Liriodendron tulipifera was exposed to gradually elevated ozone concentrations of 100-300 μg kg-1 in the naturally irradiated environment chamber. During 15 d of exposure to O3, net photosynthetic rate (PN) decreased and there was large difference between the control (C) and treatment with ozone (OT), while there was no significant difference in water use efficiency. Total chlorophyll content as well as the value of fluorescence parameter Fv/Fm decreased, while antioxidant enzyme activities related to ascorbate-glutathione cycle increased after 15 d of OT. Unchanged contents of ascorbate and glutathione indirectly suggest that the species hastened the antioxidant's oxidization/reduction cycle using enzymes instead of expanding their pool against oxidative stress. and S. Z. Ryang ... [et al.].
We tested the mode of action of Cd on photosynthesis and activities of ATP-sulfurylase (ATP-S), catalase (CAT), superoxide dismutase (SOD), ascorbate peroxidase (APX), glutathione reductase (GR), and on contents of phytochelatins (PCs) and glutathione (GSH) in two cultivars of wheat (Triticum aestivum L.) PBW-343 and WH-542 differing in yield potential. Cd treatment increased Cd content and photosynthetic activity in PBW-343 more than in WH-542. The activities of APX, GR, ATP-S, and synthesis of PCs and GSH were also increased by Cd, but the CAT and SOD activities were inhibited in both the cultivars. The efficient functioning of antioxidative enzymes, production of PCs and GSH, helped in counteracting the effects of Cd namely in PBW-343, protected photosynthetic ability, and increased the tolerance to Cd. and I. Ahmad ... [et al.].
Cr(VI) significantly reduced rates of net photosynthesis and transpiration and of stomatal conductance. Cr(VI) did not affect the Fv/Fm ratio of chlorophyll fluorescence implying that the primary photochemical processes in photosystem 2 were not affected. However, the efficiency of excitation capture by open PS2 centres, in vivo quantum yield of PS2 photochemistry, and electron transport rate were significantly reduced by Cr(VI). The coefficient of photochemical quenching was reduced with a concomitant increase in coefficient of non-photochemical quenching, suggesting reduced demand for ATP and NADPH due to inhibition of CO2 assimilation. Lipid peroxidation was increased by Cr(VI) and the activities of superoxide dismutase and catalase (CAT) were increased. However, the CAT activity was reduced by high Cr(VI) concentration. The activities of ascorbate peroxidase and glutathione reductase were significantly reduced by Cr(VI) treatment.
The aim of the present work was to investigate a new mechanism likely contributing to the toxic action of acetaminophen, especially to explore the possible inhibition of glutathione reductase through an acetaminophen-glutathione conjugate (APAP-SG). APAP-SG conjugate was synthesized by organic synthesis and purified by column chromatography. The inhibitory effect of the conjugate on two types of glutathione reductase (from yeasts and rat hepatocytes) was tested spectrophotometrically. We found that the enzyme activity was reduced similarly after the treatment with 2.96 mM acetaminophenglutathione conjugate in both yeast and hepatocyte glutathione reductases (GR); the enzyme activity was inhibited to 52.7±1.5 % (2.4±0.3 mU/ml) in yeast GR (control activity was 5.6±0.3 mU/ml) and to 48.1±8.8 % (2.2±0.2 mU/ml) in rat hepatocytes lysate GR (control activity was 5.2±0.2 mU/ml). In addition, the enzyme activity (from hepatocytes lysate) was decreased to 79±7 %, 67±2 % and 39±7 %, in 0.37, 1.48 and 3.7 mM concentration of the conjugate, respectively. We found that glutathione reductase, the essential enzyme of the antioxidant system, was dose-dependently inhibited by the product of acetaminophen metabolism - the conjugate of acetaminophen and glutathione., T. Roušar ... [et al.]., and Obsahuje bibliografii a bibliografické odkazy