333 research outputs found
Planck Fluctuations, Measurement Uncertainties and the Holographic Principle
Starting from a critical analysis of recently reported surprisingly large
uncertainties in length and position measurements deduced within the framework
of quantum gravity, we embark on an investigation both of the correlation
structure of Planck scale fluctuations and the role the holographic hypothesis
is possibly playing in this context. While we prove the logical independence of
the fluctuation results and the holographic hypothesis (in contrast to some
recent statements in that direction) we show that by combining these two topics
one can draw quite strong and interesting conclusions about the fluctuation
structure and the microscopic dynamics on the Planck scale. We further argue
that these findings point to a possibly new and generalized form of quantum
statistical mechanics of strongly (anti)correlated systems of degrees of
freedom in this fundamental regime.Comment: 19 pages, Latex, no figures, some new references, to appear
ModPhysLett
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High concentrations of morphine sensitize and activate mouse dorsal root ganglia via TRPV1 and TRPA1 receptors.
BACKGROUND: Morphine and its derivatives are key drugs in pain control. Despite its well-known analgesic properties morphine at high concentrations may be proalgesic. Particularly, short-lasting painful sensations have been reported upon dermal application of morphine. To study a possible involvement of TRP receptors in the pro-nociceptive effects of morphine (0.3 - 10 mM), two models of nociception were employed using C57BL/6 mice and genetically related TRPV1 and TRPA1 knockout animals, which were crossed and generated double knockouts. Hindpaw skin flaps were used to investigate the release of calcitonin gene-related peptide indicative of nociceptive activation. RESULTS: Morphine induced release of calcitonin gene-related peptide and sensitized the release evoked by heat or the TRPA1 agonist acrolein. Morphine activated HEK293t cells transfected with TRPV1 or TRPA1. Activation of C57BL/6 mouse dorsal root ganglion neurons in culture was investigated with calcium imaging. Morphine induced a dose-dependent rise in intracellular calcium in neurons from wild-type animals. In neurons from TRPV1 and TRPA1 knockout animals activation by morphine was markedly reduced, in the TRPV1/A1 double knockout animals this morphine effect was abrogated. Naloxone induced an increase in calcium levels similar to morphine. The responses to both morphine and naloxone were sensitized by bradykinin. CONCLUSION: Nociceptor activation and sensitization by morphine is conveyed by TRPV1 and TRPA1
Increased System Fidelity for Navy Aviation Hypoxia Training
In 2009, the Naval Aviation Survival Training Program (NASTP) Trainer Management Team (TMT) identified a need for a next-generation normobaric mask-on hypoxia trainer with enhanced capabilities due to the lack of positive air pressure provided by existing capabilities. The lack of a positive pressure-on-demand airflow delivery for current mask-on hypoxia training has been cited as a potential training gap wherein 44% of students experience air hunger (Artino, Folga, & Vacchiano, 2009). As a result, it is unclear whether students are able to recognize more subtle symptoms of hypoxia or if they are masked by air hunger. To address this, researchers have investigated an innovative technology solution to deliver representative pressure-on-demand flow rates, thereby increasing training fidelity by replicating the air delivery method of aircraft systems. This research also provided an opportunity to seek additional novel advances. Reducing the logisitical footprint and increasing portability by removing the need for compressed gases was a goal to ease implementation within higher fidelity training simulators with limited space to increase immersive training opportunities. This paper will provide an overview of the training need and the technical approach to the training device development. Additionally, the authors will discuss the engineering and human subjects testing conducted to evaluate the system. The results will include how symptoms experienced using this novel device compare to historical data from other training systems, in addition to whether the system reduces or eliminates air hunger issues
Analgesic treatment of ciguatoxin-induced cold allodynia
Ciguatera, the most common form of nonbacterial ichthyosarcotoxism, is caused by consumption of fish that have bioaccumulated the polyether sodium channel activator ciguatoxin. The neurological symptoms of ciguatera include distressing, often persistent sensory disturbances such as paraesthesias and the pathognomonic symptom of cold allodynia. We show that intracutaneous administration of ciguatoxin in humans elicits a pronounced axon-reflex flare and replicates cold allodynia. To identify compounds able to inhibit ciguatoxin-induced Na-v responses, we developed a novel in vitro ciguatoxin assay using the human neuroblastoma cell line SH-SY5Y. Pharmacological characterisation of this assay demonstrated a major contribution of Na(v)1.2 and Na(v)1.3, but not Na(v)1.7, to ciguatoxin-induced Ca2+ responses. Clinically available Nav inhibitors, as well as the K(v)7 agonist flupirtine, inhibited tetrodotoxin-sensitive ciguatoxin-evoked responses. To establish their in vivo efficacy, we used a novel animal model of ciguatoxin-induced cold allodynia. However, differences in the efficacy of these compounds to reverse ciguatoxin-induced cold allodynia did not correlate with their potency to inhibit ciguatoxin-induced responses in SH-SY5Y cells or at heterologously expressed Nav1.3, Na(v)1.6, Na(v)1.7, or Na(v)1.8, indicating cold allodynia might be more complex than simple activation of Na-v channels. These findings highlight the need for suitable animal models to guide the empiric choice of analgesics, and suggest that lamotrigine and flupirtine could be potentially useful for the treatment of ciguatera. (C) 2013 International Association for the Study of Pain. Published by Elsevier B. V. All rights reserved
A geometrical origin for the covariant entropy bound
Causal diamond-shaped subsets of space-time are naturally associated with
operator algebras in quantum field theory, and they are also related to the
Bousso covariant entropy bound. In this work we argue that the net of these
causal sets to which are assigned the local operator algebras of quantum
theories should be taken to be non orthomodular if there is some lowest scale
for the description of space-time as a manifold. This geometry can be related
to a reduction in the degrees of freedom of the holographic type under certain
natural conditions for the local algebras. A non orthomodular net of causal
sets that implements the cutoff in a covariant manner is constructed. It gives
an explanation, in a simple example, of the non positive expansion condition
for light-sheet selection in the covariant entropy bound. It also suggests a
different covariant formulation of entropy bound.Comment: 20 pages, 8 figures, final versio
Boundary conditions in the Unruh problem
We have analyzed the Unruh problem in the frame of quantum field theory and
have shown that the Unruh quantization scheme is valid in the double Rindler
wedge rather than in Minkowski spacetime. The double Rindler wedge is composed
of two disjoint regions (- and -wedges of Minkowski spacetime) which are
causally separated from each other. Moreover the Unruh construction implies
existence of boundary condition at the common edge of - and -wedges in
Minkowski spacetime. Such boundary condition may be interpreted as a
topological obstacle which gives rise to a superselection rule prohibiting any
correlations between - and - Unruh particles. Thus the part of the field
from the -wedge in no way can influence a Rindler observer living in the
-wedge and therefore elimination of the invisible "left" degrees of freedom
will take no effect for him. Hence averaging over states of the field in one
wedge can not lead to thermalization of the state in the other. This result is
proved both in the standard and algebraic formulations of quantum field theory
and we conclude that principles of quantum field theory does not give any
grounds for existence of the "Unruh effect".Comment: 31 pages,1 figur
Topological features of massive bosons on two dimensional Einstein space-time
In this paper we tackle the problem of constructing explicit examples of
topological cocycles of Roberts' net cohomology, as defined abstractly by
Brunetti and Ruzzi. We consider the simple case of massive bosonic quantum
field theory on the two dimensional Einstein cylinder. After deriving some
crucial results of the algebraic framework of quantization, we address the
problem of the construction of the topological cocycles. All constructed
cocycles lead to unitarily equivalent representations of the fundamental group
of the circle (seen as a diffeomorphic image of all possible Cauchy surfaces).
The construction is carried out using only Cauchy data and related net of local
algebras on the circle.Comment: 41 pages, title changed, minor changes, typos corrected, references
added. Accepted for publication in Ann. Henri Poincare
Soluble epoxide hydrolase limits mechanical hyperalgesia during inflammation.
RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/about/license which is similar to the 'Creative Commons Attribution Licence'. In brief you may : copy, distribute, and display the work; make derivative works; or make commercial use of the work - under the following conditions: the original author must be given credit; for any reuse or distribution, it must be made clear to others what the license terms of this work are.BACKGROUND: Cytochrome-P450 (CYP450) epoxygenases metabolise arachidonic acid (AA) into four different biologically active epoxyeicosatrienoic acid (EET) regioisomers. Three of the EETs (i.e., 8,9-, 11,12- and 14,15-EET) are rapidly hydrolysed by the enzyme soluble epoxide hydrolase (sEH). Here, we investigated the role of sEH in nociceptive processing during peripheral inflammation. RESULTS: In dorsal root ganglia (DRG), we found that sEH is expressed in medium and large diameter neurofilament 200-positive neurons. Isolated DRG-neurons from sEH(-/-) mice showed higher EET and lower DHET levels. Upon AA stimulation, the largest changes in EET levels occurred in culture media, indicating both that cell associated EET concentrations quickly reach saturation and EET-hydrolyzing activity mostly effects extracellular EET signaling. In vivo, DRGs from sEH-deficient mice exhibited elevated 8,9-, 11,12- and 14,15-EET-levels. Interestingly, EET levels did not increase at the site of zymosan-induced inflammation. Cellular imaging experiments revealed direct calcium flux responses to 8,9-EET in a subpopulation of nociceptors. In addition, 8,9-EET sensitized AITC-induced calcium increases in DRG neurons and AITC-induced calcitonin gene related peptide (CGRP) release from sciatic nerve axons, indicating that 8,9-EET sensitizes TRPA1-expressing neurons, which are known to contribute to mechanical hyperalgesia. Supporting this, sEH(-/-) mice showed increased nociceptive responses to mechanical stimulation during zymosan-induced inflammation and 8,9-EET injection reduced mechanical thresholds in naive mice. CONCLUSION: Our results show that the sEH can regulate mechanical hyperalgesia during inflammation by inactivating 8,9-EET, which sensitizes TRPA1-expressing nociceptors. Therefore we suggest that influencing the CYP450 pathway, which is actually highly considered to treat cardiovascular diseases, may cause pain side effects.Peer Reviewe
Hyperentangled States
We investigate a new class of entangled states, which we call
'hyperentangled',that have EPR correlations identical to those in the vacuum
state of a relativistic quantum field. We show that whenever hyperentangled
states exist in any quantum theory, they are dense in its state space. We also
give prescriptions for constructing hyperentangled states that involve an
arbitrarily large collection of systems.Comment: 23 pages, LaTeX, Submitted to Physical Review
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