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Conducting Studies (conducting + studies)
Selected AbstractsIn vitro reconstructed mucosa-integrating Langerhans' cellsEXPERIMENTAL DERMATOLOGY, Issue 4 2003P. Sivard Abstract:, All three-dimensional in vitro mucosal models constructed, thus far, have only been reconstituted by epithelial cells. We have developed a reconstructed oral and vaginal epithelium that integrates Langerhans' cells (LC), the dendritic cells (DC) of malpighian epithelia. The epithelium was composed of gingival or vaginal keratinocytes seeded on a de-epidermized dermis (DED) and grown in submerged culture for 2 weeks. LC precursors, obtained after differentiation of cord blood-derived CD34+ hematopoietic progenitor cells (CD34+HPC) by granulocyte macrophage-colony stimulating factor (GM-CSF), tumor necrosis factor-, (TNF-,), transforming growth factor-, (TGF-,) and Flt3-ligand (Flt3-L), were introduced after 6,8 days of culture into the reconstituted epithelium. The in vitro reconstituted mucosal epithelium formed a multilayered, well-differentiated epithelial structure, confirmed by the immunohistochemical expression of cytokeratins 4, 6, 10, 13, 14, 16 and involucrin. LC were identified in the basal and suprabasal epithelial layers by CD1a antigen, S100 protein and Langerin/CD207 expression, and by transmission electron microscopy. Type IV collagen was expressed at the chorio,epithelial junction, and most ultrastructural features of this junction were visualized by electron microscopy. This in vitro reconstructed gingiva or vagina integrating LC represents interesting models very similar to native tissues. Because LC play an important role in the mucosal immune system, our models could be useful for conducting studies on interactions with pathogenic agents (viruses, bacteria etc.), as well as in pharmacological, toxicological and clinical research. [source] A review of the effects of catch-and-release angling on black bass, Micropterus spp.: implications for conservation and management of populationsFISHERIES MANAGEMENT & ECOLOGY, Issue 2 2007M. J. SIEPKER Abstract, This paper summarises recent peer-reviewed literature addressing the effects of catch-and-release angling on black bass, Micropterus spp., to facilitate management and conservation of these fish. Traditionally, the effects of catch and release have been evaluated by measuring mortality. Many recent studies have measured sublethal effects on physiology and behaviour. There is also greater emphasis on adding more realism to sublethal catch-and-release experiments through angler involvement in research activities and by conducting studies in the field rather than in laboratory environments. Owing to these advances, there have been a number of recent findings, which are summarised here, related to air exposure, gear (e.g. circle hooks) and the weigh-in procedure that are particularly relevant to black bass anglers, tournament organisers and fishery managers. Additional research is particularly needed for: (1) population-level effects of angling for nesting fish; (2) population-level effects of tournament-associated mortality; (3) effectiveness of livewell additives for enhancing survival; (4) consequences of fish displacement in competitive events; (5) effects of weigh-in procedures and other organisational issues on fish condition and survival; and (6) reducing barotrauma. [source] Cumulative effects of in utero administration of mixtures of reproductive toxicants that disrupt common target tissues via diverse mechanisms of toxicityINTERNATIONAL JOURNAL OF ANDROLOGY, Issue 2 2010C. V. Rider Summary Although risk assessments are typically conducted on a chemical-by-chemical basis, the 1996 Food Quality Protection Act required the US Environmental Protection Agency to consider cumulative risk of chemicals that act via a common mechanism of toxicity. To this end, we are conducting studies with mixtures of chemicals to elucidate mechanisms of joint action at the systemic level with the goal of providing a framework for assessing the cumulative effects of reproductive toxicants. Previous mixture studies conducted with antiandrogenic chemicals are reviewed briefly and two new studies are described. In all binary mixture studies, rats were dosed during pregnancy with chemicals, singly or in pairs, at dosage levels equivalent to approximately one-half of the ED50 for hypospadias or epididymal agenesis. The binary mixtures included androgen receptor (AR) antagonists (vinclozolin plus procymidone), phthalate esters [di(n-butyl) phthalate (DBP) plus benzyl n-butyl phthalate (BBP) and diethyl hexyl phthalate (DEHP) plus DBP], a phthalate ester plus an AR antagonist (DBP plus procymidone), a mixed mechanism androgen signalling disruptor (linuron) plus BBP, and two chemicals which disrupt epididymal differentiation through entirely different toxicity pathways: DBP (AR pathway) plus 2,3,7,8 TCDD (AhR pathway). We also conducted multi-component mixture studies combining several ,antiandrogens'. In the first study, seven chemicals (four pesticides and three phthalates) that elicit antiandrogenic effects at two different sites in the androgen signalling pathway (i.e. AR antagonist or inhibition of androgen synthesis) were combined. In the second study, three additional phthalates were added to make a 10 chemical mixture. In both the binary mixture studies and the multi-component mixture studies, chemicals that targeted male reproductive tract development displayed cumulative effects that exceeded predictions based on a response-addition model and most often were in accordance with predictions based on dose-addition models. In summary, our results indicate that compounds that act by disparate mechanisms of toxicity to disrupt the dynamic interactions among the interconnected signalling pathways in differentiating tissues produce cumulative dose-additive effects, regardless of the mechanism or mode of action of the individual mixture component. [source] Kinetics of adsorption of 2-CEES and HD on impregnated silica nanoparticles under static conditionsAICHE JOURNAL, Issue 5 2009Amit Saxena Abstract Silica nanoparticles of high surface area (887.3 m2/g) were synthesized using aerogel route and, thereafter, impregnated with those reactive chemicals, which have already been proven to be effective against sulfur mustard (HD). Thus, developed adsorbents were tested for their potential by conducting studies on kinetics of adsorption of 2-chloroethylethyl sulfide (2-CEES) and HD under static conditions. Kinetics of adsorption was studied using linear driving force model and Fickian diffusion model. The kinetic parameters such as equilibration constant, equilibration capacity, diffusional exponent, and adsorbate-adsorbent interaction constant were also determined. Trichloroisocyanuric acid impregnated silica nanoparticles (10% w/w) showed the maximum uptake of 2-CEES (1824 mg/g) and HD (1208 mg/g). Values of diffusional exponent indicated the mechanisms to be Fickian and anomalous. Chemical interaction seemed to be another mechanism involved in the toxicant uptake rate. Hydrolysis, dehydrochlorination, and oxidation reactions were found to be the route of degradation of toxicants. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Conceptual and Design Essentials for Evaluating Mechanisms of ChangeALCOHOLISM, Issue 2007Matthew K. Nock Background:, Considerable progress has been made toward the development of evidence-based treatments for a wide range of psychological disorders; however, little is known about the mechanisms through which these treatments actually lead to clinical change. Although the use of traditional randomized controlled treatment designs and tests of statistical mediation have significantly advanced understanding of psychological treatments, they are insufficient to test mechanisms of change. Method:, This article outlines the conceptual and methodological requirements for evaluating mechanisms of change, highlights the importance of such a focus, and offers specific recommendations for research aimed at elucidating change mechanisms. Results and Conclusions:, Conceptualizing and conducting studies that test mechanisms of change requires substantial modifications to traditional research designs, but doing so will significantly enhance scientific understanding as well as the efficiency and effectiveness of clinical interventions. [source] Web-based methods in terrorism and disaster research,JOURNAL OF TRAUMATIC STRESS, Issue 2 2006William E. Schlenger This article provides an overview of the use of the Internet for conducting studies after terrorist attacks and other large-scale disasters. We begin with a brief summary of the scientific and logistical challenges of conducting such research, followed by a description of some of the most important design features that are required to produce valid findings. We then describe one approach to Internet surveys that, although not perfect, addresses many of the challenges well. We close with some thoughts about how the Internet-based methods available today are likely to develop further in coming years. [source] Modeling normal and pathological processes through skin tissue engineeringMOLECULAR CARCINOGENESIS, Issue 8 2007Marta Garcia Abstract Skin tissue engineering emerged as an experimental regenerative therapy motivated primarily by the critical need for early permanent coverage of extensive burn injuries in patients with insufficient sources of autologous skin for grafting. With time, the approach evolved toward a wider range of applications including disease modeling. We have established a skin-humanized mouse model system consisting in bioengineered human-skin-engrafted immunodeficient mice. This new model allows to performing regenerative medicine, gene therapy, genomics, and pathology studies in a human context on homogeneous samples. Starting from skin cells (keratinocytes and fibroblasts) isolated from normal donor skin or patient's biopsies, we have been able to deconstruct-reconstruct several inherited skin disorders including genodermatoses and cancer-prone diseases in a large number of skin humanized mice. In addition, the model allows conducting studies in normal human skin to gain further insight into physiological processes such as wound healing or UV-responses. © 2007 Wiley-Liss, Inc. [source] Validation of diagnostic codes for outpatient-originating sudden cardiac death and ventricular arrhythmia in Medicaid and Medicare claims data,PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, Issue 6 2010Sean Hennessy PharmD Abstract Purpose Sudden cardiac death (SD) and ventricular arrhythmias (VAs) caused by medications have arisen as an important public health concern in recent years. The validity of diagnostic codes in identifying SD/VA events originating in the ambulatory setting is not well known. This study examined the positive predictive value (PPV) of hospitalization and emergency department encounter diagnoses in identifying SD/VA events originating in the outpatient setting. Methods We selected random samples of hospitalizations and emergency department claims with principal or first-listed discharge diagnosis codes indicative of SD/VA in individuals contributing at least 6 months of baseline time within 1999,2002 Medicaid and Medicare data from five large states. We then obtained and reviewed medical records corresponding to these events to serve as the reference standard. Results We identified 5239 inpatient and 29,135 emergency department events, randomly selected 100 of each, and obtained 119 medical records, 116 of which were for the requested courses of care. The PPVs for an outpatient-originating SD/VA precipitating hospitalization or emergency department treatment were 85.3% (95% confidence interval [CI],=,77.6,91.2) overall, 79.7% (95%CI,=,68.3,88.4) for hospitalization claims, and 93.6% (95%CI,=,82.5,98.7) for emergency department claims. Conclusions First-listed SD/VA diagnostic codes identified in inpatient or emergency department encounters had very good agreement with clinical diagnoses and functioned well to identify outpatient-originating events. Researchers using such codes can be confident of the PPV when conducting studies of SD/VA originating in the outpatient setting. Copyright © 2009 John Wiley & Sons, Ltd. 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