Uniformly Strong Persistence for a Delayed Predator-Prey Model

An asymptotically periodic predator-prey model with time delay is investigated. Some sufficient conditions for the uniformly strong persistence of the system are obtained. Our result is an important complementarity to the earlier results

Puerarin Improves Diabetic Aorta Injury by Inhibiting NADPH Oxidase-Derived Oxidative Stress in STZ-Induced Diabetic Rats

Objective. Puerarin is a natural flavonoid isolated from the TCM lobed kudzuvine root. This study investigated the effect and mechanisms of puerarin on diabetic aorta in rats. Methods. Streptozotocin- (STZ-) induced diabetic rats were administered with puerarin for 3 weeks. Levels of serum insulin (INS), PGE2, endothelin (ET), glycated hemoglobin (GHb), H2O2, and nitric oxide (NO) in rats were measured by ELISA and colorimetric assay kits. The aortas were stained with H&E. Moreover, the mRNA expression of ICAM-1, LOX-1, NADPH oxidase 2 (NOX2), and NOX4 and the protein expression of ICAM-1, LOX-1, NF-κB p65, E-selectin, NOX2, and NOX4 in aorta tissues were measured by real-time PCR and Western blot, respectively. The localization of ICAM-1, NF-κB p65, NOX2, and NOX4 in the aorta tissues was also determined through immunohistochemistry. Results. Puerarin treatment exerted no effect on fasting blood glucose levels but significantly reduced the serum levels of INS, GHb, PGE2, ET, H2O2, and NO. In addition, puerarin improved the pathological alterations and inhibited the expression of ICAM-1, LOX-1, NOX2, and NOX4 at both mRNA and protein levels. Puerarin also significantly reduced the number of cells showing positive staining for ICAM-1, NOX2, NOX4, and NF-κB p65. Conclusion. Puerarin demonstrated protective effect on the STZ-induced diabetic rat aorta. The protective mechanisms may include regulation of NF-κB and inhibition of NOX2 and NOX4 followed by inhibition of cell adhesion molecule expression

Primjena Monte Carlo metode s algoritmom simuliranog opuštanja u analizi Mossbauerovih spektara

A convenient and robust procedure for Mössbauer analysis based on Monte Carlo method is described. The method uses simulated annealing approach to find the optimum Mössbauer parameters in the Lorentzian profile as initial values for the Monte Carlo search program. A succession of solutions to the function describing the spectrum is then randomly generated until the solution with the minimum chi-square with respect to the experimental data is reached. The result having the reduced chi-square close to 1 shows the validity of the method.Opisujemo pogodan i snažan postupak za analizu Mössbauerovih spektara zasnovan na Monte Carlo metodi. Primjenjuje se pristup simuliranog opuštanja za nalaženje najpovoljnijih parametara Lorentzovih profila Mossbauerovih spektara koji su početne vrijednosti za Monte Carlo program traženja. Zatim se nasumice stvara niz rješenja za funkciju koja opisuje spektar dok se ne postigne rješenje koje je u najboljem skladu s eksperimentalnim podacima. Postignuti ishod je u dobrom skladu s mjerenim spektrom, što pokazuje vrijednost metode

Natural products targeting autophagy and apoptosis in NSCLC: a novel therapeutic strategy

Lung cancer is the leading cause of cancer-related mortality worldwide, with non-small cell lung cancer (NSCLC) being the predominant type. The roles of autophagy and apoptosis in NSCLC present a dual and intricate nature. Additionally, autophagy and apoptosis interconnect through diverse crosstalk molecules. Owing to their multitargeting nature, safety, and efficacy, natural products have emerged as principal sources for NSCLC therapeutic candidates. This review begins with an exploration of the mechanisms of autophagy and apoptosis, proceeds to examine the crosstalk molecules between these processes, and outlines their implications and interactions in NSCLC. Finally, the paper reviews natural products that have been intensively studied against NSCLC targeting autophagy and apoptosis, and summarizes in detail the four most retrieved representative drugs. This paper clarifies good therapeutic effects of natural products in NSCLC by targeting autophagy and apoptosis and aims to promote greater consideration by researchers of natural products as candidates for anti-NSCLC drug discovery

Cigarette Smoke (CS) and Nicotine Delay Neutrophil Spontaneous Death via Suppressing Production of Diphosphoinositol Pentakisphosphate

Diphosphoinositol pentakisphosphate (InsP7), a higher inositol phosphate containing energetic pyrophosphate bonds, is beginning to emerge as a key cellular signaling molecule. However, the various physiological and pathological processes that involve InsP7 are not completely understood. Here we report that cigarette smoke (CS) extract and nicotine reduce InsP7 levels in aging neutrophils. This subsequently leads to suppression of Akt deactivation, a causal mediator of neutrophil spontaneous death, and delayed neutrophil death. The effect of CS extract and nicotine on neutrophil death can be suppressed by either directly inhibiting the PtdIns(3,4,5)P3/Akt pathway, or increasing InsP7 levels via overexpression of InsP6K1, an inositol hexakisphosphate (InsP6) kinase responsible for InsP7 production in neutrophils. Delayed neutrophil death contributes to the pathogenesis of CS-induced chronic obstructive pulmonary disease. Therefore, disruption of InsP6K1 augments CS-induced neutrophil accumulation and lung damage. Taken together, these results suggest that CS and nicotine delay neutrophil spontaneous death by suppressing InsP7 production and consequently blocking Akt deactivation in aging neutrophils. Modifying neutrophil death via this pathway provides a strategy and therapeutic target for the treatment of tobacco-induced chronic obstructive pulmonary disease

Reconstruction of Typhoon Structure Using 3-Dimensional Doppler Radar Radial Velocity Data with the Multigrid Analysis: A Case Study in an Idealized Simulation Context

Extracting multiple-scale observational information is critical for accurately reconstructing the structure of mesoscale circulation systems such as typhoon. The Space and Time Mesoscale Analysis System (STMAS) with multigrid data assimilation developed in Earth System Research Laboratory (ESRL) in National Oceanic and Atmospheric Administration (NOAA) has addressed this issue. Previous studies have shown the capability of STMAS to retrieve multiscale information in 2-dimensional Doppler radar radial velocity observations. This study explores the application of 3-dimensional (3D) Doppler radar radial velocities with STMAS for reconstructing a 3D typhoon structure. As for the first step, here, we use an idealized simulation framework. A two-scale simulated “typhoon” field is constructed and referred to as “truth,” from which randomly distributed conventional wind data and 3D Doppler radar radial wind data are generated. These data are used to reconstruct the synthetic 3D “typhoon” structure by the STMAS and the traditional 3D variational (3D-Var) analysis. The degree by which the “truth” 3D typhoon structure is recovered is an assessment of the impact of the data type or analysis scheme being evaluated. We also examine the effects of weak constraint and strong constraint on STMAS analyses. Results show that while the STMAS is superior to the traditional 3D-Var for reconstructing the 3D typhoon structure, the strong constraint STMAS can produce better analyses on both horizontal and vertical velocities

Volcanically-induced floral changes across the Triassic-Jurassic (T-J) transition

The End-Triassic Mass Extinction (ETME) saw the catastrophic loss of ca. 50% of marine genera temporally associated with emplacement of the Central Atlantic Magmatic Province (CAMP). However, the effects of the ETME on land is a controversial topic. Evaluation of the disparate cause(s) and effects of the extinction requires additional, detailed terrestrial records of these events. Here, we present a multidisciplinary record of volcanism and environmental change from an expanded Triassic-Jurassic (T-J) transition preserved in lacustrine sediments from the Jiyuan Basin, North China. High-resolution chemostratigraphy, palynological, kerogen, and sedimentological data reveal that terrestrial conditions responded to and were defined by large-scale volcanism. The record of sedimentary mercury reveals two discrete CAMP eruptive phases during the T-J transition. Each of these can be correlated with large, negative C isotope excursions (CIE-I of -4.7 ‰; CIE-II of -2.9 ‰), significantly reduced plant diversity (with ca. 45% and 44% generic losses respectively), enhanced wildfire (marked by increased fusinite or charcoal content), and major climatic shifts towards drier and hotter conditions (indicated by the occurrence of calcareous nodules, increased Classopollis pollen content, and PCA analysis). Our results show that CAMP eruptions may have followed a bimodal eruptive model and demonstrate the powerful ability of large-scale volcanism to alter the global C cycle and profoundly affect the climate, in turn leading to enhanced wildfires and a collapse in land plant diversity during the T-J transition

Myeloid Cell-Derived Reactive Oxygen Species Externally Regulate the Proliferation of Myeloid Progenitors in Emergency Granulopoiesis

SummaryThe cellular mechanisms controlling infection-induced emergency granulopoiesis are poorly defined. Here we found that reactive oxygen species (ROS) concentrations in the bone marrow (BM) were elevated during acute infection in a phagocytic NADPH oxidase-dependent manner in myeloid cells. Gr1+ myeloid cells were uniformly distributed in the BM, and all c-kit+ progenitor cells were adjacent to Gr1+ myeloid cells. Inflammation-induced ROS production in the BM played a critical role in myeloid progenitor expansion during emergency granulopoiesis. ROS elicited oxidation and deactivation of phosphatase and tensin homolog (PTEN), resulting in upregulation of PtdIns(3,4,5)P3 signaling in BM myeloid progenitors. We further revealed that BM myeloid cell-produced ROS stimulated proliferation of myeloid progenitors via a paracrine mechanism. Taken together, our results establish that phagocytic NADPH oxidase-mediated ROS production by BM myeloid cells plays a critical role in mediating emergency granulopoiesis during acute infection