897 research outputs found
Interacting supernovae and supernova impostors. SN 2007sv: the major eruption of a massive star in UGC 5979
We report the results of the photometric and spectroscopic monitoring
campaign of the transient SN 2007sv. The observables are similar to those of
type IIn supernovae, a well-known class of objects whose ejecta interact with
pre-existing circum-stellar material. The spectra show a blue continuum at
early phases and prominent Balmer lines in emission, however, the absolute
magnitude at the discovery of SN 2007sv (M_R = - 14.25 +/- 0.38) indicate it to
be most likely a supernova impostor. This classification is also supported by
the lack of evidence in the spectra of very high velocity material as expected
in supernova ejecta. In addition we find no unequivocal evidence of broad lines
of alpha - and/or Fe-peak elements. The comparison with the absolute light
curves of other interacting objects (including type IIn supernovae) highlights
the overall similarity with the prototypical impostor SN 1997bs. This supports
our claim that SN 2007sv was not a genuine supernova, and was instead a
supernova impostor, most likely similar to the major eruption of a luminous
blue variable.Comment: Accepted for publication in MNRAS. 15 pages, 11 figures, 5 table
Treatment of cyclic vomiting syndrome with co-enzyme Q10 and amitriptyline, a retrospective study
<p>Abstract</p> <p>Background</p> <p>Cyclic vomiting syndrome (CVS), which is defined by recurrent stereotypical episodes of nausea and vomiting, is a relatively-common disabling condition that is associated with migraine headache and mitochondrial dysfunction. Co-enzyme Q10 (Co-Q) is a nutritional supplement that has demonstrated efficacy in pediatric and adult migraine. It is increasingly used in CVS despite the complete lack of studies to demonstrate its value in treatment</p> <p>Methods</p> <p>Using an Internet-based survey filled out by subjects with CVS or their parents, the efficacy, tolerability and subject satisfaction in CVS prophylaxis were queried. Subjects taking Co-Q (22 subjects) were compared against those taking amitriptyline (162 subjects), which is the general standard-of-care.</p> <p>Results</p> <p>Subjects/parents reported similar levels of efficacy for a variety of episode parameters (frequency, duration, number of emesis, nausea severity). There was a 50% reduction in at least one of those four parameters in 72% of subjects treated with amitriptyline and 68% of subjects treated Co-Q. However, while no side effects were reported on Co-Q, 50% of subjects on amitriptyline reported side effects (P = 5 × 10<sup>-7</sup>), resulting in 21% discontinuing treatment (P = 0.007). Subjects/parents considered the benefits to outweigh the risks of treatment in 47% of cases on amitriptyline and 77% of cases on Co-Q (P = 0.008).</p> <p>Conclusion</p> <p>Our data suggest that the natural food supplement Co-Q is potentially efficacious and tolerable in the treatment of CVS, and should be considered as an option in CVS prophylaxis. Our data would likely be helpful in the design of a double-blind clinical trial.</p
Symptoms of somatization as a rapid screening tool for mitochondrial dysfunction in depression
<p>Abstract</p> <p>Aims</p> <p>Somatic symptomatology is common in depression, and is often attributed to the Freudian-inspired concept of "somatization". While the same somatic symptoms and depression are common in mitochondrial disease, in cases with concurrent mood symptoms the diagnosis of a mitochondrial disorder and related therapy are typically delayed for many years. A short screening tool that can identify patients with depression at high risk for having underlying mitochondrial dysfunction is presented.</p> <p>Methods</p> <p>Six items of the Karolinska Scales of Personality (KSP) were found to differentiate among 21 chronically-depressed Swedish subjects with low versus normal muscle ATP production rates. A screening tool consisting of the six KSP questions was validated in the relatives of American genetics clinic patients, including in 24 matrilineal relatives in families with maternally inherited mitochondrial disease and in 30 control relatives.</p> <p>Results</p> <p>Among the depressed Swedish patients, the screening tool was positive in 13/14 with low and 1/7 with normal mitochondrial function (P = 0.0003). Applied to the American relatives of patients, the screening tool was positive in 13/24 matrilineal relatives and in 1/30 control relatives (P = 2 × 10<sup>-5</sup>).</p> <p>Conclusion</p> <p>Our preliminary data suggest that a small number of specific somatic-related questions can be constructed into a valid screening tool for cases at high risk for having a component of energy metabolism in their pathogenesis.</p
The possible detection of a binary companion to a Type Ibn supernova progenitor
We present late-time observations of the site of the Type Ibn supernova (SN) 2006jc, acquired with the Hubble
Space Telescope Advanced Camera for Surveys. A faint blue source is recovered at the SN position, with
brightness mF W 435 = 26.76 0.20, mF W 555 = 26.60 0.23 and mF W 625 = 26.32 0.19 mag, although there is
no detection in a contemporaneous narrow-band Ha image. The spectral energy distribution of the late-time source
is well-fit by a stellar-like spectrum (log 3.7 Teff > and log L L > 4), subject to only a small degree of reddening
—consistent with that estimated for SN 2006jc itself at early-times. The lack of further outbursts after the
explosion of SN 2006jc suggests that the precursor outburst originated from the progenitor. The possibility of the
source being a compact host cluster is ruled out on the basis of the source’s faintness; however, the possibility that
the late-time source may be an unresolved light echo originating in a shell or sphere of pre-SN dust (within a radius
1 pc) is also discussed. Irrespective of the nature of the late-time source, these observations rule out a luminous
blue variable as a companion to the progenitor of SN 2006jc
SN 2009E: a faint clone of SN 1987A
In this paper we investigate the properties of SN 2009E, which exploded in a
relatively nearby spiral galaxy (NGC 4141) and that is probably the faintest
1987A-like supernova discovered so far. Spectroscopic observations which
started about 2 months after the supernova explosion, highlight significant
differences between SN 2009E and the prototypical SN 1987A. Modelling the data
of SN 2009E allows us to constrain the explosion parameters and the properties
of the progenitor star, and compare the inferred estimates with those available
for the similar SNe 1987A and 1998A. The light curve of SN 2009E is less
luminous than that of SN 1987A and the other members of this class, and the
maximum light curve peak is reached at a slightly later epoch than in SN 1987A.
Late-time photometric observations suggest that SN 2009E ejected about 0.04
solar masses of 56Ni, which is the smallest 56Ni mass in our sample of
1987A-like events. Modelling the observations with a radiation hydrodynamics
code, we infer for SN 2009E a kinetic plus thermal energy of about 0.6 foe, an
initial radius of ~7 x 10^12 cm and an ejected mass of ~19 solar masses. The
photospheric spectra show a number of narrow (v~1800 km/s) metal lines, with
unusually strong Ba II lines. The nebular spectrum displays narrow emission
lines of H, Na I, [Ca II] and [O I], with the [O I] feature being relatively
strong compared to the [Ca II] doublet. The overall spectroscopic evolution is
reminiscent of that of the faint 56Ni-poor type II-plateau supernovae. This
suggests that SN 2009E belongs to the low-luminosity, low 56Ni mass, low-energy
tail in the distribution of the 1987A-like objects in the same manner as SN
1997D and similar events represent the faint tail in the distribution of
physical properties for normal type II-plateau supernovae.Comment: 19 pages, 9 figures (+7 in appendix); accepted for publication in A&A
on 3 November 201
Towards the prediction of antimicrobial efficacy for hydrogen bonded, self-associating amphiphiles
Herein, we report 50 structurally related supramolecular self-associating amphiphilic (SSA) salts and related compounds. These SSAs are shown to act as antimicrobial agents, active against model Gram-positive (Methicillin-Resistant Staphylococcus aureus) and/or Gram-negative (Escherichia coli) bacteria of clinical interest. Through a combination of solution state, gas phase, solid state and in silico measurements we determine 14 different physicochemical parameters for each of these 50 structurally related compounds. These parameter sets are then used to identify molecular structure – physicochemical property – antimicrobial activity relationships for our model Gram-negative and Gram-positive bacteria, while simultaneously providing insight towards the elucidation of SSA mode of antimicrobial action
Murfreesboro Addresses
https://digitalcommons.acu.edu/crs_books/1086/thumbnail.jp
The Unusual Temporal and Spectral Evolution of SN2011ht. II. Peculiar Type IIn or Impostor?
SN2011ht has been described both as a true supernova and as an impostor. In
this paper, we conclude that it does not match some basic expectations for a
core-collapse event. We discuss SN2011ht's spectral evolution from a hot dense
wind to a cool dense wind, followed by the post-plateau appearance of a faster
low density wind during a rapid decline in luminosity. We identify a slow dense
wind expanding at only 500--600 km/s, present throughout the eruption. A faster
wind speed V ~ 900 km/s may be identified with a second phase of the outburst.
There is no direct or significant evidence for any flow speed above 1000 km/s;
the broad asymmetric wings of Balmer emission lines in the hot wind phase were
due to Thomson scattering, not bulk motion. We estimate a mass loss rate of
order 0.04 Msun/yr during the hot dense wind phase of the event. There is no
evidence that the kinetic energy substantially exceeded the luminous energy,
roughly 2 X 10^49 ergs; so the total energy was far less than a true SN. We
suggest that SN2011ht was a giant eruption driven by super-Eddington radiation
pressure, perhaps beginning about 6 months before the discovery. A strongly
non-spherical SN might also account for the data, at the cost of more free
parameters.Comment: To appear in the Astrophysical Journal, Nov. 20 issue. Expanded
discussion re SN impostors and Type IIn SNe plus two new figure
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification.
Primary familial brain calcification (PFBC) is a rare neurodegenerative disorder characterized by a combination of neurological, psychiatric, and cognitive decline associated with calcium deposition on brain imaging. To date, mutations in five genes have been linked to PFBC. However, more than 50% of individuals affected by PFBC have no molecular diagnosis. We report four unrelated families presenting with initial learning difficulties and seizures and later psychiatric symptoms, cerebellar ataxia, extrapyramidal signs, and extensive calcifications on brain imaging. Through a combination of homozygosity mapping and exome sequencing, we mapped this phenotype to chromosome 21q21.3 and identified bi-allelic variants in JAM2. JAM2 encodes for the junctional-adhesion-molecule-2, a key tight-junction protein in blood-brain-barrier permeability. We show that JAM2 variants lead to reduction of JAM2 mRNA expression and absence of JAM2 protein in patient's fibroblasts, consistent with a loss-of-function mechanism. We show that the human phenotype is replicated in the jam2 complete knockout mouse (jam2 KO). Furthermore, neuropathology of jam2 KO mouse showed prominent vacuolation in the cerebral cortex, thalamus, and cerebellum and particularly widespread vacuolation in the midbrain with reactive astrogliosis and neuronal density reduction. The regions of the human brain affected on neuroimaging are similar to the affected brain areas in the myorg PFBC null mouse. Along with JAM3 and OCLN, JAM2 is the third tight-junction gene in which bi-allelic variants are associated with brain calcification, suggesting that defective cell-to-cell adhesion and dysfunction of the movement of solutes through the paracellular spaces in the neurovascular unit is a key mechanism in CNS calcification
Functional Amyloids Composed of Phenol Soluble Modulins Stabilize Staphylococcus aureus Biofilms
Staphylococcus aureus is an opportunistic pathogen that colonizes the skin and mucosal surfaces of mammals. Persistent staphylococcal infections often involve surface-associated communities called biofilms. Here we report the discovery of a novel extracellular fibril structure that promotes S. aureus biofilm integrity. Biochemical and genetic analysis has revealed that these fibers have amyloid-like properties and consist of small peptides called phenol soluble modulins (PSMs). Mutants unable to produce PSMs were susceptible to biofilm disassembly by matrix degrading enzymes and mechanical stress. Previous work has associated PSMs with biofilm disassembly, and we present data showing that soluble PSM peptides disperse biofilms while polymerized peptides do not. This work suggests the PSMs' aggregation into amyloid fibers modulates their biological activity and role in biofilms
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