Comparative studies on the toxicological, antiinflammatory and analgesic properties of three sources of Xuedan in mice and their rapid identification by electronic tongue

Purpose: To compare the toxicological, anti-inflammatory and analgesic properties of three sources of Xuedan, viz, Hemsleya omeiensis (HO), Hemsleya giganth (HG) and Hemsleya dolichocarpa (HD) in mice, and to study their rapid identification based on electronic tongue (E-tongue).Methods: After 7 days of administration, the median lethal doses (LD50) of the three xuedan decoctions in mice were determined. In addition, the anti-inflammatory and analgesic effects of the three xuedans were evaluated in mice using xylene-induced ear edema and acetic acid-induced pain. Furthermore, Etongue technology was used to identify HO, HG and HD. Principal component analysis (PCA) and discriminant factor analysis (DFA) were used to analyze the data acquired by E-tongue.Results: The median lethal dose (LD50) values of H. omeiensis, H. gigantha and H. dolichocarpa were 32.3, 17.4 and 13.7g/kg, respectively. Compared with normal control group, the anti-inflammatory effects of Xuedan were obvious in xylene-induced ear edema (p < 0.05), and pain sensation was significantly inhibited in acetic acid-induced writhing test (p < 0.05). Furthermore, E-tongue technology effectively identified HO, HG and HD.Conclusion: H. omeiensis exhibits the highest LD50 value and best analgesic effect among the three sources of xuedan. E-tongue technology is effective and rapid in identifying HO, HG and HD.Keywords: Xuedan, Hemsleya omeiensis, Hemsleya gigantha, Hemsleya dolichocarpa, Antiinflammation, Analgesia, Electronic tongu

Effect of solvent fractions of crude extract of Liushenqu on gastrointestinal motility in guinea pigs, and the underlying mechanism(s)

Purpose: To study the effect of solvent fractions of the crude extract of liushenqu on gastrointestinal motility in guinea pigs, and the mechanism of action. Methods: The effects of solvent fractions of crude extract of liushenqu (LSQ) on receptors in guinea pig isolated small intestinal cells were determined by treatment with different receptor blockers, including diphenhydramine (0.067 mg/mL), atropine sulfate (0.064 mg/mL), propranolol hydrochloride (0.033mg/mL), phentolamine mesylate (0.04mg/mL) and ondansetron hydrochloride (0.048mg/mL), to investigate the possible pharmacological mechanism of action. Results: There was no significant change in the maximum amplitude of muscle tension before and after administration in the control group, petroleum ether fraction group, and dichlormethane fraction group, while muscle tension in the 95 % ethanol and n-butanol fractions significantly increased (p < 0.01). The mean changes in tension were significantly different from that of control group (p < 0.01), but ethyl acetate fraction showed significant intestinal muscle inhibition (p < 0.01). Addition of LSQ did not alleviate the inhibition caused by diphenhydramine, but it significantly reversed the inhibition caused by blockers of cholinergic muscarinic receptor, adrenergic alpha- and beta- receptors, and 5-HT receptor (p < 0.01). Conclusion: These results indicate that n-butanol fraction is the most effective bioactive fraction of LSQ, while ethyl acetate fraction has the opposite effect. In addition, its mechanism of action is related to increase in the amplitude of small intestine smooth muscle contraction and acceleration of small intestine peristalsis

Exponential multistability of memristive Cohen-Grossberg neural networks with stochastic parameter perturbations

© 2020 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0/.Due to instability being induced easily by parameter disturbances of network systems, this paper investigates the multistability of memristive Cohen-Grossberg neural networks (MCGNNs) under stochastic parameter perturbations. It is demonstrated that stable equilibrium points of MCGNNs can be flexibly located in the odd-sequence or even-sequence regions. Some sufficient conditions are derived to ensure the exponential multistability of MCGNNs under parameter perturbations. It is found that there exist at least (w+2) l (or (w+1) l) exponentially stable equilibrium points in the odd-sequence (or the even-sequence) regions. In the paper, two numerical examples are given to verify the correctness and effectiveness of the obtained results.Peer reviewe

Review of advanced road materials, structures, equipment, and detection technologies

As a vital and integral component of transportation infrastructure, pavement has a direct and tangible impact on socio-economic sustainability. In recent years, an influx of groundbreaking and state-of-the-art materials, structures, equipment, and detection technologies related to road engineering have continually and progressively emerged, reshaping the landscape of pavement systems. There is a pressing and growing need for a timely summarization of the current research status and a clear identification of future research directions in these advanced and evolving technologies. Therefore, Journal of Road Engineering has undertaken the significant initiative of introducing a comprehensive review paper with the overarching theme of “advanced road materials, structures, equipment, and detection technologies”. This extensive and insightful review meticulously gathers and synthesizes research findings from 39 distinguished scholars, all of whom are affiliated with 19 renowned universities or research institutions specializing in the diverse and multidimensional field of highway engineering. It covers the current state and anticipates future development directions in the four major and interconnected domains of road engineering: advanced road materials, advanced road structures and performance evaluation, advanced road construction equipment and technology, and advanced road detection and assessment technologies

Increased serum exosomal miR-134 expression in the acute ischemic stroke patients

Abstract Background The exosomal miRNAs have been emerged as biomarkers and therapeutic targets for various diseases, however, the function of exosomal miRNAs in stroke remains largely unknown. Methods The blood samples from acute ischemic stroke (AIS) patients and normal controls were collected. The exosomes were isolated from the blood samples, which were confirmed by electron microscopy and western blot with the specific exosomes biomarker CD9, CD63 and Tsg101. Results RT-qPCR analysis showed that exosomal miR-134 was significantly increased in AIS patients within 24 h after stroke onset compared with that of control group. Highly expressed exosomal miR-134 was correlated with the National Institutes of Health Stroke Scale (NIHSS) scores, infarct volume and positively associated with the worse prognosis of the stroke patients. Additionally, the exosomal miR-134 was strong positively correlated with the expression of serum interleukin 6 (IL-6) and plasma high-sensitivity C relative protein (hs-CRP). The receiver operating characteristic (ROC) curve suggested that miR-134 might be a potential factor to discriminate AIS patients from non-stroke controls. Conclusions The exosomal miR-134 as a possible novel biomarker for the diagnosis and prognosis of stroke

Pollution Characteristics, Chemical Compositions, and Population Health Risks during the 2018 Winter Haze Episode in Jianghan Plain, Central China

To determine the pollution characteristics, chemical compositions, and population health risks of PM2.5 at different pollution levels, PM2.5 samples were intensively collected during the long-lasting winter haze episode from 13–23 January 2018 in Xiantao in Jianghan Plain (JHP), central China. The higher PM2.5 levels during the severe pollution period were dominated by the WNW-NNE air-masses, whereas the lower PM2.5 concentrations during other pollution periods were mainly affected by the NE, S, and NW air-masses. The NO3−/SO42− and OC/EC ratios indicated a mixed contribution of intensive vehicle exhaust and secondary formation. The enrichment factor and geo-accumulation index for assessing the PM2.5-bound metal(loid)s contamination levels were positively correlated. Ingestion is the dominant exposure pathway of PM2.5-bound metal(loid)s for children and adults, followed by inhalation and dermal contact. As, Cr, and Pb may pose carcinogenic and non-carcinogenic risks, whereas Sb and V may only pose non-carcinogenic risks for children and adults. The population health risks may not depend on the pollution levels but depend on the PM2.5-bound metal(loid)s concentrations. PM2.5-bound metal(loid)s may pose much higher population health risks for adults compared to children. More attentions should be paid to the population health risks of PM2.5-bound metal(loid)s during a long-lasting winter haze episode in JHP

Synthesis, Biological Evaluation, DNA Binding, and Molecular Docking of Hybrid 4,6-Dihydrazone Pyrimidine Derivatives as Antitumor Agents

In the present paper, on the basis of molecular hybridization, a series of 4,6-dihydrazone pyrimidine derivatives containing the pyridine moiety were synthesized, structurally characterized, and evaluated in vitro for their antitumor activity. According to the results, all the tested compounds demonstrated broad-spectrum antitumor activity against selected tumor cell lines (MCF-7, BGC-823, A549, and BEL-7402) and no obvious toxicity toward normal cells HL-7702. In particular, compounds 10a and 10f were found to be the most promising antitumor agents among the tested compounds against BGC-823 cells (IC50 = 9.00 μM and 7.89 μM) and BEL-7402 cells (IC50 = 6.70 μM and 7.66 μM), respectively. Compounds 10a and 10f exhibited higher potency against BGC-823 and BEL-7402 than the positive control 5-FU (IC50 = 15.18 μM and 15.81 μM). Further mechanism investigations demonstrated that compounds 10a and 10f could significantly increase the level of cellular ROS and induce early apoptosis of BGC-823 cells in a dose-dependent manner. Moreover, the DNA binding results from UV/Vis, CD spectroscopy, and molecular docking studies indicated that 10a and 10f bind with DNA via groove binding and partial intercalation. These results demonstrated that 10a and 10f may serve as novel lead compounds for the discovery of more dihydrazone pyrimidine derivatives with improved antitumor potency and selectivity

Bufalin reverses ABCB1-mediated resistance to docetaxel in breast cancer

Background: Docetaxel (DCT) is widely used in clinical practice, but the drug resistance of breast cancer patients has become an important reason to limit its clinical efficacy. Chan’su is a commonly used traditional Chinese medicine for the treatment of breast cancer. Bufalin (BUF) is a bioactive polyhydroxy steroid extracted from chan’su and has strong antitumor activity, but there are few studies on reversing drug resistance in breast cancer. The aim of this study is to determine whether BUF can reverse the drug resistance to DCT and restore efficacy in breast cancer. Methodology: The reversal index of BUF was detected by Cell Counting Kit-8 (CCK-8) assays. The effects of BUF on enhancing the apoptosis of DCT were detected by flow cytometry and Western Blot (WB), and the main differential expression levels of sensitive and resistant strains were detected by high-throughput sequencing. Rhodamine 123 assay, WB and ATP Binding Cassette Subfamily B Member 1 (ABCB1) ATPase activity experiments were used to detect the effect of BUF on ABCB1. The nude mouse orthotopic model was constructed to investigate the reversal effect of BUF on DCT resistance in vivo. Results: With BUF intervention, the sensitivity of drug-resistant cell lines to DCT was increased. BUF can inhibit the expression of ABCB1 protein, increase the drug accumulation of DCT in drug-resistant strains, and reduce the ATPase activity of ABCB1. Animal experiments show that BUF can inhibit the growth of drug-resistant tumors in an orthotopic model of breast cancer and decrease the expression of ABCB1. Conclusion: BUF can reverse ABCB1-mediated docetaxel resistance in breast cancer