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Serum concentrations of advanced oxidation protein products (AOPPs) and glycation end products (AGEs) were assessed with respect to functional compromise of liver, as determined by the Child-Pugh and MELD scores. Patients with decompensated liver cirrhosis (Child-Pugh B and C) exhibited significantly higher serum concentrations of AOPPs than both patients with compensated liver cirrhosis (Child-Pugh A) and controls. The levels of plasma AGEs in all liver cirrhotic patients were higher when compared with those with the controls and this difference was statistically significant. Plasma total antioxidant status of the patients was significantly lower than that of controls. Significant positive correlations between AOPPs level and the MELD score and between the oxidative stress index and the MELD score were found in all patients with liver cirrhosis. Altered AOPPs levels in decompensated patients may influence the potency of oxidative stress and the progression of liver disease.
The aim of the study was to determine the effectiveness of total protein (AFTP), serum-ascites total protein gradient, and serum-ascites albumin gradient (SAAG) determination for the diagnostics of ascites in dogs. The examinations were conducted on 68 dogs of both sexes and different breeds, aged 5 months to 12 years, manifesting signs of ascites. All the animals underwent ECG, abdominal USG, blood testing (total protein, albumin). The concentration of total protein, albumin and leukocyte count was additionally determined in the ascites fluid. On the basis of the obtained results the dogs were divided into 3 groups depending on the disease etiology: group 1 - 38 dogs with the signs of ascites connected with cardiac insufficiency, group 2 - 23 dogs with the signs of ascites connected with neoplastic diseases, group 3 - 7 dogs with the signs of ascites connected with liver parenchyma pathology. The statistical analysis of the obtained results showed statistically significant differences between 3 examined groups in total protein concentration in ascites fluid (p=0.001), serum-ascites total protein gradient (p=0.003) and serum-ascites albumin gradient (p=0.0027). The determination of the serum-ascites total protein gradient and serum-ascites albumin gradient is a useful diagnostic test in the diversification of transudes and exudates. The serum-ascites total protein gradient and serum-ascites albumin gradient is significantly lower in the group of dogs with liver disease than in the group with cardiac insufficiency and neoplastic diseases. The serum-ascites albumin gradient is useful as a marker for portal hypertension.
Fossil catshark egg capsules, Scyliorhinotheca goederti gen. et sp. nov., are reported from a Late Eocene deep−water methane−seep calcareous deposit in western Washington State, USA. The capsules are preserved three−dimensionally and some show mineralized remnants of the ribbed capsule wall consisting of small globular crystals that are embedded in a microsparitic matrix. The globules are calcitic, but a strontium content of 2400–3000 ppm suggests that they were origi− nally aragonitic. The carbonate enclosing the egg capsules, and the capsule wall itself, show 13C values as low as −36.5‰, suggesting that formation was induced by the anaerobic oxidation of methane and hence in an anoxic environ− ment. We put forward the following scenario for the mineralization of the capsule wall: (i) the collagenous capsules expe− rienced a sudden change from oxic to anoxic conditions favouring an increase of alkalinity; (ii) this led to the precipitation of aragonitic globules within the collagenous capsule wall; (iii) subsequently the remaining capsule wall was mineralized by calcite or aragonite; (iv) finally the aragonitic parts of the wall recrystallized to calcite. The unusual globular habit of the early carbonate precipitates apparently represents a taphonomic feature, resulting from mineralization mediated by an organic matrix. Taphonomic processes, however, are at best contributed to an increase of alkalinity, which was mostly driven by methane oxidation at the ancient seep site.
Advanced oxidation protein products (AOPPs) are protein markers of oxidative stress with pro-inflammatory properties that accumulated in liver cirrhosis. In the present study, we investigated the association between chronic inflammatory response triggered by AOPPs and the severity of liver disease as assessed by the Child-Pugh score. Plasma concentrations of AOPPs and inflammatory markers such as C-reactive protein, tumor necrosis factor-α, and interleukin-6 were measured in 41 patients with HCV-related cirrhosis, 43 patients with alcohol-related liver cirrhosis (ALC), and in 30 age and sex matched controls. In comparison with controls, AOPPs were increased in HCV-related compensated (Child-Pugh A) and decompensated (Child-Pugh B-C) cirrhosis and in alcohol-related compensated cirrhosis. AOPPs level positively correlated with Child-Pugh score in alcohol-related cirrhosis but not in HCV-related cirrhosis and the correlation with the indices of chronic inflammation was stronger in ALC. In turn, AOPPs in HCV-related cirrhosis was related to inflammation to a lesser extent, but a significant correlation with antioxidant defense could be noted. In summary, liver cirrhosis was associated with increased formation of AOPPs, which differed between alcohol-related and HCV-related cirrhosis with respect to the relationship between AOPPs and antioxidant defense, stage of liver cirrhosis, and inflammatory response. The significant correlation between AOPPs accumulation and indices of chronic inflammation, more specifically TNF-α, suggests that oxidative stress may be a mediator of chronic inflammatory state in the early stage of alcohol-related cirrhosis.
The aim of the study was to assess the usefulness of vascular angiography in the diagnostics of liver vascular system diseases. The study was conducted on 3 dogs: Yorkshire terrier marked C1, German Shepherd C2 and Airedale Terrier - C3, aged 11 months, 9 and 5 years respectively. The examinations were performed as follows: the history and clinical examination, abdominal USG, morphological examination, urea and creatinine concentration, AlAT, AspAT, ALP, GGT, amylase and lipase, the concentration of total bilirubin, ammonia, total protein and albumins. All animals underwent the angiography of the liver vascular system. Additionally, in laparotomy, an oligobiopsy of the liver was performed during which liver samples were collected for histopathological examinations. Results: Dogs C1 and C3 manifested leucocytosis. Only in dog C2 the morphological examination revealed thrombocytopenia. The biochemical examinations of blood serum in dog C1 showed a decrease in the urea level. Dog C2 demonstrated an increase the activity of AspAT, AlAT, ALP and GGT, as well as hyperbilirubinemia, hypoproteinemia and hypoalbuminemia. Dogs C1 and C2 had hyperammonemia. The histopathological examination of liver samples collected during diagnostic laparotomy in dog C1 revealed a slight fibrosis of single portal spaces and dilation of central veins and sinuses, which suggested passive hyperemia. Additionally, diffuse micro- and macrofollicular lipidosis of the whole bioptate was recognized. The histopathological examination of the collected liver bioptate in dog C2 showed macro- and micronodular cirrhosis of the liver. In dog C3 a venous congestion of the liver without signs of inflammation, fibrosis or lipidosis was diagnosed. The contrast examination of the liver vascular system in dog C1 revealed an extrahepatic portosystemic shunt. A connection of the splenic vein with the caudal vena cava in the form of a short loop between the portal vein branching off and the jejunal vein was observed. Dog C2 had multiple intrahepatic portosystemic shunts. In addition, a characteristic spiral course of intrahepatic branches was observed, which suggested liver cirrhosis. The examination of the liver vascular system in dog C3 revealed no abnormalities in the structure of the liver vascular system. Clinical signs and results of laboratory tests suggest the disease but the basic examination enabling the final diagnosis and location of a shunt is portography. This method is widely used in the diagnostics of liver vascular system diseases. However, it is an invasive method and should be performed in large specialist centres.
Tumours of the gall bladder constitute 4-5% of tumours originating from the bile duct epithelium. The mucous cystadenoma is a rare benign neoplasm of the gall bladder. This study is the case presentation of a male Scottish terrier, aged 12 years. The dog presented weakness, vomiting, loss of appetite and enlargement of the abdominal cavity. The ultrasound examination showed an enlarged gall bladder, filled with heteroechogenic, amorphic contents. By the walls the contents of the bladder were hypoechogenic, about 0.3cm thick. The laboratory blood tests showed leukocytosis, an increase in AST, ALT, GGTP activity and an over 65-fold increase in ALP. In addition, hyperlipidemia was observed in the dog. The following drugs were administered: amoxycyline, ursodexycholic acid, S-adenosine-L-metionin. The control blood tests were performed every three weeks. During the entire period of the therapy significant differences in ALP and ALT activity were observed. After three weeks since the beginning of the therapy ALP activity decreased to the half of the initial value and the significant improvement of the dog’s clinical condition was noted. After the six-month therapy the administration of ursodexycholic acid was stopped for four months. The significant increase in ALP and ALT was observed in this period. Due to the worsening of biochemical blood parameters the therapy with ursodexycholic acid was restarted. On the account of old age and lack of recovery the dog was subjected to euthanasia and autopsy after an eighteen-month therapy. The postmortem examination revealed the normal size liver. The gall bladder was considerably enlarged. The wall of the bladder was irregularly thickened. Based on the histopathological examination, the mucous cystadenoma of the gall bladder was diagnosed.
Bauflo male rats were infected with Hymenolepis diminuta. On 7th, 14th, 21th, 28th and 52th day of infection blood and liver were collected to determine AACo, AspAt, AlAt in the blood serum and in liver homogenates. In the course of teniosis in rats the activitics of all examined enzymes show changes in the serum and in liver homogenates. The most pronounced ones occur between the 7th and 21st day of infection. In the authors' opinion this is related to the highest pathogenicity of H. diminuta and especially with toxic action at this time. Determination of AACo activity proved to be a useful test to follow up the dynamics of organ changes in the course of hymenolepidosis.
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