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Original Article

In vitro effects of rosmarinic acid on glutathione reductase and glucose 6-phosphate dehydrogenase

, , , , &
Pages 587-594 | Received 27 Jul 2008, Accepted 09 Apr 2009, Published online: 09 May 2011

Figures & data

Figure 1.  Structure of rosmarinic acid.

Figure 1.  Structure of rosmarinic acid.

Figure 2.  Inhibition kinetics of bovine kidney cortex glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against oxidized glutathione (GSSG) as varied substrate and rosmarinic acid (RA) (0.1–0.4 mM) as inhibitor at different fixed NADPH (0.1 mM) concentrations.

Figure 2.  Inhibition kinetics of bovine kidney cortex glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against oxidized glutathione (GSSG) as varied substrate and rosmarinic acid (RA) (0.1–0.4 mM) as inhibitor at different fixed NADPH (0.1 mM) concentrations.

Figure 3.  Inhibition kinetics of bovine kidney cortex glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against NADPH as varied substrate and rosmarinic acid (RA) (0.1–0.6 mM) as inhibitor at different fixed oxidized glutathione (GSSG) (0.7 mM) concentrations.

Figure 3.  Inhibition kinetics of bovine kidney cortex glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against NADPH as varied substrate and rosmarinic acid (RA) (0.1–0.6 mM) as inhibitor at different fixed oxidized glutathione (GSSG) (0.7 mM) concentrations.

Figure 4.  Inhibition kinetics of bovine liver glutathione reductase (GR). Inhibition kinetics of Lineweaver–Burk double reciprocal plot of initial velocity against oxidized glutathione (GSSG) as varied substrate and rosmarinic acid (RA) (0.1–0.4 mM) as inhibitor at different fixed NADPH (0.1 mM) concentrations.

Figure 4.  Inhibition kinetics of bovine liver glutathione reductase (GR). Inhibition kinetics of Lineweaver–Burk double reciprocal plot of initial velocity against oxidized glutathione (GSSG) as varied substrate and rosmarinic acid (RA) (0.1–0.4 mM) as inhibitor at different fixed NADPH (0.1 mM) concentrations.

Figure 5.  Inhibition kinetics of bovine liver glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against NADPH as varied substrate and rosmarinic acid (RA) (0.1–0.6 mM) as inhibitor at different fixed oxidized glutathione (GSSG) (0.7 mM) concentrations.

Figure 5.  Inhibition kinetics of bovine liver glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against NADPH as varied substrate and rosmarinic acid (RA) (0.1–0.6 mM) as inhibitor at different fixed oxidized glutathione (GSSG) (0.7 mM) concentrations.

Figure 6.  Inhibition kinetics of yeast glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against oxidized glutathione (GSSG) as varied substrate and rosmarinic acid (RA) (0.1–0.4 mM) as inhibitor at different fixed NADPH (0.1 mM) concentrations.

Figure 6.  Inhibition kinetics of yeast glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against oxidized glutathione (GSSG) as varied substrate and rosmarinic acid (RA) (0.1–0.4 mM) as inhibitor at different fixed NADPH (0.1 mM) concentrations.

Figure 7.  Inhibition kinetics of yeast glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against NADPH as varied substrate and rosmarinic acid (RA) (0.1–0.6 mM) as inhibitor at different fixed oxidized glutathione (GSSG) (0.7 mM) concentrations.

Figure 7.  Inhibition kinetics of yeast glutathione reductase (GR). Lineweaver–Burk double reciprocal plot of initial velocity against NADPH as varied substrate and rosmarinic acid (RA) (0.1–0.6 mM) as inhibitor at different fixed oxidized glutathione (GSSG) (0.7 mM) concentrations.

Figure 8.  Inhibition kinetics of sheep brain cortex glucose 6-phosphate dehydrogenase (G6PD). Lineweaver–Burk double reciprocal plot of initial velocity against glucose 6-phosphate (G6P) as varied substrate and rosmarinic acid (RA) (0–2 mM) as inhibitor at different fixed NADP+ (0.1 mM) concentrations.

Figure 8.  Inhibition kinetics of sheep brain cortex glucose 6-phosphate dehydrogenase (G6PD). Lineweaver–Burk double reciprocal plot of initial velocity against glucose 6-phosphate (G6P) as varied substrate and rosmarinic acid (RA) (0–2 mM) as inhibitor at different fixed NADP+ (0.1 mM) concentrations.

Figure 9.  Inhibition kinetics of sheep brain cortex glucose-6-phosphate dehydrogenase (G6PD). Lineweaver–Burk double reciprocal plot of initial velocity against NADP+ as varied substrate and rosmarinic acid (RA) (0–2 mM) as inhibitor at different fixed glucose 6-phosphate (G6P) (0.4 mM) concentrations.

Figure 9.  Inhibition kinetics of sheep brain cortex glucose-6-phosphate dehydrogenase (G6PD). Lineweaver–Burk double reciprocal plot of initial velocity against NADP+ as varied substrate and rosmarinic acid (RA) (0–2 mM) as inhibitor at different fixed glucose 6-phosphate (G6P) (0.4 mM) concentrations.

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