[ZHANG Wei-hua's clinical experience of Zhenjing Anshen method in treatment of insomnia].

The paper summarizes professor ZHANG Wei-hua's clinical experience in treatment of insomnia with Zhenjing Anshen (calming-down the spirit) method. It is believed that insomnia results from the unstable spirit in pathogenesis of TCM. The basic therapeutic principle is regulating the spirit, in which, stabilizing the primary spirit and tranquilizing the heart spirit are emphasized. Main acupoints are Baihui (GV 20), Sishencong (EX-HN 1) and Yintang (GV 24+) to stabilize the primary spirit, located on the head; and Shenmen (HT 7) located on the wrist to calm-down the heart spirit, as well as Sanyinjiao (SP 6) and Yongquan (KI 1) in the lower extremities to benefit yin and balance yang, and then to house the spirit eventually. The needles are inserted in different depths and to various directions. The external application of herbal plaster is combined at Yongquan (KI 1) and the supplementary acupoints are selected in terms of syndrome differentiation. This therapy is simple in acupoint selection and very effective in treatment of insomnia.

[Professor ZHANG Wei-hua's clinical experience in chronic somatic pain treated with zhidong needling techniques].

The paper summarizes professor ZHANG Wei-hua's clinical experience for the treatment of chronic somatic pain with zhidong needling techniques. In terms of the characteristics of chronic somatic pain, professor ZHANG has integrated zhidong needling with acupuncture kinetic therapy. The satisfactory therapeutic effects are obtained by selecting the painful points and regions as the treatment sites and the specific techniques of zhidong needling depending on the size of affected area, the depth of illness, the size and shape of the cord-like muscle, etc. Five techniques of zhidong needling are used accordingly with twirling, pulling, lifting and thrusting, surrounding needling methods involved, as well as with the manipulation speed, direction and frequency considered.

MiR-195 alleviates oxygen-glucose deprivation/reperfusion-induced cell apoptosis via inhibition of IKKα-mediated NF-κB pathway.

OBJECTIVES: Increasing evidence confirmed that miRNA plays a critical role in the occurrence and development of ischemic stroke. Here, the aim of this study was to examine the function and mechanisms of miR-195 in vascular endothelial cell apoptosis induced by oxygen-glucose deprivation (OGD). METHODS: This study intended to use OGD to simulate ischemia in vitro. The mRNA expression of miR-195, IKKα and NF-κB in human umbilical vein endothelial cells (HUVECs) were detected by RT-qPCR. The proliferation and apoptosis ability of HUVECs were evaluated using MTT assay, colony formation assay and flow cytometry, respectively. Western blot was applied to examine related protein expression. The interaction between miR-195 and IKKα was verified by dual-luciferase reporter gene assay. RESULTS: OGD significantly inhibited cell viability and induced cell apoptosis in HUVECs. Meanwhile, OGD treatment notably decreased the expression of miR-195, as well as enhanced NF-κB expression. Moreover, miR-195 directly interacted with IKKα and suppressed its expression. Mechanically, overexpression of miR-195 exhibited pro-proliferation and anti-apoptotic effect on HUVECs treated with OGD through targeting IKKα-mediated NF-κB pathway. At the molecular level, through suppressing IKKα/NF-κB pathway, miR-195 inhibited the expression of pro-apoptotic protein Bax and active caspase-3, but increased the expression of anti-apoptotic Bcl-2 in HUVECs. CONCLUSIONS: Our finding uncovers the protective effect of miR-195 on the biological behavior of HUVECs via suppression of the NF-κB pathway induced by IKKα, which may provide a new potential strategy for ischemic stroke clinical treatment.

OOCHIP: Compartmentalized Microfluidic Perfusion System with Porous Barriers for Enhanced Cell-Cell Crosstalk in Organ-on-a-Chip.

Improved in vitro models of human organs for predicting drug efficacy, interactions, and disease modelling are crucially needed to minimize the use of animal models, which inevitably display significant differences from the human disease state and metabolism. Inside the body, cells are organized either in direct contact or in close proximity to other cell types in a tightly controlled architecture that regulates tissue function. To emulate this cellular interface in vitro, an advanced cell culture system is required. In this paper, we describe a set of compartmentalized silicon-based microfluidic chips that enable co-culturing several types of cells in close proximity with enhanced cell-cell interaction. In vivo-like fluid flow into and/or from each compartment, as well as between adjacent compartments, is maintained by micro-engineered porous barriers. This porous structure provides a tool for mimicking the paracrine exchange between cells in the human body. As a demonstrating example, the microfluidic system was tested by culturing human adipose tissue that is infiltrated with immune cells to study the role if the interplay between the two cells in the context of type 2 diabetes. However, the system provides a platform technology for mimicking the structure and function of single- and multi-organ models, which could significantly narrow the gap between in vivo and in vitro conditions.

In-situ monitoring of phenol in surface waters by diffusive gradients in thin films technique based on the nanocomposites of zero-valent iron@biochar.

The nano-sized zero valent iron assisted biochar from hazelnut shell (nZVI@biochar) was prepared and assessed for the feasibility as the binding agent in diffusive gradients in thin-films (DGT) technique. The 1.5% agarose solution containing the optimal nZVI@biochar dose of 15 g L-1 was used to prepare the nZVI@biochar binding gel which owned a high capacity (1010 ± 50 µg disc-1) and a rapid uptake within 30 min. The elution efficiency of phenol from the loaded binding gel was up to 99.3% using the mixture of 1% hydroxylamine hydrochloride and 0.05 mol L-1 HCl. The phenol uptake of nZVI@biochar-DGT increased linearly with the increase of deployment time (R2 = 0.9938) and was in accord with the theoretical values from DGT equation, while there was no notable interference of the sample matrixes on the phenol uptake of nZVI@biochar-DGT in the spiked freshwaters. The good performance of nZVI@biochar-DGT was found under a range of pH (4.1-10.2), ionic strength (as pNaNO3) (0.155-4), and dissolved organic matter up to 20 mg L-1. In field, the monitoring of nZVI@biochar-DGT was more representative than the results from the grab-sampling with better precision and lower sampling frequency, which can provide reliable information, reduce the cost of human resources, and improve efficiency. These illustrate that the nZVI@biochar is more suitable as the binding agent of DGT for uptake of phenol and nZVI@biochar-DGT is an effective tool to monitor in-situ phenol in waters.

Adipose-on-a-chip: a dynamic microphysiological in vitro model of the human adipose for immune-metabolic analysis in type II diabetes.

Infiltration of immune cells into adipose tissue is associated with chronic low-grade inflammation in obese individuals. To better understand the crosstalk between immune cells and adipocytes, in vivo-like in vitro models are required. Conventionally transwell culture plates are used for studying the adipocyte-immune cell interaction; however, the static culture nature of this approach falls short of closely recapitulating the physiological environment. Here we present a compartmentalized microfluidic co-culture system which provides a constant-rate of nutrient supply as well as waste removal, resembling the microvascular networks of the in vivo environment. Human adipocytes and U937 cells were co-cultured in close proximity in an enclosed system. The porous barrier between the adjacent compartments comprises an array of microchannels, which enables paracrine interaction between cells in adjacent compartments and improved perfusion-based long term cell feeding. Human pre-adipocytes were fully differentiated into adipocytes on the chip and remained viable for several weeks. Upon co-culturing with immune cells, adipocytes showed a tendency to develop insulin resistance. The immune-metabolic correlation has been studied by monitoring adiponectin and IL-6 expression, as well as glucose uptake upon treatment with insulin. Our microfluidic system can be potentially used to develop physiologically relevant adipose tissue models to study obesity-associated diseases such as insulin resistance and type 2 diabetes and therefore, facilitate drug development to treat these diseases.

[Chemical characteristics and source assessment of rainwater at Shenyang].

To understand the origin and chemical characteristics of precipitation in Shenyang, about 25 rainwater samples were collected in 2007. The pH of samples varied from 4.89 to 8.02, with the volume-weighted average of 6.89. The results showed that the concentration of the sum of anions and cations in Shenyang was higher than those in southern cities such as Hangzhou, whereas the acidification of rainwater was not very serious in Shenyang. The volume-weighted average concentrations of SO4(2-) and Cl(-) were 330.00 microeq x L(-1) and 85.05 microeq x L(-1), with the percent contribution to anions of 60.32% and 15.55%, respectively. Ca2+ and NH4(+) were the main cations with contribution of 49.51% and 29.78%, respectively. The seasonal variations of ions showed that the concentrations were higher in autumn and winter than in spring and summer. Investigations of fractional acidity (FA), neutralization factors (NF), and correlation coefficients among ionic constituents indicated that high pH values were controlled by the neutralization caused by the alkaline materials but not by the absence of acidic materials. Results of NF indicated that NH4(+) and Ca(2+) were the dominant neutralization substances. Calculation of enrichment factors for rainwater components relative to soil and seawater indicated that SO4(2-) and NO3(-) were mostly attributed by the anthropogenic activities, 53.1% of Cl(-) originated from sea sources, and NH4(+) and K(+) came from the soils and human activities.