• 제목/요약/키워드: 벌사상자

검색결과 6건 처리시간 0.015초

AGS 위암세포에서 Akt/GSK-3β/p53 신호경로 조절을 통한 벌사상자 에탄올 추출물의 G1 Cell Cycle Arrest 유도 효과 (Ethanol Extract from Cnidium monnieri (L.) Cusson Induces G1 Cell Cycle Arrest by Regulating Akt/GSK-3β/p53 Signaling Pathways in AGS Gastric Cancer Cells)

  • 임은경;김은지;김보민;김상용;하성호;김영민
    • 한국식품영양과학회지
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    • 제46권4호
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    • pp.417-425
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    • 2017
  • 벌사상자는 여성의 생식기 질환이나 화농성 피부염에 주로 사용되어온 한약재로, 최근 들어 암과 관련된 연구가 많이 이루어짐에 따라 벌사상자의 항암 효과에 대한 관심이 높아지고 있다. 벌사상자의 대표적인 성분인 osthole, xanthotoxol 등은 벤젠고리 화합물로 에탄올과 같은 유기용매에 잘 용해된다. 이에 따라 본 연구에서는 AGS 위암세포에서 벌사상자 에탄올 추출물(CME)에 대한 세포주기 정지 유도 효과를 확인하고자 하였다. CME 처리에 의한 AGS 위암세포의 증식 억제 유도 효과 및 세포독성 효과를 확인하기 위하여 MTT assay와 LDH release assay를 실시한 결과, 농도 및 시간 의존적으로 세포생존율이 감소하였으며, 농도 의존적인 세포독성 효과를 확인하였다. 또한, CME의 농도가 증가할수록 AGS 위암세포의 형태학적 변화가 관찰되었다. 이러한 세포증식 억제 유도 효과가 세포주기 정지에 의한 것인지 확인하기 위하여 CME를 농도별로 24시간 동안 처리한 후 세포주기를 측정하였다. 그 결과 G1기의 세포가 농도 의존적으로 증가함을 확인하였다. 그리고 CME의 처리가 세포주기와 관련된 단백질에 미치는 영향을 알아보기 위하여 western blot analysis를 실시하여 G1기 세포주기 정지와 관련된 신호 단백질들의 발현 변화를 확인하였다. 그 결과 CME의 처리가 세포 증식과 분열에 중요한 역할을 하는 p-Akt와 p-GSK-$3{\beta}$의 발현을 저해하는 것을 확인하였고, 이에 따라 p53의 발현과 활성이 증가하여 p21의 발현이 증가함을 확인하였다. 또한, p21의 증가에 따른 cyclin E의 발현 감소와 CDK2의 비활성화 상태인 p-CDK(T14), p-CDK(Y15)의 발현 증가를 확인하였다. 이와 같은 CME의 세포주기 억제 유도 효과가 일어나는 신호경로를 확인하기 위하여 LY294002(PI3K/Akt 저해제), BIO(GSK-$3{\beta}$ 저해제), Pifithrin-${\alpha}$(p53 저해제)를 CME와 각각 또는 병행 처리한 후 MTT assay, 세포주기 측정, western blot analysis를 진행하였다. 그 결과 LY294002의 처리는 CME 처리군과 유사하게 세포생존율을 저해시키고 G1기 정지를 유도했으며, 세포주기 단백질을 조절하였다. 또한, GSK-$3{\beta}$와 p53 저해제를 처리하였을 때 CME를 병행 처리했음에도 불구하고 세포증식 억제나 G1기 정지와 같은 항암 효과가 나타나지 않았으며, 관련 신호경로 단백질의 변화도 관찰되지 않았다. 이러한 결과는 CME의 처리가 Akt/GSK-$3{\beta}$/p53 신호경로를 조절하여 cyclin E의 발현을 감소시키고 CDK2의 활성을 억제함으로써 G1기 세포주기 정지를 유도함을 확인하였다.

강활과 벌사상자 추출물의 피부 미백효과 (Skin Whitening Effects of Angelica koreana and Cnidium monnieri Extracts)

  • 조완구;김청택
    • 디지털융복합연구
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    • 제12권4호
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    • pp.419-425
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    • 2014
  • 본 연구의 목적은 강활과 벌사상자 추출물에 의한 피부 멜라닌 형성 저해와 안정성과 자극성 시험을 통하여 기능성 화장품의 사용 물질 가능성을 평가하고자 하였다. 본 실험에 사용된 추출물은 White-$AK^{TM}$이고 INCI 명칭은 Osthole이다. White-$AK^{TM}$의 주성분은 쿠마린이고 EC50 값은 마우스 멜라노마 B16 세포 시험에서 2.7ppm이였다. White-$AK^{TM}$는 알부틴보다 100배 낮은 농도에서 저해 효과를 보였다. 미백 효과의 주 기작은 티로시나제-관련 유전자 발현을 저해하는 것으로 생각되었다. White-$AK^{TM}$ 5% 용액을 함유한 기본적인 에센스 처방을 피부에 적용 시 피부자극을 경감시켰다. White-$AK^{TM}$은 불투명한 용기에서 4주간 자외선 하에서 100%의 회수율을 보였고 $50^{\circ}C$에서 4주간 97%의 회수율을 보였다. 따라서 피부 미백효과와 자극성 경감효과가 있고 자외선 조건하에서 안정한 White-$AK^{TM}$은 화장품 처방에서 기능성 원료로 사용될 수 있을 것으로 사료된다.

Leydig Cell의 항산화에 미치는 벌사상자와 사상자의 비교연구 (The Antioxidant Activity of Cnidii Fructus and Torilis Fructus in Leydig cells)

  • 오지훈;김도림;박수연;장문석;박성규
    • 대한본초학회지
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    • 제29권6호
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    • pp.111-116
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    • 2014
  • Objectives : The purpose of this study was to estimate the antioxidant activity of water extract of Cnidii Fructus (CF) and Torilis Fructus (TF) in Leydig cells. Methods : Free radical scavenging activity of CF and TF against 2,2-diphenyl-1-picrylhydrazyl (DPPH) was determined spectrophotometrically. We investigated the effect of CF and TF in Leydig cells by MTT assay. The protective effects of CF and TF against hydrogen peroxide-induced oxidative stress in Leydig cells. Superoxide dismutase (SOD), and catalase activity assays were performed in Leydig cells. Results : The results showed that CF scavenged DPPH radical in a dose-dependent manner by up to 81.2%, TF scavenged DPPH radical in a dose-dependent manner by up to 63.8%. CF showed cell viability as 121.0, 132.7, 126.6% in 5, 10, $100{\mu}g/ml$ concentrations. TF showed cell viability as 127.5, 111.8% in 5, $100{\mu}g/ml$ concentraions, respectively. The hydrogen peroxide-induced cytotoxicity of Leydig cells were protected to 86.3% by CF at concentration of $10{\mu}g/ml$ and protected to 83.5% by TF at concentration of $100{\mu}g/ml$. Both CF and TF at all concentrations, SOD activity was not significantly changed. Catalase activity was significantly increased at 10, $100{\mu}g/ml$ concentrations of CF, respectively. TF's catalase activity showed no significant difference from that of the control. Conclusions : These results suggest that CF, as an antioxidant, protects Leydig cells in hydrogen peroxide-induced oxidative stress. know that "Kwangjebikeup" played a role in settlement and spreading of foreign knowledge to civilians.

벌사상자 Ethyl Acetate 분획물의 항염증활성연구 (Ethyl Acetate Fraction of Cnidium monnieri(L). Cussion Suppresses PAM plus A23187-induced Inflammation Reaction through Blockade of NF-κB and MAPK activation)

  • 강옥화;김상영;권동렬
    • 생약학회지
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    • 제46권3호
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    • pp.195-202
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    • 2015
  • Cnidium monnieri (L). Cussion is used as a tonic agent in traditional oriental medicine. However, the molecular mechanism of mast cell-mediated anti-inflammatory modulation has not been fully understood. The aim of the present study was to demonstrate the effects of Cnidium monnieri (L). Cussion eathyl acetate fraction on the expression of pro-inflammatory cytokines, as well as to elucidate its mechanism of action in the human mast cell line (HMC-1). Cells were stimulated with phorbol 12-myristate 13-acetate (PMA) plus A23187 in the presence or absence of Cnidium monnieri (L). Cussion eathyl acetate fraction. Cnidium monnieri (L). Cussion eathyl acetate fraction significantly inhibited the PMA plus A23187-induction of inflammatory cytokines such as tumor necrosis factor (TNF)-$\alpha$, interleukin (IL)-6 and IL-8. Moreover, EtOAc fraction attenuated cyclooxygenase (COX)-2 expression. In activated HMC-1 cells, phosphorylation of extra-signal response kinase (ERK) 1/2 decreased after treatment with EtOAc fraction. Moreover EtOAc fraction inhibited PMA plus A23187-induced nuclear factor (NF)-${\kappa}B$ activation, $I{\kappa}B$ degradation. EtOAc fraction suppressed the expression of TNF-$\alpha$, IL-6, IL-8 through a decrease in the ERK 1/2, as well as activation of NF-${\kappa}B$. These results indicated that Cnidium monnieri (L). Cussion EtOAc fraction exerted a regulatory effect on inflammatory reactions mediated by mast cells.

DNA 염기서열과 미각패턴 분석을 이용한 사상자와 벌사상자의 감별 (Comparison between Torilis japonica and Cnidium monnieri Using DNA Sequencing and Taste Pattern Analysis)

  • 김영화;김영선;채성욱;이미영
    • 대한본초학회지
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    • 제28권6호
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    • pp.9-14
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    • 2013
  • Objectives : Cnidii Fructus is prescribed as the fruit of Cnidium monnieri (L.) Cusson or Torilis japonica (Houtt.) DC. in Korea pharmacopoeia. Although there are differences in the composition of useful components, two species have been used without distinction. In order to discriminate them, DNA sequencing and taste pattern analysis were used in this study. Methods : Primers ITS 1 and ITS 4 were used to amplify the intergenic transcribed spacer(ITS) region of nuclear ribosomal DNA from seven T. japonica and six C. monnieri samples. Taste pattern of samples were measured by using taste-sensing system SA402B equipped with five foodstuff sensors(CT0, C00, AAE, CA0, and AE1). The five initial taste(sourness, bitterness, astringency, umami, and saltiness) and three aftertaste(aftertaste of bitterness, astringency, and umami) of two species were compared. Results : According to the results of ITS region sequence analysis, two species showed 94 base pairs differences. The similarity of two sequences was 85%. From the taste pattern analysis, sourness, bitterness, aftertaste of bitterness(aftertaste-B), and umami showed a different pattern. Especially, bitterness and aftertaste-B of C. monnieri were significantly higher than T. japonica. In addition, two species were shown to have two markedly different clustering by these two flavors. Conclusion : T. japonica and C. monnieri were effectively discriminated using DNA sequencing and taste pattern analysis. These methods can be used to identify the origin of traditional medicine in order to maintain therapeutic efficacy.

벌사상자의 위염 치료 적용에 대한 네트워크 약리학적 분석 (Network Pharmacological Analysis of Cnidii Fructus Treatment for Gastritis)

  • 김영식;이승호
    • 동의생리병리학회지
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    • 제38권1호
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    • pp.22-26
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    • 2024
  • The purpose of this study was to identify the applicability, main compounds, and target genes of Cnidii Fructus (CF) in the treatment of gastritis using network pharmacology. The compounds in CF were searched in Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) and a database of medicinal materials and chemical compounds in Northeast Asian traditional medicine (TM-MC). The target gene information of the compounds was collected from pubchem and cross-compared with the gastritis-related target gene information collected from Genecard to derive the target genes. Gene ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were performed on the derived target genes. Afterwards, network analysis between compounds and disease target genes was performed using cytoscape. We identified 121 active compounds and 139 target genes associated with gastritis. Pathways derived from the GO biological process and KEGG pathway DB primarily focus on target genes related to inflammation (IL-6, IL-8, TNF production, NF-κB transcription factor activity, and NF-κB signaling pathway) and cell death (PI3K-Akt, FoxO). Major targets for CF treatment of gastritis include TP53, TNF, BCL2, EGFR, NFKB1, ABCB1, PPARG, PTGS2, IL6, IL1B, and SOD1, along with major compounds such as coumarin, osthol, hexadecanoic acid, oleic acid, linoleic acid, and stigmasterol. This study provided CF's applicability for gastritis, related compounds, and target information. Evaluating CF's effectiveness in a preclinical gastritis model suggests its potential use in clinical practice for digestive system diseases.