药物防治蝇害的研究进展

蝇害已经成为危害规模化畜禽养殖的重要问题。文章回顾了防治蝇害的三代杀虫剂的发展过程和存在的问题 ;展望了作为新一代环境友好防治蝇害药物的昆虫生长调节剂的开发前景。     

The failure of selenium supplementation to prevent copper-induced liver damage in Fischer 344 rats.

This study evaluates the ability of selenium (Se) supplementation to prevent experimental copper (Cu)-induced hepatocellular damage. Weanling male Fischer 344 rats were randomly assigned to groups of 15, 3 groups (A,B,C) were fed Cu-loaded diets (containing 2000 microg/g copper, added as CuSO4) and different levels of Se (added as Na2SeO3 x 5H2O) as follows: A) Cu-loaded/Se adequate diet (0.4 microg/g Se, fed basis); B) Cu-loaded/Se-supplemented diet (2 microg/g Se); and C) Cu-loaded/Se-deficient diet (< 0.2 microg/g). Three additional groups (D,E,F) were fed diets containing adequate levels of Cu (14 microg/g Cu, fed basis) and different levels of Se as follows: D) Cu-adequate/Se-adequate diet; E) Cu-adequate/Se-supplemented diet (2 microg/g Se); and F) Cu-adequate/Se-deficient (< 0.2 microg/g) diet. After 4, 8, and 12 weeks on the experimental diets, liver samples were processed for histology, histochemistry, metal analysis, glutathione peroxidase (GSH-Px) measurement, and quantification of malondialdehyde (MDA). Morphologic changes characteristic of Cu-associated hepatitis, without an increase in hepatic MDA levels, were seen in all Cu-loaded rats in each sampling. Similar changes occurred in rats fed Se-adequate, Se-supplemented and Se-deficient diets. This study demonstrates that Fischer 344 rats fed 2000 microg/g Cu develop morphologic changes due to Cu toxicity without evidence of lipid peroxidation. Furthermore, Se supplementation does not result in protection against Cu-induced liver injury.     

Mycoplasma hyopneumoniae colonization of pigs sired by different boars

Differences in Mycoplasma hyopneumoniae colonization were evaluated in experimentally inoculated pigs sired by 3 different boars of the same genetic line. Forty-six pigs were used, including a treatment group and positive and negative control groups. The pigs were intratracheally inoculated with an M. hyopneumoniae suspension or with Friis media as a placebo. To evaluate differences in the magnitude of colonization during a 35-day period, nasal and tracheal swabs were collected weekly and tested by nested polymerase chain reaction (N-PCR). Temperature, weight and circulating antibodies were measured for 35 days. At 11 and 35 d postinoculation the pigs were necropsied and macroscopic and microscopic lesions were determined. A section of bronchus was tested by the indirect immunofluorescence test (IFAT), scanning electron microscopy (SEM) and N-PCR. The N-PCR results from the nasal and tracheal swabs showed that the pigs sired by one boar (B3) had a distinctive colonization pattern, different from that of the pigs from the other 2 boars and from the positive controls. SEM studies demonstrated that at 35 d postinoculation a higher proportion of B3 pigs had lower numbers of mycoplasmas attached to the cilia compared with B1 and B2 offspring. No significant differences were observed in temperature and weight gain among groups by ANOVA; however, with use of a 2 × 2 table, temperature differences were observed between pigs sired by boars B1 and B2 at 4 d postinoculation. No pigs seroconverted, showed gross or microscopic lesions, or had positive IFAT results. These results provide evidence of differences in patterns of colonization between pigs sired by different boars, suggesting a possible genetic effect.     

Capnographic documentation of nasoesophageal and nasogastric feeding tube placement in dogs

Objective: To evaluate the ability of capnography to document proper placement of nasoesophageal (NE) and nasogastric (NG) feeding tubes. This study was conducted in 3 phases. Phase I of this study was designed in order to test the efficacy of capnography to distinguish placement of a feeding tube in the alimentary tract versus the respiratory tract. Phase II was designed in order to document that carbon dioxide (CO₂) could be measured through a polyvinyl chloride (PVC) feeding tube. Phase III was performed in order to evaluate the technique of continuous monitoring during insertion of the feeding tube into the esophagus and stomach as would be performed during a clinical‐tube placement. Design: Prospective study. Setting: Research laboratory. Animals: 24 adult dogs. Interventions: In Phase I, sedated dogs were instrumented with an intratracheal catheter and an 8 French feeding tube placed nasally into the distal esophagus and later advanced into the stomach. In Phase II, dogs were anesthetized and an 8 French feeding tube was placed down the endotracheal tube, then into the esophagus and later advanced into the stomach. In Phase III, sedated dogs were instrumented with an 8 French feeding tube inserted intranasally and then advanced to the level of the nasopharynx, distal esophagus and, lastly, the stomach. Fluoroscopy was used in order to determine location of the feeding tube. Measurements and main results: Phase I measurements included respiratory rate and CO₂ from the trachea, esophagus, and stomach and pH of gastric fluid sample. Phase II measurements included respiratory rate and CO₂ from the endotracheal tube, feeding tube in the endotracheal tube, feeding tube in the distal esophagus, and feeding tube in the stomach. Phase III data collection included respiratory rate and CO₂ as the tube was passed through the nasal cavity, nasopharynx, esophagus and stomach. Phase I fluid samples were collected from 5 of the 9 dogs and had pH values from 1.68 to 4.20. In both phases, values for the respiratory rate and CO₂ from the esophagus and stomach were 0 ± 0, significantly lower (P < 0.001) than the values from the trachea. In Phase II, there was no significant difference between the respiratory rates (P = 0.886) and CO₂ (P = 0.705) readings obtained from the endotracheal tube compared to readings from the feeding tube in the endotracheal tube. In Phase III, there was a significant difference (P < 0.001) between the respiratory rates and CO₂ readings obtained from the nasal cavity and the nasopharynx when compared to those readings obtained from the esophagus and stomach. Measurement of CO₂ and respiratory rate resulted in a reading of 0 every time the feeding tube was in the esophagus or stomach. Conclusions: Capnography may be used in order to detect airway placement of NE and NG tubes.     

The Application of GIS in Small Watershed Classification in Loess Plateau

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图书馆工作人员应该转变的六个观念

文章认为，要使图书馆工作适应新的技术革命和社会主义市场经济的需要，就必须转变观念。当前需要转变的观念有以下六个方面:图书馆由藏书中心变成文献资料中心、信息中心、智力开发中心;从关门办馆到开门办馆:从无偿服务到有偿服务:从独自办馆到馆际协作:从手工操作到运用现代技术手段:从与世无争到积极竞争。     

北京黑猪和长白猪脂肪代谢的比较

猪在断奶后的生长期内,体内脂肪逐渐增加,和其它家畜相比,猪更倾向沉积体脂。但猪体脂的沉积还要受遗传、年龄、日粮营养水平等因素的影响。在饲粮消化能量(DE)水平保持在3000—3200Kcal/kg,蛋白质含量为14％—15％的饲养条件下,我们分别测定了纯系北京黑猪(肉脂兼用型,平均瘦肉率为51％)和纯系长白猪(瘦肉型猪、平均瘦肉率为62％)的某些脂肪合成酶活性和脂肪代谢的一些生化指标。北京黑猪(公母各半)脂肪组织(背膘)中苹果酸酶(ME),葡萄糖—6—磷酸脱氢酶(G—6—PDH),异柠檬酸脱氢酶(ICDH)三种NADPH—生成酶活性随体重增加而升高,差异极其显著(P<0.001)。体重90kg的酶活性比56kg约高三倍。脂纺组织中上述NADPH生成酶活性北京黑猪比长白猪(体重均为90kg,公母各半)高一倍(P<0.001)。给北京黑猪(30头,公母各半,起始体重为60kg)注谢重组猪生长激素(rPGH,每天每头2mg,连续注谢28天),除表现生长加快,脂肪率下降约21％—23％外,其脂肪组织中NADPH生成酶活性降低十分明显(P<0.001)。苹果酸酶,葡萄糖—6—磷酶脱氢酶,异柠檬酸脱氢酶,三种酶总活性比对照组降低20％。血精中三酰甘油,游离脂肪酸,总胆固醇,高密度脂蛋白(HDL)胆固醇、乳糜微粒,极低密度脂蛋白(VLDL)胆固醇含量,6月龄时,北京黑猪明显高于长白猪(P<0.001—0.0005);而4月龄时,北京黑猪血清中三酰甘油,高密度脂蛋白胆固酶含量则均明显低于长白猪。北京黑猪血清中三酰甘油,高密度脂蛋白胆固醇含量,随月龄(4月龄—6月龄)增长而增加(P<0.0005)。而长白猪则相反,随月龄而呈下降趋势(P<0.05—0.0005)。两种猪的脂蛋白电泳和含量测定未见有年龄和品种间的差异。     

近冰点温度贮藏草莓的研究

草莓呼吸旺盛,果皮薄易受伤,难以贮藏。利用近冰点温度贮藏可以明显地抑制草莓的呼吸作用,结合小袋包装的气密性,改善了包装内部的气体组成,提高草莓果实周围的相对湿度并减少空气对流,从而抑制了草莓在贮藏过程中糖分、水分的损耗,减少了糖酸比值的下降。保持了一定的感观指标,可使草莓的贮藏时间延长。     

靠接换砧矫治枳砧甜橙缺铁黄化研究

靠接红桔、酸桔和枸头橙砧,矫治枳砧甜橙缺铁黄化有明显效果。其中,以枸头橙效果最好,以下依次为酸桔和红桔,靠接砧苗后树势逐年恢复,产量成倍增加,靠接红桔、酸桔和枸头橙分别比对照增产3.3、1.4和1.5倍;对提高果实含糖量、果汁率和降低含酸量亦有良好效果。     

Porcine reproductive and respiratory syndrome virus: morphological, biochemical and serological characteristics of Quebec isolates associated with acute and chronic outbreaks of porcine reproductive and respiratory syndrome.

Cytolytic and noncytolytic strains of the porcine reproductive and respiratory syndrome virus (PRRSV) were isolated in primary cultures of porcine alveolar macrophages (PAM) from lung homogenates of stillborn fetuses or blood samples of dyspneic piglets collected from Quebec pig farms having experienced acute or chronic outbreaks of PRRS. Serological identification of the virus was confirmed by indirect immunofluorescence and indirect protein A-gold immunoelectron microscopy using reference antiserum prepared from experimentally-infected specific pathogen free (SPF) piglets and monoclonal antibodies (MoAbs) directed against the p15 nucleocapsid (N) protein of the reference ATCC-VR2332 isolate. Intracytoplasmic enveloped viral particles that tended to accumulate into cytoplasmic vesicles were observed in the infected PAM; no budding was demonstrated at the level of the cytoplasmic membrane. The extracellular virions appeared as pleomorphic but mostly spherical enveloped particles, 50-72 nm in diameter (averaged diameter of 50 particles was 58.3 nm), with an isometric core about 25-30 nm. Buoyant density of the virus in CsCL density gradients was estimated to 1.18-1.20 g/mL. No hemagglutinating activity was demonstrated. Analysis of semipurified virions of isolate IAF-exp91 by radioimmunoprecipitation (RIPA) and Western immunoblotting experiments, using reference rabbit and porcine hyperimmune sera, revealed four major viral proteins, a predominant 15 kD N protein and three other proteins with predicted M(r_ of 19, 26 and 42 kD. Progeny viral particles produced in PRRSV-infected PAM in the presence of tunicamycin lacked the 42 kD protein, thus confirming its N-glycosylated nature. Immunoprecipitation experiments using the anti-ATCC-VR2332 MoAbs confirmed the close antigenic relationships between Quebec and American reference isolates of PRRSV.