Inhibition of GluN2B-containing NMDA receptors in early life combined with social stress in adulthood leads to alterations in prefrontal PNNs in mice.

Perineuronal nets (PNNs) are specialized extracellular matrix (ECM) structures present in the central nervous system (CNS) and have been identified as significant regulators of developmental plasticity in the developing cortex. PNNs are particularly enriched in the cortex surrounding parvalbumin-expressing (PV+) cells. A growing body of evidence suggests that the abnormalities in PV+ neurons and PNNs are associated with various neurological disorders, including schizophrenia, which is a neurodevelopmental defect disease. The N-methyl-D-aspartate receptor (NMDAR) selective antagonist is frequently employed to establish animal models of schizophrenia in laboratory settings. The crucial involvement of GluN2B-containing NMDARs in the development of CNS has been extensively established. However, the role of GluN2B in the pathophysiology of schizophrenia has yet to be thoroughly investigated. The present study inhibited GluN2B function through intraperitoneal infusion of the GluN2B selective antagonist ifenprodil into juvenile mice aged 3-4 weeks, followed by the administration of social stress when these mice reached 9 weeks of age. Then, immunofluorescence staining was employed to examine the changes in the PNNs and PV+ cells, an acoustic startle and prepulse inhibition test was used to detect activities of the PV+ cells, and Western blot was used to quantify the protein expression levels of GluN2A and GluN2B in the prefrontal cortex (PFC). The study revealed that in the PFC of mice subjected to GluN2B antagonist treatment in early life and social stress in adulthood, there was an increase in the number of PV+ cells wrapped by PNNs, and a decrease in the activation of PV+ cells during the prepulse inhibition test, which is an indicator of sensory gating functions, as well as changes in the protein expression levels of GluN2A and GluN2B, which resulted in an increase in the ratio of GluN2A to GluN2B. These aberrations in the mice are comparable to those observed in animal models and patients with schizophrenia. The findings suggest that even a transient hypofunction of GluN2B in early life poses a significant risk for the emergence of schizophrenia symptoms in adulthood.

The influence of temperature on the emissions of organophosphate ester flame retardants from polyisocyanurate foam: Measurement and modeling.

The material-phase diffusion coefficient (Dm) and material/air partition coefficient (Kma) are the key parameters controlling the emissions of semivolatile organic compounds (SVOCs) from source materials. In indoor environments, air temperature is subject to change and can significantly affect the emission rates of SVOCs from building materials and consumer products. In this study, the emissions of organophosphate ester flame retardants (OPEFRs) from customized polyisocyanurate foam materials were measured in 44-mL microchambers at 23, 35, and 55 °C. The values of Dm and Kma at different temperatures were determined. The results showed that the increase of temperature can significantly enhance the emissions of OPEFRs from the foam materials, and the emissions of OPEFRs were found to transfer from SVOC-type to volatile organic compound (VOC)-type with the increase of temperature. A correlation for OPEFRs between the steady-state emission rate and temperature and correlations between Dm, Kma, and temperature were obtained. The research results shed light on the effect of temperature on the mechanisms governing emissions of SVOCs.

A general mechanistic model for predicting the fate and transport of phthalates in indoor environments.

A mechanistic model that considers particle dynamics and their effects on surface emissions and sorptions was developed to predict the fate and transport of phthalates in indoor environments. A controlled case study was conducted in a test house to evaluate the model. The model-predicted evolving concentrations of benzyl butyl phthalate in indoor air and settled dust and on interior surfaces are in good agreement with measurements. Sensitivity analysis was performed to quantify the effects of parameter uncertainties on model predictions. The model was then applied to a typical residential environment to investigate the fate of di-2-ethylhexyl phthalate (DEHP) and the factors that affect its transport. The predicted steady-state DEHP concentrations were 0.14 µg/m3 in indoor air and ranged from 80 to 46 000 µg/g in settled dust on various surfaces, which are generally consistent with the measurements of previous studies in homes in different countries. An increase in the mass concentration of indoor particles may significantly enhance DEHP emission and its concentrations in air and on surfaces, whereas increasing ventilation has only a limited effect in reducing DEHP in indoor air. The influence of cleaning activities on reducing DEHP concentration in indoor air and on interior surfaces was quantified, and the results showed that DEHP exposure can be reduced by frequent and effective cleaning activities and the removal of existing sources, though it may take a relatively long period of time for the levels to drop significantly. Finally, the model was adjusted to identify the relative contributions of gaseous sorption and particulate-bound deposition to the overall uptake of semi-volatile organic compounds (SVOCs) by indoor surfaces as functions of time and the octanol-air partition coefficient (Koa ) of the chemical. Overall, the model clarifies the mechanisms that govern the emission of phthalates and the subsequent interactions among air, suspended particles, settled dust, and interior surfaces. This model can be easily extended to incorporate additional indoor source materials/products, sorption surfaces, particle sources, and room spaces. It can also be modified to predict the fate and transport of other SVOCs, such as phthalate-alternative plasticizers, flame retardants, and biocides, and serves to improve our understanding of human exposure to SVOCs in indoor environments.

Measurements of Parameters Controlling the Emissions of Organophosphate Flame Retardants in Indoor Environments.

Emission of semivolatile organic compounds (SVOCs) from source materials usually occurs very slowly in indoor environments due to their low volatility. When the SVOC emission process is controlled by external mass transfer, the gas-phase concentration in equilibrium with the material ( y0) is used as a key parameter to simplify the source models that are based on solid-phase diffusion. A material-air-material (M-A-M) configured microchamber method was developed to rapidly measure y0 for a polyisocyanurate rigid foam material containing organophosphate flame retardants (OPRFs). The emission test was conducted in 44 mL microchambers for target OPFRs, including tris(2-chloroethyl) phosphate (CASRN: 115-96-8), tris(1-chloro-2-propyl) phosphate (CASRN: 13674-84-5), and tris(1,3-dichloro-2-propyl) phosphate (CASRN: 13674-87-8). In addition to the microchamber emission test, two other types of tests were conducted to determine y0 for the same foam material: OPFR diffusive tube sampling tests from the OPFR source foam using stainless-steel thermal desorption tubes and sorption tests of OPFR on an OPFR-free foam in a 53 L small chamber. Comparison of parameters obtained from the three methods suggests that the discrepancy could be caused by a combination of theoretical, experimental, and computational differences. Based on the y0 measurements, a linear relationship between the ratio of y0 to saturated vapor pressure concentration and material-phase mass fractions has been found for phthalates and OPFRs.

Fate and Transport of Phthalates in Indoor Environments and the Influence of Temperature: A Case Study in a Test House.

A case study in a test house was conducted to investigate the fate and transport of benzyl butyl phthalate (BBzP) and di-2-ethylhexyl phthalate (DEHP) in residential indoor environments and the influence of temperature. Total airborne concentrations of phthalates were sensitive to indoor temperatures, and their steady-state concentration levels increased by a factor of 3 with an increase in temperature from 21 to 30 °C. Strong sorption of phthalates was observed on interior surfaces, including dust, dish plates, windows, mirrors, fabric cloth, and wood. Equilibrium partitioning coefficients for phthalates adsorbed to these surfaces were determined, and their values decreased with increasing temperature. For impervious surfaces, dimensionless partitioning coefficients were calculated and found to be comparable to reported values of the octanol-air partition coefficients of phthalates, Koa, suggesting that an organic film may develop on these surfaces. In addition, sorption kinetics was studied experimentally, and the equilibration time scale for impervious surfaces was found to be faster than that of fabric cloth. Finally, using an indoor fate model to interpret the measurement results, there was good agreement between model predictions and the observed indoor air concentrations of BBzP in the test house.

Emission of phthalates and phthalate alternatives from vinyl flooring and crib mattress covers: the influence of temperature.

Emissions of phthalates and phthalate alternatives from vinyl flooring and crib mattress covers were measured in a specially designed chamber. The gas-phase concentrations versus time were measured at four different temperatures, that is, 25, 36, 45, and 55 °C. The key parameter that controls the emissions (y0, gas-phase concentration in equilibrium with the material phase) was determined, and the emissions were found to increase significantly with increasing temperature. Both the material-phase concentration (C0) and the chemical vapor pressure (Vp) were found to have great influence on the value of y0. The measured ratios of C0 to y0 were exponentially proportional to the reciprocal of temperature, in agreement with the van't Hoff equation. A emission model was validated at different temperatures, with excellent agreement between model calculations and chamber observations. In residential homes, an increase in the temperature from 25 to 35 °C can elevate the gas-phase concentration of phthalates by more than a factor of 10, but the total airborne concentration may not increase that much for less volatile compounds. In infant sleep microenvironments, an increase in the temperature of mattress can cause a significant increase in emission of phthalates from the mattress cover and make the concentration in the infant's breathing zone about four times higher than that in the bulk room air, resulting in potentially high exposure.

Improved method for measuring and characterizing phthalate emissions from building materials and its application to exposure assessment.

Phthalate emission from vinyl floorings was measured in specially designed stainless steel chambers. Phthalate concentrations increased and reached steady state after 2 to 5 days for all experiments. By having a high ratio of emission surface to sorption surface, avoiding mass loss of phthalates onto sampling pathways, and improving air mixing inside the chamber, the time to reach steady state was significantly reduced, compared to previous studies (1 to 5 months). An innovative approach was developed to determine y0, the gas-phase concentration of phthalates in equilibrium with the material phase, which is the key parameter controlling phthalate emissions. Target phthalate material-phase concentration (C0) and vapor pressure (Vp) were explicitly measured and found to have great influences on the y0 value. For low phthalate concentrations in materials, a simple partitioning mechanism may linearly relate y0 and C0, but cannot be evoked for high-weight phthalate percentages. In addition, the sorption kinetics and adsorption isotherm of phthalates on stainless steel chamber surfaces were determined experimentally. Independently measured or calculated parameters were used to validate a semivolatile organic compounds (SVOCs) emission model, with excellent agreement between model predictions and the observed chamber concentrations in gas and stainless steel phases. With the knowledge of y0 and emission mechanisms, human exposure to phthalates from tested floorings was assessed; the levels were comparable to previous studies. This work developed a rapid, novel method to measure phthalate emissions; emission measurement results can be connected to exposure assessment and help health professionals estimate screening-level exposures associated with SVOCs and conduct risk-based prioritization for SVOC chemicals of concern.

Influence of sand grain diameter and wind velocity on lift-off velocities of sand particles.

In this paper, the velocities of sand particles near the sand bed in the saltation cloud were measured in a wind tunnel through an improved experimental scheme of the Particle Image Velocimetry (PIV) system. The influences of the diameter of sand particles in the saltation cloud and wind velocity on the probability distribution function (PDF) of lift-off velocities of sand particles were investigated. Results demonstrate that for the sand particles saltating above the sand bed with the mean grain diameter (d m = 0.3 mm), smaller and larger ones have the same velocity distribution, and wind velocity has no obvious influence on the distribution shape of the lift-off velocities, i.e., the PDFs of the horizontal and vertical lift-off velocities both follow a lognormal distribution, but the diameter of sand particles in the saltation cloud and wind velocity have an influence on the parameters of the PDF of horizontal and vertical lift-off velocities. Eventually, we present formulas to describe the PDF of lift-off velocities of sand particles with regard to the influence of wind velocity and the diameter of sand particles in the saltation cloud above the sand bed with d m = 0.3 mm.