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The article presents the results of the development of molecular dynamics models of modifications of polypropylene (PP) material in the plasma of a radio-frequency (RF) discharge and a copper coating deposit by magnetron sputtering on the surface of a polyethylene (PE) material. The model of the RF plasma modification process describes changes in the surface layers of the PP material upon interaction with low-energy plasma ions: the nature of the breaking of covalent bonds in macromolecules, the chemical composition of sputtered particles, and changes in the ordering of the supramolecular structure. The model of the vacuum metallization process describes the processes of the introduction of metal atoms into the polymer structure, the change in the conformation of macromolecules, the formation of macroradicals with uncompensated chemical bonds, and the formation of an interfacial layer between the polymer and the metal coating.

The purpose of this work is to investigate the effect of radio-frequency (RF) plasma modification in a plasma-forming reactive air gas on changes in the chemical structure of polyethylene (PE) based materials. As a result of plasma modification, the relative content of carbon and oxygen atoms linked by a double bond, as well as carbon and nitrogen atoms linked by a single bond, significantly increases on the surface of PE materials, which is evidence of the formation of carbonyl, carboxyl, aldehyde, and amino groups. [ABSTRACT FROM AUTHOR]

The aim of this work is to scientifically substantiate the mechanisms of plasma-chemical modification of polymeric materials in radio-frequency (RF) low-pressure discharge plasma. Using the method of molecular dynamics, a model describing the mechanisms of formation of oxygen- and nitrogen-containing functional groups on the surface of polymeric materials as a result of plasma modification was developed. The established mechanisms include multistep chemical reactions with the formation of alkyl dioxyl and alkoxyl radicals and unstable hydroperoxide groups. [ABSTRACT FROM AUTHOR]

Oxidative stress, accompanied by mitochondrial dysfunction, is a key mechanism involved in the pathogenesis of Parkinson's disease (PD). Both carnosine and lipoic acid are potent antioxidants, the applicability of which in therapy is hindered by their limited bioavailability. This study aimed to evaluate the neuroprotective properties of a nanomicellar complex of carnosine and lipoic acid (CLA) in a rotenone-induced rat model of PD. Parkinsonism was induced via the administration of 2 mg/kg rotenone over the course of 18 days. Two doses of intraperitoneal CLA (25 mg/kg and 50 mg/kg) were administered alongside rotenone to assess its neuroprotective effect. At 25 mg/kg CLA decreased muscle rigidity and partially restored locomotor activity in animals that received rotenone. Furthermore, it caused an overall increase in brain tissue antioxidant activity, accompanied by a 19% increase in neuron density in the substantia nigra and increased dopamine levels in the striatum relative to animals that only received rotenone. Based on the acquired results, it may be concluded that CLA have neuroprotective properties and could potentially be beneficial in PD treatment when used in conjunction with the base therapy.

Intracerebroventricular (ICV) administration of ouabain, an inhibitor of the Na, K-ATPase, is an approach used to study the physiological functions of the Na, K-ATPase and cardiotonic steroids in the central nervous system, known to cause mania-like hyperactivity in rats. We describe a mouse model of ouabain-induced mania-like behavior. ICV administration of 0.5 µl of 50 µM (25 pmol, 14.6 ng) ouabain into each lateral brain ventricle results in increased locomotor activity, stereotypical behavior, and decreased anxiety level an hour at minimum. Fast-scan cyclic voltammetry showed that administration of 50 µM ouabain causes a drastic drop in dopamine uptake rate, confirmed by elevated concentrations of dopamine metabolites detected in the striatum 1 h after administration. Ouabain administration also caused activation of Akt, deactivation of GSK3β and activation of ERK1/2 in the striatum of ouabain-treated mice. All of the abovementioned effects are attenuated by haloperidol (70 µg/kg intraperitoneally). Observed effects were not associated with neurotoxicity, since no dystrophic neuron changes in brain structures were demonstrated by histological analysis. This newly developed mouse model of ouabain-induced mania-like behavior could provide a perspective tool for studying the interactions between the Na,K-ATPase and the dopaminergic system.