Load-Aware Traffic Control in Software-Defined Enterprise Wireless Local Area Networks

With the growing popularity of Bring Your Own Device (BYOD), modern enterprise Wireless Local Area Networks (WLANs) deployments always consist of multiple Access Points (APs) to meet the fast-increasing demand for wireless access. In order to avoid network congestion which leads to issues such as suboptimal Quality of Service (QoS) and degraded user Quality of Experience (QoE), intelligent network traffic control is needed. Software Defined Networking (SDN) is an emerging architecture and intensively discussed as one of the most promising technologies to simplify network management and service development. In the SDN architecture, network management is directly programmable because it is decoupled from forwarding layer. Leveraging SDN to the existing enterprise WLANs framework, network services can be flexibly implemented to support intelligent network traffic control. This thesis studies the architecture of software-defined enterprise WLANs and how to improve network traffic control from a client-side and an AP-side perspective. By extending an existing software-defined enterprise WLANs framework, two adaptive algorithms are proposed to provide client-based mobility management and load balancing. Custom protocol messages and AP load metric are introduced to enable the proposed adaptive algorithms. Moreover, a software-defined enterprise WLAN system is designed and implemented on a testbed. A load-aware automatic channel switching algorithm and a QoS-aware bandwidth control algorithm are proposed to achieve AP-based network traffic control. Experimental results from the testbed show that the designed system and algorithms significantly improve the performance of traffic control in enterprise WLANs in terms of network throughput, packet loss rate, transmission delay and jitter

Effects of K-877, a novel selective PPARα modulator, on small intestine contribute to the amelioration of hyperlipidemia in low-density lipoprotein receptor knockout mice

Peroxisome proliferator-activated receptor α (PPARα) is a well-known therapeutic target for treating hyperlipidemia. K-877 is a novel selective PPARα modulator (SPPARMα) that enhances PPARα transcriptional activity with high selectivity and potency, resulting in reduced plasma lipid levels. This study aimed to evaluate the effects of K-877 on hyperlipidemia in low-density lipoprotein receptor knockout (Ldlr−/−) mice, a mouse model of atherosclerosis. We revealed that K-877 administration significantly decreased plasma triglyceride (TG) and total cholesterol (TC) levels and increased plasma high-density lipoprotein cholesterol (HDL-C) levels in Ldlr−/− mice. K-877 administration to Ldlr−/− mice efficiently increased the gene expression of PPARα and its target genes related to fatty acid oxidation in the liver and small intestine. The same treatment significantly increased ATP-binding cassette a1 gene expression in the liver and small intestine and reduced Niemann Pick C1-like 1 gene expression in the small intestine, suggesting that K-877 administration induced HDL-C production in the liver and small intestine and reduced cholesterol absorption in the small intestine. In conclusion, K-877 administration had pronounced effects on the liver and small intestine in Ldlr−/− mice. K-877 is an attractive PPARα-modulating drug for treating hyperlipidemia that works equally well in both the liver and small intestine

Octacosanol and policosanol prevent high-fat diet-induced obesity and metabolic disorders by activating brown adipose tissue and improving liver metabolism

Brown adipose tissue (BAT) is an attractive therapeutic target for treating obesity and metabolic diseases. Octacosanol is the main component of policosanol, a mixture of very long chain aliphatic alcohols obtained from plants. The current study aimed to investigate the effect of octacosanol and policosanol on high-fat diet (HFD)-induced obesity. Mice were fed on chow, or HFD, with or without octacosanol or policosanol treatment for four weeks. HFD-fed mice showed significantly higher body weight and body fat compared with chow-fed mice. However, mice fed on HFD treated with octacosanol or policosanol (HFDo/p) showed lower body weight gain, body fat gain, insulin resistance and hepatic lipid content. Lower body fat gain after octacosanol or policosanol was associated with increased BAT activity, reduced expression of genes involved in lipogenesis and cholesterol uptake in the liver, and amelioration of white adipose tissue (WAT) inflammation. Moreover, octacosanol and policosanol significantly increased the expression of Ffar4, a gene encoding polyunsaturated fatty acid receptor, which activates BAT thermogenesis. Together, these results suggest that octacosanol and policosanol ameliorate diet-induced obesity and metabolic disorders by increasing BAT activity and improving hepatic lipid metabolism. Thus, these lipids represent promising therapeutic targets for the prevention and treatment of obesity and obesity-related metabolic disorders

An adaptive mobility manager for Software-Defined Enterprise WLANs

In current Enterprise WLANs (EWLANs), mobility management remains a challenging issue due to the rapid growth of mobile user number and varying traffic load. With conventional mobility managers, client handoff are based on signal strength of APs which often leads to imbalanced traffic load among APs. Software Defined Networking (SDN) has gained increasing popularity as a novel network architecture. Leveraging SDN to existing EWLANs, mobility management can be improved efficiently. In this paper, we present an adaptive mobility manager which utilises dynamic hysteresis of AP load to make handoff decisions. With proposed solution, network throughput is improved significantly compared to the conventional handoff algorithm

An adaptive load balancing application for software-defined enterprise WLANs

In current Enterprise WLANs (EWLANs), traffic load on access points (APs) is often unevenly distributed as wireless stations (WS) independently select the AP with best signal strength to associate with, which leads to issues such as sub-optimal network throughput and degradation of user quality of experience (QoE). Existing load balancing solutions based on the received signal strength indicator (RSSI) continue to exhibit inefficiencies. Software Defined Networking (SDN) promises to provide flexibility and programmability for network management. Leveraging SDN to existing EWLANs, the efficiency of load balancing can be improved significantly. This paper propose an adaptive load balancing solution which proactively balance network traffic based on AP load and RSSI. Experiment results show that both packet loss rate and network throughput are improved significantly compared to the conventional load balancing algorithm

Fabrication of Monodisperse Flower-Like Coordination Polymers (CP) Microparticles by Spray Technique

In this manuscript, we have developed an efficient spraying method to successfully fabricate a series of flower-like coordination polymers (CP) microparticles, including Co/BDC (1,4-benzenedicarboxylate) metal organic frameworks (MOF) and infinite coordination polymers (ICP) microparticles, as well as Ni-Co/BDC MOF and Zn/DOBDC (2,5-dioxido-1,4-benzenedicarboxylate) MOF. The spraying method has shown high efficiency and universality in synthesizing the flower-like CP. The crystalline structure can be adjusted by varying the solvent composition in the spraying process. SEM observation demonstrated the MOF and ICP microparticles possess the similar flower-like structure, which is composed of nanoflakes with smooth surface, and the flower-like microparticles could be monodisperse with as low as 5% polydispersity. Moreover, the fabrication of the flower-like CP microparticles by spraying has a wide operation window, because there is no need to precisely control the experiment conditions, like solvents, concentration, and spray order. Due to the practicality of spray technique, this work would pave the way for the manufacture of the flower-like materials and have great potential in applications of catalysis, sensor, energy storage, and so on

Enterohepatic Transcription Factor CREB3L3 Protects Atherosclerosis via SREBP Competitive Inhibition

動脈硬化発症を制御する転写因子の相互作用を発見. 京都大学プレスリリース. 2020-12-09.Background and Aims: cAMP responsive element-binding protein 3 like 3 (CREB3L3) is a membrane-bound transcription factor involved in the maintenance of lipid metabolism in the liver and small intestine. CREB3L3 controls hepatic triglyceride and glucose metabolism by activating plasma fibroblast growth factor 21 (FGF21) and lipoprotein lipase. In this study, we intended to clarify its effect on atherosclerosis. Methods: CREB3L3-deficifient, liver-specific CREB3L3 knockout, intestine-specific CREB3L3 knockout, both liver- and intestine-specific CREB3L3 knockout, and liver CREB3L3 transgenic mice were crossed with LDLR−/− mice. These mice were fed with a Western diet to develop atherosclerosis. Results: CREB3L3 ablation in LDLR−/− mice exacerbated hyperlipidemia with accumulation of remnant APOB-containing lipoprotein. This led to the development of enhanced aortic atheroma formation, the extent of which was additive between liver- and intestine-specific deletion. Conversely, hepatic nuclear CREB3L3 overexpression markedly suppressed atherosclerosis with amelioration of hyperlipidemia. CREB3L3 directly upregulates anti-atherogenic FGF21 and APOA4. In contrast, it antagonizes hepatic sterol regulatory element-binding protein (SREBP)-mediated lipogenic and cholesterogenic genes, and regulates intestinal liver X receptor-regulated genes involved in the transport of cholesterol. CREB3L3 deficiency results in the accumulation of nuclear SREBP proteins. Because both transcriptional factors share the cleavage system for nuclear transactivation, full-length CREB3L3 and SREBPs in the endoplasmic reticulum (ER) functionally inhibit each other. CREB3L3 promotes the formation of the SREBP-insulin induced gene 1 (SREBP-INSIG1) complex to suppress SREBPs for ER-Golgi transport, resulting in ER retention and inhibition of proteolytic activation at the Golgi, and vice versa. Conclusions: CREB3L3 has multi-potent protective effects against atherosclerosis owing to new mechanistic interaction between CREB3L3 and SREBPs under atherogenic conditions

The Peroxisome Proliferator-Activated Receptor α (PPARα) Agonist Pemafibrate Protects against Diet-Induced Obesity in Mice

Peroxisome proliferator-activated receptor α (PPARα) is a therapeutic target for hyperlipidemia. Pemafibrate (K-877) is a new selective PPARα modulator activating PPARα transcriptional activity. To determine the effects of pemafibrate on diet-induced obesity, wild-type mice were fed a high-fat diet (HFD) containing pemafibrate for 12 weeks. Like fenofibrate, pemafibrate significantly suppressed HFD-induced body weight gain; decreased plasma glucose, insulin and triglyceride (TG) levels; and increased plasma fibroblast growth factor 21 (FGF21). However, compared to the dose of fenofibrate, a relatively low dose of pemafibrate showed these effects. Pemafibrate activated PPARα transcriptional activity in the liver, increasing both hepatic expression and plasma levels of FGF21. Additionally, pemafibrate increased the expression of genes involved in thermogenesis and fatty acid oxidation, including Ucp1, Cidea and Cpt1b in inguinal adipose tissue (iWAT) and the mitochondrial marker Elovl3 in brown adipose tissue (BAT). Therefore, pemafibrate activates thermogenesis in iWAT and BAT by increasing plasma levels of FGF21. Additionally, pemafibrate induced the expression of Atgl and Hsl in epididymal white adipose tissue, leading to the activation of lipolysis. Taken together, pemafibrate suppresses diet-induced obesity in mice and improves their obesity-related metabolic abnormalities. We propose that pemafibrate may be useful for the suppression and improvement of obesity-induced metabolic abnormalities

Highly Transparent, Conductive, and Bendable Ag Nanowire Electrodes with Enhanced Mechanical Stability Based on Polyelectrolyte Adhesive Layer

In this paper, a highly transparent, conductive, and bendable Ag nanowire (AgNW)-based electrode with excellent mechanical stability was prepared through the introduction of an adhesive polyelectrolyte multilayer between AgNW networks and a polyethylene terephthalate (PET) substrate. The introduction of the adhesive layer was performed based on a peel–assembly–transfer procedure, and the adhesive polyelectrolyte greatly improved the mechanical stability of the AgNW transparent conductive films (TCFs) without obviously attenuating the morphology and optoelectrical properties of the AgNW networks. The as-prepared AgNW TCFs simultaneously possess high optical transparency, good conductivity, excellent flexibility, and remarkable mechanical stability. It is believed that the proposed strategy would pave a new way for preparing flexible transparent electrodes with a long-term stability, which is significant in the development and practical applications of flexible transparent electronic devices operated in severe environments