Neurochemically distinct populations of the bed nucleus of stria terminalis modulate innate fear response to weak threat evoked by predator odor stimuli

Anxiety and trauma-related disorders are characterized by significant alterations in threat detection, resulting in inadequate fear responses evoked by weak threats or safety stimuli. Recent research pointed out the important role of the bed nucleus of stria terminalis (BNST) in threat anticipation and fear modulation under ambiguous threats, hence, exaggerated fear may be traced back to altered BNST function. To test this hypothesis, we chemogenetically inhibited specific BNST neuronal populations (corticotropin-releasing hormone - BNSTCRH and somatostatin - BNSTSST expressing neurons) in a predator odor-evoked innate fear paradigm. The rationale for this paradigm was threefold: (1) predatory cues are particularly strong danger signals for all vertebrate species evoking defensive responses on the flight-avoidance-freezing dimension (conservative mechanisms), (2) predator odor can be presented in a scalable manner (from weak to strong), and (3) higher-order processing of olfactory information including predatory odor stimuli is integrated by the BNST. Accordingly, we exposed adult male mice to low and high predatory threats presented by means of cat urine, or low- and high-dose of 2-methyl-2-thiazoline (2MT), a synthetic derivate of a fox anogenital product, which evoked low and high fear response, respectively. Then, we tested the impact of chemogenetic inhibition of BNSTCRH and BNSTSST neurons on innate fear responses using crh- and sst-ires-cre mouse lines. We observed that BNSTSST inhibition was effective only under low threat conditions, resulting in reduced avoidance and increased exploration of the odor source. In contrast, BNSTCRH inhibition had no impact on 2MT-evoked responses, but enhanced fear responses to cat odor, representing an even weaker threat stimulus. These findings support the notion that BNST is recruited by uncertain or remote, potential threats, and CRH and SST neurons orchestrate innate fear responses in complementary ways

Solvothermal Crystallization of Ag/AgxO-AgCl Composites: Effect of Different Chloride Sources/Shape-Tailoring Agents

In the present work, AgCl microcrystals were obtained by solvothermal crystallization to investigate the effect of H+, Na+, K+, and different shape-tailoring agents (non-ionic: polyvinylpyrrolidone vs. anionic: sodium dodecyl sulfate) on the textural and photocatalytic properties of the samples. The crystallization process resulted in secondary products, such as AgxO or Ag, AgClO3, AgClO4, which were further transformed during the photocatalytic tests. The most efficient photocatalyst (assessed for methyl orange degradation) was synthesized using HCl, as a chloride source and polyvinylpyrrolidone, as a shape-tailoring agent. Therefore, the ability of polyvinylpyrrolidone to enhance the photocatalytic activity was also investigated, and it was found that the addition of 0.6 g polyvinylpyrrolidone resulted in the most efficient photocatalyst. Moreover, AgxO, being a charge separator, could play a critical role in the photocatalytic process, while reversibly transforming to Ag back and forth

Shape tailoring of AgBr microstructures: effect of the cations of different bromide sources and applied surfactants

Investigations regarding AgBr-based photocatalysts came to the center of attention due to their high photosensitivity. The present research focuses on the systematic investigation regarding the effect of different alkali metal cation radii and surfactants/capping agents applied during the synthesis of silver-halides. Their morpho-structural and optical properties were determined via X-ray diffractometry, diffuse reflectance spectroscopy, scanning electron microscopy, infrared spectroscopy, and contact angle measurements. The semiconductors' photocatalytic activities were investigated using methyl orange as the model contaminant under visible light irradiation. The correlation between the photocatalytic activity and the obtained optical and morpho-structural properties was analyzed using generalized linear models. Moreover, since the (photo)stability of Ag-based photoactive materials is a crucial issue, the stability of catalysts was also investigated after the degradation process. It was concluded that (i) the photoactivity of the samples could be fine-tuned using different precursors and surfactants, (ii) the as-obtained AgBr microcrystals were transformed into other Ag-containing composites during/after the degradation, and (iii) elemental bromide did not form during the degradation process. Thus, the proposed mechanisms in the literature (for the degradation of MO using AgBr) must be reconsidered

Synthesis, characterization, and challenges faced during the preparation of zirconium pillared clays

In this study, Zr-pillared montmorillonite clays (Zr-PILCs) were synthesized using two different precursor materials: raw montmorillonite (CM) and sodium ion-saturated montmorillonite (Na-CM) at different Zr/clay ratios (2.5, 5 and 10 mmol/g). To study the effect of Zr concentration and clay pre-treatment with NaCl on pillaring, the modified clay samples were characterized in detail using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), high-resolution transmission electron microscopy (HRTEM), scanning transmission electron microscopy and energy-dispersive X-ray spectroscopy (STEM-EDX). The XRD analysis showed the increase of basal spacing of Zr-PILCs prepared from both precursor materials: from 1.26 to 1.74 nm in the case of CM, and from 1.13 to 1.93 nm for Na-CM. Results from FT-IR revealed new bands ascribed to Zr-O bonds in the range of 400–500 cm−1 in Zr-pillared samples obtained from Na-CM at Zr/clay ratios of 2.5 and 5 mmol/g. The distribution and nature of Zr species in between the silicate layers were studied using STEM-EDX and HAADF imaging. They were found to be separated by a distance of 1.5–3 nm and their thickness lies in the range of 1–2 nm. Pillared clays prepared from pre-treatment with NaCl were more thermally stable at higher temperatures

Response Time Curves of Ion-Selective Electrodes

The response characteristics of different types of ion-selective electrodes were investigated thoroughly for obtaining kinetic information for the electrode response. On the basis of response time data or supposed electrode mechanisms, the ion-selective electrodes have been divided into different groups. For the evaluation of the response time curves of electrodes, at which the rate-determining step is the diffusion of the appropriate ion in the electrode membrane phase (neutral carrier-, and covered surface electrodes), a diffusion model has been used. The response characteristics of electrodes operating on ion-exchange equilibria (e.g., precipitate based electrodes etc.) have been interpreted with the help of a first-order kinetic equation. In addition to this, a so-called multielectrode model has been worked out for the general interpretation of the electrode response if the rate determining sequence of the overall potential determining step is covered by a diffusion process through the adhering laminary layer at the electrode surface. © 1976, American Chemical Society. All rights reserved

Systematic investigation of experimental parameters on nitrogen incorporation into carbon nanotube forests

Nitrogen doping carbon nanotubes can enhance their beneficial physical and chemical properties, rendering them more desirable for various applications, e.g., in electronics. In this study, we used catalytic chemical vapor deposition to synthesize carbon na-no-tube forests on different substrates. The samples were prepared in the presence of compounds containing nitrogen (ammonia, acetonitrile, tripropylamine, and their mixture with acetone) that were introduced into the reactor by bubbling or injection. Of the two different nitrogen introduction methods, the direct injection of a liquid nitrogen precursor promoted the synthesis of bamboo-structured carbon nanotube forests more efficiently. It was found in the injection experiments that the amount of precursor affected the extent of nitrogen incorporation. The presence of various nitrogen species in CNTs was also identified, and the manner in which temperature and the presence of hydrogen both influence nitrogen incorporation into the carbon na-no-tubes was observed

Spectroscopic in Situ Imaging of Acid Coextraction Processes in Solvent Polymeric Ion-Selective Electrode and Optode Membranes

Time-dependent processes induced by acidic solutions in solvent polymeric membranes with a H+-selective chromoionophore are studied in a spectropotentiometric setup. They are important for understanding the response time of anion-selective optodes and the response of H+-selective electrodes at low pH when anion interference is potential determining. The extent of anion - proton coextraction is characterized with extraction experiments on thin optical films (optodes) containing the same components and described by theory. Imaging experiments indicate rapid diffusion processes and unusual nonlinear steady-state concentration profiles that are explained by parallel extraction of undissociated acid into the membrane. Long-term potential drifts of the respective electrode are detected and related to the diffusion processes

Rapid Synthesis Method of Ag₃PO₄ as Reusable Photocatalytically Active Semiconductor

The widespread use of Ag3PO4 is not surprising when considering its higher photostability compared to other silver-based materials. The present work deals with the facile precipitation method of silver phosphate. The effects of four different phosphate sources (H3PO4, NaH2PO4, Na2HPO4, Na3PO4·12 H2O) and two different initial concentrations (0.1 M and 0.2 M) were investigated. As the basicity of different phosphate sources influences the purity of Ag3PO4, different products were obtained. Using H3PO4 did not lead to the formation of Ag3PO4, while applying NaH2PO4 resulted in Ag3PO4 and a low amount of pyrophosphate. The morphological and structural properties of the obtained samples were studied by X-ray diffractometry, diffuse reflectance spectroscopy, scanning electron microscopy, infrared spectroscopy, and X-ray photoelectron spectroscopy. The photocatalytic activity of the materials and the corresponding reaction kinetics were evaluated by the degradation of methyl orange (MO) under visible light. Their stability was investigated by reusability tests, photoluminescence measurements, and the recharacterization after degradation. The effect of as-deposited Ag nanoparticles was also highlighted on the photostability and the reusability of Ag3PO4. Although the deposited Ag nanoparticles suppressed the formation of holes and reduced the degradation of methyl orange, they did not reduce the performance of the photocatalyst