미역(Undaria pinnatifida) 포자를 사용한 생태독성 시험법은 연중 상시 이용하기에 어렵다. 미역 의 암배우체는 실험실에서 배양할 수 있기 때문에, 포자의 단점을 보완하고 상시 생태독성 시 험에 사용할 수 있다. 따라서 미역의 암배우체를 생태독성 시험에 활용하기 위해 다양한 환경 조건에 노출된 미역의 암배우체 생존율과 상대성장률의 변화를 분석하였다. 미역 암배우체는 염분(5~40 psu), 온도(5~30℃), pH (2~10), 광량(0~120 μmol photon m-2 s-1)에 노출되었다. 암배 우체의 생존율은 최고 평균값을 기준으로 온도 20℃, 염분 27.5 psu, pH 8, 광량 30 μmol photon m-2 s-1에서 가장 높았다. 상대성장률은 최고 평균값을 기준으로 온도 15℃, 염문 35 psu, pH 9, 광량 60 μmol photon m-2 s-1에서 가장 높았다. 본 연구결과를 통해 미역 암배우체의 생존율과 상대성장률을 활용하여 연안환경을 상시 신속하게 평가하기 위한 효율적인 방법으로 활용이 기대된다.

Toxicity of seven environment friendly agricultural materials (EFAM), which have been used in the domestic market were evaluated on honeybee (Apis mellifera) and asian multicolored ladybird beetle (Harmonia axyridis). Three EFAMs made from plant extract agents (Wangjoongwang Eco, Bogum Eco and Bestop Eco) and four EFAMs made from microbial utilizing agents (Worldstar Eco, Goodmorning, Bluechip and Cameleon) were investigated as EFAMs. In evaluation of toxicity on honeybee, the RT25 values of 3 EFAMs made from plant extract agents ranged from 1 to 3 days. Therefore, honeybee should be released 1-3 days after application of these EFAMs. Meanwhile, the four agricultural materials made from microbial utilizing agents did not show any mortality against honeybee. In evaluating the toxicity to adult and larva ladybird beetles, all seven EFAMs made from plant extract agents and microbial utilizing agents to show any mortality.

To evaluate the protective effect of Ajuga multiflora BUNGE (AMB) extract on the toxicity of lead acetate (LA), environmental pollutant, cell viability was measured by XTT assay using cultured NIH3T3 fibroblasts. And also, the effect of antioxidant, butylated hydroxytoluene (BHT) on LA-induced cytotoxicity was analysed. For the protective effect of AMB extract on LA-induced cytotoxicity, NIH3T3 fibroblasts were pretreated with 80 or 90 μg/mL of AMB extract for 2 hours before the treatment of LA. And also, the antioxidative effects of AMB extract against LA-induced cytotoxicity were assessed by DPPH-radical scavenging activity, superoxide dismutase (SOD)-like activity and inhibitory activity of lipid peroxidation (LP). In this study, LA significantly decreased cell viability dose-dependently compared with control, and then XTT50 value was determined at 46.1 μM of LA. In the effect of BHT against LA-induced cytotoxicity, it effectively prevented toxic effect of LA by the significant increase of cell viability. In the protective effect of AMB extract on LA-induced cytotoxicity, it significantly increased cell viability which was decreased by LA-induced cytotoxicity, and also it showed the antioxidative effects such as DPPH-radical scavenging activity, SOD-like activity and inhibitory activity of LP. From these results, it is suggested that the cytotoxicity of LA is involved in oxidative stress, and AMB extract effectively prevented the cytotoxicity induced by LA via an antioxidative effect. Conclusively, the natural substance such as AMB extract may be alternative resources for the prevention or treatment of diseases related with oxidative stress.