1,202 research outputs found

    Statistical mechanical evaluation of spread spectrum watermarking model with image restoration

    Get PDF
    In cases in which an original image is blind, a decoding method where both the image and the messages can be estimated simultaneously is desirable. We propose a spread spectrum watermarking model with image restoration based on Bayes estimation. We therefore need to assume some prior probabilities. The probability for estimating the messages is given by the uniform distribution, and the ones for the image are given by the infinite range model and 2D Ising model. Any attacks from unauthorized users can be represented by channel models. We can obtain the estimated messages and image by maximizing the posterior probability. We analyzed the performance of the proposed method by the replica method in the case of the infinite range model. We first calculated the theoretical values of the bit error rate from obtained saddle point equations and then verified them by computer simulations. For this purpose, we assumed that the image is binary and is generated from a given prior probability. We also assume that attacks can be represented by the Gaussian channel. The computer simulation retults agreed with the theoretical values. In the case of prior probability given by the 2D Ising model, in which each pixel is statically connected with four-neighbors, we evaluated the decoding performance by computer simulations, since the replica theory could not be applied. Results using the 2D Ising model showed that the proposed method with image restoration is as effective as the infinite range model for decoding messages. We compared the performances in a case in which the image was blind and one in which it was informed. The difference between these cases was small as long as the embedding and attack rates were small. This demonstrates that the proposed method with simultaneous estimation is effective as a watermarking decoder

    Association of Glycative Stress With Motor and Muscle Function

    Get PDF
    Glycative stress is a type of biological stress caused by non-enzymatic glycation reactions, which include advanced glycation end product (AGE) formation, AGE accumulation, glycation-driven dysfunction of proteins and cellular signaling, inflammation, oxidation, and tissue damage. Increased glycative stress derived from hyperglycemia and lifestyle disorders is a risk factor in metabolic and age-related diseases, such as type 2 diabetes, cardiovascular disease, cancer, Alzheimer’s disease, osteoporosis, and dementia. Studies have shown that AGE accumulation is correlated with the age-related loss of muscle mass and power output, also called sarcopenia. Mechanistically, dysfunctions of contractile proteins, myogenic capacity, and protein turnover can cause glycative stress-induced skeletal muscle dysfunction. Because the skeletal muscle is the largest metabolic organ in the body, maintaining skeletal muscle health is essential for whole-body health. Increasing awareness and understanding of glycative stress in the skeletal muscle in this review will contribute to the maintenance of better skeletal muscle function

    LPS-Toll-Like Receptor-Mediated Signaling on Expression of Protein S and C4b-Binding Protein in the Liver

    Get PDF
    Protein S (PS), mainly synthesized in hepatocytes and endothelial cells, plays a critical role as a cofactor of anticoagulant activated protein C (APC). PS activity is regulated by C4b-binding protein (C4BP), structurally composed of seven α-chains (C4BPα) and a β-chain (C4BPβ). In this paper, based primarily on our previous studies, we review the lipopolysaccharide (LPS)-induced signaling which affects expression of PS and C4BP in the liver. Our in vivo studies in rats showed that after LPS injection, plasma PS levels are significantly decreased, whereas plasma C4BP levels first are transiently decreased after 2 to 12 hours and then significantly increased after 24 hours. LPS decreases PS antigen and mRNA levels in both hepatocytes and sinusoidal endothelial cells (SECs), and decreases C4BP antigen and both C4BPα and C4BPβ mRNA levels in hepatocytes. Antirat CD14 and antirat Toll-like receptor (TLR)-4 antibodies inhibited LPS-induced NFκB activation in both hepatocytes and SECs. Furthermore, inhibitors of NFκB and MEK recovered the LPS-induced decreased expression of PS in both cell types and the LPS-induced decreased expression of C4BP in hepatocytes. These data suggest that the LPS-induced decrease in PS expression in hepatocytes and SECs and LPS-induced decrease in C4BP expression in hepatocytes are mediated by MEK/ERK signaling and NFκB activation and that membrane-bound CD14 and TLR-4 are involved in this mechanism

    An Investigation of Vocal Learning Propensity in Zebra Finch (Taeniopygia guttata)

    Full text link
    The investigator attempted to predict the vocal learning propensity from either family pedigree or early vocal babbling (subsong). Pedigree trees suggest the possibility that vocal learning ability may depend on family. We failed to predict vocal learning propensity from subsong, but suggested that subsong may influence vocal learning outcome

    Altered autonomic nervous system activity as a potential etiological factor of premenstrual syndrome and premenstrual dysphoric disorder

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Premenstrual syndrome (PMS) encompasses a wide variety of cyclic and recurrent physical, emotional, and behavioral symptoms occurring during the late luteal phase of the menstrual cycle and abating shortly following the beginning of menses. Although PMS is widely recognized, its etiopathogenesis is not yet understood. The present study investigates whether the activity of the autonomic nervous system, which plays a vital role in orchestrating physiological homeostasis within the human body, is altered during the menstrual cycle of women with different degrees of premenstrual symptomatology.</p> <p>Methods</p> <p>Sixty-two women in their 20s to 40s with regular menstrual cycles participated in this study. All subjects were examined during the follicular and late luteal phases. Cycle phase was determined by the onset of menstruation and oral temperature and was verified by concentrations of ovarian hormones, estrone, and pregnanediol in a urine sample taken early in the morning. Autonomic nervous system activity was assessed by means of heart-rate variability (HRV) power spectral analysis during supine rest. The Menstrual Distress Questionnaire was used to evaluate physical, emotional, and behavioral symptoms accompanying the menstrual cycle of the subjects. The subjects were categorized in three groups, Control, PMS, and premenstrual dysphoric disorder (PMDD) groups, depending on the severity of premenstrual symptomatology.</p> <p>Results</p> <p>No intramenstrual cycle difference in any of the parameters of HRV was found in the Control group, which had no or a small increase in premenstrual symptoms. In contrast, Total power and high frequency power, which reflect overall autonomic and parasympathetic nerve activity, respectively, significantly decreased in the late luteal phase from the follicular phase in the PMS group. As for the PMDD group, which had more severe symptoms premenstrually, heart-rate fluctuation as well as all components of the power spectrum of HRV were markedly decreased regardless of the menstrual cycle compared to those of the other two groups.</p> <p>Conclusion</p> <p>Several theories have been proposed to explain the underlying mechanisms of PMS with its complex web of bio-psycho-social factors. Although causes and consequences continue to elude, the present study provides intriguing and novel findings that the altered functioning of the autonomic nervous system in the late luteal phase could be associated with diverse psychosomatic and behavioral symptoms appearing premenstrually. In addition, when symptoms become more severe (as seen in women with PMDD), the sympathovagal function might be more depressed regardless of the menstrual cycle.</p

    Diffusion analysis with triexponential function in liver cirrhosis

    Get PDF
    13301甲第4213号博士(保健学)金沢大学博士論文要旨Abstract 要約Outline 以下に掲載:Journal of Magnetic Resonance Imaging 38(1) pp.148-153 2013. International Society for Magnetic Resonance in Medicine. 共著者:Tatsuya Hayashi, Tosiaki Miyati, Junji Takahashi, Kei Fukuzawa, Hironobu Sakai, Masakatsu Tano, Satoshi Saito

    心筋細胞の拍動同期現象に関する数理モデル

    Get PDF
    学位の種別: 課程博士審査委員会委員 : (主査)東京大学教授 時弘 哲治, 東京大学教授 稲葉 寿, 東京大学教授 吉田 朋広, 東京大学教授 新井 仁之, 東京大学教授 WILLOX RALPH, お茶の水女子大学准教授 群 宏University of Tokyo(東京大学
    corecore