHR chimaeric transcript is expressed in all eight alveolar rhabdomyosarcomas investigated. Immunoprecipitation experiments detect the predicted fusion protein. These findings indicate that the t(2;13) generates a potentially tumorigenic fusion transcription factor consisting of intact PAX3 DNA binding domains, a truncated fork head DNA binding domain and C-terminal FKHR regions.
Assuntos
Proteínas de Ligação a DNA/genética , Rabdomiossarcoma Alveolar/genética , Fatores de Transcrição/genética , Translocação Genética , Sequência de Aminoácidos , Sequência de Bases , Cromossomos Humanos Par 13 , Cromossomos Humanos Par 2 , Clonagem Molecular , DNA de Neoplasias , Proteína Forkhead Box O1 , Fatores de Transcrição Forkhead , Humanos , Dados de Sequência Molecular , Proteínas de Neoplasias/genética , Fator de Transcrição PAX3 , Fatores de Transcrição Box Pareados , Reação em Cadeia da Polimerase , RNA Mensageiro , Homologia de Sequência de Aminoácidos , Células Tumorais CultivadasRESUMO
AIM: Cerebral vasospasm is a leading cause of death and disability following aneurysmal subarachnoid hemorrhage (SAH). Nitric oxide (NO) is a potent mediator of vasodilation, and citrulline is a known contributor to NO production. The leukocytosis inflammatory response can increase vasoconstrictive compounds that may also contribute to vasospasm. Dexamethasone is a glucocorticosteroid commonly administered after SAH, which may alter the production of leukocytes and citrulline. The goal of this project was to study the effects of dexamethasone on leukocytosis, citrulline, and angiographic vasospasm. METHODS: Experimental SAH was induced in 18 New Zealand white rabbits. Intravenous dexamethasone was administered to one group (N.=9) at 2 mg/kg/day. A placebo group (N.=9) was given a saline infusion with otherwise identical procedures. CSF citrulline, leukocytes, protein, and glucose, as well as plasma citrulline were measured at baseline and 3 days post-SAH in a blinded fashion. Basilar artery angiography was performed at baseline and repeated 3 days post-SAH. RESULTS: The change in CSF citrulline from day 0 to day 3 was significantly lower in the dexamethasone group compared to controls (P=0.002). The change in CSF white blood cells was also significantly lower (P=0.005). There was no significant change in plasma citrulline levels or angiographic vasospasm. CONCLUSION: Dexamethasone significantly decreases CSF citrulline and CSF leukocytosis after experimental SAH. It is possible this could lead to a relative vasoconstriction and vasodilation, respectively. These processes could cancel-out opposing effects of dexamethasone on cerebral vasospasm, partially contributing to the recognized, multifactorial, inconsistent effects of glucocorticoids on vasospasm.
Assuntos
Citrulina/líquido cefalorraquidiano , Dexametasona/uso terapêutico , Glucocorticoides/uso terapêutico , Leucócitos/efeitos dos fármacos , Hemorragia Subaracnóidea/tratamento farmacológico , Vasoespasmo Intracraniano/tratamento farmacológico , Animais , Dexametasona/farmacologia , Modelos Animais de Doenças , Glucocorticoides/farmacologia , Óxido Nítrico/líquido cefalorraquidiano , Coelhos , Hemorragia Subaracnóidea/líquido cefalorraquidiano , Hemorragia Subaracnóidea/complicações , Vasoespasmo Intracraniano/líquido cefalorraquidiano , Vasoespasmo Intracraniano/etiologia , Vasoespasmo Intracraniano/metabolismoRESUMO
Congenital abnormalities of the reproductive tract of male sheep were surveyed at three abattoirs in the south west of England during the period June 2000-January 2004. A total of 7307 rams were examined [6521 lambs (prepubescent) and hoggets (aged from their first autumn after birth until first shorn) and 786 adult rams mature rams that had been exposed to ewes]. A total of 156 congenital lesions were detected, 87 of which occurred in lambs. Testicular hypoplasia was the most common lesion occurring in 69 lambs as well as eight hoggets ('microtestes' were recognized in nine other animals in which the testis was disproportionately smaller than the epididymis). The second most common lesion found was notched scrotum occurring in 34 animals (27 young rams and seven adults). Some cases of notched scrotum were accompanied by hypospadias which was seen in a total of seven lambs and eight hoggets. Other lesions, detected in five or less animals (less than approximately 0.05% of the animals examined), included cryptorchidism and various abnormalities of the epididymis (segmental aplasia of the epididymis, blind efferent ducts and epididymal cyst) and congenital scrotal hernia. The overall prevalence of congenital lesions of 2.21% emphasizes the importance of undertaking breeding soundness examinations of young rams before they are put with the flock.
Assuntos
Genitália Masculina/anormalidades , Doenças dos Ovinos/epidemiologia , Ovinos/anormalidades , Matadouros , Animais , Criptorquidismo/epidemiologia , Criptorquidismo/veterinária , Inglaterra/epidemiologia , Epididimo/anormalidades , Hipospadia/epidemiologia , Hipospadia/veterinária , Masculino , Escroto/anormalidades , Maturidade Sexual , Doenças dos Ovinos/diagnóstico por imagem , Testículo/anormalidades , UltrassonografiaRESUMO
Among the proteins regulating vesicular traffic, the small, Ras-like GTPases have received particular attention. Several recent reports indicate that another class of GTP-binding (G) protein, the heterotrimeric G proteins, also participates in the regulation of vesicular traffic. Thus, studies using transfected cells and cell-free systems show that a pertussis toxin-sensitive trimeric G protein, G(i3), is involved in the formation of secretory vesicles from the Golgi complex. These results raise the intriguing possibility that signal transduction processes across intracellular membranes play a role in vesicle formation, and provide important clues about the molecular machinery involved in this process.
RESUMO
The Golgi apparatus is a highly complex organelle comprised of a stack of cisternal membranes on the secretory pathway from the ER to the cell surface. This structure is maintained by an exoskeleton or Golgi matrix constructed from a family of coiled-coil proteins, the golgins, and other peripheral membrane components such as GRASP55 and GRASP65. Here we find that TMP21, p24a, and gp25L, members of the p24 cargo receptor family, are present in complexes with GRASP55 and GRASP65 in vivo. GRASPs interact directly with the cytoplasmic domains of specific p24 cargo receptors depending on their oligomeric state, and mutation of the GRASP binding site in the cytoplasmic tail of one of these, p24a, results in it being transported to the cell surface. These results suggest that one function of the Golgi matrix is to aid efficient retention or sequestration of p24 cargo receptors and other membrane proteins in the Golgi apparatus.
Assuntos
Complexo de Golgi/metabolismo , Proteínas de Membrana/metabolismo , Transporte Proteico/fisiologia , Animais , Anticorpos , Autoantígenos , Complexo de Golgi/química , Proteínas da Matriz do Complexo de Golgi , Proteínas de Membrana/análise , Proteínas de Membrana/imunologia , Proteínas de Transporte Nucleocitoplasmático , Ligação Proteica/fisiologia , Coelhos , Fator de Crescimento Transformador alfa/análise , Fator de Crescimento Transformador alfa/metabolismo , Técnicas do Sistema de Duplo-Híbrido , LevedurasRESUMO
Membrane traffic between the endoplasmic reticulum (ER) and Golgi apparatus and through the Golgi apparatus is a highly regulated process controlled by members of the rab GTPase family. The GTP form of rab1 regulates ER to Golgi transport by interaction with the vesicle tethering factor p115 and the cis-Golgi matrix protein GM130, also part of a complex with GRASP65 important for the organization of cis-Golgi cisternae. Here, we find that a novel coiled-coil protein golgin-45 interacts with the medial-Golgi matrix protein GRASP55 and the GTP form of rab2 but not other Golgi rab proteins. Depletion of golgin-45 disrupts the Golgi apparatus and causes a block in secretory protein transport. These results demonstrate that GRASP55 and golgin-45 form a rab2 effector complex on medial-Golgi essential for normal protein transport and Golgi structure.
Assuntos
Complexo de Golgi/enzimologia , Proteínas de Membrana/metabolismo , Transporte Proteico/fisiologia , Proteína rab2 de Ligação ao GTP/metabolismo , Animais , Autoantígenos , Complexo de Golgi/química , Complexo de Golgi/ultraestrutura , Proteínas da Matriz do Complexo de Golgi , Células HeLa , Humanos , Rim/citologia , Proteínas de Membrana/análise , Proteínas de Membrana/genética , Camundongos , Dados de Sequência Molecular , Ratos , Técnicas do Sistema de Duplo-Híbrido , Leveduras , Proteína rab2 de Ligação ao GTP/análiseRESUMO
Bilateral testicular haemorrhage was detected in a 5-year-old Bleu du Maine ram in an abattoir survey of male reproductive tracts in sheep; the ultrasonographic and histologic features of the lesions are described.
Assuntos
Hemorragia/veterinária , Doenças dos Ovinos/diagnóstico , Doenças Testiculares/veterinária , Animais , Hemorragia/diagnóstico por imagem , Hemorragia/patologia , Masculino , Ovinos , Doenças dos Ovinos/diagnóstico por imagem , Doenças dos Ovinos/patologia , Doenças Testiculares/diagnóstico por imagem , Doenças Testiculares/patologia , UltrassonografiaRESUMO
Bilateral testicular enlargement was recognized in a young lamb; both gonads were largely replaced by a mass composed of multiple cystic spaces. Positive immunohistochemical staining for factor VIII-related protein indicated that the cysts were lined by endothelial cells. The precise nature and origin of the lesions is unclear; they might represent hamartomas or benign tumours or may be a result of lymphatic obstruction.
Assuntos
Linfangioma/veterinária , Doenças dos Ovinos/diagnóstico , Neoplasias Testiculares/veterinária , Animais , Diagnóstico Diferencial , Linfangioma/diagnóstico , Masculino , Ovinos , Doenças dos Ovinos/diagnóstico por imagem , Doenças dos Ovinos/patologia , Neoplasias Testiculares/diagnóstico , UltrassonografiaRESUMO
OBJECTIVES: The objectives of this study were to quantify the sensitivity and specificity of visual assessment of radiographs of the canine elbow in detecting ulnar trochlear notch sclerosis, to establish interobserver and intra-observer variation for the presence and grade of sclerosis and to quantify the effect of radiographic exposure on observer grading. METHODS: Mediolateral elbow radiographs were obtained from Labrador retrievers (n=34) aged between six and 18 months. Radiographs from dogs with an arthroscopic diagnosis of fragmented medial coronoid process (n=17) and those from a control population (n=17) were subjected to observer grading for the presence or absence of and the grade of ulnar trochlear notch sclerosis. Interobserver and intra-observer variation and observer sensitivity and specificity were calculated. Digital data from the ulnar trochlear notch were correlated with mean observer grade to quantify the effect of radiographic exposure on observer grade. RESULTS: Interobserver agreement was "fair" (kappa=0.251 to 0.369) and intra-observer agreement was "moderate" to "substantial" (kappa=0.462 to 0.667). The sensitivity of observer assessment was 72 per cent with a specificity of 22 per cent. Mean observer grade was not significantly correlated with the degree of radiographic exposure (P=0.70). CLINICAL SIGNIFICANCE: Ulnar trochlear notch sclerosis is a phenomenon associated with fragmented medial coronoid process. However, interobserver agreement in grading this feature is only fair, being identified by observers with moderate sensitivity but with relatively poor specificity. This low specificity may predispose to overdiagnosis in clinical cases. Intra-observer agreement is moderate to substantial, suggesting that individuals can reliably quantify this radiological feature on multiple occasions. The ability of observers to assess the degree of sclerotic change is not significantly affected by radiographic exposure.
Assuntos
Doenças do Cão/diagnóstico por imagem , Artropatias/veterinária , Ulna/patologia , Animais , Competência Clínica/estatística & dados numéricos , Doenças do Cão/patologia , Cães , Feminino , Artropatias/diagnóstico por imagem , Masculino , Variações Dependentes do Observador , Radiografia , Esclerose/diagnóstico por imagem , Esclerose/veterinária , Sensibilidade e Especificidade , Ulna/diagnóstico por imagem , Médicos Veterinários/normasRESUMO
In recent years, a large number of coiled-coil proteins localised to the Golgi apparatus have been identified using antisera from human patients with a variety of autoimmune conditions [1]. Because of their common method of discovery and extensive regions of coiled-coil, they have been classified as a family of proteins, the golgins [1]. This family includes golgin-230/245/256, golgin-97, GM130/golgin-95, golgin-160/MEA-2/GCP170, giantin/macrogolgin and a related group of proteins - possibly splice variants - GCP372 and GCP364[2][3][4][5][6][7][8][9][10][11]. GM130 and giantin have been shown to function in the p115-mediated docking of vesicles with Golgi cisternae [12]. In this process, p115, another coiled-coil protein, is though to bind to giantin on vesicles and to GM130 on cisternae, thus acting as a tether holding the two together [12] [13]. Apart from giantin and GM130, none of the golgins has yet been assigned a function in the Golgi apparatus. In order to obtain clues as to the functions of the golgins, the targeting to the Golgi apparatus of two members of this family, golgin-230/245/256 and golgin-97, was investigated. Each of these proteins was shown to target to the Golgi apparatus through a carboxy-terminal domain containing a conserved tyrosine residue, which was critical for targeting. The domain preferentially bound to Rab6 on protein blots, and mutations that abolished Golgi targeting resulted in a loss of this interaction. Sequence analysis revealed that a family of coiled-coil proteins from mammals, worms and yeast contain this domain at their carboxyl termini. One of these proteins, yeast Imh1p, has previously been shown to have a tight genetic interaction with Rab6 [14]. On the basis of these data, it is proposed that this family of coiled-coil proteins functions in Rab6-regulated membrane-tethering events.
Assuntos
Autoantígenos/metabolismo , Proteínas de Transporte/metabolismo , Complexo de Golgi/metabolismo , Proteínas de Membrana , Proteínas rab de Ligação ao GTP , Proteínas ras/metabolismo , Sequência de Aminoácidos , Animais , Autoantígenos/química , Autoantígenos/genética , Sítios de Ligação , Proteínas da Matriz do Complexo de Golgi , Proteínas de Fluorescência Verde , Células HeLa , Humanos , Proteínas Luminescentes/genética , Proteínas Luminescentes/metabolismo , Camundongos , Dados de Sequência Molecular , Mutação , Ligação Proteica , Estrutura Terciária de Proteína , Proteínas Recombinantes de Fusão/genética , Proteínas Recombinantes de Fusão/metabolismo , Homologia de Sequência de AminoácidosRESUMO
Membrane fission occurs in eukaryotic cells whenever a vesicle is produced or a larger subcellular compartment is divided into smaller discrete units. Recent evidence suggests this fission event is promoted by enzymes that generate phosphatidic acid and thereby cause a distortion of the lipid bilayer.
Assuntos
Proteínas Adaptadoras de Transdução de Sinal , Membranas Intracelulares/fisiologia , Fusão de Membrana/fisiologia , Fatores de Transcrição , Animais , Ácido Araquidônico/metabolismo , Proteínas de Transporte/metabolismo , Membranas Intracelulares/metabolismo , Lisofosfolipídeos/metabolismo , Ácido Palmítico/metabolismo , Domínios de Homologia de srcRESUMO
We have investigated the mechanism of activation of an inactive but functionally intact hamster thymidine kinase (TK) gene by the chemical carcinogen N-methyl-N'-nitro-N-nitrosoguanidine. Following carcinogen treatment of TK- RJK92 Chinese hamster cells, aminopterin-resistant (HATr) colonies appeared at a frequency 50-fold higher than in untreated controls. More than 80% of these HATr variants expressed TK enzymatic activity and were divided into high- and low-activity classes. In all TK+ variants, TK expression was correlated with demethylation in the 5' region of the TK gene and the appearance a 1,400-nucleotide TK mRNA. Using high-performance liquid chromatography to measure the level of genomic methylation, we found that four of five high-activity lines demonstrated extensive genomic hypomethylation (approximately 25% of normal level) that was associated with demethylation of all TK gene copies. Restriction endonuclease analysis of 15 low-activity lines revealed four instances of sequence alterations in the far-5' region of the TK gene and one instance of a tandem low-copy amplification. In these lines, the structurally altered gene copy was demethylated. Thus, we propose that a chemical carcinogen can activate TK expression by several different mechanisms. Focal demethylation with or without gene rearrangement was associated with low TK activity, whereas demethylation throughout the genome was associated with high TK activity.
Assuntos
Genes/efeitos dos fármacos , Metilnitronitrosoguanidina/farmacologia , Timidina Quinase/genética , Animais , Sequência de Bases , Divisão Celular/efeitos dos fármacos , Linhagem Celular , Cricetinae , Cricetulus , Variação Genética , Metilação , Hibridização de Ácido Nucleico , PlasmídeosRESUMO
Alveolar rhabdomyosarcomas are pediatric solid tumors with a hallmark cytogenetic abnormality: translocation of chromosomes 2 and 13 [t(2;13) (q35;q14)]. The genes on each chromosome involved in this translocation have been identified as the transcription factor-encoding genes PAX3 and FKHR. The NH2-terminal paired box and homeodomain DNA-binding domains of PAX3 are fused in frame to COOH-terminal regions of the chromosome 13-derived FKHR gene, a novel member of the forkhead DNA-binding domain family. To determine the role of the fusion protein in transcriptional regulation and oncogenesis, we identified the PAX3-FKHR fusion protein and characterized its function(s) as a transcription factor relative to wild-type PAX3. Antisera specific to PAX3 and FKHR were developed and used to examine PAX3 and PAX3-FKHR expression in tumor cell lines. Sequential immunoprecipitations with anti-PAX3 and anti-FKHR sera demonstrated expression of a 97-kDa PAX3-FKHR fusion protein in the t(2;13)-positive rhabdomyosarcoma Rh30 cell line and verified that a single polypeptide contains epitopes derived from each protein. The PAX3-FKHR protein was localized to the nucleus in Rh30 cells, as was wild-type PAX3, in t(2;13)-negative A673 cells. In gel shift assays using a canonical PAX binding site (e5 sequence), we found that DNA binding of PAX3-FKHR was significantly impaired relative to that of PAX3 despite the two proteins having identical PAX DNA-binding domains. However, the PAX3-FKHR fusion protein was a much more potent transcriptional activator than PAX3 as determined by transient cotransfection assays using e5-CAT reporter plasmids. The PAX3-FKHR protein may function as an oncogenic transcription factor by enhanced activation of normal PAX3 target genes.
Assuntos
Cromossomos Humanos Par 13 , Cromossomos Humanos Par 2 , Proteínas de Ligação a DNA/genética , Neoplasias Pulmonares/genética , Proteínas de Fusão Oncogênica/genética , Rabdomiossarcoma Alveolar/genética , Fatores de Transcrição/genética , Translocação Genética , Animais , Sequência de Bases , Sítios de Ligação , Linhagem Celular , Núcleo Celular/metabolismo , Chlorocebus aethiops , Proteínas de Ligação a DNA/biossíntese , Proteína Forkhead Box O1 , Fatores de Transcrição Forkhead , Expressão Gênica , Humanos , Dados de Sequência Molecular , Sondas de Oligonucleotídeos , Proteínas de Fusão Oncogênica/biossíntese , Fator de Transcrição PAX3 , Fatores de Transcrição Box Pareados , Biossíntese de Proteínas , Fatores de Transcrição/biossíntese , Transcrição Gênica , TransfecçãoRESUMO
The maximum length and depth of the longitudinal section, and the maximum width and depth of the transverse section of the gall bladders of 32 dog cadavers were measured ultrasonographically; the contents of the gall bladder were then aspirated and its actual volume measured. The volume of the gall bladder was estimated from the ultrasonographic measurements by using formulae suggested for assessment of the volumes of the urinary bladder in human beings and the gall bladder of dogs, and these formulae were compared with a formula derived from the measurements made in this study. In 21 of the dogs, the measurements were repeated twice so that their reproducibility could be evaluated. All the formulae gave good estimations of the volume of the dogs' gall bladders, but the formula for the human urinary bladder volume was better than the other two. The actual volume of the gall bladder was related to the dogs' bodyweight. There were no significant differences between the repeated measurements of the maximum length and depth of the longitudinal section or the width of the transverse section of the gall bladder, but there were significant variations in the depth of the transverse section.
Assuntos
Cães/anatomia & histologia , Vesícula Biliar/anatomia & histologia , Animais , Cães/fisiologia , Vesícula Biliar/diagnóstico por imagem , Vesícula Biliar/fisiologia , Valores de Referência , Reprodutibilidade dos Testes , Ultrassonografia/veterináriaRESUMO
Dendritic cells (DCs) throughout the female reproductive tract (FRT) were examined for phenotype, HIV capture ability and innate anti-HIV responses. Two main CD11c+ DC subsets were identified: CD11b+ and CD11blow DCs. CD11b+CD14+ DCs were the most abundant throughout the tract. A majority of CD11c+CD14+ cells corresponded to CD1c+ myeloid DCs, whereas the rest lacked CD1c and CD163 expression (macrophage marker) and may represent monocyte-derived cells. In addition, we identified CD103+ DCs, located exclusively in the endometrium, whereas DC-SIGN+ DCs were broadly distributed throughout the FRT. Following exposure to GFP-labeled HIV particles, CD14+ DC-SIGN+ as well as CD14+ DC-SIGN- cells captured virus, with â¼30% of these cells representing CD1c+ myeloid DCs. CD103+ DCs lacked HIV capture ability. Exposure of FRT DCs to HIV induced secretion of CCL2, CCR5 ligands, interleukin (IL)-8, elafin, and secretory leukocyte peptidase inhibitor (SLPI) within 3 h of exposure, whereas classical pro-inflammatory molecules did not change and interferon-α2 and IL-10 were undetectable. Furthermore, elafin and SLPI upregulation, but not CCL5, were suppressed by estradiol pre-treatment. Our results suggest that specific DC subsets in the FRT have the potential for capture and dissemination of HIV, exert antiviral responses and likely contribute to the recruitment of HIV-target cells through the secretion of innate immune molecules.
Assuntos
Células Dendríticas/imunologia , Genitália Feminina/imunologia , Infecções por HIV/imunologia , HIV/imunologia , Imunidade Inata , Antígeno CD11c/metabolismo , Moléculas de Adesão Celular/metabolismo , Células Cultivadas , Quimiocina CCL2/metabolismo , Células Dendríticas/virologia , Elafina/metabolismo , Estradiol/farmacologia , Feminino , HIV/patogenicidade , Infecções por HIV/transmissão , Humanos , Interleucina-8/metabolismo , Lectinas Tipo C/metabolismo , Receptores de Lipopolissacarídeos/metabolismo , Fagocitose , Receptores CCR5/metabolismo , Receptores de Superfície Celular/metabolismo , Inibidor Secretado de Peptidases Leucocitárias/metabolismoRESUMO
REASONS FOR PERFORMING STUDY: An alternative technique of radiographing the pelvis in the standing horse is required, to avoid the risks associated with general anaesthesia. HYPOTHESIS: That lateral oblique radiography in the standing horse would be a useful technique in the investigation of pelvic injury. OBJECTIVES: To describe the technique of lateral oblique pelvic radiography in the standing horse and demonstrate the feasibility and usefulness of this technique. METHODS: A technique for lateral oblique radiography in the standing horse was devised and retrospective review made of radiographic findings in 18 clinical cases. RESULTS: The caudal iliac shaft, greater trochanter of the femur, femoral head, acetabulum and coxofemoral articulation on the side under investigation were visualised consistently using this technique. Of the 18 cases, 3 iliac shaft fractures, 1 acetabular fracture, 2 coxofemoral luxations and 4 horses with new bone formation around the coxofemoral joint and/or proximal femur were identified. CONCLUSIONS: Lateral oblique radiography in the standing, conscious horse can be used to investigate conditions affecting the caudal iliac shaft, coxofemoral articulation and proximal femur in the horse. POTENTIAL RELEVANCE: The technique is straightforward, noninvasive and useful in the investigation of horses with suspected pelvic injury. However, not all pelvic injuries would be identified, and normal radiographic findings do not rule out injury or fractures elsewhere in the pelvis.
Assuntos
Fraturas Ósseas/veterinária , Cavalos/lesões , Ossos Pélvicos/diagnóstico por imagem , Pelve/diagnóstico por imagem , Animais , Feminino , Fraturas Ósseas/diagnóstico , Fraturas Ósseas/diagnóstico por imagem , Masculino , Pelve/lesões , Radiografia , Estudos RetrospectivosRESUMO
OBJECTIVES: To evaluate the clinical, clinical pathology, diagnostic imaging, microbiological and pathological features of cholangitis/cholangiohepatitis in the dog. METHODS: The study design was a retrospective review of cases of bacterial cholangitis/cholangiohepatitis presented to the University of Bristol during the period 1995 to 2000. The diagnosis was made based on hepatic histopathological findings and positive bile culture results. RESULTS: Four dogs met the inclusion criteria. Common presenting signs included anorexia (n=4), jaundice (n=4), vomiting (n=4) and pyrexia (n=2). All four dogs had a leucocytosis or neutrophilia reported at some time in their history along with serum bilirubin elevation. In addition, serum alkaline phosphatase and alanine transaminase activity was increased in all of the dogs in which it was measured both before and at the time of referral. In general, the diagnostic imaging findings were non-specific. Organisms cultured from bile aspirates were Escherichia coli (n=3), Clostridium species (n=2) and a faecal Streptococcus species (n=1). Two cases resolved with medical treatment alone; two with concurrent cholecystitis required cholecystectomy. Following surgery, both of these cases showed a resolution of clinical signs. CLINICAL SIGNIFICANCE: This report highlights the fact that bacterial cholangitis/cholangiohepatitis with or without concurrent cholecystitis should be considered as a potential differential in dogs presenting with signs referable to biliary tract disease.