In the presence of different concentrations of GSH, ME was inhibited by cadmium to a far smaller extent,

the inhibition being both dose- and time-dependent on GSH concentration Selleck RG7422 ( Figure 3). The effect of different concentrations of BSA on ME activity without cadmium and in the presence of 1 mM cadmium during a 24 h incubation are shown in Figure 4. Like GSH, BSA protected ME activity. The addition of BSA to the incubation medium at a concentration of 20 μg per ml to ME increased enzyme activity to about 130%, as shown for GSH in Figure 3. In the presence of different concentrations of BSA, ME was inhibited by cadmium to a much lesser extent, the inhibition being both dose- and time-dependent on the different concentrations of BSA. BSA is a 70 kDa protein containing about 7% cysteine in an amino acid structure and can protect enzyme activity as a non-specific chaperone ( Figure 4). Figure 5 shows the effect of GSH at 2 mM concentration Buparlisib supplier and in the presence of 2 mM cadmium during a 48-hour incubation with NADP-dependent ME from shrimp abdominal muscle. In the presence of 2 mM of GSH and 2 mM cadmium, the inhibition was time-dependent; GSH can also protect ME activity against higher concentrations of cadmium. Figure 6 illustrates the effect of 20 μg BSA per ml added to ME during

incubation for 48 hours and of 2 mM cadmium on NADP-dependent ME activity from shrimp abdominal muscle. In the presence of 2 mM cadmium, the inhibition was time-dependent; BSA can also protect ME activity against higher concentrations of cadmium ( Figure 6). Glutathione (GSH) is present in many living systems and often alleviates the adverse effect of xenobiotics, but it is unclear how

it affects the inhibition of some enzymes by cadmium (Cd). An intracellular glutathione concentration of up to 8 mM mafosfamide reflects a dynamic balance between reduced glutathione and oxidized glutathione (Griffith 1999). Oxidized glutathione is reduced intracellularly to GSH by glutathione reductase in a NADPH-dependent reaction (Kehrer & Lund 1994). Under physiological conditions and depending on NADPH availability, the GSH/GSSG ratio can reach 100 (Griffith 1999). However, if certain compounds (e.g. malic enzyme, isocitrate dehydrogenase, glucose-6-phosphate dehydrogenase) limit the glutathione reductase reaction or NADPH synthesis, oxidized glutathione can accumulate. As shown earlier, the activity of malic enzyme in the abdominal muscle of Crangon crangon is about 20 times greater than that of glucose-6-phosphate dehydrogenase. In crustaceans, moreover, both malic enzyme and isocitrate dehydrogenase are more significant as a source of NADPH in somatic muscles ( Skorkowski et al. 1980). The present investigation was undertaken to establish the effects of cadmium on the activity of shrimp muscle ME.