The anti-proliferative effect of turmeric and rooibos extracts on human Hodgkin lymphoma cells

The toxicity and limited success of many chemotherapies used in modern medicine to treat cancer has created a large demand for safer, more effective treatments. In many forms of traditional medicine, whole plant extracts have been safely used to treat a wide range of diseases, however there is limited scientific evidence that explains the extent to which such extracts are effective and how they work. Recent screening of both turmeric and rooibos extracts suggest that these natural health products (NHPs) have anti-proliferative properties in a range of human lymphoma cell lines. WST-1 assays were used to evaluate the effects of turmeric and rooibos extracts (water and ethanolic) on the metabolic viability of KM-H2 human Hodgkin lymphoma cells. Results showed ethanolic and cold water extracts of both turmeric and rooibos to be most effective in reducing cell viability in a time- and dose-dependent manner. Trypan blue exclusion assays were further used to determine if the reduction in viability corresponded to a decrease in the proliferation and/or an increase in the death of these cells. The extracts utilized in this assay were applied to cells both individually and in combination to determine the existence of any synergistic effects. Analysis of the growth curves produced from this data will demonstrate the time and dose required for the optimal efficacy of these extracts in reducing the viability of KM-H2 cells. Future work will include discovering the mode of anti-cancer action, assessing whether or not the effective extracts are selective (non-toxic to normal cells), and determining the efficacy in animal models. If these NHPs prove to be both safe and efficacious through the duration of the pre-clinical evaluation, they may improve both current chemotherapy treatment options and the quality of life for patients with Hodgkin lymphoma

Lack of evidence for western flower thrips biotypes base don intra and inter-strain variation in gut bacteria

Western flower thrips is a polyphagous insect, which during the last 30 years has become a world wide pest. It was found earlier that these thrips are associated with a type of Erwinia species gut bacteria. In this study we examine the variation of bacteria within and between thrips individuals and try to find evidence for biotypes in western flower thrips regarding the type of gut bacteria. The existence of biotypes in this thrips species has been suggested by different authors. For example, thrips populations have been found that differ in resistance against pesticides and in their ability to transmit plant viruses. With biotypes we mean groups of individuals (strains, populations, lines) of a species which differ in one or more traits with other groups of that species. The gut bacteria of thrips are acquired by young thrips larvae via the host plant and have a beneficial effect on thrips development and oviposition. We studied thrips strains from different countries and host plants, and the isofemale lines that were created from them, on bean plant leaves. All thrips lines that we studied contained Erwinia species gut bacteria. Morphological and biochemical characteristics of gut bacteria from the thrips isofemale lines were similar to the Erwinia type strain from the reference, a thrips strain cultured on chrysanthemum in Amsterdam (TAC 93.XII.8). Per isofemale line we studied five thrips individuals and per thrips we studied four bacterial colonies, with RAPD markers. The genetic variation between bacteria isolated from thrips was as large among isofemale lines as within isofemale lines. No evidence for thrips biotypes was found. Bacteria within one thrips individual show a stronger degree of similarity than bacteria from different thrips individuals within a single rearing. This is probably due to a bottleneck caused by the limited number of successful infections of bacteria into the gut of the thrip

Bloques de hormigón con revestimiento para cara vista

Not availableDe día en día va adquiriendo un gran incremento la fabricación y empleo de bloques de hormigón con revestimiento para cara vista. Actualmente, se fabrican tres tipos de estos bloques s con revestimiento tipo terrazo, de plástico, y de cemento con superficie pulida

Resource Management in Diffserv On DemAnd (RODA) PHR

The purpose of this draft is to present the Resource Management in Diffserv (RMD) On DemAnd (RODA) Per Hop Reservation (PHR) protocol. The RODA PHR protocol is used on a per-hop basis in a Differentiated Services (Diffserv) domain and extends the Diffserv Per Hop Behavior (PHB) with resource provisioning and control

Vascular responses to radiotherapy and androgen-deprivation therapy in experimental prostate cancer

Background: Radiotherapy (RT) and androgen-deprivation therapy (ADT) are standard treatments for advanced prostate cancer (PC). Tumor vascularization is recognized as an important physiological feature likely to impact on both RT and ADT response, and this study therefore aimed to characterize the vascular responses to RT and ADT in experimental PC. Methods: Using mice implanted with CWR22 PC xenografts, vascular responses to RT and ADT by castration were visualized in vivo by DCE MRI, before contrast-enhancement curves were analyzed both semi-quantitatively and by pharmacokinetic modeling. Extracted image parameters were correlated to the results from ex vivo quantitative fluorescent immunohistochemical analysis (qIHC) of tumor vascularization (9 F1), perfusion (Hoechst 33342), and hypoxia (pimonidazole), performed on tissue sections made from tumors excised directly after DCE MRI. Results: Compared to untreated (Ctrl) tumors, an improved and highly functional vascularization was detected in androgen-deprived (AD) tumors, reflected by increases in DCE MRI parameters and by increased number of vessels (VN), vessel density ( VD), and vessel area fraction ( VF) from qIHC. Although total hypoxic fractions ( HF) did not change, estimated acute hypoxia scores ( AHS) – the proportion of hypoxia staining within 50 μm from perfusion staining – were increased in AD tumors compared to in Ctrl tumors. Five to six months after ADT renewed castration-resistant (CR) tumor growth appeared with an even further enhanced tumor vascularization. Compared to the large vascular changes induced by ADT, RT induced minor vascular changes. Correlating DCE MRI and qIHC parameters unveiled the semi-quantitative parameters area under curve ( AUC) from initial time-points to strongly correlate with VD and VF, whereas estimation of vessel size ( VS) by DCE MRI required pharmacokinetic modeling. HF was not correlated to any DCE MRI parameter, however, AHS may be estimated after pharmacokinetic modeling. Interestingly, such modeling also detected tumor necrosis very strongly. Conclusions: DCE MRI reliably allows non-invasive assessment of tumors’ vascular function. The findings of increased tumor vascularization after ADT encourage further studies into whether these changes are beneficial for combined RT, or if treatment with anti-angiogenic therapy may be a strategy to improve the therapeutic efficacy of ADT in advanced PC.publishedVersio

A prospective methicillin resistant staphylococcus aureus typing system for infection control : design and effectiveness

The uptake of Gadomer-17, as probed by fast dynamic T(1) measurements, was used to assess the vascular permeability surface-area product per leakage volume of tissue (k(Tofts)) of human glioma xenografts implanted in mice. With this approach we could discriminate between two types of glioma xenograft lines with a known difference in the perfused vascular architecture and degree of hypoxia. The T(1) data were analyzed according to the Tofts-Kermode compartment model. The fast-growing E102 tumor demonstrated a homogeneous distribution of the vascular permeability surface area across the tumor (mean k(Tofts) value = 0.18 +/- 0.05 min(-1)). The slowly growing E106 tumor showed a more heterogeneous pattern. Three perfused tumor areas with differences in vascular permeability surface area could be distinguished: a well-perfused periphery with high k(Tofts) values (0.24 +/- 0.04 min(-1)), perfused capillaries inside the tumor with low k(Tofts) values (0.108 +/- 0.026 min(-1)), and perfused capillaries adjacent to necrotic regions with high k(Tofts) values (0.29 +/- 0.10 min(-1)). On a different series of tumors, the hypoxic fractions were measured, and these were significantly higher in E106 tumors (0.14 +/- 0.05) compared to tumors of the E102 line (0.03 +/- 0.02)

Исследование микроструктуры безобжиговых периклазоуглеродистых огнеупоров при использовании в качестве заполнителя различного вида периклаза

У статті представлено результати досліджень мікроструктури периклазовуглецевих зразків, у яких в якості наповнювача використовували різні види периклазу. Петрографічні дослідження показали, що зразки щільні та міцні, як на плавленому, так і на спеченому периклазі.In clause the results of researches of microstructure magnesia-carbon refractors are submitted, at which in quality filler used different kind magnesia. Microstructures of samples strong and dense, both on melted, and on sintered periclase have shown, that

Rab3D is critical for secretory granule maturation in PC12 cells.

Neuropeptide- and hormone-containing secretory granules (SGs) are synthesized at the trans-Golgi network (TGN) as immature secretory granules (ISGs) and complete their maturation in the F-actin-rich cell cortex. This maturation process is characterized by acidification-dependent processing of cargo proteins, condensation of the SG matrix and removal of membrane and proteins not destined to mature secretory granules (MSGs). Here we addressed a potential role of Rab3 isoforms in these maturation steps by expressing their nucleotide-binding deficient mutants in PC12 cells. Our data show that the presence of Rab3D(N135I) decreases the restriction of maturing SGs to the F-actin-rich cell cortex, blocks the removal of the endoprotease furin from SGs and impedes the processing of the luminal SG protein secretogranin II. This strongly suggests that Rab3D is implicated in the subcellular localization and maturation of ISGs

New Modularity of DAP-Kinases: Alternative Splicing of the DRP-1 Gene Produces a ZIPk-Like Isoform

DRP-1 and ZIPk are two members of the Death Associated Protein Ser/Thr Kinase (DAP-kinase) family, which function in different settings of cell death including autophagy. DAP kinases are very similar in their catalytic domains but differ substantially in their extra-catalytic domains. This difference is crucial for the significantly different modes of regulation and function among DAP kinases. Here we report the identification of a novel alternatively spliced kinase isoform of the DRP-1 gene, termed DRP-1β. The alternative splicing event replaces the whole extra catalytic domain of DRP-1 with a single coding exon that is closely related to the sequence of the extra catalytic domain of ZIPk. As a consequence, DRP-1β lacks the calmodulin regulatory domain of DRP-1, and instead contains a leucine zipper-like motif similar to the protein binding region of ZIPk. Several functional assays proved that this new isoform retained the biochemical and cellular properties that are common to DRP-1 and ZIPk, including myosin light chain phosphorylation, and activation of membrane blebbing and autophagy. In addition, DRP-1β also acquired binding to the ATF4 transcription factor, a feature characteristic of ZIPk but not DRP-1. Thus, a splicing event of the DRP-1 produces a ZIPk like isoform. DRP-1β is highly conserved in evolution, present in all known vertebrate DRP-1 loci. We detected the corresponding mRNA and protein in embryonic mouse brains and in human embryonic stem cells thus confirming the in vivo utilization of this isoform. The discovery of module conservation within the DAPk family members illustrates a parsimonious way to increase the functional complexity within protein families. It also provides crucial data for modeling the expansion and evolution of DAP kinase proteins within vertebrates, suggesting that DRP-1 and ZIPk most likely evolved from their ancient ancestor gene DAPk by two gene duplication events that occurred close to the emergence of vertebrates