Background : Adenophora triphylla var japonica is a perennial herb that belongs to Campanulaceae. Radix Adenophorae is a dried rhizome of A. triphylla and same genus plant. It has contains chemicals such as cycloartenyl acetate, lupenone, β-sitosterol, taraxerone, octacosanoic acid, and praeruptorin A. Radix Adenophorae considered to be effective regulating humoral and cellular immunity, antimutation, restraining adenocarcinoma cell, strengthening cardiac function, allaying a fever, and easing pain and cough. In this study, we tried to establish a mass production system of A. triphylla which has high economic value as a medicinal herb by plant tissue culture in order to cultivate standard varieties. Methods and Results : In this study, A. triphylla internode was used as a explant and it was surface sterilized by 1% sodium hypochlorite for 5 minutes, consequently several times washed with ddH2O. Further it was placed in to MS medium including with axillary bud. The 1/2MS, B5, SH was used in this research. And the plant growth regulator of 0.1 - 2 ㎎/ℓ auxins (NAA, IBA) and cytokines (BA) were used respectively to achieve multiple shoots. The whole study was carried out in the department of Herbal crop research, Eumseong, RDA. Conclusion : In this study we obtained, 6.2 multi-shoots per an explant, and the shoot growth was also favorable in the presence of 1.0 ㎎/ℓ BA and 1.0 ㎎/ℓ IBA.

Background : Ligusticum chuanxiong Hort is a perennial herb of the Umbelliferae family and an important traditional oriental medicinal plant. The compounds contained in L. chuanxiong can be divided into five kinds, essential oil, alkaloids, phenolic acids, phthalide lactones, and other constituents. These compounds have cardiovascular and cerebrovascular effects, antioxidants, neuroprotection, anti-fibrinolytic, antidotes, anti-inflammatory and antitumor activities. In this study, we anticipated to establish the in vitro propagation system of L. chuanxiong, which is a high economic value as medicinal herb, by plant tissue culture to solve the problem of root stocks contamination. Methods and Results : The whole study was carried out in the department of Herbal crop research, Eumseong, RDA. In this study, L. chuanxiong nodes was used as an explant and it was surface sterilized by 2% sodium hypochlorite for 1 minutes, then washed with ddH2O several times. Further the surface sterilized nodes were placed on MS basal media. Multiple shoots were induced on MS, SH, WPM media with 0.1 - 2 ㎎/ℓ auxin (NAA, IBA) and cytokine (BA). In this study we obtained 4.6 multi-shoots per an explant, and growth of the shoot was also favorable in the presence of 1.0 ㎎/ℓ BA. Subsequent transfer of these regenerated shoots on 1/2 MS media resulted in root formation. The rooted plantlets were able to grow in soil after 3 weeks of acclimatization. Conclusion : The optimal conditions for in vitro propagation of L. chuanxiong were established through this experiment.

Background : Cnidium officinale Makino is a perennial herb of the family Umbelliferae, and an important traditional oriental medicinal plant in China, Japan and Korea. Cnidii Rhizoma, the dried rhizome of C. officinale have been used as traditional oriental medicine in Korea. It has been shown that the cnidii rhizomes are used in the treatment of pain, inflammation, menstrual disturbance, and anti-vitamin deficiency disease, and also act as a blood pressure depressant. In this study, we anticipated to establish the mass propagation system of C. officinale, which is a high economic value as medicinal herb, by plant tissue culture to solve the problem of root stocks contamination. Methods and Results : The whole study was carried out in the department of Herbal crop research, Eumseong, RDA. In this study, C. officinale root bud was used as a explant and it was surface sterilized by 1% sodium hypochlorite for 3 minutes, then several times washed with ddH2O. Multiple shoots were induction them on MS, B5, SH media with 0.1 - 2 ㎎/ℓ auxin (NAA, IBA) and cytokine (BA, Zeatin). In this study we obtained, 7.4 multi-shoots per an explant, and the shoot growth was also favorable in the presence of 0.2 ㎎/ℓ Zeatin. Subsequent transfer of these regenerated shoots on 1/2 SH media resulted in root formation. Rooted plantlets were able to grow in soil after a short period of acclimatization. Conclusion : This experiment was comducted to identify the optimal in vitro propagation condition of C. officinale.