Fig. 1. Photography of (A) un-inoculated sterilized medium, (B) spent mushroom medium (SMS) after 1st harvest, (C) SMS after 3rd harvest, and (D) harvested shiitake.
Fig. 2. Comparison of (A) total polyphenol, (B) total flavonoids, (C) total sugar and (D) reducing sugar contents of the hot-water extracts prepared from (1) un-inoculated sterilized medium, (2) SMS after 1st harvest, (3) SMS after 3rd harvest and (4) harvested shiitake. Data are presented as the mean ± SD of three determinations. Different superscript letters within a column differ significantly by Duncan’s multiple range test (p<0.05).
Fig. 3. Comparison of anti-oxidant activities of the hot-water extracts prepared from (1) un-inoculated sterilized medium, (2) SMS after 1st harvest, (3) SMS after 3rd harvest and (4) harvested shiitake. Data are presented as the mean ± SD of three determinations. Different superscript letters within a column differ significantly by Duncan’s multiple range test (p<0.05).
Fig. 4. Comparison of α-glucosidase inhibitory activity of the hot-water extracts prepared from (1) un-inoculated sterilized medium (0.5 mg/ml), (2) SMS after 1st harvest (0.5 mg/ml), (3) SMS after 3rd harvest (0.5 mg/ml), (4) harvested shiitake (0.5 mg/ml), (5) acarbose (0.5 mg/ml) and (6) acarbose (0.0625 mg/ml). Data are presented as the mean ± SD of three determinations. Different superscript letters within a column differ significantly by Duncan’s multiple range test (p<0.05).
Fig. 5. Comparison of anti-coagulation activities of the hot-water extracts prepared from un-inoculated sterilized medium, spent mushroom medium (SMS) and harvested shiitake.
Table 1. Calculated RC50 of the hot-water extracts prepared from un-inoculated sterilized medium, spent mushroom medium (SMS) and harvested shiitake
Table 2. Platelet aggregation inhibitory activities of the hot-water extracts prepared from un-inoculated sterilized medium, spent mushroom medium (SMS) and harvested shiitake
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