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671.
Marjory B. Brooks John Randolph Karen Warner Sharon Center 《Veterinary clinical pathology / American Society for Veterinary Clinical Pathology》2009,38(3):306-315
Background: Clinical diagnosis of platelet dysfunction is complex and technically challenging. The wide repertoire of platelet responses requires a test panel to assess different parameters of platelet reactivity. While “global” hemostasis analyzers and whole blood assays have potential for testing platelet function, their ability to evaluate platelet procoagulant activity is ill‐defined. Objectives: The aim of this study was to determine whether platelet procoagulant deficiency, the pathophysiologic defect of Scott syndrome, could be detected in point‐of‐care and whole blood assays. Methods: Study subjects were 4 Scott syndrome‐affected German Shepherds and 8 control dogs. We evaluated 2 point‐of‐care instruments: the platelet function analyzer (PFA‐100) and thromboelastograph (TEG). TEG analysis was performed on recalcified citrated whole blood with and without tissue‐factor activation. A whole blood flow cytometric assay was configured to detect thrombin‐induced platelet P‐selectin expression and platelet‐derived microparticle release. Cytometric samples were analyzed after 1 hour and 1 day of storage. Results: We found no significant differences between Scott and control dogs in PFA‐100 COL/ADP closure times or in any TEG parameter in tissue‐factor–activated samples. In nonactivated samples, mean clotting time (K) and time to maximal rate of thrombus generation were significantly prolonged in Scott dogs; however, values overlapped with those of control dogs. Cytometric analysis of samples from Scott dogs showed significantly diminished platelet‐derived microparticle release. Samples from all dogs reanalyzed after 1 day of storage had nonspecific increases in basal P‐selectin expression and vesiculation. Conclusion: A whole blood cytometric assay to detect stimulated platelet microparticle release can be used to screen for Scott syndrome. However, platelet activation artifacts preclude overnight storage for next‐day analysis. 相似文献
672.
673.
Songming Zhu Brooks Saucier James Durfey Shulin Chen Bill Dewey 《Aquacultural Engineering》1999,20(4):317-244
Water recirculating systems have been used in the shellfish industry for depuration and wet-storage. Knowledge of shellfish excretion characteristics is critical to recirculating system design. In this study, the excretion rate of total ammonia nitrogen (TAN), total Kjeldahl nitrogen (TKN), and 5-day biochemical oxygen demand (BOD5) from Manila clams (Tapes philippinarum) were investigated under both laboratory and commercial conditions. The laboratory tests were conducted under temperatures ranging from 3 to 30°C. The experimental results showed that temperature was a key factor in determining the excretion rate of all the above parameters. The relationship between TAN excretion rate (RTAN) and temperature (T) can be represented by an exponential function (RTAN=0.57×1.25T). For the temperature range between 3 and 20°C, the daily mean excretion rates of TAN, TKN and BOD5 ranged between 1.5–46.1, 4.8–131.0 and 57.4–219.4 mg per kilogram of the clams (wet weight with shell on), respectively. There were linear correlations between TAN, TKN and BOD5 production rates. The data presented in this paper can be used to estimate waste generation from a given shellfish processing operation and to size the waste treatment components for a recirculating depuration (or wet-storage) system. 相似文献
674.
Karen J Murchie Sascha E Danylchuk Christopher E Pullen Edd Brooks Aaron D Shultz Cory D Suski y J Danylchuk & Steven J Cooke 《Aquaculture Research》2009,40(13):1538-1550
Throughout their circumtropical distribution, bonefish ( Albula spp.) play a vital role in local economies as a highly prized sport fish. Recent interest in stock enhancement to sustain bonefish fisheries has led to the recognition that there currently are no data on how to live capture large numbers of adults (potential broodstock), transport them to captive facilities and how to handle them to ensure high survival. The objective of this study was to develop strategies for the capture and relocation of wild bonefish to a marine research holding facility to enable basic research and explore the potential for culturing bonefish for stock enhancement. Bonefish Albula vulpes (Linnaeus, 1758) were captured as they entered or left tidal creeks on Eleuthera, The Bahamas using seine nets and then transported by boat or truck to the laboratory. The relocation process evoked secondary stress responses at the metabolic, osmoregulatory and haematological levels as indicated by changes in blood glucose, lactate, haematocrit and ion values, relative to control fish. Physical and behavioural disturbances were also observed in bonefish that were unable to acclimate to laboratory conditions. Successful laboratory acclimation and long-term holding of wild bonefish was achieved through an adaptive learning process, whereby we identified a series of strategies and handling techniques to facilitate the acclimation of wild adult bonefish to captivity. This knowledge will enable future laboratory research on bonefish and is a prerequisite to the culture of this highly prized sport fish, and other sub-tropical and tropical marine species. 相似文献