990 resultados para G1
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Esta pesquisa tem como objeto os fatores que influenciam a mensuração glicêmica realizada pela enfermagem em pacientes que recebem insulina contínua intravenosa utilizando glicosímetros portáteis à beira leito. Vários fatores podem influenciar a mensuração glicêmica, tais como a amostra sanguínea, a calibração do aparelho, a estocagem das fitas-teste, o hematócrito dos pacientes, o uso de vasoaminas e falhas do operador. A partir da Tese de que: A identificação dos fatores que influenciam a mensuração glicêmica realizada pela enfermagem através de glicosímetros é determinante para a eficiência das barreiras de salvaguarda voltadas para a minimização de falhas na sua execução, a fim de garantir resultados glicêmicos confiáveis e, consequentemente, realizar a titulação da insulina com segurança, teve-se como objetivo geral propor ações de enfermagem que funcionem como barreiras para diminuir as falhas nas mensurações glicêmicas realizadas pela enfermagem em pacientes que recebem infusão contínua de insulina. Espera-se contribuir com ações para garantir a adequação e o controle rigoroso da insulina administrada. Estudo observacional, transversal, prospectivo com abordagem quantitativa na análise dos dados, em uma unidade intensiva cirúrgica cardiológica de um hospital público do Rio de Janeiro. As variáveis do estudo foram submetidas a tratamentos estatísticos não paramétricos e às medidas de associação. Foram investigados 42 pacientes com observação de 417 glicemias. Predominaram pacientes do sexo feminino (57,14%), média de idade de 48 (15,85) anos, sem insuficiência renal e sem tratamento dialítico (90,48%). Observou-se PAM com média de 77(10,29) mmHg, uso de vasoaminas (80,95%), PaO2 ≥ 90mmHg em 85,71% e hematócrito <35% em 71,42%. Encontrou-se uma incidência de hipoglicemia de 35,7%, sendo a população dividida em dois grupos, o primeiro (G1) com pacientes que apresentaram hipoglicemia ≤ 60mg/dl (n=15), e o segundo (G2), com pacientes sem hipoglicemia (n=27). O hematócrito baixo foi a característica clínica que apresentou maior associação com a hipoglicemia. Pacientes com esta condição apresentaram 5,60 vezes mais risco de apresentarem hipoglicemia. O uso de vasoaminas elevou 3,3 vezes o risco de hipoglicemia em pacientes com estas medicações. A realização de cirurgias de emergência, a presença de insuficiência renal com tratamento dialítico, e a elevação da PaO2 acima de 90mmHg também apresentaram associação positiva com a hipoglicemia. Das 417 mensurações observadas, predominou o uso de amostra sanguínea de origem arterial. Observou-se que em todas as etapas da técnica de mensuração houve desvio de execução, com exceção de compressão da polpa digital. Os desvios observados que mostraram associação positiva (RR>1) para pacientes com hipoglicemia foram: a falta de calibração do glicosímetro, a falta de verificação da validade/integridade da fita teste, a falta da higienização das mãos e a falta da coleta de até 1 ml de sangue. Construiu-se uma revisão da técnica de mensuração glicêmica com enfoque nos fatores que podem comprometer o resultado glicêmico levando em conta o risco de hipoglicemia. Tornou-se evidente que a compreensão apropriada dos fatores que influenciam a glicemia e a mensuração glicêmica é indispensável para o enfermeiro na obtenção de resultados glicêmicos confiáveis, e assim, evitar erros na titulação das doses de insulina administrada.
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The influences of age, size, and condition of spawning females on fecundity and oocyte quality were analyzed for the Patagonian stock of Argentine Hake (Merluccius hubbsi). Samples of mature females were collected in the spawning area as part of 2 research surveys conducted in January 2010 and 2011, during the peak of the reproductive season. Batch fecundity (BF) ranged between 40,500 (29 cm total length [TL]) and 2,550,000 (95 cm TL) hydrated oocytes, and was positively correlated with TL, gutted weight, age, hepatosomatic index (HSI), and the relative condition factor (Kn). Relative fecundity ranged between 85 and 1040 hydrated oocytes g–1 and showed significant positive relationships with gutted weight, HSI, and Kn; however, coefficients of determination were low for all regressions. Dry weights of samples of 100 hydrated oocytes ranged between 1.8 and 3.95 mg and were positively correlated with all variables analyzed, including batch and relative fecundity. Multiple regression models created with data of the morphophysiological characteristics of females supported maternal influences on fecundity and egg weights. Within the studied size range (29–95 cm TL), larger individuals had better somatic and egg condition, mainly revealed by higher HSI and hydrated oocytes with larger oil droplets (275.71μm [standard error 1.49]). These results were associated with the higher feeding activity of larger females during the spawning season in comparison with the feeding activity of young individuals (<5 years old); the better nutritional state of larger females, assumed to result from more feeding, was conducive to greater production of high-quality eggs.
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Blooms of the brevetoxin-producing dinoflagellate Karenia brevis have been linked to high mortality of bottlenose dolphins Tursiops truncatus on Florida’s Gulf of Mexico coast. A clear understanding of trophic transfer of brevetoxin from its algal source up the food web to top predators is needed to assess exposure of affected dolphin populations. Prey fish constitute a means of accumulating and transferring brevetoxins and are potential vectors of brevetoxin to dolphins frequently exposed to K. brevis blooms. Here we report results of brevetoxin analyses of the primary fish species consumed by long-term resident bottlenose dolphins inhabiting Sarasota Bay, Florida. Fish collected during K. brevis blooms in 2003 to 2006 were analyzed by competitive enzyme-linked immunosorbent assay (ELISA) and had brevetoxin concentrations ranging from 4 to 10844 ng PbTx-3 eq g–1 tissue. Receptor binding assay (RBA) and liquid chromatography–mass spectrometry (LC-MS) analysis confirmed toxicity and the presence of parent brevetoxins and known metabolites. Fish collected in the absence of K. brevis blooms tested positive for brevetoxin by ELISA and RBA, with concentrations up to 1500 ng PbTx-3 eq g–1 tissue. These findings implicate prey fish exposed to K. brevis blooms as brevetoxin vectors for their dolphin predators and provide a critical analysis of persistent brevetoxin loads in the food web of dolphins repeatedly exposed to Florida red tides.
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草地生态系统中,放牧对调节物质流动和营养循环起着关键的作用。内蒙古地区已有上千年的游牧历史,放牧是该地区重要的草地利用方式之一。然而,近50年来,由于人口的剧增以及对草原的不合理利用与管理,使得内蒙古草原发生了严重的退化与沙漠化。理解放牧对氮循环的定量影响,对我们更合理地利用草地、防治生态系统的进一步退化以及探求最佳恢复途径都具有重要的意义。中国科学院内蒙古草原生态系统定位站精准设置的5种放牧强度处理(0.00, 1.33, 2.67, 4.00, 5.33 羊/公顷)为我们的研究提供了理想的平台。2005、2006年生长季期间,在经过16年不同放牧强度处理的一个典型草原样地上,我们测定了氮素输入(氮沉降、生物固氮)、转化(净氮矿化)、输出(反硝化及氨气挥发)速率等N循环的重要参量。同时,测定了微生物生物量碳、氮(Cmic,Nmic)及微生物呼吸(Rmic),研究了微生物在氮循环中的作用。另外,还测定了植物、土壤、固氮体中的15N自然丰度值,探讨了其对不同放牧强度的响应格局与机理。 结果表明,干湿混合沉降物全氮浓度最高达11.53 mg N l–1,沉降量最高为1.77 kg N ha–1m–1。月均氮沉降量与浓度正相关,它们与降水量均关系密切,前者更密切。结皮面积所占比例很小,不超过8%。结皮含氮量为1.01-1.43 g N kg–1,受放牧的影响不显著,但随放牧强度的增加有降低的趋势。土壤结皮能固氮,但固氮量不超过土壤氮含量的1倍。地耳的固氮量为结皮的10-20倍,故是主要的固氮体。尽管地耳含氮量受放牧影响不显著,但放牧是不放牧条件下地耳氮含量的1.58倍。 土壤NH4+-N浓度随季节变化范围为1.71-9.45 µg N g–1,它们在各放牧处理之间的差异不显著。土壤NO3–-N浓度变幅为0.27-11.21 µg N g–1。总无机氮浓度在不放牧条件下的变幅为2.69-14.57 µg N g–1,占总氮的0.49-2.6%;放牧条件下的变幅为2.49-8.66 µg N g–1,占总氮的0.35-1.21%。总无机氮浓度随季节和放牧强度的变化趋势与硝态氮相似,表现为2005年夏季期间有逐渐增加的趋势,而在2006年整个生长季期间有逐渐降低的趋势。不放牧比放牧条件下含氮量高,但在4个放牧处理之间的差异不显著。净氮矿化速率的变幅为–0.61-0.27 µg N g–1d–1,峰值通常出现在7月。净氮矿化速率在各处理间没有一致性差异,但中牧(2.67、4.00 羊/公顷)通常比重牧(5.33 羊/公顷)下的值高。净氮硝化速率通常很低,波动在–0.32-0.16 µg N g–1之间,2005年夏季及2006年春秋季的值相对较高。净氮硝化速率在各放牧处理之间差异不显著,但重牧条件下的值通常最低。累积净氮转化量在年际间差异大,2005年总体上遵循正态分布模式,而2006年随着放牧强度的增加有直线下降的趋势,2006年比2005年的累积量高。土壤温度和湿度比放牧强度对净氮矿化的影响更加显著。放牧强度通过调节这两个土壤因子对氮动态而产生间接影响。 反硝化和N2O的释放速率低,前者变幅为0.33-6.21µg N kg–1 d–1,后者为0.42-11.28 µg N kg–1 d–1。释放量夏季较强,春秋较弱。放牧对反硝化释放影响不显著,只在2005年对N2O释放影响显著。尽管如此,反硝化和N2O释放速率整体表现出在不放牧比放牧条件下高的趋势,且比最高放牧强度5.33 羊/公顷下的反硝化速率显著高。然而,它们在4个放牧处理之间的差异始终不显著。累积反硝化和N2O释放存在年际变化,2006年的值显著高。它们随着放牧强度的递增有逐渐降低的趋势,这在2006年表现得尤为明显,这种结果主要归因于土壤总氮量在长期放牧条件下随放牧压力的增加而逐渐降低。 氨气挥发速率变幅为0.88-3.52 g N ha–1d–1,高峰值出现在5月,2005比2006年同期的速率大。两年间放牧强度对氨气挥发的影响都较弱,2005年影响更弱。不放牧条件下的氨气挥发量通常最低,这在生长季的前期表现得更为明显,中牧及重牧条件下通常最高。放牧能影响氨气挥发与氨态氮,硝态氮及总无机氮浓度之间的关系,即不放牧条件下相关性显著,而放牧条件下相关性不显著。年际间氨气挥发速率与无机氮浓度之间的关系趋势相反,2005年负相关,2006年正相关。在水分充足的2006年,所有处理条件下氨气挥发与土壤水分及温度之间显著相关,但在单独每个放牧处理下,相关性不显著。 Cmic变幅大,为13.97-350.45 μg C g–1,占土壤总有机碳的1.58-8.35%。最高和最低值分别出现在夏季和春季。它们在各处理间差异不显著,不放牧下的值相对偏高。Cmic与土壤有机C和全N、前期的立枯、凋落量及含N量、优势种前期的地上生物量、根系生物量、土壤温度以及水分之间关系密切。氮素状态如氨态氮、总无机氮含量、反硝化以及N2O释放速率,氨气挥发速率与Cmic之间关系密切。Nmic占土壤全氮的0.41-2.74%,不受季节和放牧强度的显著影响。Nmic与可溶性N,表土层根系全N,立枯有机C,地上生物量之间关系密切。氮循环过程中氨气挥发速率受Nmic的影响。Rmic随季节而变化,通常5月份值最高。Rmic随着放牧强度的增加有稍降低的趋势。Rmic与土壤可溶性C、有机C,不同土层根系有机C,凋落物、立枯量及其C、N含量、全N,地上生物量,优势种前期的生物量,土壤温度之间关系密切。土壤氮循环动态如氨态氮、硝态氮、总无机氮浓度及反硝化速率与Rmic之间关系密切。 土壤、植物、地耳、生物结皮的δ15N值与放牧强度之间相关关系不显著。然而,放牧有增加表层土和植物的δ15N值而降低表土、地耳、结皮的δ15N值的趋势。表层土δ15N值与前一年生长季末期硝态氮及总无机氮浓度,反硝化速率及累积氨气挥发之间密切相关。 土壤碳含量的变幅为10.44-17.19 g C kg–1,全氮量的变幅为0.54-0.82 g N kg–1。长期的高强度放牧降低了土壤碳、氮储量。根系碳、氮含量分别为土壤碳、氮含量的40-50和10倍。立枯和凋落物有机碳含量变幅为446.94-507.01 g C kg–1,与放牧强度之间关系不密切;氮含量变幅为4.58-7.18 g N kg–1,与放牧强度之间显著负相关。优势种木地肤、冷蒿的含碳量与放牧强度之间相关不显著,但含氮量与之显著相关。 综述以上结果,不同放牧强度对内蒙草地生态系统氮循环中不同过程产生影响的程度各不相同,这种影响主要是通过它与土壤环境因子如温度、水分的联合作用而间接产生。
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供体细胞的同步化处理可能改变其表观遗传特性,进而影响胚胎的克隆效率。研究同步化处理对小鼠胎儿成纤维细胞(mouse embryonicf ibroblasts,MEFs)组蛋白H3K9甲基化、乙酰化及组蛋白H3K4单甲基化、三甲基化表达的影响。分离培养MEFs,增殖稳定的第3代MEFs分别用5mL/L血清饥饿处理4d或15mL/LDM-SO处理2d使细胞处于增殖抑制期,通过免疫组化染色和Image-J图像处理软件,相对定量比较不同处理情况下组蛋白H3K9甲基化、乙酰化和组蛋白H3K4单甲基化、三甲基化变化情况。Ki-67染色检测结果表明,两种同步化处理可使细胞处于G0期或G1期。DMSO处理使MEFs组蛋白H3K9乙酰化表达水平升高,而5mL/L血清饥饿处理则使其表达水平下降;此外,两种同步化处理均导致组蛋白H3K9甲基化和H3K4单甲基化表达下降,但不影响组蛋白H3K4三甲基化的表达水平。研究结论表明:同步化处理可改变MEFs组蛋白乙酰化和甲基化表达水平,进而有可能影响胚胎克隆效率。
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2003年8月—2005年8月,对无量山大寨子5个黑长臂猿群体的结构和组成进行了观察。当一个群体在早晨鸣叫或依次通过树冠时,记录群体的结构和组成。每个群体都由1个成年雄性、2个成年雌性及其后代组成。2003年8月平均群体大小为6·2只;到2005年8月,平均群体大小发展为6·4只,其中有2个亚成年雄性从出生群迁出,且有3只幼猿出生。在3个群体(G1、G2和G3)中两个成年雌性都成功繁殖了后代。同一群体内两个成年雌性间无攻击或等级行为。2005年4月15日,当一只亚成年雌性进入G3的领域后,两只成年雌性对其进行追逐驱赶,并且干扰其与成年雄性配合进行二重唱,成年雄性没有直接驱赶流浪的亚成年雌性,10天后这只亚成年雌性离开了G3的领域。亚成年雄性经常与群体其他成员保持一定距离,并且在出生地通过独唱练习鸣叫。黑长臂猿可能通过亚成年雄性和雌性的迁出,及成年雌性对外来流浪雌性的驱赶维持这种一夫二妻的群体结构。
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以雄性银鲫为实验材料 ,通过雌二醇 (Estradiol- 1 7β,E2 )的多次诱导 ,使得 E2 诱导产物成为血清中的主要蛋白。而后 ,在快速蛋白液相色谱 (FPL C)系统上 ,利用高交换量的阴离子交换层析 Q柱 ,成功的从血清中提纯了与雌性特异蛋白相一致的 E2 诱导产物。糖、磷、脂蛋白分析表明 ,它是一类糖磷脂蛋白大分子。同时 ,它能被 Mg2 + - Ethylenediamine tetraaceticacid(Mg2 + - EDTA)部分沉淀 ,这进一步证明 ,与雌性特异蛋白相一致的
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采用 RAPD方法 ,对两个人工雌核发育红白锦鲤群体进行了多态性及分子标记分析。结果表明 ,同一雌核发育群体具有基本一致的扩增产物 ,而不同雌核发育群体间的扩增产物则有较大不同 ;并从 3 0个随机引物的扩增谱带中找到了 7个引物 (Opo- 7,Opo- 9,Opo- 1 2 ,Opo- 1 4,Opj- 4,Opj- 8和 Opj- 1 0 )的扩增谱带可以作为两个不同雌核发育群体间的遗传标记。由 UPGMA聚类法构建的分支系统树清晰地反映了两个雌核发育群体及其个体间的相互关系。
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在描述鳞片、背鳍条和矢耳石三种材料轮纹特征的基础上 ,比较了这些年龄鉴定材料在判读错鄂裸鲤年龄和反映生长特征上的异同。在个体早期生长阶段 ,耳石轮纹阻断、8龄以上个体鳞片上年轮环纹的缺失和背鳍条出现轮纹的重叠是影响错鄂裸鲤年龄准确判读的主要因素。采用耳石和鳞片的体长退算数据 ,VonBertalanffy方程较好地描述了错鄂裸鲤的生长。由于背鳍条的生长在个体的生长过程中始终呈现为负的异速生长 ,因此耳石、鳞片在解释个体生长时优于鳍条
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国家重点基础研究计划 ( 973)项目 (G1 9990 5 390 8); 中国科学院生物特别支持费 (STZ 0 0 1 3)资助
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分别取行天然雌核发育繁殖的银鲫和两性生殖的彩鲫的卵母细胞为材料 ,提取总RNA ,分离mRNA ,进而反转录合成cDNA并定向插入λgtllSfi Not克隆载体 ,经体外包装构建了银鲫与彩鲫卵母细胞的表达型cDNA文库。测试结果表明库容量分别达到 3 1× 1 0 6(银鲫 )和 1 6× 1 0 6(彩鲫 )。进一步人工合成CyclinA1 保守引物 ,采用PCR扩增文库的方法 ,克隆了银鲫 (1 61 6bp)与彩鲫 (1 62 6bp)的CyclinA1 全长cDNA。序列分析结果表明 :两种鱼编
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取源于武汉两个不同渔场两尾白鲢的卵子,经紫外照射遗传物质失活的鲤鱼精子刺激雌核发育和热休克诱导第二极体保留的基因组操作技术,获得了两个不同的人工雌核发育白鲢群体。采用聚丙烯酰胺垂直板电泳技术,分析了这两个不同人工雌核发育白鲢群体(分别称为Hy-G1和Hy-G2)内不同个体的肝脏、肌肉组织以及红细胞中乳酸脱氢酶(LDH)、苹果酸脱氢酶(MDH)、酯酶(EST)、超氧化物歧化酶(SOD)等几种同工酶的表达谱式,并与普通繁殖的同龄白鲢进行了比较。结果表明,各个雌核发育白鲢群体内不同个体间的酶谱表现出很大程度的一
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Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) is one of the TNF superfamily members, participating in many biological processes including cell proliferation and apoptotic death. In this study, a TRAIL gene was cloned from a perciform fish, the mandarin fish Siniperca chuatsi, a major cultured fish in China's aquaculture, and is named as SCTRAIL for S. chuatsi TRAIL. The full-length cDNA of SCTRAIL is 1359 bp, encoding a 283-amino-acid protein. This deduced protein contains the CYS231, a 23-mer fragment of transmembrane region, a glycosylation site and a TNF family signature, all of which are conserved among TRAIL members. SCTRAIL gene consists of six exons, with five intervening introns, spaced over approximately 9 kb of genomic sequence. Southern blotting demonstrated that the SCTRAIL gene is present as a single copy in mandarin fish genome. A 620 bp promoter region obtained by genome walking contains a number of putative transcription factor binding sites, such as Oct-1, Sp-1, NF-1, RAP-1, C/EBPaLp, NF-kappa B and AP-1. The SCTRAIL is constitutively expressed in all the analyzed tissues, as revealed by RT-PCR, which is confirmed by Western blotting analysis using polyclonal antibody against bacteria-derived recombinant SCTRAIL protein. As an apoptosis-inducing ligand, the overexpression of SCTRAIL but not the mutant SCTRAIL-C203S in HeLa cells induced changes characteristic of apoptosis, including chromatin condensation, nucleus fragmentation, DNA ladder, and increase of sub-G0/G1 cells in FACS analysis. (c) 2007 Elsevier Ltd. All rights reserved.
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C-Phycocyanin (C-PC) from blue-green algae has been reported to have various pharmacological characteristics, including antiinflammatory and anti-tumor activities. In this study, we expressed the beta-subunit of C-PC (ref to as C-POP) in Escherichia coli. We found that the recombinant C-PC/beta has anti-cancer properties. Under the treatment of 5 mu M of the recombinant C-PC/beta, four different cancer cell lines accrued high proliferation inhibition and apoptotic induction. Substantially, a lower response occurred in non-cancer cells. We investigated the mechanism by which C-PC/beta inhibits cancer cell proliferation and induces apoptosis. We found that the C-PC/beta interacts with membrane-associated beta-tubulin and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). Under the treatment of the C-PC/beta, depolymerization of microtubules and actin-filaments were observed. The cells underwent apoptosis with an increase in caspase-3, and caspase-8 activities. The cell cycle was arrested at the G0/G1 phase under the treatment of C-PC/beta. In addition, the nuclear level of GAPDH decreased significantly. Decrease in the nuclear level of GAPDH prevents the cell cycle from entering into the S phase. Inhibition of cancer cell proliferation and induction of apoptosis may potentate the C-POP as a promising cancer prevention or therapy agent. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
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共轭树枝状大分子在电致发光、薄膜晶体管、非线性光学以及光合成过程人工模拟中具有潜在的应用前景。然而,为了实现上述应用,我们需要探讨新的合成方法和更深入地探讨树枝状大分子内部电子或能量的传输过程。本人在王佛松院士和王献红研究员的悉心指导下,对官能化苯乙炔树枝状大分子的合成及性质进行了初步的研究。主要工作总结如下:一、采用新的合成方案合成苯乙炔树枝状大分子。利用树脂固载的重复“收敛/发散”的合成方案合成高溶解性苯乙炔类树枝状大分子,每次重复后,代数以2的指数次方在增长、每一步的分离纯化都是相当容易的,产物只需充分冲洗,即可达到分离纯化的目的,克服了收敛和发散中存在的缺陷。这个方案的另一个重要进步在于其中心及末梢都容易官能化,在其中心或末端连上不同的电活性或光活性基团可实现这种树枝大分子的多方面应用。二、氧化还原活性的苯乙炔树枝状大分子的合成。将苯乙炔树状大分子的中心键合上具有氧化还原活性的二茂铁基团,得到一代、二代、四代电活性树枝状大分子。三、氧化还原活性的苯乙炔树枝大分子的电化学性质。对所合成的一代、二代、四代电活性树枝状大分子进行计时安培方法和循环伏安测试分别得到扩散系数D_0和标准电子转移速率常数k_0,它们都随着树枝状大分子代数的增长呈现明显的衰减现象。通过电化学方法揭示了随着树枝状大分子代数的增加,电极与氧化还原电对之间的电子转移呈现了明显的衰减关系。树枝状大分子Fc-G1, Fc-G2和Fc-G4的计算机优化构象表明随着代数的增长氧化还原电对被包埋得更加紧密,这种包埋程度的差异强烈地影响了氧化还原电对与电极之间的电子传输速率。