Depression-like Behavior Induced by Repeated Administration of Dexamethasone to Lipopolysaccharide-inflamed Mice.

BACKGROUND: Over the years, animal models of depression have been developed by loading chronic stress, inducing neuroinflammation, or administering drugs that induce depression; however, these results have poor reproducibility. Therefore, it is necessary to develop animal models that exhibit definitive symptoms of depression for studies on potential therapeutics. OBJECTIVE: This study was aimed at investigating depression-like symptoms and their pathogenesis in lipopolysaccharide (LPS)-inflamed mice treated with dexamethasone (DEX). METHODS: Male ICR mice were injected with LPS, followed by injection with DEX a day later and each day for 6 consecutive days. Depression-like behavior, expression of the glial markers glial fibrillary acidic protein (GFAP) and ionized calcium-binding adapter molecule 1 (Iba1), and the number of the immature neuronal marker doublecortin (DCX)-positive cells were assessed using tail-suspension test (TST), forced swim test (FST), western blot analysis, and immunohistochemical analysis. RESULTS: Mice in the LPS+DEX group had significantly longer immobility time in the TST and FST than did those in the LPS- or DEX-only and control groups on day 7 post-LPS administration. GFAP and Iba1 expression was significantly elevated in the hippocampus of mice in the LPS group than in those of mice in the control group. Moreover, a significantly lower number of DCX-positive cells was observed in the hippocampal dentate gyrus of mice in the LPS+DEX group compared with that in mice in the LPS- or DEX-only and control groups on day 7 after LPS administration. CONCLUSION: Repeated DEX administration to LPS-inflamed mice may induce definitive depression-like symptoms by decreasing the number of immature neurons in the hippocampal dentate gyrus. This novel mouse model of depression was produced by repeated administration of steroids to inflamed mice.

Water spectral pattern as holistic marker for water quality monitoring.

Online water quality monitoring technologies have been improving continuously. At the moment, water quality is defined by the respective range of few chosen parameters. However, this strategy requires sampling and it cannot provide evaluation of the entire water molecular system including various solutes. As it is nearly impossible to monitor every single molecule dissolved in water, the objective of our research is to introduce a complimentary approach, a new concept for water screening by observing the water molecular system changes using aquaphotomics and Quality Control Chart method. This approach can continuously provide quick information about any qualitative change of water molecular arrangement without taking into account the reason of the alteration of quality. Different species and concentrations of solutes in aqueous systems structure the water solvent differently. Aquaphotomics investigates not the characteristic absorption bands of the solute in question, but the solution absorption at vibrational bands of water's covalent and hydrogen bonds that have been altered by the solute. The applicability of the proposed concept is evaluated by monitoring the water structural changes in different aqueous solutions such as acid, sugar, and salt solutions at millimolar concentration level and in ground water. The results show the potential of the proposed approach to use water spectral pattern monitoring as bio marker of water quality. Our successful results open a new venue in water quality monitoring by offering a quick and cost effective method for continuous screening of water molecular arrangement. Instead of the regular analysis of individual physical or chemical parameters, with our method - as a complementary tool - the structural changes of water molecular system used as a mirror reflecting even small disturbances in water can indicate the necessity of further detailed analysis by conventional methods.

Water revealed as molecular mirror when measuring low concentrations of sugar with near infrared light.

Near infrared spectroscopy is an overtone spectroscopy regarded as a quick and non-destructive method that provides analytical solutions for components that represent approximately 1% or more of the total mass of the investigated composite samples. Aquaphotomics offers the possibility for disentanglement of information remaining hidden in the spectra when conventional data evaluation methods are used, since this concept utilizes changes of the water structure induced by the measured solute as specific molecular vibrations at water bands. Here, near infrared technique and aquaphotomics are applied for non-destructive identification and quantification of mono- and di-saccharide solutes at 100-0.02 mM concentration that is accepted as unachievable with near infrared spectroscopy. The results presented in this study support the aquaphotomics' water molecular mirror concept that explores spectral changes related to water molecular rearrangements caused by minute changes of the solutes in the aqueous systems. The method provides quick and accurate alternative for classical analytical measurements of saccharides even at millimolar concentration levels.