Table 2.
Antioxidative activities of the fermented rice extracts†
| Rice extract‡ | Inhibition of linoleic acid peroxidation |
Scavenging of DPPH radical |
|||
|---|---|---|---|---|---|
| Absorbance at 500 nm | Inhibition (%) | Absorbance at 517 nm | Inhibition (%) | ||
| Control | 1.059 ± 0.054 | 0 | 3.098 ± 0.254 | 0 | |
| BHT | 0.097 ± 0.004a | 90.8 | 0.325 ± 0.027a | 89.5 | |
| UBRE | 0.509 ± 0.051e | 51.9 | 2.447 ± 0.151f | 21 | |
| MRRE | 0.163 ± 0.024b | 84.6 | 0.504 ± 0.034b | 84.6 | |
| PLRE | 0.223 ± 0.032c | 78.9 | 1.115 ± 0.092c | 64 | |
| CSRE | 0.431 ± 0.022d | 59.3 | 1.379 ± 0.102d | 45.2 | |
| ABRE | 0.485 ± 0.024e | 54.2 | 1.902 ± 0.112e | 38.6 | |
†Values in each column with the same superscript are not significantly different at p<0.05. Values are expressed as mean ± SD (n = 3). ‡The extracts from rice fermented with the mycelia of Monascus ruber, Phellinus linteus, Cordyceps sinensis and Agaricus blazei are termed as MRRE, PLRE, CSRE and ABRE, respectively. UBRE, used as an internal control, means the extract from unpolished brown rice, source material. See sample concentration in Materials and Methods. BHT was used at a dose of 200 µg.