Effects of <i>Moringa oleifera</i> Leaf Extract on Diabetes-Induced Alterations in Paraoxonase 1 and Catalase in Rats Analyzed through Progress Kinetic and Blind Docking
In our study, we aimed to evaluate the effects of <i>Moringa oleifera</i> leaves extract on rat paraoxonase 1 (rPON1) and catalase (rCAT) activities in alloxan-induced diabetic rats. Our study included three groups; group C (control, n = 5); group D (diabetic, n = 5); and group DM (<i...
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| Main Authors: | , , , , , , |
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| Format: | Book |
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MDPI AG,
2020-09-01T00:00:00Z.
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| Summary: | In our study, we aimed to evaluate the effects of <i>Moringa oleifera</i> leaves extract on rat paraoxonase 1 (rPON1) and catalase (rCAT) activities in alloxan-induced diabetic rats. Our study included three groups; group C (control, n = 5); group D (diabetic, n = 5); and group DM (<i>M. oleifera</i> extract-supplemented diabetic rats, n = 5). Daily oral administration of <i>M. oleifera</i> extract at 200 mg/kg doses produced an increase in endogenous antioxidants. Serum rPON1 (lactonase) and liver cytosol catalase activities were determined by a spectrophotometric assay using progress curve analysis. We found a decrease in the Vm value of rPON1 in diabetic rats, but dihydrocoumarin (DHC) affinity (Km) was slightly increased. The value of Vm for the DM group was found to be reduced approximately by a factor of 3 compared with those obtained for group C, whereas Km was largely changed (96 times). Catalase activity was significantly higher in the DM group. These data suggest that the activation of rPON1 and rCAT activities by <i>M. oleifera</i> extracts may be mediated via the effect of the specific flavonoids on the enzyme structure. In addition, through molecular blind docking analysis, rPON1 was found to have two binding sites for flavonoids. In contrast, flavonoids bound at four sites in rCAT. In conclusion, the data suggest that compounds from <i>M. oleifera</i> leaves extract were able to influence the catalytic activities of both enzymes to compensate for the changes provoked by diabetes in rats. |
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| Item Description: | 10.3390/antiox9090840 2076-3921 |