PubMed · 1789866
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S A Merchant, V Patel. 1991. "Sonographic sliding".. https://doi.org/10.7863/jum.1991.10.8.444
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The purpose of this study was to examine whether postural stability depends only on the support base perimeter, that is the stability area, when body balance is perturbed by respiration. To this end, seven normal subjects were asked to breathe quietly, breathe deeply and to hold their breath (apnoea). They were asked to maintain a standing posture (Sta), and two sitting postures differing by the ischio femoral contact with the seat (Sit100 and Sit30). In other words, these three postures differed not only by the stability area, but also by pelvis mobility. The thoracic perimeter, displacement of the centre of pressure (CP) and iliac crest acceleration (Ah), taken as an index of pelvis mobility, of seven normal subjects were recorded. The results showed that the sway path (SP) was longer in seated subjects than in standing ones, and in Sit100 than in Sit30. The distance between the CP extreme positions (Delta Xp) varied in the opposite direction to SP. Iliac crests and thoracic displacements were shown to be in phase in Sit condition, and did not display any particular pattern in Sta. It was concluded that postural steadiness depends on the postural chain mobility in addition to stability area. As pelvis and lumbar column mobility are related, it is proposed that both contribute to postural chain mobility, owing to respiratory perturbation being compensated.
OBJECTIVE: To characterize the clinical, clinicopathologic, and imaging findings in dogs with intestinal lymphangiectasia and to compare the histologic grade of lymphangiectasia with clinicopathologic and imaging abnormalities. DESIGN: Retrospective study. ANIMALS: 17 dogs with a histologic diagnosis of intestinal lymphangiectasia. PROCEDURE: Medical records of dogs with a histologic diagnosis of intestinal lymphangiectasia were reviewed for signalment, history, clinical signs, results of exploratory laparotomy, and clinicopathologic, radiographic, ultrasonographic, and histologic findings. RESULTS: Mean age of dogs was 8.3 years; the most common clinical signs were diarrhea, anorexia, lethargy, vomiting, and weight loss. Abnormal physical examination findings included dehydration, ascites, and signs of pain on palpation of the abdomen. The most notable clinicopathologic findings were low serum ionized calcium concentration and hypoalbuminemia. Abdominal ultrasonography was performed in 12 dogs and revealed intestinal abnormalities in 8 dogs and peritoneal effusion in 7 dogs. Exploratory laparotomy revealed abnormalities in 9 of 16 dogs including thickened small intestine, dilated lacteals, lymphadenopathy, and adhesions. On histologic examination of the small intestine, concurrent inflammation was observed in 15 of 17 dogs, crypt ectasia in 5 of 17, and lipogranulomas in 2 of 17. CONCLUSIONS AND CLINICAL RELEVANCE: Intestinal lymphangiectasia in dogs appears to be a heterogeneous disorder characterized by various degrees of panhypoproteinemia, hypocholesterolemia, lymphocytopenia, and imaging abnormalities. In most dogs, the severity of hypoalbuminemia appears to offer the best correlation with severity of histologic lesions of lymphangiectasia. Imaging abnormalities are common in dogs with intestinal lymphangiectasia but are not specific enough to differentiate this disorder from other gastrointestinal disorders, nor are they predictive of histologic severity.
A drug delivery system (DDS) consisting of lipopolysaccharide (LPS) as a drug and 2-hydroxyethyl methacrylate (HEMA)-diethylene glycol dimethacrylate (2G) or -polyethylene glycol dimethacrylate (4G, 9G) copolymer was prepared, and used for the efficient preparation of an experimental animal model of chronic hyper-endotoxemia. The release profiles of LPS in the in-vitro test were greatly influenced by the composition of HEMA-2G, 4G, 9G in the copolymer. It was found that LPS release from the DDS continued gradually and constantly throughout 2 weeks. In the in-vivo experiment with rats, the DDS maintained a high blood concentration level of LPS for 3 days. These results strongly suggest the possibility of convenient and reproducible preparation of a chronic hyper-endotoxemia animal model.