Necessary Mechanisms (necessary + mechanism)

Distribution by Scientific Domains


Selected Abstracts


Antisense oligodeoxynucleotide-induced suppression of basal forebrain NMDA-NR1 subunits selectively impairs visual attentional performance in rats

EUROPEAN JOURNAL OF NEUROSCIENCE, Issue 1 2001
Janita Turchi
Abstract It is generally agreed that basal forebrain neuronal circuits contribute to the mediation of the ability to detect, select and discriminate signals, to suppress the processing of irrelevant information, and to allocate processing resources to competing tasks. Rats were trained in a task designed to assess sustained attention, or in a cued discrimination task that did not tax attentional processes. Animals were equipped with guide cannula to infuse bilaterally antisense oligodeoxynucleotides (ODNs) against the N -methyl- d -aspartate (NMDA) NR1 subunits, or missense ODNs, into the substantia innominata of the basal forebrain. Infusions of antisense or missense ODNs did not affect cued visual discrimination performance. Infusions of antisense ODNs dose-dependently impaired sustained attention performance by selectively decreasing the animals' ability to detect signals while their ability to reject nonsignal trials remained unchanged. The detrimental attentional effects of antisense infusions were maximal 24 h after the third and final infusion, and performance returned to baseline 24 h later. Missense infusions did not affect attentional performance. Separate experiments demonstrated extensive suppression of NR1 subunit immunoreactivity in the substantia innominata. Furthermore, infusions of antisense did not produce neurotoxic effects in that region as demonstrated by the Fluoro-Jade method. The present data support the hypothesis that NMDA receptor (NMDAR) stimulation in the basal forebrain, largely via glutamatergic inputs originating in the prefrontal cortex, represents a necessary mechanism to activate the basal forebrain corticopetal system for mediation of attentional performance. [source]


Regulated transcription of the immediate-early gene Zif268: Mechanisms and gene dosage-dependent function in synaptic plasticity and memory formation

HIPPOCAMPUS, Issue 5 2002
Bruno Bozon
Abstract The immediate-early gene Zif268 is a member of the Egr family of inducible transcription factors. Data from gene expression studies have suggested that this gene may play a critical role in initial triggering of the genetic machinery that has long been considered a necessary mechanism for maintenance of the later phases of LTP and also for the consolidation or stabilization of long-lasting memories. Until recently, however, the data supporting this assumption have been based primarily on circumstantial evidence, with no direct evidence to suggest that Zif268 is required for long-lasting synaptic plasticity and memory. In this report, we review our own data using Zif268 mutant mice; we show that although the early phase of dentate gyrus LTP is normal in these mice, the later phases are not present, and the ability of the mice to maintain learned information over a 24-h period is deficient. In addition, we present new information showing a task-dependent gene dosage effect in Zif268 heterozygous mice. We show that spatial learning is particularly sensitive to reduced levels of Zif268, as one-half of the complement of Zif268 in heterozygous mice is insufficient to maintain spatial long-term memories. Hippocampus 2002;12:570,577. © 2002 Wiley-Liss, Inc. [source]


Decentralisation, Governance and Health-System Performance: ,Where You Stand Depends on Where You Sit'

DEVELOPMENT POLICY REVIEW, Issue 6 2010
Andrew Mitchell
Advocates of local government often argue that when decentralisation is accompanied by adequate mechanisms of accountability, particularly those responsive to local preferences, improved service delivery will result. From the perspective of the health sector, the appropriate degree of decentralisation and the necessary mechanisms of accountability depend upon the achievement of health system goals. Drawing on evidence from six countries (Bolivia, Chile, India, Pakistan, Philippines, Uganda), this article comes to the conclusion that a balance between centralisation of some functions and decentralisation of others, along with improved mechanisms of accountability, is needed to achieve health system objectives. [source]


Molecular Diversity of Vasotocin-Dependent Aquaporins Closely Associated with Water Adaptation Strategy in Anuran Amphibians

JOURNAL OF NEUROENDOCRINOLOGY, Issue 5 2010
M. Suzuki
Anuran amphibians represent the first vertebrates that adapted to terrestrial environments, and are successfully distributed around the world, even to forests and arid deserts. Many adult anurans have specialised osmoregulatory organs, in addition to the kidney (i.e. the ventral pelvic skin to absorb water from the external environments and a urinary bladder that stores water and reabsorbs it in times of need). Aquaporin (AQP), a water channel protein, plays a fundamental role in these water absorption/reabsorption processes. The anuran AQP family consists of at least AQP0-AQP5, AQP7-AQP10 and two anuran-specific types, designated as AQPa1 and AQPa2. For the three osmoregulatory organs, AQP3 is constitutively located in the basolateral membrane of the tight-junctioned epithelial cells, allowing water transport between the cytoplasm of these cells and the neighbouring tissue fluid at all times. On the other hand, AQPs at the apical side of the tight epithelial cells are different among these organs, and are named kidney-type AQP2, ventral pelvic skin-type AQPa2 and urinary bladder-type AQPa2. All of them show translocation from the cytoplasmic pool to the apical plasma membrane in response to arginine vasotocin, thereby regulating water transport independently in each osmoregulatory organ. It was further revealed that, in terrestrial and arboreal anurans, the bladder-type AQPa2 is expressed in the pelvic skin, together with the pelvic skin-type AQPa2, potentially facilitating water absorption from the pelvic skin. By contrast, Xenopus has lost the ability to efficiently produce pelvic skin-type AQPa2 (AQP-x3) because Cys-273 of AQP-x3 and/or Cys-273-coding region of AQPx3 mRNA attenuate gene expression at a post-transcriptional step, presumably leading to the prevention of excessive water influx in this aquatic species. Collectively, the acquisition of two forms of AQPa2 and the diversified regulation of their gene expression appears to provide the necessary mechanisms for the evolutionary adaptation of anurans to a wide variety of ecological environments. [source]


Using the Bell Labs security framework to enhance the ISO 17799/27001 information security management system

BELL LABS TECHNICAL JOURNAL, Issue 3 2007
Andrew R. McGee
The global information technology (IT) industry recognizes the need for standards to improve the quality and consistency of security for IT products and services. As such, the International Organization for Standardization/ International Electrotechnical Commission (ISO/IEC) 27000 series is focusing on the requirements, security controls, and implementation guidance for an organization's information security management system (ISMS). This guidance establishes general principles that can be used in various industries and government; however, standardized techniques are also needed to identify, implement, and operate security controls as part of the ISMS life cycle. The Bell Labs Security Framework identifies both the minimal and differentiating security controls by decomposing an IT product or service into a layered hierarchy of equipment and facilities groupings and examining the types of activities that occur at each layer in a standardized manner. Furthermore, the Bell Labs Security Framework security dimensions provide the necessary mechanisms to implement and operate the selected controls. The Bell Labs Security Framework enhances the ISO/IEC 27000 series by providing a comprehensive end-to-end approach to implementing IT security. © 2007 Alcatel-Lucent. [source]