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Subsequent Translocation (subsequent + translocation)

Distribution by Scientific Domains

Medical Sciences	50%
Life Sciences	50%

Selected Abstracts

Cytolethal distending toxin (CDT): a bacterial weapon to control host cell proliferation?

FEMS MICROBIOLOGY LETTERS, Issue 2 2001
Jean de Rycke
Abstract Cytolethal distending toxins (CDT) constitute a family of genetically related bacterial protein toxins able to stop the proliferation of numerous cell lines. This effect is due to their ability to trigger in target cells a signaling pathway that normally prevents the transition between the G2 and the M phase of the cell cycle. Produced by several unrelated Gram-negative mucosa-associated bacterial species, CDTs are determined by a cluster of three adjacent genes (cdtA, cdtB, cdtC) encoding proteins whose respective role is not yet fully elucidated. The CDT-B protein presents sequence homology to several mammalian and bacterial phosphodiesterases, such as DNase I. The putative nuclease activity of CDT-B, together with the activation by CDT of a G2 cell cycle checkpoint, strongly suggests that CDT induces an as yet uncharacterized DNA alteration. However, the effective entry of CDT into cells and subsequent translocation into the nucleus have not yet been demonstrated by direct methods. The relationship between the potential DNA-damaging properties of this original family of toxins and their role as putative virulence factors is discussed. [source]

Gastrointestinal effects of nonsteroidal anti-inflammatory drugs

FUNDAMENTAL & CLINICAL PHARMACOLOGY, Issue 3 2003
Brendan J. R. Whittle
Abstract Non-steroidal anti-inflammatory drugs (NSAIDs) causes extensive damage to the gastrointestinal (GI) tract. The underlying mechanisms of gastric injury include topical irritant actions that disrupt the epithelial barrier, as well as the inhibition of cyclo-oxygenase (COX), which is predominantly the COX-1 isoform in the mucosa. This damage can be attenuated by antisecretory agents or by mucosal protective agents such as the synthetic prostanoids or nitric oxide (NO) donors. Compounds designed to attenuate topical irritancy, or have protective agents incorporated, such as NO-containing NSAIDs, the CINODs (cyclo-oxygenase-inhibiting NO-donating drugs) show reduced mucosal injury. NSAIDs also cause injury in the small intestine, which appears to result from initial COX inhibition, with subsequent translocation of indigenous bacteria, induction of NO synthase and production of the cytotoxic moiety, peroxynitrite. The COX-2 selective agents, the coxibs, which inhibit prostanoid biosynthesis at inflammatory sites, but not the endogenous protective prostanoids in the gut formed by COX-1, have proved so far to be a successful therapeutic approach to reducing NSAIDs GI damage. The clinical outcome of the use of the second generation of coxibs, and the newer NO NSAIDs is now awaited. [source]

Modulation of the inflammatory response to cardiopulmonary bypass by dopexamine and epidural anesthesia

ACTA ANAESTHESIOLOGICA SCANDINAVICA, Issue 10 2002
F. Bach
Background: Cardiopulmonary bypass (CPB) induces a systemic inflammatory reaction. Microcirculation-dependent alteration of the gut mucosal barrier with subsequent translocation of endotoxins is a postulated mechanism for this inflammatory response. This study was designed to elucidate whether two different approaches to modulate splanchnic perfusion may influence systemic inflammation to CPB. Methods: We examined 40 patients scheduled for elective coronary bypass surgery in a prospective, randomized study. One group (DPX) received dopexamine (1 µg · kg,1 · min,1) continuously after induction of anesthesia until 18 h after CPB. The control group (CON) received equal volumes of NaCl 0.9% in a time-matched fashion. In a third group (EPI) a continuous epidural infusion of bupivacaine 0.25% [(body height (cm) , 100) · 10,1=ml·h,1] was administered for the whole study period. Procalcitonin (PCT), tumor necrosis factor (TNF-,), soluble TNF receptor, human soluble intercellular adhesion molecule-1, C-reactive protein (CRP) and leukocyte count were measured as parameters of inflammation. Results: All parameters significantly increased following CPB. Increases of PCT, TNF-, and leukocyte count were significantly attenuated in the DPX and EPI groups at different time points. However, neither splanchnic blood flow nor oxygen delivery and consumption were different when compared with the CON-group. Conclusion: These results do suggest that mechanisms other than an improved splanchnic blood flow by DPX and EPI treatment have to be considered for the anti-inflammatory effects. [source]

Translocations: Providing Outcomes for Wildlife, Resource Managers, Scientists, and the Human Community

RESTORATION ECOLOGY, Issue 2 2008
Kevin A. Parker
Abstract The World Conservation Union (1987) defines a translocation as a release of animals with the intention of establishing, reestablishing, or augmenting an existing population. Despite frequent use as a tool for the management of threatened and endangered wildlife, the full benefits of translocations often go unrealized. In this article, I demonstrate how translocations can achieve outputs for conservation management, conservation science, and the wider human community, using North Island (NI) Saddleback or Tieke (Philesturnus rufusater) as an illustrative example. From a conservation management perspective, NI Saddleback have been salvaged from a relic population of less than 500 birds on 484-ha Hen Island to a metapopulation of approximately 6,000 birds on 13 offshore islands and at two mainland New Zealand sites. These translocations have reduced the risk of global extinction for this species and helped restore the ecosystems involved. All these translocations have occurred in the past 42 years from known source populations and with known numbers of birds released. The resulting replicated serial population bottlenecks provide numerous scientific opportunities for conservation and biological research. Although the first Saddleback translocations were to reserves closed to the public, subsequent translocations have been to open reserves, providing the wider human community with an opportunity to see and be actively involved in the management of a threatened endemic species. This has raised the profile of both NI Saddleback and other species and has provided wider community conservation benefits. These three outputs illustrate the value of translocations for resource management and conservation science and for increasing community interest, participation, and investment in biological conservation. [source]