Gravitational lensing of gravitational waves: A statistical perspective

In this paper, we study the strong gravitational lensing of gravitational waves (GWs) from a statistical perspective, with particular focus on the high frequency GWs from stellar binary black hole coalescences. These are most promising targets for ground-based detectors such as Advanced Laser Interferometer Gravitational Wave Observatory (aLIGO) and the proposed Einstein Telescope (ET) and can be safely treated under the geometrical optics limit for GW propagation. We perform a thorough calculation of the lensing rate, by taking account of effects caused by the ellipticity of lensing galaxies, lens environments, and magnification bias. We find that in certain GW source rate scenarios, we should be able to observe strongly lensed GW events once per year ($\sim1~\text{yr}^{-1}$) in the aLIGO survey at its design sensitivity; for the proposed ET survey, the rate could be as high as $\sim80~\text{yr}^{-1}$. These results depend on the estimate of GW source abundance, and hence can be correspondingly modified with an improvement in our understanding of the merger rate of stellar binary black holes. We also compute the fraction of four-image lens systems in each survey, predicting it to be $\sim30$ per cent for the aLIGO survey and $\sim6$ per cent for the ET survey. Finally, we evaluate the possibility of missing some images due to the finite survey duration, by presenting the probability distribution of lensing time delays. We predict that this selection bias will be insignificant in future GW surveys, as most of the lens systems ($\sim90$ per cent) will have time delays less than $\sim1$ month, which will be far shorter than survey durations.Comment: 10 pages, 5 figures, 1 table. Revised to match version published in MNRA

Systemically administered liposome-encapsulated Ad-PEDF potentiates the anti-cancer effects in mouse lung metastasis melanoma

BACKGROUND: The use of adenoviral vector for gene therapy is still an important strategy for advanced cancers, however, the lack of the requisite coxsackie-adenovirus receptor in cancer cells and host immune response to adenovirus limit the application of adenoviral vector in vivo. METHOD: We designed the antiangiogenic gene therapy with recombinant PEDF adenovirus (Ad-PEDF) encapsulated in cationic liposome (Ad-PEDF/Liposome), and investigated the anti-tumor efficacy of Ad-PEDF/Liposome complex on inhibition of tumor metastasis. RESULTS: We found that systemic administration of Ad-PEDF/liposome was well tolerated and resulted in marked suppression of tumor growth, and was more potent than uncoated Ad-PEDF to induce apoptosis in B16-F10 melanoma cells and inhibit murine pulmonary metastases in vivo. After Ad-luciferase was encapsulated with liposome, its distribution decreased in liver and increased in lung. The anti-Ad IgG level of Ad-PEDF/Liposome was significantly lower than Ad-PEDF used alone. CONCLUSION: The present findings provide evidences of systematic administration of cationic liposome-encapsulated Ad-PEDF in pulmonary metastatic melanoma mice model, and show an encouraging therapeutic effect for further exploration and application of more complexes based on liposome-encapsulated adenovirus for more cancers

Alterations in amino acid levels and metabolite ratio of spinal cord in rat with myocardial ischemia-reperfusion injury by proton magnetic resonance spectroscopy

Abstract Objectives The mechanism behind spinal metabolites and myocardial ischemia-reperfusion (IR) injury is not well understood. Proton magnetic resonance spectroscopic analysis of spinal cord extracts provides a quick evaluation of the specific metabolic activity in rats with myocardial IR injury. We investigated the relationship between the IR-related variables and the changes in spinal metabolites. Methods Proton magnetic resonance spectroscopy (1H-MRS) was used to assess the spinal metabolites of adult rats with and without myocardial IR injury (n=6 per group). Myocardial IR injury was reproduced using intermittent occlusion of the left anterior descending coronary artery. We studied the relationship between the metabolite ratio measurement and IR-related variables. All rats underwent 1H-MRS, with the ratio of interest placed in different spinal cord segments to measure levels of twelve metabolites including N-acetylaspartate (NAA), taurine (Tau),glutamate (Glu),gamma amino acid butyric acid (GABA),creatine (Cr), and myoinositol (MI), etc. Results Rats with myocardial IR injury had higher concentration of Tau in the upper thoracic spinal cord (p< 0.05), and lower concentration of Gly and Glu in the cervical segment of the spinal cord (p< 0.05), when compared to the Control group. The ratios of glutamate/taurine (Glu/Tau), Glu/(GABA+Tau) and Glu/Total were significantly different between the IR group and the Control group in the upper thoracic spinal cord (p< 0.05). So were the ratios of Glu/(GABA+Tau) in the cervical segment (p< 0.05),and Glu/Tau and Glu/(GABA+Tau) in the lower thoracic spinal cord (p< 0.05). Conclusions These findings suggest that myocardial IR injury may be related to spinal biochemical alterations. It is speculated that these observed changes in the levels of spinal metabolites may be involved in the pathogenesis and regulation of myocardial IR injury. Keywords: myocardial ischemia-reperfusion injury; spinal cord; metabolomics; proton nuclear magnetic resonanc

Comprehensive study of the blazars from Fermi-LAT LCR: The log-normal flux distribution and linear RMS-Flux relation

Fermi-LAT LCR provide continuous and regularly-sampled gamma-ray light curves, spanning about 14 years, for a large sample of blazars. The log-normal flux distribution and linear RMS-Flux relation of the light curves for a few of Fermi blazar have been examined in previous studies. However, the probability that blazars exhibit log-normal flux distribution and linear RMS-Flux relation in their gamma-ray light curves has not been systematically explored. In this study, we comprehensively research on the distribution of gamma-ray flux and the statistical characteristics on a large sample of 1414 variable blazars from the Fermi-LAT LCR catalog, including 572 FSRQs, 477 BL Lacs, and 365 BCUs, and statistically compare their flux distributions with normal and log-normal distributions. The results indicate that the probability of not reject log-normal is 42.05% for the large sample, and there is still 2.05% probability of not reject normality, based on the joint of Kolmogorov-Smirnov, Shapiro-Wilk and Normality tests. We further find that the probability that BL Lacs conforms to the log-normal distribution is higher than that of FSRQs. Besides, after removing sources with less than 200 data points from this large sample, a sample of 549 blazars, which is still a large sample comparing to the previous studies, was obtained. Basing on dividing the light curves into segments every 20 points (or 40 points, or one year), we fitted the linear RMS-Flux relation of this three different sets, and found that the Pearson correlation coefficients are all close to 1 of the most blazars. This result indicates a strong linear correlation between the RMS and the flux of this 549 blazars. The log-normal distribution and linear RMS-Flux relation indicate that the variability of gamma-ray flux for most blazars is non-linear and multiplicative process.Comment: 13pages, 5figures, Accepted for publication in RA

Relativistic quantum transport theory of hadronic matter: the coupled nucleon, delta and pion system

We derive the relativistic quantum transport equation for the pion distribution function based on an effective Lagrangian of the QHD-II model. The closed time-path Green's function technique, the semi-classical, quasi-particle and Born approximation are employed in the derivation. Both the mean field and collision term are derived from the same Lagrangian and presented analytically. The dynamical equation for the pions is consistent with that for the nucleons and deltas which we developed before. Thus, we obtain a relativistic transport model which describes the hadronic matter with $N$, $\Delta$ and $\pi$ degrees of freedom simultaneously. Within this approach, we investigate the medium effects on the pion dispersion relation as well as the pion absorption and pion production channels in cold nuclear matter. In contrast to the results of the non-relativistic model, the pion dispersion relation becomes harder at low momenta and softer at high momenta as compared to the free one, which is mainly caused by the relativistic kinetics. The theoretically predicted free $\pi N \to \Delta$ cross section is in agreement with the experimental data. Medium effects on the $\pi N \to \Delta$ cross section and momentum-dependent $\Delta$-decay width are shown to be substantial.Comment: 66 pages, Latex, 12 PostScript figures included; replaced by the revised version, to appear in Phys. Rev.

CircNet: a database of circular RNAs derived from transcriptome sequencing data

Circular RNAs (circRNAs) represent a new type of regulatory noncoding RNA that only recently has been identified and cataloged. Emerging evidence indicates that circRNAs exert a new layer of post-transcriptional regulation of gene expression. In this study, we utilized transcriptome sequencing datasets to systematically identify the expression of circRNAs (including known and newly identified ones by our pipeline) in 464 RNA-seq samples, and then constructed the CircNet database (http://circnet.mbc.nctu.edu.tw/) that provides the following resources: (i) novel circRNAs, (ii) integrated miRNA-target networks, (iii) expression profiles of circRNA isoforms, (iv) genomic annotations of circRNA isoforms (e.g. 282 948 exon positions), and (v) sequences of circRNA isoforms. The CircNet database is to our knowledge the first public database that provides tissue-specific circRNA expression profiles and circRNA–miRNA-gene regulatory networks. It not only extends the most up to date catalog of circRNAs but also provides a thorough expression analysis of both previously reported and novel circRNAs. Furthermore, it generates an integrated regulatory network that illustrates the regulation between circRNAs, miRNAs and genes

Transcutaneous electrical acupoint stimulation for reducing cognitive dysfunction in lumbar spine surgery: A randomized, controlled trail

ObjectiveThis study aimed to evaluate the effect of perioperative transcutaneous electrical acupoint stimulation (TEAS) on postoperative cognitive dysfunction (POCD) in older patients with lumbar spine surgery.MethodsOlder patients (aged 60–80 years old) receiving lumbar spine surgery under general anesthesia were randomly divided into group A, 3-day intervention group; group B, 7-day intervention group; control group C, sham TEAS group, selected “Baihui” (GV 20) and “Dazhui” (GV 14) point was intervened once 30 min before operation with “HANS” transcutaneous electrical stimulation device, and then once a day after operation for 30 min each time. The primary outcome was the incidence of postoperative cognitive impairment assessed by the use of the Mini Mental Rating Scale (MMSE), patients developed POCD according to the Z score method. The secondary outcome was serum interleukin-6 (IL-6), tumor Necrosis factor α (TNF-α), neuron-specific enolase (NSE), and S100β protein levels.ResultsThree days after surgery, the incidence of POCD in groups A((22.4%)) and B ((18.3%)) were lower than those in group C ((42.9%)) (P &lt; 0.05). There was no significant difference between groups A and B (P &gt; 0.05). Seven days after surgery, the incidence of POCD in group B (18.3%) was lower than that in groups A (26.5%) and B (42.9%), and the comparison between groups B and C was statistically significant (P &lt; 0.05). On the 3rd and 7th days after surgery, the levels of IL-6, TNF-α, NSE, and S100β in the two TEAS groups were lower than those in the sham TEAS group (P &lt; 0.01), but higher than the preoperative levels in the three groups (P &lt; 0.01).ConclusionIt seems that Perioperative TEAS intervention could reduce the level of inflammatory factors IL-6, TNF-α in the blood of older patients with lumbar spine surgery, and reduce the incidence of POCD.Clinical trial registrationwww.chictr.org.cn, identifier ChiCTR2200063030