Table 3.
Plant species | % Inhibition activity unboiled | % Inhibition activity boiled |
---|---|---|
Brassica juncea | 20.1 ± 1.50 | 16.6 ± 1.67 |
Cinnamomum zeylanicum | 32.39 ± 1.91 | 28.59 ± 1.78 |
Coriandrum sativum | −33.33 ± 1.43 | −23.98 ± 1.27a |
Cuminum cyminum | −7.14 ± 1.12 | 1.16 ± 1.14a |
Curcuma longa | 52.2 ± 1.65 | 47.78 ± 1.98a |
Elettaria cardamomum | −33.33 ± 1.67 | −26.89 ± 1.67a |
Foeniculum officinale | 28.79 ± 1.22 | 26.73 ± 1.75 |
Myristica fragrans | −5.81 ± 1.45 | −5.74 ± 1.44 |
Syzygium aromaticum | 58.10 ± 1.24 | 52.82 ± 1.45a |
Trigonella foenum‐graecum | 8.69 ± 1.35 | 7.78 ± 1.19 |
Acarbose | 87.67 ± 1.76 | NA |
Preincubation chromogenic method from Geethalakshmi et al. (2010) was adapted, and the final concentrations of the crude extracts were 1 mg/ml. The amylase inhibition was analyzed by amount of maltose production from starch at 517 nm after incubation at 37°C. Acarbose was used as the standard inhibitor. Results were presented as mean ± standard deviation, and mean was taken as the average of three readings of three different experiments. “‐” indicates a promotion of pancreatic amylase activity.
NA, not applicable.
The inhibitory activity in boiled extract is significantly (p < 0.05) different to the corresponding unboiled extract.