Asymmetric long period fiber gratings fabricated by use of CO₂laser to carve periodic grooves on the optical fiber

Author name used in this publication: Peng, Gang-DingAuthor name used in this publication: Wang, Yi-Ping2006-2007 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe

Glucagon-Like Peptide-1 Modulates Neurally-Evoked Mucosal Chloride Secretion in Guinea Pig Small Intestine In Vitro.

Glucagon-like peptide-1 (GLP-1) acts at the G protein-coupled receptor, GLP-1R, to stimulate secretion of insulin and to inhibit secretion of glucagon and gastric acid. Involvement in mucosal secretory physiology has received negligible attention. We aimed to study involvement of GLP-1 in mucosal chloride secretion in the small intestine. Ussing chamber methods, in concert with transmural electrical field stimulation (EFS), were used to study actions on neurogenic chloride secretion. ELISA was used to study GLP-1R effects on neural release of acetylcholine (ACh). Intramural localization of GLP-1R was assessed with immunohistochemistry. Application of GLP-1 to serosal or mucosal sides of flat-sheet preparations in Ussing chambers did not change baseline short-circuit current (Isc), which served as a marker for chloride secretion. Transmural EFS evoked neurally mediated biphasic increases in Isc that had an initial spike-like rising phase followed by a sustained plateau-like phase. Blockade of the EFS-evoked responses by tetrodotoxin indicated that the responses were neurally mediated. Application of GLP-1 reduced the EFS-evoked biphasic responses in a concentration-dependent manner. The GLP-1 receptor antagonist exendin-(9 –39) suppressed this action of GLP-1. The GLP-1 inhibitory action on EFS-evoked responses persisted in the presence of nicotinic or vasoactive intestinal peptide receptor antagonists but not in the presence of a muscarinic receptor antagonist. GLP-1 significantly reduced EFS-evoked ACh release. In the submucosal plexus, GLP-1R immunoreactivity (IR) was expressed by choline acetyltransferase- IR neurons, neuropeptide Y-IR neurons, somatostatin-IR neurons, and vasoactive intestinal peptide-IR neurons. Our results suggest that GLP-1R is expressed in guinea pig submucosal neurons and that its activation leads to a decrease in neurally evoked chloride secretion by suppressing release of ACh at neuroepithelial junctions in the enteric neural networks that control secretomotor functions

Excitation Dependent Phosphorous Property and New Model of the Structured Green Luminescence in ZnO

published_or_final_versio

Foraminiferal biostratigraphy and palaeoenvironmental analysis of the mid-Cretaceous limestones in the southern Tibetan plateau

This study of mid-Cretaceous foraminifera from the Linzhou, the Coqen and the Xigaze Basins in the southern Tibetan Plateau has provided the first high resolution biostratigraphic description of these limestones and interpretation of their paleoenvironmental settings. The fossil assemblages are dominated primarily by orbitolinid larger benthic foraminifera. We reassessed the identification of many taxa, dividing the South Tibetan sedimentary successions of Aptian to Early Cenomanian age into eight new foraminiferal biozones (TLK1 a–h): (i) (TLK1a) a shallow reefal environment corresponding to planktonic foraminifera zone (PZ) Aptian 1–2, dominated by Palorbitolina and Praeorbitolina spp.; (ii) (TLK1b) a transgressive, reefal to forereefal environment corresponding to PZ Aptian 3, characterized by the first appearance of Mesorbitolina parva; (iii) (TLK1c) a shallow reefal to backreef environment of Late Aptian (PZ Aptian 4) age, characterized by the first appearance of Mesorbitolina texana; (iv) (TLK1d) a transgressive phase of forereef to an inner neritic environment of Albian (PZ Albian 1) age, characterized by the first appearance of Cuneolina pavonia; (v) (TLKe) an open-marine reefal environment of Albian (PZ Albian 2) age, with assemblages dominated by flat to slightly conical orbitolinids, characterized by the first appearance of Palorbitolinoides hedini; (vi) (TLK1f) a shallow, open-marine reefal to forereef environment of Middle Albian (PZ Albian 3) age, dominated by flat and convex orbitolinids, and characterized by the first appearance of Mesorbitolina aperta; (vii) (TLK1g) a reefal to forereef environment of end Albian (PZ Albian 4) age, characterized by the appearance of Conicorbitolina cf. cuvillieri and Pseudochoffatella cuvillieri, and in which Early Aptian species of Praeorbitolina cf. wienandsi have been recorded for the first time from the Late Albian; (viii) (TLK1h) a shallow reefal environment of Early Cenomanian age characterized by the first appearance of Conicorbitolina sp. A and Nezzazata conica. The eight new biozones provided biostratigraphic correlation of the Langshan, Sangzugang and Takena Formations in the Lhasa terrane, while the observed evolution of the environmentally controlled microfacies corresponds closely with the current, inferred global sea-level variation of the period. The almost continuous sedimentary sequences studied allowed previously defined orbitolinid phylogenetic linages to be confirmed

Inscription of polymer optical fiber Bragg grating at 962 nm and its potential in strain sensing

Author name used in this publication: Zhi Feng ZhangAuthor name used in this publication: Xiao Ming TaoAuthor name used in this publication: Guang Feng Wang2010-2011 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe

Could Public Restrooms Be an Environment for Bacterial Resistomes?

PMCID: PMC3547874This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

Adenosine-mono-phosphate-activated protein kinase-independent effects of metformin in T cells

The anti-diabetic drug metformin regulates T-cell responses to immune activation and is proposed to function by regulating the energy-stress-sensing adenosine-monophosphate-activated protein kinase (AMPK). However, the molecular details of how metformin controls T cell immune responses have not been studied nor is there any direct evidence that metformin acts on T cells via AMPK. Here, we report that metformin regulates cell growth and proliferation of antigen-activated T cells by modulating the metabolic reprogramming that is required for effector T cell differentiation. Metformin thus inhibits the mammalian target of rapamycin complex I signalling pathway and prevents the expression of the transcription factors c-Myc and hypoxia-inducible factor 1 alpha. However, the inhibitory effects of metformin on T cells did not depend on the expression of AMPK in T cells. Accordingly, experiments with metformin inform about the importance of metabolic reprogramming for T cell immune responses but do not inform about the importance of AMPK

Automatic alignment of surgical videos using kinematic data

Over the past one hundred years, the classic teaching methodology of "see one, do one, teach one" has governed the surgical education systems worldwide. With the advent of Operation Room 2.0, recording video, kinematic and many other types of data during the surgery became an easy task, thus allowing artificial intelligence systems to be deployed and used in surgical and medical practice. Recently, surgical videos has been shown to provide a structure for peer coaching enabling novice trainees to learn from experienced surgeons by replaying those videos. However, the high inter-operator variability in surgical gesture duration and execution renders learning from comparing novice to expert surgical videos a very difficult task. In this paper, we propose a novel technique to align multiple videos based on the alignment of their corresponding kinematic multivariate time series data. By leveraging the Dynamic Time Warping measure, our algorithm synchronizes a set of videos in order to show the same gesture being performed at different speed. We believe that the proposed approach is a valuable addition to the existing learning tools for surgery.Comment: Accepted at AIME 201

Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase

Background Statins are first-line therapy for cardiovascular disease prevention, but their systemic effects across lipoprotein subclasses, fatty acids, and circulating metabolites remain incompletely characterized. Objectives This study sought to determine the molecular effects of statin therapy on multiple metabolic pathways. Methods Metabolic profiles based on serum nuclear magnetic resonance metabolomics were quantified at 2 time points in 4 population-based cohorts from the United Kingdom and Finland (N = 5,590; 2.5 to 23.0 years of follow-up). Concentration changes in 80 lipid and metabolite measures during follow-up were compared between 716 individuals who started statin therapy and 4,874 persistent nonusers. To further understand the pharmacological effects of statins, we used Mendelian randomization to assess associations of a genetic variant known to mimic inhibition of HMG-CoA reductase (the intended drug target) with the same lipids and metabolites for 27,914 individuals from 8 population-based cohorts. Results Starting statin therapy was associated with numerous lipoprotein and fatty acid changes, including substantial lowering of remnant cholesterol (80% relative to low-density lipoprotein cholesterol [LDL-C]), but only modest lowering of triglycerides (25% relative to LDL-C). Among fatty acids, omega-6 levels decreased the most (68% relative to LDL-C); other fatty acids were only modestly affected. No robust changes were observed for circulating amino acids, ketones, or glycolysis-related metabolites. The intricate metabolic changes associated with statin use closely matched the association pattern with rs12916 in the HMGCR gene (R2 = 0.94, slope 1.00 ± 0.03). Conclusions Statin use leads to extensive lipid changes beyond LDL-C and appears efficacious for lowering remnant cholesterol. Metabolomic profiling, however, suggested minimal effects on amino acids. The results exemplify how detailed metabolic characterization of genetic proxies for drug targets can inform indications, pleiotropic effects, and pharmacological mechanisms