新疆细毛羊及新西兰罗姆尼羊的引种适应性观察

一、种羊场基本情况丰都大塘坝种羊场位于川东,地处北纬29°.30′—30°.21′,东经107°.41′—108°.09′之间,荒山草坡全县351255亩,禾本科、豆科、菊科等牧草为主,且有许多绵羊喜吃的灌木。年平均气温为18.4℃,最高43.5℃,最低-11℃,年日照为1344.9小时;年降雨量为1400—1600毫米,风速大,为1.1m/s。无霜期达293天,属亚热带高温多湿性多雨区。

Capillary Zone Electrophoresis of Native Amino Acids with Indirect Ultraviolet Detection

Aim To strdy the separation of native amino acids using capillary zone electro- pboresis (CZE) with indirect ultraviolet detecition. Methods 13 native amino acids were sepa- rated by capillary electrophoresis with indirect detection . The experiments were carried out with homemade CE apparatus under the following operating conditior conditions: a fused-silica capillary col- umn of 50.0cm effect length and of 75m i.d. was used. 7 organic acids were used as BGAE, and a positive potential of separation in CZE with indirect detection. After optimizing for l3 native amino acids were established. Conclusion The choice of BGAe is an important factor influencing the efficiency of separation in CZE with indiect detection .After optimizing the separation conditions a baseline separation for 13 native amino acids is obtained.

Differential gene expression during capillary morphogenesis in a microcarrier-based three-dimensional in vitro model of angiogenesis with focus on chemokines and chemokine receptors

AIM:To globally compare the gene expression profiles during the capillary morphogenesis of human microvascular endothelial cells (HMVECs) in an in vitro angiogeness system with affymetrix oligonucleotide array. METHODS: A microcarrier-based in vitro angiogenesis system was developed, in which ECs migrated into the matrix, proliferated, and formed capillary sprouts. The sprouts elongated, branched and formed networks. The total RNA samples from the HMVECs at the selected time points (0.5, 24, and 72 h) during the capillary morphogenesis were used for microarray analyses, and the data were processed with the softwares provided by the manufacturers. The expression patterns of some genes were validated and confirmed by semi-quantitative RT-PCR. The regulated genes were grouped based on their molecular functions and expression patterns, and among them the expression of chemokines and chemokine receptors was specially examined and their functional implications were analyzed. RESULTS: A total of 1 961 genes were up- or downreg-ulated two-folds or above, and among them, 468 genes were up- or down-regulated three-folds or above. The regulated genes could be grouped into categories based on their molecular functions, and were also clustered into six groups based on their patterns of expression. As for chemokines and chemokine receptors, CXCL1/GRO-α, CXCL2/GRO-β, CXCL5/ENA-78, CXCL6/GCP2, IL-8/CXCL8, CXCL12/SDF-1, CXCL9/Mig, CXC11/ITAC, OOCL1/fractalkine, CCL2/MCP-1, CCL3, CCL5/RANTES, CCL7, CCL15, CCL21, CCL23, CCL28, and CCR1, CCR9, CXCR4 were identified. Moreover, these genes demonstrated different changing patterns during the capillary morphogenesis, which implied that they might have different roles in the sequential process. Among the chemokines identified, CCL2/MCP-1, CCL5/RANTES and CX3CL1 were specially up-regulated at the 24-h time point when the sprouting characterized the morphological change. It was thus suggested that they might exert crucial roles at the early stage of angiogenesis. CONCLUSION: The present study demonstrates a global profile of gene expression during endothelial capillary morphogenesis, and the results provide us much information about the molecular mechanisms of angiogenesis, with which further evaluation of individual genes can be conducted.

Density, Viscosity, and Excess Properties for Binary Mixture of Diethylene Glycol Monoethyl Ether ＋ Water from 293.15 to 333.15 K at Atmospheric Pressure

Densities and viscosities were measured as a function of composition for binary liquid mixture of diethylerie glycol monoethyl ether [CH3CH2O（CH2）2O（CH2）2OH] ＋ water from 293.15 to 333.15 K at atmospheric pressure, with a capillary pycnometer and Ubbelohde capillary viscometer respectively. From the experimental data, the excess molar volume V^E, viscosity deviation △η, and the excess energy of activation for viscous flow △G^＊E were calculated. These data were correlated by the Redlich-Kister type equations to obtain the coefficients and standard deviations. The results showed a strong molecular interaction between diethylene glycol monoethyl ether and water.

Histology of the Body Wall of the Piscine Leech, Cystibranchus mastacembeli （Hirudinea： Piscicolidae）

The histology of the body wall of the fish parasitic leech, Cystibranchus masstacembeli Rahemo, 1989 collected from freshwater eel, Mastacembelus simach was investigated. The body wall found consists of five layers, namely： cuticle, epidermis, dennis, muscle layer and botryoidal tissue. Cuticle is very thin layer, casting was evident in some sections, annulation was also seen in longitudinal sections, some time with sensory structures inside the crypts. Epidermis with hammer-shaped ceils, these cells are broad towards the outer and narrower towards their inner ends. In some sections intensively stained haematoxylin-eosin granules from which neck-like tubes leads with filiform projections outward to open to the exterior by minute apertures. Dermis is thicker than epidermis, with distinct large cells connected by a connective tissue and some muscle fibers, also large vacuoles or empty vesicles were detected which are haemocoelomic capillaries, which along with those situated in the epidermis make a respiratory membrane of this leech. Muscle layer consists of outer circular and inner longitudinal, the later is more abundant and occupies more space than the circular. Botryoidal tissue fills the spaces between body wall and inner intestinal or crop diverticulae, its tissue is composed of more or less rounded cells, more eosinophilic cytoplasm but with dark nuclei, intermingled with small oblique or radial muscle fibers, haemocoelomic spaces were also evident in this layer.

A new method of immobilizing HEK293 cells on the inner wall of a capillary column as stationary phase for drug screening

It is a new strategy to immobilize cells on the inner wall of a capillary column and use affinity capillary electrophoresis（ACE） to study receptor-ligand interactions or to screen natural products and compounds synthesized by combinatorial chemistry. In this paper, we developed a new method of immobilizing HEK293 cells on the inner wall of a capillary column. Four important experimental conditions were optimized, including cell injection density, PLL concentration, cell culturing time and sterile processing method. Immobilized cell-coated capillary columns prepared under the optimized experimental conditions exhibited good uniformity, stability and durability, which were suitable for capillary electrophoresis. The method could also be used to immobilize HEK293 cells over-expressing certain membrane receptors on the inner wall of a capillary. In this way, cell-coated capillary columns could be applied to ACE drug screening targeting certain membrane proteins.

Study of parameters affecting infection risk from contaminated injectable products using multiple spot contamination model: a case study of insulin vials

Infections of patients from consumption of contaminated pharmaceutical products constituted major health risk problems. Medicinal products are liable to microbial intrusion during in-use application. The current study focused on repeated contamination with constant level of microbiological burden by two bacteria viz. Staphylococcus aureus and Pseudomonas aeruginosa were used as dose-response models for infection through two different routes of administration. Nine different forms of insulin vials were subjected to this type of simulation study at constant assumed level of contaminations, preservative efficacy test(PET) and dose potency. Multi-spot contamination imitation study showed that initial fast rise in contamination, followed shortly by longer but steeper slope which finally turned into higher rate of contamination during the few last doses of the unit dosage forms, where the volume of the product became increasingly and progressively very small. When the probability of infection curves was constructed, both S. aureus and P. aeruginosa showed same pattern, with notably higher risk from septicemia route of the latter rather than subcutaneous route of the former. The present simulation study showed that continuous use of the same contaminated syringe progressively increased the risk of infection, especially at final few doses(between 3th and 10 th last doses depending on the dosage form sizes in the vials and the administration volumes) of the product. Small volume parenterals(SVP) are especially products at higher risk than the larger volume ones.