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Aims: This study was aimed to use Coffea arabica, Salvia rhytidea and Bonium persicum extracts against Leishmania major and L. tropica promastigotes to compare various concentrations of these plant extracts. In addition, their cytotoxicity and antioxidant activities were also evaluated. Study Design: This study was performed experimentally using various concentrations of three medicinal plant extracts compared to control groups. Methodology: Fresh seeds of C. arabica and B. persicum and leaves of S. rhytidea were powdered and each plant material was extracted by ethyl alcohol via warm maceration method. Complete medium was used to prepare nine final concentrations (1-1000 µg/ml) for experiments. The cytotoxicity and antioxidant activities of the ethanolic extracts were evaluated using colorimetric cell viability WST1 and DPPH assays. All experiments were performed in triplicate and analyzed by t-test. The optical density (OD) values as measured by enzyme-linked immunosorbent assay (ELISA) were used to calculate the IC50 values. Selectivity index (SI) of the plant extracts was not attributed to cytotoxicity when it was ≥ 10. Results: The results indicated that B. persicum extract had potent antileishmanial activity against the promastigotes of both Leishmania species based on a dose-dependent response (
ABSTRACT
Objective: To develop a protocol for breaking of seed dormancy and increasing the seed germination rate of Bunium persicum. Methods: The seeds were treated with 3.1, 6.3, 12.5, 25, 50 and 100 μmol/L of benzyl aminopurine, gibberellic acid (GA
ABSTRACT
<p><b>OBJECTIVE</b>To develop a protocol for breaking of seed dormancy and increasing the seed germination rate of Bunium persicum.</p><p><b>METHODS</b>The seeds were treated with 3.1, 6.3, 12.5, 25, 50 and 100 µmol/L of benzyl aminopurine, gibberellic acid (GA3), thidiazuron (TDZ) and forchlorfenuron. Then, seeds were transferred to two different temperature conditions including room temperature (25 °C) and chilling temperature (2-5 °C).</p><p><b>RESULTS</b>The treatment of moist seeds with chilling temperature (2-5 °C) broke seed dormancy and showed maximum germination, which was 54.7% after 60 d treatment. Also, the treatment of dry seeds with chilling temperature broke seed dormancy with 9.3% germination rate after 120 d. Treatment of seeds with different level of plant growth regulators showed that under moist-room condition, there was evidence of higher and lower seed germination rate: GA3 (100 µmol/L) with 46.7% and TDZ (50 µmol/L) with 6.67% respectively. In addition, the results showed that under moist-chilling condition, TDZ (6.3 µmol/L) with 53.3% seed germination rate had higher influence on breaking seed dormancy. Treatment of seeds with combination of TDZ and GA3 under moist-chilling condition revealed higher rate of breaking of seed dormancy when 6.3 µmol/L TDZ was combined with 100 µmol/L GA3, showing 93.7% germination rate.</p><p><b>CONCLUSIONS</b>The effect of plant growth regulators coupled with chilling temperature on breaking of seed dormancy could provide a large number of seedlings while the long juvenile time which is the next restricting factor of plantation still remained. Thus, the subsequent growth of seedlings to provide a large number of corms is necessary for successful plantation.</p>
ABSTRACT
Objective: To develop a protocol for breaking of seed dormancy and increasing the seed germination rate of Bunium persicum. Methods:The seeds were treated with 3.1, 6.3, 12.5, 25, 50 and 100 μmol/L of benzyl aminopurine, gibberellic acid (GA3), thidiazuron (TDZ) and forchlorfenuron. Then, seeds were transferred to two different temperature conditions including room temperature (25 °C) and chilling temperature (2-5 °C). Results: The treatment of moist seeds with chilling temperature (2-5 °C) broke seed dormancy and showed maximum germination, which was 54.7%after 60 d treatment. Also, the treatment of dry seeds with chilling temperature broke seed dormancy with 9.3%germination rate after 120 d. Treatment of seeds with different level of plant growth regulators showed that under moist-room condition, there was evidence of higher and lower seed germination rate:GA3 (100 μmol/L) with 46.7%and TDZ (50 μmol/L) with 6.67%respectively. In addition, the results showed that under moist-chilling condition, TDZ (6.3 μmol/L) with 53.3%seed germination rate had higher influence on breaking seed dormancy. Treatment of seeds with combination of TDZ and GA3 under moist-chilling condition revealed higher rate of breaking of seed dormancy when 6.3 μmol/L TDZ was combined with 100 μmol/L GA3, showing 93.7%germination rate. Conclusions:The effect of plant growth regulators coupled with chilling temperature on breaking of seed dormancy could provide a large number of seedlings while the long juvenile time which is the next restricting factor of plantation still remained. Thus, the subsequent growth of seedlings to provide a large number of corms is necessary for successful plantation.