Fiber-optic parametric amplifier and oscillator based on intracavity parametric pump technique

Chinese Government Scholarship of Postgraduates' Oversea Study For Building High-Level UniversityA cost-effective fiber optical parametric amplifier (FOPA) based on the laser intracavity pump technique has been proposed and demonstrated experimentally. The parametric process is realized by inserting a 1 km highly nonlinear dispersion-shifted fiber (HNL-DSF) into a fiber ring-laser cavity that consists of a high-power erbium-doped fiber (EDF) amplifier and two highly reflective fiber Bragg gratings. Compared with the conventional parametric pump schemes, the proposed pumping technique is free from a tunable semiconductor laser as the pump source and also the pump phase modulation. When the oscillating power of 530 mW in the EDF laser cavity is achieved to pump the HNL-DSF, a peak parametric gain of 27.5 dB and a net gain over 45 nm are obtained. Moreover, a widely tunable fiber-optic parametric oscillator is further developed using the FOPA as a gain medium. (C) 2009 Optical Society of Americ

Uterine electromyography for discrimination of labor imminence in women with threatened preterm labor under tocolytic treatment

[EN] As one of the main aims of obstetrics is to be able to detect imminent delivery in patients with threatened preterm labor, the techniques currently used in clinical practice have serious limitations in this respect. The electrohysterogram (EHG) has now emerged as an alternative technique, providing relevant information about labor onset when recorded in controlled checkups without administration of tocolytic drugs. The studies published to date mainly focus on EHG-burst analysis and, to a lesser extent, on whole EHG window analysis. The study described here assessed the ability of EHG signals to discriminate imminent labor (The ability of EHG recordings to predict imminent labor (<7days) was analyzed in preterm threatened patients undergoing tocolytic therapies by means of EHG-burst and whole EHG window analysis. The non-linear features were found to have better performance than the temporal and spectral parameters in separating women who delivered in less than 7days from those who did not.Mas-Cabo, J.; Prats-Boluda, G.; Perales Marín, AJ.; Garcia-Casado, J.; Alberola Rubio, J.; Ye Lin, Y. (2019). Uterine electromyography for discrimination of labor imminence in women with threatened preterm labor under tocolytic treatment. Medical & Biological Engineering & Computing. 57:401-411. https://doi.org/10.1007/s11517-018-1888-yS40141157Aboy M, Cuesta-Frau D, Austin D, Micó-Tormos P (2007) Characterization of sample entropy in the context of biomedical signal analysis. Conf Proc IEEE Eng Med Biol Soc:5942–5945. https://doi.org/10.1109/IEMBS.2007.4353701Aboy M, Hornero R, Abásolo D, Álvarez D (2006) Interpretation of the Lempel-Ziv complexity measure in the context of biomedical signal analysis. IEEE Trans Biomed Eng 53:2282–2288. https://doi.org/10.1109/TBME.2006.883696Chkeir A, Fleury MJ, Karlsson B, Hassan M, Marque C (2013) Patterns of electrical activity synchronization in the pregnant rat uterus. Biomed 3:140–144. https://doi.org/10.1016/j.biomed.2013.04.007Crandon AJ (1979) Maternal anxiety and neonatal wellbeing. J Psychosom Res 23:113–115. https://doi.org/10.1016/0022-3999(79)90015-1Devedeux D, Marque C, Mansour S, Germain G, Duchêne J (1993) Uterine electromyography: a critical review. Am J Obstet Gynecol 169:1636–1653. https://doi.org/10.1016/0002-9378(93)90456-SFele-Žorž G, Kavšek G, Novak-Antolič Ž, Jager F (2008) A comparison of various linear and non-linear signal processing techniques to separate uterine EMG records of term and pre-term delivery groups. Med Biol Eng Comput 46:911–922. https://doi.org/10.1007/s11517-008-0350-yFergus P, Cheung P, Hussain A, al-Jumeily D, Dobbins C, Iram S (2013) Prediction of preterm deliveries from EHG signals using machine learning. PLoS One 8:e77154. https://doi.org/10.1371/journal.pone.0077154Garfield RE, Maner WL (2006) Biophysical methods of prediction and prevention of preterm labor: uterine electromyography and cervical light-induced fluorescence—new obstetrical diagnostic techniques. In: Preterm Birth pp 131–144Garfield RE, Maner WL (2007) Physiology and electrical activity of uterine contractions. Semin Cell Dev Biol 18:289–295. https://doi.org/10.1016/j.semcdb.2007.05.004Garfield RE, Maner WL, MacKay LB et al (2005) Comparing uterine electromyography activity of antepartum patients versus term labor patients. Am J Obstet Gynecol 193:23–29. https://doi.org/10.1016/j.ajog.2005.01.050Goldenberg RL, Culhane JF, Iams JD, Romero R (2008) Epidemiology and causes of preterm birth. Lancet 371:75–84. https://doi.org/10.1016/S0140-6736(08)60074-4American College of Obstetricians and Gynecologists and Committee on Practice Bulletins— Obstetrics (2012) Practice bulletin no. 127. Obstet Gynecol 119(6):1308–1317.Hadar E, Biron-Shental T, Gavish O, Raban O, Yogev Y (2015) A comparison between electrical uterine monitor, tocodynamometer and intra uterine pressure catheter for uterine activity in labor. J Matern Neonatal Med 28:1367–1374. https://doi.org/10.3109/14767058.2014.954539Hans P, Dewandre P, Brichant JF, Bonhomme V (2005) Comparative effects of ketamine on Bispectral Index and spectral entropy of the electroencephalogram under sevoflurane anaesthesia. Br J Anaesth 94:336–340. https://doi.org/10.1093/bja/aei047Hassan M, Terrien J, Marque C, Karlsson B (2011) Comparison between approximate entropy, correntropy and time reversibility: application to uterine electromyogram signals. Med Eng Phys 33:980–986. https://doi.org/10.1016/j.medengphy.2011.03.010Hassan M, Terrien J, Muszynski C et al (2013) Better pregnancy monitoring using nonlinear correlation analysis of external uterine electromyography. IEEE Trans Biomed Eng 60:1160–1166. https://doi.org/10.1109/TBME.2012.2229279Horoba K, Jezewski J, Matonia A, Wrobel J, Czabanski R, Jezewski M (2016) Early predicting a risk of preterm labour by analysis of antepartum electrohysterograhic signals. Biocybern Biomed Eng 36:574–583. https://doi.org/10.1016/j.bbe.2016.06.004Lawn JE, Wilczynska-Ketende K, Cousens SN (2006) Estimating the causes of 4 million neonatal deaths in the year 2000. Int J Epidemiol 35:706–718. https://doi.org/10.1093/ije/dyl043Lemancewicz A, Borowska M, Kuć P, Jasińska E, Laudański P, Laudański T, Oczeretko E (2016) Early diagnosis of threatened premature labor by electrohysterographic recordings—the use of digital signal processing. Biocybern Biomed Eng 36:302–307. https://doi.org/10.1016/j.bbe.2015.11.005M L WLM, LR C (2012) Noninvasive uterine electromyography for prediction of preterm delivery. Am J Obstet Gynecol 204:1–20. https://doi.org/10.1016/j.ajog.2010.09.024.NoninvasiveManer WL, Garfield RE (2007) Identification of human term and preterm labor using artificial neural networks on uterine electromyography data. Ann Biomed Eng 35:465–473. https://doi.org/10.1007/s10439-006-9248-8Maner WL, Garfield RE, Maul H, Olson G, Saade G (2003) Predicting term and preterm delivery with transabdominal uterine electromyography. Obstet Gynecol 101:1254–1260. https://doi.org/10.1016/S0029-7844(03)00341-7Marque C, Gondry J (1999) Use of the electrohysterogram signal for characterization of contractions during pregnancy. IEEE Trans Biomed Eng 46:1222–1229Maul H, Maner WL, Olson G, Saade GR, Garfield RE (2004) Non-invasive transabdominal uterine electromyography correlates with the strength of intrauterine pressure and is predictive of labor and delivery. J Matern Fetal Neonatal Med 15:297–301Mischi M, Chen C, Ignatenko T, de Lau H, Ding B, Oei SGG, Rabotti C (2018) Dedicated entropy measures for early assessment of pregnancy progression from single-channel electrohysterography. IEEE Trans Biomed Eng 65:875–884. https://doi.org/10.1109/TBME.2017.2723933Most O, Langer O, Kerner R, Ben David G, Calderon I (2008) Can myometrial electrical activity identify patients in preterm labor? Am J Obstet Gynecol 199:378. https://doi.org/10.1016/j.ajog.2008.08.003Petrou S (2005) The economic consequences of preterm birth during the first 10 years of life. BJOG 112:10–15. https://doi.org/10.1111/j.1471-0528.2005.00577.xRabotti C, Sammali F, Kuijsters N, et al (2015) Analysis of uterine activity in nonpregnant women by electrohysterography: a feasibility study. In: Proc Annu Int Conf IEEE Eng Med Biol Soc EMBS pp 5916–5919Schlembach D, Maner WL, Garfield RE, Maul H (2009) Monitoring the progress of pregnancy and labor using electromyography. Eur J Obstet Gynecol Reprod Biol 144:2–8. https://doi.org/10.1016/j.ejogrb.2009.02.016Sikora J, Matonia A, Czabański R et al (2011) Recognition of premature threatening labour symptoms from bioelectrical uterine activity signals. Arch Perinat Med 17:97–103Vinken MPGC, Rabotti C, Mischi M, van Laar JOEH, Oei SG (2010) Nifedipine-induced changes in the electrohysterogram of preterm contractions: feasibility in clinical practice. Obstet Gynecol Int 2010:325635. https://doi.org/10.1155/2010/325635Vrhovec J, Lebar AM (2012) An uterine electromyographic activity as a measure of labor progression. Appl EMG Clin Sport Med 243–268. doi: https://doi.org/10.5772/25526Vrhovec J, Macek-Lebar A, Rudel D (2007) Evaluating uterine electrohysterogram with entropy. 11th Mediterr Conf Med Biomed Eng Comput 144–147. https://doi.org/10.1007/978-3-540-73044-6_36Ye-Lin Y, Bueno-Barrachina JM, Prats-boluda G, Rodriguez de Sanabria R, Garcia-Casado J (2017) Wireless sensor node for non-invasive high precision electrocardiographic signal acquisition based on a multi-ring electrode. Measurement 97:195–202. https://doi.org/10.1016/J.MEASUREMENT.2016.11.009Ye-Lin Y, Garcia-Casado J, Prats-Boluda G, Alberola-Rubio J, Perales A (2014) Automatic identification of motion artifacts in EHG recording for robust analysis of uterine contractions. Comput Math Methods Med 2014:1–11. https://doi.org/10.1155/2014/470786Zhang XS, Roy RJ, Jensen EW (2001) EEG complexity as a measure of depth of anesthesia for patients. IEEE Trans Biomed Eng 48:1424–1433. https://doi.org/10.1109/10.96660

Salsolinol Facilitates Glutamatergic Transmission to Dopamine Neurons in the Posterior Ventral Tegmental Area of Rats

Although in vivo evidence indicates that salsolinol, the condensation product of acetaldehyde and dopamine, has properties that may contribute to alcohol abuse, the underlying mechanisms have not been fully elucidated. We have reported previously that salsolinol stimulates dopamine neurons in the posterior ventral tegmental area (p-VTA) partly by reducing inhibitory GABAergic transmission, and that ethanol increases glutamatergic transmission to VTA-dopamine neurons via the activation of dopamine D1 receptors (D1Rs). In this study, we tested the hypothesis that salsolinol stimulates dopamine neurons involving activation of D1Rs. By using whole-cell recordings on p-VTA-dopamine neurons in acute brain slices of rats, we found that salsolinol-induced increase in spike frequency of dopamine neurons was substantially attenuated by DL-2-amino-5-phosphono-valeric acid and 6, 7-dinitroquinoxaline-2, 3-dione, the antagonists of glutamatergic N-Methyl-D-aspartic acid and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors. Moreover, salsolinol increased the amplitude of evoked excitatory postsynaptic currents (EPSCs) and the frequency but not the amplitude of spontaneous EPSCs. Additionally, SKF83566, a D1R antagonist attenuated the salsolinol-induced facilitation of EPSCs and of spontaneous firing of dopamine neurons. Our data reveal that salsolinol enhances glutamatergic transmission onto dopamine neurons via activation of D1Rs at the glutamatergic afferents in dopamine neurons, which contributes to salsolinol's stimulating effect on p-VTA dopamine neurons. This appears to be a novel mechanism which contributes toward rewarding properties of salsolinol

Plasminogen Activator Inhibitor-1 4G/5G Gene Polymorphism and Coronary Artery Disease in the Chinese Han Population: A Meta-Analysis

Background: The polymorphism of plasminogen activator inhibitor-1 (PAI-1) 4G/5G gene has been indicated to be correlated with coronary artery disease (CAD) susceptibility, but study results are still debatable. Objective and Methods: The present meta-analysis was performed to investigate the association between PAI-1 4G/5G gene polymorphism and CAD in the Chinese Han population. A total of 879 CAD patients and 628 controls from eight separate studies were involved. The pooled odds ratio (OR) for the distribution of the 4G allele frequency of PAI-1 4G/5G gene and its corresponding 95 % confidence interval (CI) was assessed by the random effect model. Results: The distribution of the 4 G allele frequency was 0.61 for the CAD group and 0.51 for the control group. The association between PAI-1 4G/5G gene polymorphism and CAD in the Chinese Han population was significant under an allelic genetic model (OR = 1.70, 95 % CI = 1.18 to 2.44, P = 0.004). The heterogeneity test was also significant (P,0.0001). Meta-regression was performed to explore the heterogeneity source. Among the confounding factors, the heterogeneity could be explained by the publication year (P = 0.017), study region (P = 0.014), control group sample size (P = 0.011), total sample size (P = 0.011), and ratio of the case to the control group sample size (RR) (P = 0.019). In a stratified analysis by the total sample size, significantly increased risk was only detected in subgroup 2 under an allelic genetic model (OR = 1.93, 95% CI = 1.09 to 3.35, P = 0.02)

Synthesis of Tapered CdS Nanobelts and CdSe Nanowires with Good Optical Property by Hydrogen-Assisted Thermal Evaporation

The tapered CdS nanobelts and CdSe nanowires were prepared by hydrogen-assisted thermal evaporation method. Different supersaturation leads to two different kinds of 1D nanostructures. The PL measurements recorded from the as-prepared tapered CdS nanobelts and CdSe nanowires show only a bandgap emission with relatively narrow full-width half maximum, which means that they possess good optical property. The as-synthesized high-quality tapered CdS nanobelts and CdSe nanowires may be excellent building blocks for photonic devices

Analytic philosophy for biomedical research: the imperative of applying yesterday's timeless messages to today's impasses

The mantra that "the best way to predict the future is to invent it" (attributed to the computer scientist Alan Kay) exemplifies some of the expectations from the technical and innovative sides of biomedical research at present. However, for technical advancements to make real impacts both on patient health and genuine scientific understanding, quite a number of lingering challenges facing the entire spectrum from protein biology all the way to randomized controlled trials should start to be overcome. The proposal in this chapter is that philosophy is essential in this process. By reviewing select examples from the history of science and philosophy, disciplines which were indistinguishable until the mid-nineteenth century, I argue that progress toward the many impasses in biomedicine can be achieved by emphasizing theoretical work (in the true sense of the word 'theory') as a vital foundation for experimental biology. Furthermore, a philosophical biology program that could provide a framework for theoretical investigations is outlined

Observation of a ppb mass threshoud enhancement in \psi^\prime\to\pi^+\pi^-J/\psi(J/\psi\to\gamma p\bar{p}) decay

The decay channel $\psi^\prime\to\pi^+\pi^-J/\psi(J/\psi\to\gamma p\bar{p})$ is studied using a sample of $1.06\times 10^8$ $\psi^\prime$ events collected by the BESIII experiment at BEPCII. A strong enhancement at threshold is observed in the $p\bar{p}$ invariant mass spectrum. The enhancement can be fit with an $S$-wave Breit-Wigner resonance function with a resulting peak mass of $M=1861^{+6}_{-13} {\rm (stat)}^{+7}_{-26} {\rm (syst)} {\rm MeV/}c^2$ and a narrow width that is $\Gamma<38 {\rm MeV/}c^2$ at the 90% confidence level. These results are consistent with published BESII results. These mass and width values do not match with those of any known meson resonance.Comment: 5 pages, 3 figures, submitted to Chinese Physics

IgCaller for reconstructing immunoglobulin gene rearrangements and oncogenic translocations from whole-genome sequencing in lymphoid neoplasms

Immunoglobulin (Ig) gene rearrangements and oncogenic translocations are routinely assessed during the characterization of B cell neoplasms and stratification of patients with distinct clinical and biological features, with the assessment done using Sanger sequencing, targeted next-generation sequencing, or fluorescence in situ hybridization (FISH). Currently, a complete Ig characterization cannot be extracted from whole-genome sequencing (WGS) data due to the inherent complexity of the Ig loci. Here, we introduce IgCaller, an algorithm designed to fully characterize Ig gene rearrangements and oncogenic translocations from short-read WGS data. Using a cohort of 404 patients comprising different subtypes of B cell neoplasms, we demonstrate that IgCaller identifies both heavy and light chain rearrangements to provide additional information on their functionality, somatic mutational status, class switch recombination, and oncogenic Ig translocations. Our data thus support IgCaller to be a reliable alternative to Sanger sequencing and FISH for studying the genetic properties of the Ig loci.We are indebted to the Genomics Core Facility of the Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) for the technical support, to R. Siebert and D. Huebschmann for sharing the CSR regions, and to K. Stamatopoulos, E. Vlachonikola and F. Psomopoulos for their helpful comments on the manuscript. We thank R. Eils, P. Lichter, C. von Kalle, S. Fröhling, H. Glimm, M. Zapatka, S. Wolf, K. Beck, and J. Kirchhof for infrastructure and pipeline development within DKFZ-HIPO and NCT POP. This study was supported by the Instituto de Salud Carlos III and the European Regional Development Fund “Una manera de hacer Europa” (PMP15/00007 to E.C.), the “la Caixa” Foundation (CLLEvolution-LCF/PR/HR17/52150017, Health Research 2017 Program HR17-00221 to E.C.), the National Institute of Health “Molecular Diagnosis, Prognosis, and Therapeutic Targets in Mantle Cell Lymphoma” (P01CA229100 to E.C.), and CERCA Programme/Generalitat de Catalunya. F.N. is supported by a pre-doctoral fellowship of the Ministerio de Economía y Competitividad (BES-2016-076372). F.M. is supported by the Memorial Sloan Kettering Cancer Center NCI Core Grant (P30 CA 008748). E.C. is an Academia Researcher of the “Institució Catalana de Recerca i Estudis Avançats” (ICREA) of the Generalitat de Catalunya. This work was partially developed at the Centre Esther Koplowitz (CEK, Barcelona, Spain).Peer ReviewedPostprint (published version