• Title/Summary/Keyword: Pinellia

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Development of Herbicide(Paraquat) Tolerant Plant Through Tissue Culture- 1. Mechanism of Plant Tolerance to Paraquat (농약(제초제)(農藥(除草劑)) Paraquat에 대한 저항성(抵抗性) 식물체(植物體) 선발육성(選拔育成)- 제1보(第1報) Paraquat에 대한 식물(植物)의 내성기작(耐性機作))

  • Kim, K.U.;Kim, D.U.;Kwon, S.T.
    • Korean Journal of Weed Science
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    • v.6 no.2
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    • pp.191-200
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    • 1986
  • The study was conducted to screen paraquat-tolerant plant species among crops and weeds, using the response of plant like leaf disc discoloration, visual injury and dry weight in the presence of paraquat. Mechanism of paraquat-tolerance was investigated in strains of soybean through evaluating activities of superoxide dismutase and peroxidase and the multiplication of callus derived from soybean cotyledon. In crops, Kwanggyo has been selected as a paraquat-tolerant variety among soybean cultivars tested, and Hood as a susceptible one. In weeds, Polygonum aviculare, Chenopodium album and Pinellia ternata were evaluated as the paraquat resistant species, providing the possibility for the donor plant species for paraquat resistance. Activity of superoxide dismutase known to detoxify paraquat was markedly greater in Kwanggyo, a paraquat-tolerant cultivar than in Hood, a susceptible one. In addition, the similar response like superoxide dismutase was observed in peroxidese activity. The greater inhibition of callus multiplication was determined in Hood, a susceptible one than a tolerant one, Kwnggyo. Based on all the informations, it is strongly proposed that paraquat tolerance in soybean is due to destruction of $O_2^-$ by elevated concentration of superoxide dismutase in the tolerant cultivar.

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A Flora of Vascular Plants in Mt. Cheongnyangsan (Bonghwa-gun, Andong-si) (청량산(봉화군, 안동시)의 관속식물상)

  • Nam, Bo Mi;Kim, Jae Young;Jeong, Seon;Lee, Jae-Hyeon;Nam, Myoung Ja;Oh, Byoung-Un;Chung, Gyu Young
    • Korean Journal of Plant Resources
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    • v.28 no.5
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    • pp.616-634
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    • 2015
  • This study was carried out to elucidate the distribution of vascular plants and their usefulness of Mt. Cheongnyangsan (870 m) in Gyeongsangbuk-do. The vascular plants that were collected 16 times 2006 and 2014 consisted a total of 614 taxa; 97 families, 330 genera, 541 species, 3 subspecies, 61 varieties and 9 forms. For the Korean endemic plants, 21 taxa were recorded and 8 taxa of Vulnerable Species (VU) and 5 taxa of Least Concerned species (LC) categorized by the Korean Forest Service as rare plants were investigated in this region. Furthermore, Ⅴ, Ⅳ, Ⅲ degrees of floristic regional indicator plants designated by the Korean Ministry of Environment included 2 taxa, 10 taxa and 18 taxa, respectively. Moreover, four species of distributional interesting plants, Aconitum austro-koreense Koidz., Allium spirale Willd., Dipsacus japonicus Miq. and Pinellia tripartita (Blume) Schott, in Mt. Cheongnyangsan were discovered by this study. Among them, edible, pasturing, medicinal, ornamental, timber, dye, fiber and unknown usefulness plants included 234 taxa, 213 taxa, 174 taxa, 62 taxa, 16 taxa, 12 taxa, 11 taxa and 167 taxa, respectively. In addition, 32 taxa of naturalized plants were observed.

Effect of Hot Water Extracts from Medicinal Plants on the Mutagenicity of Indirect Mutagens (간접변이원의 돌연변이원성에 대한 생약재 열수 추출물의 효과)

  • Song, Geun-Seoub;Ahn, Byung-Yong;Lee, Kap-Sang;Maeng, Il-Kyung;Choi, Dong-Seong
    • Korean Journal of Food Science and Technology
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    • v.29 no.6
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    • pp.1288-1294
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    • 1997
  • For screening antimutagenic effects, the effects of 95 medicinal plants on the mutagenicity of aflatoxin $B_1$ $(AFB_1)$ and benzo(a)pyrene [B(a)P] were investigated using the SOS chromotest with Escherichia coli PQ37. The mutagenicity induced by $AFB_1$ or B(a)P was reduced over 26% by 2 kinds and 8 kinds of medicinal plant, respectively. Eight plants (Bupleurum falcatum, Corydalis ternata, Gasfrodia elata, Ostericum koreanum, Pinellia ternatia, Poncirus trifoliata, Prunus armeniaca and Rehmannia glutinosa) were also shown to have inhibitory effects on both $AFB_1$ and B(a)P. The mutagenicity induced by $AFB_1$ or B(a)P was increased over 20% by 46 kinds and 2 kinds, respectively, and 8 medicinal plants (Chrysanthemum indicum, Cinnamomum cassia, Cyperus rotundus, Morus bombycis, Patrinia scabiosaefolia, Petasites japonicus, Polygonum multiflorium, Thyja orientalis) increased significantly the mutagenicity of both mutagens. However the 8 plants themself did not show the mutagenicity in SOS Chromotest with S-9 mix alone. This result suggests that the above 8 plants may have the co-mutagenic activities. In two bacterial mutation system, SOS Chromotest and Ames test, the mutagenic or antimutagenic activities of some medicinal plants wire similar except Ostricum koreanum, Eugenia caryophyllata and Scutellaria baicalensis.

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A monitoring for the establishment of microbial limit of herbal medicine(I) (한약재의 미생물허용한도 설정을 위한 모니터링(I))

  • Lee, Ju-Hyun;Jeon, Won-Kyung;Go, Byoung-Seob;Chun, Jin-Mi;Lee, A-Yeong;Kim, Ho-Gyoung
    • Korean Journal of Oriental Medicine
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    • v.12 no.1
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    • pp.49-57
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    • 2006
  • Objectives : This study has attempted to establish an organized system for the microbiological quality of raw materials which are important factors in preparing the standard for microbial limits. Methods : This study has first set up microbial contamination limit test. total aerobic microbial count and total fungi count, int accordance with testing method of the Korea Pharmacopeia 8th edition in order to establish an inspection standard for microbial contamination. Results : The microbial contamination of 18 items that are highly prone to contamination by three regions(Seoul, Daejeon, Gyeongsangbuk-do), As a result, Morus alba Linne and Rehmannia glutimosa Liboschitz var. purpurea Makino showed as high contaminated by WHO's Microbial Contamination Limit standard. In case of Yukjin medicine in the Theory of Herb Medicinal Properties, total bacterial contamination rate showed as 17.7%, total fungal contamination rate showed as 41.2% and total aerobic mircobial count and total fungi count on Ephedra sinica Stapf. Pinellia ternate Breitenbach, Evodia officinalis Dode showed as high measured. The microbial conatmination rate materials which make up Yukmijihwanghwan were mostly high therefore the total aerobic microbial count was measured as high in case of Yukmijihwanghwan, the characteristics about microbial contamination strain is to be researched. Conclusions : By combining the basic data and experimental results related to microbial contamination of herb medicine, the most ideal storage standards for herb medicine has been attempted to be presented.

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Effects of OMC-2010 constituents on cytokine productions in mouse spleen cells (OMC-2010 구성약재가 마우스의 비장세포 cytokine 생성에 미치는 영향)

  • Bae, Gi-Sang;Kim, Hyun Sik;Park, Kyoung-Chel;Choi, Sun-Bok;Jo, Il-Joo;Lee, Chang-Hyuk;Seo, Sang-Wan;Kim, Jong-Jin;Shin, Yong-Kook;Kim, Min Sun;Park, Kyu Hwan;Song, Ho-Joon;Park, Sung-Joo
    • The Korea Journal of Herbology
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    • v.27 no.6
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    • pp.49-54
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    • 2012
  • Objective : We recently reported that OMC-2010 has an immuno-modulatory effects via inhibiting tumor necrosis factor (TNF)-${\alpha}$ and interleukin (IL)-5. However, we did not find out which constituents play an important role in immuno-modulatory effect of OMC-2010. Thus, this study was performed to estimate the effects of constituents of OMC-2010 on cytokine production in mouse spleen cells, then ultimately reach to find out effective constituents regulating splenic cytokine production. Methods : Mouse spleen cells were pre-treated with water and ethanol extract of constituents of OMC-2010 such as Rehmannia glutinosa (RG), Pinellia ternata (PT), Citrus unshiu Markovich (CUM), Glycyrrhiza uralensis (GU), Platycodon grandiflorum (PG), Schisandra chinensis (SC). After 1 h, the cells were stimulated with lipopolysaccharide (LPS, 1 ${\mu}g/ml$) for 48 h. Then the cells were harvested for real-time reverse transcription polymerase chain reaction to detect cytokine productions. Results : The water extract of RG extract significantly inhibited the LPS-induced inTNF-${\alpha}$ and IL-5 mRNA expressions, but the water extract of PT, CUM, GU, PG, and SC did not. The ethanol extract of RG, PT, and SC significantly inhibited the LPS-induced TNF-${\alpha}$, and IL-5 mRNA expressions, but the ethanol extract of CUM, GU, and PG did not. Conclusions : Theses results could suggest that the water extract of RG and the ethanol extract of RG, PT, and SC inhibited the expression of TNF-${\alpha}$ and IL-5, which means that the possible candidate of OMC-2010 water extract's action might be RG, and ethanol extract's action might be RG, PR, and SC.

Effects of OMC-2010 Constituents Extract on the Ovalbumin-Induced Allergic Asthma in Mice (OMC-2010 구성약재 배합추출물 투여가 Ovalbumin으로 유도한 마우스 알레르기성 기관지 천식에 미치는 영향)

  • Jo, Il-Joo;Bae, Gi-Sang;Choi, Sun-Bok;Song, Ho-Joon;Park, Sung-Joo;Seo, Sang Wan;Ok, Joo An;Kim, Min Sun;Baek, Sun Jong;Bae, Ik Hyun;Kim, Hyun Sik
    • The Korea Journal of Herbology
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    • v.28 no.5
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    • pp.87-93
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    • 2013
  • Objectives : We recently have reported that constituents of OMC-2010 have an immuno-modulatory effects via inhibiting tumor necrosis factor (TNF)-alpha and interleukin (IL)-5. In this study, based on previous data, we investigated the effects of combinations with each OMC constituents on splenocyte cytotoxicity, cytokine productions, and ovalbumin (OVA) induced experimental allergic asthma. Methods : Mouse splenocytes were pre-treated with ethanol extract of constituents of Rehmannia glutinosa (RG), Pinellia ternata (PT), Schisandra chinensis (SC). We made 4 combinations using RG, PT, and SC (A;1:1:1, B;2:1:1, C;1:2:1, D;1:1:2). The cells were pretreated with A, B, C, or D for 1 h, then stimulated with lipopolysaccharide (LPS, $1{\mu}g/ml$) for 48 h. Then the cells were harvested for real-time reverse transcription polymerase chain reaction to detect cytokine productions. Then using effective combination from RG, PR and SC, we administrated the combination orally, then challenged with OVA to induce asthma. Then we analyzed the airway hyper-reactivity (AHR), lung histology and lung TNF-${\alpha}$ and IL-5 mRNA. Results : A. B. C. and D did not showed significant cytotoxicity on splenocytes. Pre-treatment of A inhibited the expression of TNF-${\alpha}$ and IL-5 significantly, but not B, C, and D. In experimental asthma, administration of A significantly inhibited the increase of AHR, lung damage, TNF-${\alpha}$ and IL-5 expression. Conclusions : Theses results could suggest that inhibitory effects of the ideal combination with RG, PT and SC (1:1:1) could be applied to treatment of asthma and study of asthma mechanisms.