• 제목/요약/키워드: IL-6 inhibitory activity

검색결과 435건 처리시간 0.03초

음양곽과 $\alpha$ -MSH에 의한 B16 Melanoma 세포의 멜라닌화와 Retinoic Acid의 억제 효과 (Inhibitory Effects of Retinoic Acid and Melanization of B16 Melanoma Cell by Epimedium koreanum Nakai and $\alpha$ -MSH)

  • 천현자;김일광;우원홍
    • 대한화학회지
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    • 제44권6호
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    • pp.533-540
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    • 2000
  • 음양곽 물추출액과 $\alpha$-melanocyte stimulating hormone ($\alpha$-MSH)에 의한 B16 melanoma 세포의 멜라닌화를 비교 조사하였으며, retinoic acid (RA)에 의한 억제효과도 연구하였다. B16 melanoma 세포(1×$10^5$개 정도)를 $\alpha$-MSH로 처리하고 72시간 배양한 결과 $\alpha$-MSH 처리농도에 비례하여 tyrosinase 활성도와 melanin 생성이 증가되었으며, 8 ng/mL 처리시 tyrosinase 활성도는 350%, melanin 함량은 290% 이상이었다. 음양곽 물추출액으로 처리한 경우에는, 100 ${\mu}g$/mL 처리시 tyrosinase 활성도는 200%, melanin 함량은 180% 이상이었다. 위 조건에 RA를 가하면, $\alpha$-MSH의 경우 tyrosinase 활성도는 350%에서 210%로, melanin 함량은 290%에서 250%로 억제되었다. 음양곽 물추출물의 경우 tyrosinase 활성도는 200%에서 100%로, melanin 함량은 180%에서 120%로 억제되었다. 이 결과는 음양곽 물추출액이 cAMP 신호전달 경로를 통하여 B16 melanoma 세포의 멜라닌화를 촉진하며, RA는 그것을 억제하는 것으로 해석된다.

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문주란의 항염효과와 화장료적 특성 (Anti-inflammatory Activity of Crinum asiaticum Linne var. Japonicum Extract and its Application as a Cosmeceutical Ingredient)

  • 김기호;김영희;김기수;박선희;이수희;김영진;김영실;김종헌
    • 대한화장품학회지
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    • 제32권1호
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    • pp.59-64
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    • 2006
  • 문주란(Crinum asiaticum Linne var. japonicum)은 한국, 말레이지아 등 동남아시아 지역에서 관절통, 해열, 궤양 치료, 국부의 소염 및 해열 등의 목적에 민간요법 등으로 오래 전부터 사용되어 오고 있다. 본 연구에서는 이러한 문주란의 화장료 조성물로서의 가능성을 확인하기 위하여 iNOS (inducible nitric oxide synthase) 억제 그리고 PGE2, IL-6, and IL-8 방출 억제에 의한 항염 효능을 측정하였다. pH를 3.5로 조절하고 95% ethanol을 사용하여 추출한 후, HPLC 실험으로 문주란의 주성분이 면역조절물질로 잘 알려진 lycorine이며 대략 1% 정도 함유한 것을 확인하였고 그 함량은 문주란의 추출 부위 및 추출방법에 따라 달랐다. 리포다당(lipopolysaccharide, LPS)에 의해 활성화된 생쥐 대식세포(RAW 264.7 cells)에서 생성되는 NO 형성의 억제능을 측정한 항염실험에서, 문주란 에탄을 추출물은 투여량에 비례하는 저해능을 가지고 있음을 확인할 수 있었다($IC_{50} = 83.5 {\mu}g/mL$). 또한 RT-PCR법을 이용하여 문주란 에탄을 추출물이 iNOS 유전자 발현도 억제함을 확인하였다. 또한, 문주란 추출물은 전혀 세포독성을 보이지 않았으며 오히려 LPS에 대하여 세포증식효과를 나타내었다(세포생존율 약 $10{\sim}60%$ 증가). 인간의 섬유아세포에서 과산화수소에 의해 활성화된 PGE2, IL-6 및 IL-8 방출 억제효능 측정 실험에서는 0.05%와 1% 농도 이상에서 (PGE2와 IL-6의 분비가) 거의 완전히 억제됨을 확인할 수 있었고, 나아가서 IL-8의 경우는 모든 실험농도 범위에서 완전히 억제되었다(>0.0025%). 이러한 결과로부터 문주란의 추출물이 충분한 항염 효과를 가지고 있음을 확인할 수 있었다.

모려로부터 추출된 conchiolin의 LPS로 유도된 RAW 264.7 세포에서의 항염증 효과 (Inhibitory Effect of Oyster Conchioloin on Pro-inflammatory Mediator in Lipopolysaccharide;Activated Raw 264.7 Cells)

  • 박상미;조용걸;이종록;이철원;김학주;권영규;김상찬
    • 동의생리병리학회지
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    • 제22권4호
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    • pp.878-883
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    • 2008
  • Conchiolin is a complex protein which is secreted by the mollusc's outer epithelium to be the organic basis of mollusc shell. This study is to investigate a potential anti-inflammatory activity of conchiolin of oyster shell (COS). We tested the effects of COS on the lipopolysaccharide (LPS)-induced production of nitric oxide (NO) and prostaglandin E2 (PGE 2) in a murine macrophage cell line, RAW 264.7. COS inhibited production of NO and PGE2 in a dose dependent manner and also decreased the expression of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), tumor necrosis $factor-{\alpha}$ ($TNF-{\alpha}$) and interleukin-6 (IL-6). These results suggest that COS can inhibit production of pro-inflammatory mediators and might be a useful source to treat inflammation.

소(牛) 식도구 평활근의 Adrenergic receptor 존재부위에 관한 연구 (Localization of adrenergic receptors in bovine esophageal groove)

  • 강동묵;조제열;박전홍;양일석
    • 대한수의학회지
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    • 제33권4호
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    • pp.617-622
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    • 1993
  • The preliminary studies on the localization of adrenoceptors were performed on smooth muscle strips of bovine esophageal groove. The mechanical activity of the muscle strip was recorded isometrically in vitro.w In the bottom circular muscle strips. the excitatory ${\alpha}-adrenergic$ responses were not blocked by tetrodotoxin$(2.1{\times}10^{-6}M)$ and denervation which was carried by cold storage of strips for 48 hrs in Tyrode's solution at $5-6{^{\circ}C}$ without oxygen supply. These excitatory ${\alpha}-adrenergic$ responses were partially blocked by atropine. In the lip longitudinal muscle strips, the inhibitory${\beta}-adrenergic$ responses were not blocked by pretreatment of tetrodotoxin and atropine. The results suggest that ${\beta}-adrenergic$ receptors mediating relaxations are located on the postsynaptic smooth muscle cells, whereas ${\beta}-adrenergic$ receptors mediating contractions are located both in the smooth muscle cells and in the cholinergic neurones.

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내독소에 의한 말초혈액 단핵구의 IL-8 및 IL-$1{\beta}$ 유전자 발현에서 산소기 역할에 관한 연구 (Role of Oxygen Free Radical in the Expression of Interleukin-8 and Interleukin-$1{\beta}$ Gene in Mononuclear Phagocytic Cells)

  • 강민종;김재열;박재석;이승준;유철규;김영환;한성구;심영수
    • Tuberculosis and Respiratory Diseases
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    • 제42권6호
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    • pp.862-870
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    • 1995
  • 연구배경: 산소기의 작용은 과거에는 세포독성이 주로 알려져 있었던 반면, 최근 들어 산소기의 세포내 신호전달체계에서의 역할에 많은 사람의 관심이 모이고 있다. 여러 cytokine의 전사인자(transcription factor)로 작용하는 $NF{\kappa}B$는 기저상태에서는 세포질에 존재하는데 $I{\kappa}B$와 결합되어 핵내로의 이동이 억제되고 있다. 여러 연구에 의해 $NF{\kappa}B$$I{\kappa}B$로부터의 분리는 외부자극에 의해 생성된 산소기에 의한 것으로 알려졌는데, 이렇게 하여 분리된 $NF{\kappa}B$가 핵내로 이동하면 핵내에서 전사인자로 작용하여 여러 유전자의 전사를 증가시키는 것이 보고되었다. IL-8 유전자는 5'flanking promotor region에 $NF{\kappa}B$-like motif가 있어 핵내 $NF{\kappa}B$ activity의 증가로 IL-8 유전자의 전사가 증가되는 것으로 알려졌고, 또한 내독소는 핵내의 $NF{\kappa}B$ activity의 증가와 함께 호중구에서의 산소기의 분비를 가져온다. 이러한 사실로부터 내독소에 의한 IL-8 유전자의 발현은 세포내에서 생성된 산소기에 의해 $NF{\kappa}B$$I{\kappa}B$로부터 분리되어 핵내로 이동하고 이로 인해 IL-8 유전자의 전사가 증가되는 가설을 생각할 수 있다. 저자들은 이러한 가설 검정의 첫번째 단계로써 체내 염증반응에서 중요한 역할을 하는 말초혈액 단핵구의 IL-8 및 IL-$1{\beta}$ 유전자 발현에 세포내의 산소기가 관여하는지의 여부를 평가하고자 본 연구를 시행하였다. 방법: Ficoll-Hypaque density gradient 법과 plastic 부착법을 이용하여 말초혈액 단핵구를 분리하였다. 외부에서 투여한 산소기의 농도에 따른 IL-8 및 IL-$1{\beta}$ mRNA 발현의 유무를 관찰하기 위하여 $H_2O_2$를 0, 10, 100, $300{\mu}M/L$, 1mM/L의 농도로 투여하고 6시간이 경과한후 IL-8 및 IL-$1{\beta}$에 대한 Northern blot analysis를 시행하였다. 시간에 따른 IL-8 및 IL-$1{\beta}$ mRNA 변화를 관찰하고자 $H_2O_2$$100{\mu}M/L$의 농도로 투여하고 0, 2, 4, 6, 8, 24시간이 경과한 후 Northern blot analysis를 시행하였다. 항산화제가 내독소에 의한 IL-8과 IL-$1{\beta}$ mRNA 발현에 미치는 영향을 평가하기 위하여 TMTU(10 mM/L) 1시간; PDTC($100{\mu}M/L$) 1시간, NAC(10 mM/L) 2.5시간, ME(10mM/(L) 2.5시간, Desferrioxamine(100mM/L) 15시간 동안 전처치 한 디음 내독소를 투여허여 4시간이 경과한 후 IL-8 및 IL-$1{\beta}$ mRNA에 대한 Northern blot analysis를 시행하였다. 결과: $H_2O_2$농도 및 시간에 따른 말초혈액 단핵구에서의 IL-8 및 IL-$1{\beta}$ mRNA의 발현에는 유의한 차이가 관찰되지 않았지만 항산화제로 전처치하였을 때 내독소에 의한 말초혈액 단핵구에서의 IL-8 및 IL-$1{\beta}$ mRNA의 발현이 억제되었고 그 억제정도는 TMTU에서 가장 현저하였다. 결론: 이상의 결과에서 말초혈액 단핵구에서의 IL-8 및 IL-$1{\beta}$ mRNA 발현에 $H_2O_2$가 아닌 다른 산소기가 일부 관여할 것으로 생각된다.

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Effects of Dexamethasone and DHEA on the Responses of Rat Cerebral Cortical Astrocytes to Lipopolysaccharide and Antimycin A

  • Choi, Sang-Hyun;Kim, Hyung-Gun;Kim, Chang-Keun;Park, Nan-Hyang;Choi, Dong-Hee;Shim, In-Sop;Chun, Boe-Gwun
    • The Korean Journal of Physiology and Pharmacology
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    • 제3권2호
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    • pp.127-135
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    • 1999
  • As part of a study on the effects of dexamethasone and dehydroepiandrosterone (DHEA) on the biological roles of astrocytes in brain injury, this study evaluated the effects of dexamethasone and DHEA on the responses of primary cultured rat cortical astrocytes to lipopolysaccharide (LPS) and antimycin A. Dexamethasone decreased spontaneous release of LDH from astrocytes, and the dexamethasone effect was inhibited by DHEA. However, the inhibitory effect of DHEA on the dexamethasone-induced decrease of LDH release was not shown in astrocytes treated with LPS, and antimycin A-induced LDH release was not affected by dexamethasone or DHEA. Unlike dexamethasone, DHEA increased MTT value of astrocytes and also attenuated the antimycin A-induced decrease of MTT value. Glutamine synthetase activity of astrocytes was not affected by DHEA or LPS but increased by dexamethasone, and the dexamethasone- dependent increase was attenuated by DHEA. However, antimycin A markedly decreased glutamine synthetase activity, and the antimycin A effect was not affected by dexamethasone or DHEA. Basal release of $[^3H]arachidonic$ acid from astrocytes was moderately increased by LPS and markedly by antimycin A. Dexamethasone inhibited the basal and LPS-dependent releases of $[^3H]arachidonic$ acid, but neither dexamethasone nor DHEA affected antimycin A-induced $[^3H]arachidonic$ acid release. Basal IL-6 release from astrocytes was not affected by dexamethasone or DHEA but markedly increased by LPS and antimycin A. LPS-induced IL-6 release was attenuated by dexamethasone but was little affected by DHEA, and antimycin A-induced IL-6 release was attenuated by DHEA as well as dexamethasone. At the concentration of dexamethasone and DHEA which does not affect basal NO release from astrocytes, they moderately inhibited LPS-induced NO release but little affected antimycin A-induced decrease of NO release. Taken together, these results suggest that dexamethasone and DHEA, in somewhat different manners, modulate the astrocyte reactivity in brain injuries inhibitorily.

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유백피, 토복령 추출물 혼합물의 항산화, 항염, 항균 및 난소세포 보호효과 (Antioxidant, anti-inflammatory, antibacterial and ovoprotective effects of mixture of Ulmi cortex and Smilacis rhizoma extracts)

  • 전상규;안정윤;박수미;박선동;이주희
    • 대한한의학방제학회지
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    • 제28권1호
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    • pp.41-51
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    • 2020
  • Objectives : US extract is a mixture of each extract of Ulmi cortex and Smilacis rhizoma. In this study, we investigated the antioxidant, anti-inflammatory, antibacterial, and ovoprotective effects of US extract in in vitro model to identify potential candidates for improving female reproductive function. Methods : The antioxidant activity of US extract was measured using 1,1-diphenyl- 2-picrylhydrazyl free radical and superoxide anion radical scavenging assays. The anti-inflammatory effect of US extract on lipopolysaccharide (LPS)-stimulated RAW 264.7 cells were determined with a nitric oxide (NO) assay, enzyme linked immunosorbent assays, and western blots analysis. The antibacterial activity of US extract against vaginitis infection microorganisms were determined with disc diffusion and minimum inhibitory concentration assays. The ovoprotective effect of US extract on 4-vinylcyclohexene diepoxide (VCD)-induced ovotoxicity in CHO-K1 cells were evaluated with a cell viability assay. Result : US extract showed good antioxidant capacity and inhibited LPS-induced NO production as well as iNOS and COX-2 expression and secretion of pro-inflammatory cytokine IL-6 without affecting the cell viability. It showed significant clear zones for Staphylococcus aureus and Candida albicans but did not indicate the clear zones for Escherichia coli and Enterococcus faecium. VCD-induced ovotoxicity in CHO-K1 cells was significantly reduced by US extract pre-treatment. Conclusions : These results demonstrate that US extract has antioxidant activity, anti-inflammatory effects on the LPS-stimulated macrophages, antibacterial activity against vaginitis infection microorganisms, and protective effects on the ovarian cells against VCD-induced ovotoxicity. These findings suggest that the US extract can be used as new prescriptions, supplements, functional foods, and cosmetics for improving female reproductive function.

Analyzing of the Essential Oil Chemical Constituents in Artemisia lavandulaefolia and its Pharmacological Property on Antibacterial Activity

  • Kim, Kyong-Heon;Kim, Baek-Cheol;Lee, Hwa-Jung;Jeong, Seung-Il;Kim, Hong-Jun;Ju, Young-Sung
    • 한방안이비인후피부과학회지
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    • 제17권3호
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    • pp.26-32
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    • 2004
  • Objective: The aim of this work is to investigate the antibacterial activity of the essential oil obtained from Artemisia lavandulaefolia (A. lavandulaefolia), as the development of microbial resistance to antibiotics make it essential to constantly look for new and active compounds effective against pathogenic bacteria. Method: The aerial parts of A. lavandulaefolia (1 kg) were subjected to steam distillation for 3 h, using a modified Clevenger type apparatus in order to obtain essential oil. Diethyl ether was the extracting solvent kept at 25?. The essential oil were analyzed by gas chromatography (GC) and gas chromatography/mass spectrometry (GC/MS). The essential oil and the composition were tested for antimicrobial activities against 15 different genera of oral bacteria. Ninety-nine compounds accounting for 94.74$\%$</TEX> of the oil were identified. The main compounds in the oil were 1,8-cineole (5.63$\%$), yomogi alcohol (4.49$\%$), camphor (4.92$\%$), a-caryophyllene (16.10$\%$), trans-a-famesene (5.09$\%$), a-terpineol (3.91$\%$), borneol (5.27$\%$), cis-chrysanthenol (6.98$\%$), and a-humulene oxide (3.33$\%$). The essential oil and its compounds were tested for antimicrobial activity against 10 different genera of oral bacteria. Conclusion: The essential oil of A. lavandulaefolia exhibited considerable inhibitory effects against all obligate anaerobic bacteria (MICs, 0.025 - 0.05 ㎎/ml) tested, while their major compounds demonstrated various degrees of growth inhibition

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Comparative study on antioxidant activity of Gold 1, a new strain of Pyropia yezoensis

  • Jimin Hyun;Sang-Woon Lee;Hyeon Hak Jeong;Jae-Il Kim
    • Fisheries and Aquatic Sciences
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    • 제26권2호
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    • pp.158-168
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    • 2023
  • The global output of Pyropia yezoensis (dried seaweed or laver, also called 'Gim' in Korea) has been reduced over the half-decade due to the wide spread of red rot disease, a serious algal disease affecting P. yezoensis. Recently, Gold 1 (G1), which is a resistant strain of P. yezoensis to red rot disease, was developed and commercialized in South Korea, yet its physiological activity has not been investigated. In this study, a comparative study was performed on G1 and commercially available strain of P. yezoensis (CP) for their antioxidative activities. Aqueous extract of G1 showed more marked 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) radical scavenging activity compared to that of CP. In 293T cells, antioxidant activity against H2O2-induced reactive oxygen species (ROS) formation was only observed in G1 extract. In addition, G1 extract showed more potent inhibitory effect on H2O2-induced apoptotic cell death than CP extract, as examined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and fluorescence microscopy. Expression levels of various apoptosis-related genes, including B-cell lymphoma 2-associated X protein, p53, capase-3, and inflammatory cytokines, in H2O2-treated cells were significantly decreased by the treatment of G1. Taken together, the present study suggests that a new strain of red seaweed G1 can recover oxidative stress effectively by improving the imbalance of ROS generation and has a potential to be used a functional ingredient as an antioxidant source.

Lipopolysaccharide로 유도된 Raw264.7 cell에서 Rhododendron mucronulatum Turcz. Flower으로부터 분리한 myricetin에 의한 염증 억제효과 (Anti-inflammatory Effect of Myricetin from Rhododendron mucronulatum Turcz. Flowers in Lipopolysaccharide-stimulated Raw 264.7 Cells)

  • 최무영;홍신협;조준효;박혜진;조재범;이재은;김동희;김병오;조영제
    • 생명과학회지
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    • 제26권11호
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    • pp.1245-1252
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    • 2016
  • 진달래꽃으로부터 Sephadex LH-20 및 MCI gel CHP-20 column chromatography로 정제한 결과 항염증 활성을 가지는 myricetin을 분리, 동정하였다. Myricetin은 농도 의존적으로 NO 발현을 억제하였고, $50{\mu}M$ 농도에서 약 40%의 억제효과를 나타내었다. Myricetin의 iNOS와 COX-2의 발현억제력은, $25{\mu}M$ 농도에서 각각 20% 및 80%의 protein 발현 억제효과를 나타내었다. 또한 myricetin의 염증반응의 cytokine을 측정하여 $TNF-{\alpha}$, $IL-1{\beta}$, IL-6 및 $PGE_2$의 억제력을 살펴본 결과, 농도 의존적으로 발현억제 효과를 나타내었으며, $50{\mu}M$ 농도에서 각각 70%, 80%, 80% 및 95%의 발현 억제효과를 나타내었다. 따라서 진달래 꽃잎에서 분리한 myricetin은 LPS로 유도되어진 대식세포주인 Raw 264.7 세포에서 염증반응의 억제효과를 기대할 수 있었다.