不同海拔高度西藏高原牦牛若干血液生理常值的比较

本试验对西藏藏北高原那曲(海拔4500米)牦牛,藏南河谷林芝(海拔3000米)牦牛进行了某些高原生理特性对比研究。测定了红细胞总数、红细胞压积、血液总量、血红蛋白含量及其电泳分析、血清蛋白含量及其电泳分析等。测定结果表明,生活在高海拔的藏北那曲牦牛,其红细胞总数、红细胞压积、血液总量、血红蛋白均极明显地高于较低海拔的藏南河谷牦牛,而其红细胞容积的立方微米数值较小,红细胞内血红蛋白的平均重量较轻,并发现变异血红蛋白(A_3)。根据本文分析,其主要归因于高海拔、低氧压。雄性牦牛的变异血红蛋白数量高于雄牦牛,差异极显著(P相似文献   

Cecotrophy behavior and use of urea as non-protein nitrogen (NPN) source for capybara (Hydrochoerus hydrochaeris)

Fifteen female adult capybaras, with initial average body weight (BW) of 32.7 (±?5.8) kg, were kept in individual pens to evaluate effect of supplementation of concentrate feed and its supply time on cecotrophy behavior frequency. The animals were allocated in a completely randomized design, with five animals per treatment, receiving three diets: grass only, grass and grain corn offered in a single meal, and grass and grain corn offered in two daily meals; all cecotrophy acts were recorded. Later, in a second experiment, five capybaras received five levels of urea in their diet: 0, 10, 20, 30, and 40 g urea/100 kg BW, replacing soybean meal as true protein source, in a 5?×?5 Latin square design. The animals were weighed and their blood was collected every 2 weeks. The frequency of cecotrophy (Ps?<?0.05) was higher when the capybaras were fed grass only (0.5?±?0.07 acts/h) than when they received grass and corn in a single meal (0.3?±?0.05 acts/h) and grass and corn supplied in separate meals (0.1?±?0.03 acts/h). With increased urea in their diet, the capybaras showed initial signs of chronic intoxication, together with increments in serum urea (r?=?0.87, P?<?0.05) and a decreasing trend in daily weight gain (r?=??0.38, P?=?0.06). Therefore, when including concentrate feeds in capybara diet, these must be mixed with roughage in a single meal to avoid high decrease in the frequency of cecotrophy behavior and increase in dry matter intake. The replacement of soybean meal with urea in capybara diet is not recommended.     

Agarose gel electrophoresis of cerebrospinal fluid proteins of dogs after sample concentration using a membrane microconcentrator technique

BACKGROUND: Cerebrospinal fluid (CSF) is produced in the cerebral ventricles through ultrafiltration of plasma and active transport mechanisms. Evaluation of proteins in CSF may provide important information about the production of immunoglobulins within the central nervous system as well as possible disturbances in the blood-brain barrier. OBJECTIVE: The objective of this study was to measure the concentration and fractions of protein in CSF samples using a membrane microconcentrator technique followed by electrophoresis, and to compare the protein fractions obtained with those in serum. METHODS: CSF samples from 3 healthy dogs and 3 dogs with canine distemper virus infection were concentrated using a membrane microconcentrator having a 0.5 to 30,000 d nominal molecular weight limit (Ultrafree, Millipore, Billerica, MA, USA). Protein concentration was determined before and after concentration. Agarose gel electrophoresis was done on concentrated CSF samples, serum, and serial dilutions of one of the CSF samples. RESULTS: Electrophoretic bands were clearly identified in densitometer tracings in CSF samples with protein concentrations as low as 1.3 g/dL. The higher CSF protein concentration in dogs with distemper was mainly the result of increased albumin concentration. CONCLUSION: The microconcentrating method used in this study enables characterization of the main protein fractions in CSF by routine electrophoresis and may be useful for interpreting the underlying cause of changes in CSF protein concentrations.     

Antiproliferative Activity of Fucan Nanogel

Sulfated fucans comprise families of polydisperse natural polysaccharides based on sulfated L-fucose. Our aim was to investigate whether fucan nanogel induces cell-specific responses. To that end, a non toxic fucan extracted from Spatoglossum schröederi was chemically modified by grafting hexadecylamine to the polymer hydrophilic backbone. The resulting modified material (SNFuc) formed nanosized particles. The degree of substitution with hydrophobic chains was close to 100%, as estimated by elemental analysis. SNFfuc in aqueous media had a mean diameter of 123 nm and zeta potential of −38.3 ± 0.74 mV, as measured by dynamic light scattering. Nanoparticles conserved their size for up to 70 days. SNFuc cytotoxicity was determined using the MTT assay after culturing different cell lines for 24 h. Tumor-cell (HepG2, 786, H-S5) proliferation was inhibited by 2.0%–43.7% at nanogel concentrations of 0.05–0.5 mg/mL and rabbit aorta endothelial cells (RAEC) non-tumor cell line proliferation displayed inhibition of 8.0%–22.0%. On the other hand, nanogel improved Chinese hamster ovary (CHO) and monocyte macrophage cell (RAW) non-tumor cell line proliferation in the same concentration range. The antiproliferative effect against tumor cells was also confirmed using the BrdU test. Flow cytometric analysis revealed that the fucan nanogel inhibited 786 cell proliferation through caspase and caspase-independent mechanisms. In addition, SNFuc blocks 786 cell passages in the S and G2-M phases of the cell cycle.     

Effects of TiO<Subscript>2</Subscript> Nanoparticles on the Neotropical Cladoceran <Emphasis Type="Italic">Ceriodaphnia silvestrii</Emphasis> by Waterborne and Dietary Routes

The impact of nanoparticles (NPs) in zooplankton is poorly studied, particularly when organisms are exposed through diet. Food, constituted mainly by unicellular algae, can act as an important route of contamination for zooplankton. Since unicellular algae have a high surface area in relation to their volume, NPs can interact with their cell membranes and walls, as well as with exopolysaccharides secreted by them. In the present research, we investigated both the acute effects of waterborne titanium dioxide nanoparticles (TiO₂ NPs), and its chronic effects via dietary exposure on the Neotropical freshwater zooplankton Ceriodaphnia silvestrii Daday, 1902 (Crustacea: Cladocera). The observed acute effects served as support for chronic tests, in which we investigated the effects of TiO₂ NPs on survival and life history parameters (body length, numbers of eggs, and neonates produced) of cladoceran adult females, using the freshwater cosmopolitan chlorophycean Raphidocelis subcapitata as source of contamination of TiO₂ NPs for zooplankton. R. subcapitata cells were exposed to concentrations of 0, 0.01, 1, and 10 mg L^?1 of TiO₂ NPs for 96 h, and then provided as food for females of C. silvestrii until the third brood was released. Significant toxic effects were observed in body length and total number of neonates and eggs produced by females of C. silvestrii at concentrations of 1 and 10 mg L^?1 of TiO₂ NPs. Survival was the most sensitive parameter when exposure was given via food. From the concentration of 0.01 mg L^?1 of TiO₂ NPs, there was a decrease in the survival of C. silvestrii females. The quantification of TiO₂ NPs in algae evidenced that they have retained NPs in their cells, being, therefore, an important route of exposure and toxicity of TiO₂ NPs to the studied microcrustacean.