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以克山病病区粮配成基础饲料,另在基础饲料中分别补充Se或VE,或Se+VE喂养大鼠,在细胞及亚细胞水平上以Ca代谢为主研究并比较了Se和VE在克山病病因中的作用。测量了心肌细胞和心肌线粒体的Ca代谢及有关指标、心肌线粒体能量转换功能及心肌组织自由基含量。结果表明,在低Se病区粮中补充Se或VE均能在一定程度上预防病区粮中致病因素对心肌细胞及线粒体的损伤;并且补充Se或VE均能使心肌组织中自由基含量减少。提示Se和VE是通过清除体内过量自由基预防细胞和线粒体的损伤的。但值得注意的是,实验中所用病区粮VE含量不低于甚至高于非病区对照粮,在低Se情况下,所补VE的量需要相当大(如本实验中补充200μg/g)才能较明显地预防心肌细胞和心肌线粒体的损伤。通过对这些结果的分析,进一步肯定低Se是克山病形成的重要因素之一。  相似文献   
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Pharmacokinetic (PK) and immunohistochemistry (IHC) assays are essential to the evaluation of the safety and efficacy of therapeutic monoclonal antibodies (mAb) during drug development. These methods require reagents with a high degree of specificity because low concentrations of therapeutic antibody need to be detected in samples containing high concentrations of endogenous human immunoglobulins. Current assay reagent generation practices are labor-intensive and time-consuming. Moreover, these practices are molecule-specific and so only support one assay for one program at a time. Here, we describe a strategy to generate a unique assay reagent, 10C4, that preferentially recognizes a panel of recombinant human mAbs over endogenous human immunoglobulins. This “panel-specific” feature enables the reagent to be used in PK and IHC assays for multiple structurally-related therapeutic mAbs. Characterization revealed that the 10C4 epitope is conformational, extensive and mainly composed of non-CDR residues. Most key contact residues were conserved among structurally-related therapeutic mAbs, but the combination of these residues exists at low prevalence in endogenous human immunoglobulins. Interestingly, an indirect contact residue on the heavy chain of the therapeutic appears to play a critical role in determining whether or not it can bind to 10C4, but has no affect on target binding. This may allow us to improve the binding of therapeutic mAbs to 10C4 for assay development in the future. Here, for the first time, we present a strategy to develop a panel-specific reagent that can expedite the development of multiple clinical assays for structurally-related therapeutic mAbs.  相似文献   
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Background

The main goal of this study is to examine the distributions of illness conditions and resulting medical expenditures and their associated factors. To achieve this goal, an in-house survey was conducted in August of 2012 in rural Beijing, the capital city of China.

Results

The survey was conducted in Nanjianchang and Beijianchang, which are two villages 20 KM away from Miyun, a satellite city of Beijing. Data was collected on 346 households, which included 834 members. Variables measured included household characteristics, household head characteristics, illness conditions, and medical expenditures. Illness conditions and corresponding expenditure were measured for inpatient treatment, outpatient treatment, and self-treatment separately. Multivariate analysis suggested that the presence of inpatient treatment was associated with household head characteristics including age, gender, and education. The presence of a high level of outpatient treatment was associated with household head characteristics including gender and education. The presence of a high level of self-treatment was significantly associated with household size. In the analysis of overall out-of-pocket (OOP) medical expenditure, only age of household head was borderline significant. In the analysis of OOP inpatient expenditure, age and gender of household head were borderline significant. The OOP outpatient expenditure was associated with household size, presence of members older than 60, household head''s gender, marital status, and occupation. The OOP self-treatment expenditure was not associated with any household characteristic.

Conclusions

For the surveyed households, medical expenditure made up a considerable proportion of the total consumption. This study suggested that the presence of illness conditions and resulting OOP medical expenditure were associated with certain household and household head characteristics. Such results may help identify the subgroup that is the most affected by illness conditions. As this study collected recent data on inpatient, outpatient, and self-treatment separately, it may provide a useful complement to the existing studies.  相似文献   
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A novel cephalosporin derivative of monohydroguaiaretic acid (cephem-M(3)N, 7) was synthesized and found to possess anticancer activity against human leukemia (K562), breast carcinoma (MCF7), human lung cancer (A549), human colon cancer (Colo205) and pancreatic cancer cells (Capan2 and MiaPaCa2). A tumor targeting fusion protein (dsFv3-beta-lactamase) was also used in conjunction with cephem-based M(3)N 7 and its potency toward K562, MCF7, A549, Colo205, Capan2, and MiaPaCa2 was found to approach that of the free M(3)N (4). In the presence of dsFv3-beta-lactamase, tumor cells were found to be much more susceptible to conjugate 7 than normal human embryonic lung (HEL) cells and normal fibroblasts (Hef522). These notions provide a new approach to the use of nordihydroguaiaretic acid (NDGA) and its derivatives for antitumor therapy.  相似文献   
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广藿香是著名药材,青枯病是威胁广藿香生产和质量的主要病害。针对从广藿香茎叶中分离出的1株有抑菌活性的内生真菌Alternaria sp. GHX-P17,研究其代谢产物对广藿香青枯病的防治作用及耐病机制。在室内通过人工接种Alternaria sp. GHX-P17菌株与喷施粗提物稀释液2种方式,于不同时间调查广藿香青枯病的发病率和严重度,并计算其病情指数(disease index,DI)。同时,对处理后不同时间的广藿香苯丙氨酸解氨酶(phenylalanine ammonia lyase,PAL)、过氧化物酶(peroxidase,POD)和超氧化物歧化酶(superoxide dismutase,SOD)3种保护酶活性进行测定。结果表明:(1)Alternaria sp. GHX-P17处理后青枯病DI显著降低,与对照比较,204 h后DI降低为27.16%,方差分析呈显著性差异(P<0.05)。(2)随着处理时间延长,青枯病严重度升高缓慢,严重度等级降低,到204 h时,处理组的严重度明显低于对照,防治效果达到74.65%。(3)处理后的广藿香3种保护酶PAL、POD和SOD活性增强,但3种酶活性高峰出现时间不同。PAL随时间逐渐升高; POD先升高后降低,然后又升高,出现2个峰值; SOD快速升高后逐渐降低。这表明内生真菌菌株Alternaria sp. GHX-P17可以提高广藿香3种保护酶活性,延缓了青枯菌的侵染过程,降低了青枯病的发病程度。该研究结果为植物内生真菌次级代谢产物活性成分研究及生物农药开发提供了参考。  相似文献   
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The genus Aurelia is one of the major contributors to jellyfish blooms in coastal waters, possibly due in part to hydroclimatic and anthropogenic causes, as well as their highly adaptive reproductive traits. Despite the wide plasticity of cnidarian life cycles, especially those recognized in certain Hydroza species, the known modifications of Aurelia life history were mostly restricted to its polyp stage. In this study, we document the formation of polyps directly from the ectoderm of degenerating juvenile medusae, cell masses from medusa tissue fragments, and subumbrella of living medusae. This is the first evidence for back-transformation of sexually mature medusae into polyps in Aurelia sp.1. The resulting reconstruction of the schematic life cycle of Aurelia reveals the underestimated potential of life cycle reversal in scyphozoan medusae, with possible implications for biological and ecological studies.  相似文献   
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