• 제목/요약/키워드: Artemisia annua Linne

검색결과 3건 처리시간 0.019초

식물세포배양기술을 이용한 약용식물 개똥쑥 세포주 유도 및 세포주 추출물의 wound healing effect (Effect of Artemisia annua Linne callus induced by plant cell culture technology on wound healing)

  • 오승택;정해수;조문진;송미영;모상현;서효현
    • 한국산학기술학회논문지
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    • 제15권9호
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    • pp.5628-5636
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    • 2014
  • 현재 많은 나라들은 자생식물을 활용한 산업소재를 개발하는 데 지대한 관심을 가지고 있다. 특히 화장품 산업은 친환경, 자연친화적인 소재를 찾는데 집중하고 있는 추세이다. 우수한 생리활성 물질을 포함한 식물을 식물세포배양기술을 이용하여 대량으로 배양하고 그 함유물을 고농도로 얻음으로 효과적인 소재로 개발하려고 노력하고 있다. 이에 본 연구는 항암, 항균, 항산화, 항염 등의 효능이 입증되어 세계적으로 주목받고 있는 개똥쑥을 선택하여 식물세포배양기술을 이용해 유도한 캘러스의 화장품 소재로서의 가능성을 확인하고자 하였다. 약 6개월 동안 식물세포배양기술로 개똥쑥 캘러스를 유도하였고, 유도된 캘러스를 얻어 열수 및 에탄올 추출하여 약 2개월간 다양한 효능을 시험하였다. HPLC 분석을 통하여 열수 및 에탄올 추출물의 유효성분에 차이를 보임을 확인하였다. 또한 효능평가에서도 차이를 보였다. 개똥쑥 캘러스 에탄올 추출물을 처리하였을 경우 항염관련 단백질인 COX-2의 발현을 50% 이상 감소시키고 wound healing assay를 통해 상처 치유능이 70%정도 증가함을 확인하였다. 이를 통해 개똥쑥 캘러스 추출물이 자연친화적, 친환경적인 소재로써 항염 및 상처치료 관련 제품에 기여할 것으로 예상된다.

약초 추출액의 닭콕시듐 Eimeria tenella 대한 항콕시듐 효과 (Anticoccidial Effect of Herb Extracts against Eimeria tenella)

  • 김병기
    • 한국임상수의학회지
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    • 제12권1호
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    • pp.911-916
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    • 1995
  • Ionophorous antibiotics have been used popularly for the protection of avian coccidiosis, though Halo-fuginone which is derived from an extract of the Dichroa febrifuga, was developed as an antimalarial and anticoccidial agent. The antibiotics are regarded as the causes of residues in the avian products, therefore the author has tried to find out more safe herbal materials for the control of avian coccidiosis. Thus, the extracts of 5 kinds of herbs, roots of Pulsatilla koreana Nakai and Sophora flavescens Aiton, nuts of Quisqualis indica Linne, whole herbs of Artemisia annua Linne and Polygonum aviculare Linne, were investigated on the efficacy against E tenella. Survival rates, bloody diarrhea, lesion scores, body-weight gains and feed conversion rate were investigated at the 1st and the 2nd week after infection. The bloody diarrhea in the groups treated with P koreana, A annua, Q indica and P aviculare were milder than those in the groups treated with S flavescens and infected control. The lesion score in the groups treat.4 with herb extracts(2.00$\pm$0.82~2.65$\pm$0.89) were lower than those in the control group (2.80$\pm$0.7l). But, there was not significant in all infected groups. The body weight gai in the groups treated with P koreana, S flavescens, A annua and Q indica(291.74$\pm$15.76~303.43$\pm$51.90) were higher than that in the control group (283.71$\pm$16.53) but there was not significant. In a conclusion, analyzing the data of the survival rates, bloody diarrheal symptoms, lesion scores, body weight gains and oocyst excretions, the extract of S flavescens, P koreana, A annua and Q indica were effective. The further research on the above herbal materials will have been carried out by the author and the other researchers by means of the chemical analysis of the components.

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Hep3B 간암세포에서 개똥쑥 추출물에 의한 Cell Cycle Arrest 효과 (Cell Cycle Arrest Effects by Artemisia annua Linné in Hep3B Liver Cancer Cell)

  • 김은지;김근태;김보민;임은경;김상용;하성호;김영민;유제근
    • KSBB Journal
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    • 제30권4호
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    • pp.175-181
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    • 2015
  • Cells proliferate via repeating process that growth and division. This process is G1, S, G2 and M four phases consists. Monitoring the progression of the cell cycle is a specific step that to be a continuous process is repeated to adjust the start of the next step. At this time, this process is called a Checkpoint. Currently, there are three known checkpoints that G1-S phase, G2-M phase, and the M phase. In this study, we confirmed that cell cycle arrest effects by ethanol extracts of Artemisia annua Linne (AAE) in Hep3B liver cancer cells. AAE was regulated proteins which involved in cell cycle such as pAkt, pMDM2, p53, p21, pCDK2 (T14/Y15). AAE induced cell cycle arrest in G1 checkpoint through phosphorylation of CDK2. Akt and p53 upstream is inhibited by AAE and p53 activated by non-activated pMDM2, p53 inhibitor. Thereby, activated p53 is transcript to p21 and activated p21 protein is combined with Cyclin E-pCDK2 complex. Therefore, we confirmed that AAE-induced cell cycle arrest was occurred by p21-Cyclin E-pCDK2 complex by inhibition of pAkt signal. Because of this cell cycle can't pass to S phase from G1 phase.