FREE INTERACTOR MATRIX METHOD FOR CONTROL PERFORMANCE ASSESSMENT OF MULTI-VARIATE SYSTEMS

In this paper, an alternative method for the assessment of multi-vitiate control loop performance with consider twocircumstances. First, known time delays between each pair of inputs and outputs, and second, without relying on any a priori knowledge about the process model or timedelays. The performance of the control loop is calculated from data driven autoregressive moving average (ARMA) and prediction error model. It is clear that the limited data in scalar measure used for performance assessment results tends to steady-state as time tends to infinity, but large number of samples gives risen in scalar measures and tends to infinity as time samples tends to infinity and therefore it becomes difficult to calculate the performance index. In this paper, the later problem is solved by considering initial part of scalar measures with steady value for next-to-next time samples to calculate the control-loop performance index which would be utilized to decide healthy working of the control loop. Simulation example is included to show the performance index of multi-variate control loop

13-Series resolvins mediate the leukocyte-platelet actions of atorvastatin and pravastatin in inflammatory arthritis

This work was supported by funding from the European Research Council under the European Union’s Horizon 2020 research and innovation program (Grant 677542), a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society (Grant 107613/Z/15/Z), and the Barts Charity (Grant MGU0343). This work was also funded, in part, by Medical Research Council Advance Course Masters (Grant MR/J015741/1). The authors declare no conflicts of interest

O-C Study of 545 Lunar Occultations from 13 Double Stars

International audienceIn this article, we have studied the reports of lunar occultations by this project observation's teams (named APTO) in comparison with other observations of the objects. Thirteen binary stars were selected for this study. All the previous observations of these stars were also collected. Finally, an analysis of O-C of all reports were performed

Observational and Theoretical Studies of 27 δ Scuti Stars with Investigation of the Period–luminosity Relation

The multi-color CCD photometric study of 27 δ Scuti stars is presented. By using approximately three years of photometric observations, we obtained the times of maxima and magnitude changes during the observation time interval for each star. The ephemerides of our δ Scuti stars were calculated based on the Markov Chain Monte Carlo (MCMC) method using the observed times of maxima and the period of the stars’ oscillations. We used the Gaia EDR3 parallaxes to calculate the luminosities and also the absolute magnitudes of these δ Scuti stars. The fundamental physical parameters of all the stars in our sample such as masses and radii were estimated. We determined the pulsation modes of the stars based on the pulsation constants. Moreover, the period–luminosity (P–L) relation of δ Scuti stars was investigated and discussed. Then, by using a machine learning classification, new P–L relations for fundamental and overtone modes are presented. © 2021. The Astronomical Society of the Pacific. All rights reserved.This work was supported by the Ministry of Science and Education, FEUZ-2020-0030. Popov A.A. acknowledges support by the Ministry of Science and Higher Education of the Russian Federation under the grant 075-15-2020-780. The machine learning section of this study has been performed according to the scientific agreement with Raderon Lab Inc. (https:// raderonlab.ca) with contract number R\AST\2021\1001. The authors would like to appreciate Dr. Fahri Alicavus and Dr. Somayeh Khakpash for their contributions to the research. Also, great thanks to Paul D. Maley for editing the text. The authors would like to thank the reviewer for comments and suggestions that helped to improve the paper

Regional genome transcriptional response of adult mouse brain to hypoxia

<p>Abstract</p> <p>Background</p> <p>Since normal brain function depends upon continuous oxygen delivery and short periods of hypoxia can precondition the brain against subsequent ischemia, this study examined the effects of brief hypoxia on the whole genome transcriptional response in adult mouse brain.</p> <p>Result</p> <p>Pronounced changes of gene expression occurred after 3 hours of hypoxia (8% O₂) and after 1 hour of re-oxygenation in all brain regions. The hypoxia-responsive genes were predominantly up-regulated in hindbrain and predominantly down-regulated in forebrain - possibly to support hindbrain survival functions at the expense of forebrain cognitive functions. The up-regulated genes had a significant role in cell survival and involved both shared and unshared signaling pathways among different brain regions. Up-regulation of transcriptional signaling including hypoxia inducible factor, insulin growth factor (IGF), the vitamin D3 receptor/retinoid X nuclear receptor, and glucocorticoid signaling was common to many brain regions. However, many of the hypoxia-regulated target genes were specific for one or a few brain regions. Cerebellum, for example, had 1241 transcripts regulated by hypoxia only in cerebellum but not in hippocampus; and, 642 (54%) had at least one hepatic nuclear receptor 4A (HNF4A) binding site and 381 had at least two HNF4A binding sites in their promoters. The data point to HNF4A as a major hypoxia-responsive transcription factor in cerebellum in addition to its known role in regulating erythropoietin transcription. The genes unique to hindbrain may play critical roles in survival during hypoxia.</p> <p>Conclusion</p> <p>Differences of forebrain and hindbrain hypoxia-responsive genes may relate to suppression of forebrain cognitive functions and activation of hindbrain survival functions, which may coordinately mediate the neuroprotection afforded by hypoxia preconditioning.</p

Differences in Muscle Protein Synthesis and Anabolic Signaling in the Postabsorptive State and in Response to Food in 65–80 Year Old Men and Women

Women have less muscle than men but lose it more slowly during aging. To discover potential underlying mechanism(s) for this we evaluated the muscle protein synthesis process in postabsorptive conditions and during feeding in twenty-nine 65–80 year old men (n = 13) and women (n = 16). We discovered that the basal concentration of phosphorylated eEF2Thr56 was ∼40% less (P<0.05) and the basal rate of MPS was ∼30% greater (P = 0.02) in women than in men; the basal concentrations of muscle phosphorylated AktThr308, p70s6kThr389, eIF4ESer209, and eIF4E-BP1Thr37/46 were not different between the sexes. Feeding increased (P<0.05) AktThr308 and p70s6kThr389 phosphorylation to the same extent in men and women but increased (P<0.05) the phosphorylation of eIF4ESer209 and eIF4E-BP1Thr37/46 in men only. Accordingly, feeding increased MPS in men (P<0.01) but not in women. The postabsorptive muscle mRNA concentrations for myoD and myostatin were not different between sexes; feeding doubled myoD mRNA (P<0.05) and halved that of myostatin (P<0.05) in both sexes. Thus, there is sexual dimorphism in MPS and its control in older adults; a greater basal rate of MPS, operating over most of the day may partially explain the slower loss of muscle in older women

Differences in Muscle Protein Synthesis and Anabolic Signaling in the Postabsorptive State and in Response to Food in 65–80 Year Old Men and Women

Women have less muscle than men but lose it more slowly during aging. To discover potential underlying mechanism(s) for this we evaluated the muscle protein synthesis process in postabsorptive conditions and during feeding in twenty-nine 65–80 year old men (n = 13) and women (n = 16). We discovered that the basal concentration of phosphorylated eEF2Thr56 was ∼40% less (P<0.05) and the basal rate of MPS was ∼30% greater (P = 0.02) in women than in men; the basal concentrations of muscle phosphorylated AktThr308, p70s6kThr389, eIF4ESer209, and eIF4E-BP1Thr37/46 were not different between the sexes. Feeding increased (P<0.05) AktThr308 and p70s6kThr389 phosphorylation to the same extent in men and women but increased (P<0.05) the phosphorylation of eIF4ESer209 and eIF4E-BP1Thr37/46 in men only. Accordingly, feeding increased MPS in men (P<0.01) but not in women. The postabsorptive muscle mRNA concentrations for myoD and myostatin were not different between sexes; feeding doubled myoD mRNA (P<0.05) and halved that of myostatin (P<0.05) in both sexes. Thus, there is sexual dimorphism in MPS and its control in older adults; a greater basal rate of MPS, operating over most of the day may partially explain the slower loss of muscle in older women