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The redox state of NADH/NADPH balance (nicotinamide adenine dinucleotide/nicotinamide adenine dinucleotide phosphate) is crucial in cellular homeostasis. Recent studies reported that sodium halide ions (NaX, X = F - , Cl - , Br - and I - ) stimulated NAD(P)H in Vibrio fischeri (VF). However, it remained unanswered whether this pattern applied in salts with other cations, e.g., K + , Mg 2+ and Ca 2+ , whose aquatic concentrations were increased by anthropogenic activities and climate change. Currently, VF were incubated with chloride salts, including KCl, MgCl 2 and CaCl 2 , and effects were measured in a time-dependent fashion. Both NADH and NADPH showed stimulation that increased over time, and the greatest maximum stimulation at 24 h was CaCl 2  > MgCl 2  > KCl. The changes of NADH/NADPH ratios over time in CaCl 2 , MgCl 2 and KCl were descendent, ascendant and stable, respectively. Simultaneously, FMN:NAD(P)H reaction catalyst (luciferase, in the form of expression levels of lux A and lux B), adenosine triphosphate and the expression levels of its regulating gene adk were also stimulated. The luminescence showed even more significant stimulations than the overall redox reaction. Together with earlier reported effects of NaCl, the chloride salts commonly disturbed the redox state and influenced the adaption of organisms to challenging environments., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Earlier reports studied the time-dependent effects of imidazolium-based ionic liquids ([amim]X) in the aspect of biochemical explanation and that of key contributor in mixture effects. Presently, the effects of N-alkylpyridinium-based ILs ([apyr]BF4) were studied combining the above two aspects, i.e., the time-dependent effects of [bpyr]BF4, [hpyr]BF4 and [opyr]BF4 on luminescence and biochemical indicators in Vibrio qinghaiensis sp.-Q67, and those of the mixtures. In individual results, the inhibition on luminescence increased over concentrations and the side chain length, showing concentration- and side chain-dependence. Moreover, the inhibition of [apyr]BF4 decreased from 0.25 to 24h, showing a time-dependence. Notably, [hpyr]BF4 stimulated the luminescence at 24h. The biochemical effects, including inhibition and stimulation, were well correlated to those on luminescence. In mixture results, the inhibition on luminescence was lower than the predicted effects by concentration addition model which was based on individual results. Moreover, the mixture stimulation on luminescence was significantly higher than individual ones, and the mixture stimulation on biochemical indicators was even greater than that on luminescence. In mixture effects, [bpyr]BF4 was the positive contributor, and [hpyr]BF4 was the negative contributor. Similarities and differences between [amim]X and [apyr]BF4 indicated underlying mechanisms of the commonly observed hormetic effects of ionic liquids., (Copyright © 2016. Published by Elsevier B.V.)

The excess of halide ions (F − , Cl − , Br − , I − ) can cause adverse effects. Earlier studies demonstrated time-dependent stimulations of organic salts with halide ions on photobacteria. Therefore, inorganic ones with halide ions ( e.g. , NaX, X = F − , Cl − , Br − , I − ) were assumed to cause similar effects. In the present study, Vibrio fischeri was exposed to NaX. Results showed that the contents of favin mono-nucleotide (FMN), nicotinamide adenine dinucleotide (NADH), and nicotinamide adenine dinucleotide phosphate (NADPH) were stimulated by NaX with a time-dependent fashion. The maximum stimulations on FMN at 24 h were 172%, 168%, 211% and 298% of the control (p < 0.05) in NaF, NaCl, NaBr and NaI, respectively, with an order of NaF ≈ NaCl < NaBr < NaI. The maximum stimulations on NAD(P)H at 24 h followed similar orders. Similar time-dependent stimulatory effects were observed in the FMN:NAD(P)H reaction catalyst (luciferase, in the form of expression levels of lux A and lux B), adenosine triphosphate and the expression levels of its regulating gene adk . The luminescent stimulations were significantly higher than the biochemical ones despite of similar time-dependence and stimulation order among NaX. The overall results showed a common hormetic pattern in sodium halide salts. [ABSTRACT FROM AUTHOR]

Applications of 1-alkyl-3-methylimidazolium salts ([amim]X) in pharmaceuticals call for studies on the biological effects. Previously, [amim]Cl and [amim]Br caused time-dependent stimulatory effects on Vibrio qinghaiensis sp.-Q67 (Q67). Further studies are still needed to answer the question whether [amim]X with other anions have similar effects, and to explain such stimulatory effects. Here, effects of four [amim]BF 4 with different alkyl side chains on Q67 were investigated. At the apical level, they inhibited luminescence at high concentrations and the toxicities decreased with time increasing from 0.25 to 12 h. Meanwhile, they stimulated luminescence at low concentrations, and the stimulations increased over time. The maximum stimulations followed an order of [emim]BF 4 > [bmim]BF 4 > [hmim]BF 4 > [omim]BF 4 . Compared with [emim]BF 4 , imidazole caused lower stimulations, while NaBF 4 caused significantly higher ones. Overview on effects of [amim]BF 4 , imidazole and NaBF 4 indicated significant anionic contributions. At biochemical and molecular levels, favin mono-nucleotide (FMN) and nicotinamide adenine dinucleotide (NADH) increased over time, and expressions of lux A and lux B (encoding luciferase that catalyzes FMN:NADH reaction) in Q67 showed up-regulations, suggesting an overall enhancement of the bioactivities. Moreover, superoxide dismutase and catalase showed inductions with up-regulations on their encoding genes, indicating improved antioxidant responses. [ABSTRACT FROM AUTHOR]