• 제목/요약/키워드: $PGE_1$

검색결과 861건 처리시간 0.029초

면역세포 활성에 대한 Substance P의 영향 (Effects of Substance P on the Activities of Immune Cell)

  • 김형섭;오귀옥;임종득
    • Journal of Periodontal and Implant Science
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    • 제26권2호
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    • pp.376-395
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    • 1996
  • The neuropeptide substance P(SP) has been recognized to modulate immune systems, with close proximity between peptidergic sensory nerve endings and immune cells. These include the macrophage and neutrophil activation, IL-2 production in T cell, augmentation of Ig synthesis, mast cell degranulation, $PGE_2$ and collagenase secretion in synoviocytes. In this study I examined SP-induced various biological activities such as antimicrobial action, cytokine production, and mast cell degranulation in the presence or absence of other inflammatory cell activators. Antimicrobial studies showed that undifferentiated HL-60 cells were not affected by SP. However, SP significantly enhanced antimicrobial action of TPA-treated or dbcAMP-treated HL-60 cells which had been differentiated into PMN or macrophage/monocyte. I could not find synergistic relationship between SP and LPS in parallel experiments of the above. SP did not induce IL-l production from murine macrophage cell line RAW264.7 whether costimulated with LPS or not. Mast cell degranulation was occured only when stimulated with high dose ($10^{-5}M$) of SP and the degree of this activation was slightly reduced by simultaneous application of $MIP-1{\alpha}$. In addition, CGRP which is known to be a common coexisting neuropeptide with SP within specific fibers did not augment the function of SP on mast cell degranulation. These results suggest that immunoregulatory activities of SP could be mediated through direct upregulation of various functions of immune cells and also upregulation of responsiveness of immune cells to other immune activators.

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인체폐암세포의 증식 및 prostaglandin E2 생성에 미치는 청조구폐탕의 영향에 관한 연구 (Antiproliferative Effect of Chungjogupae-tang Treatment was Associated with the Inhibition of Prostaglandin E2 Release in Human Lung Carcinoma Cells)

  • 임재형;김훈;변미권;감철우;박동일
    • 동의생리병리학회지
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    • 제20권4호
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    • pp.966-972
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    • 2006
  • The effect of water extract of Chungjogupae-tang (CJGPT) was investigated _on the growth of human lung carcinoma A549 cells. Methods: MTT assay and fluorescent microscope peformed to compare and examine the efficacy of CJGPT treatment on the cytostaticity of lung cancer cells in proportion to time and doses, and DAPI staining and Western blot analysis were used to examine their effect on apoptosis. In addition, the quantitative RT-PCR was used to examine to lung cancer cells growth, and Prostaglandin E2 activity were measured. Results: Exposure of A549 cells to CJGPT respited in the growth inhibition and apoptosis in a dose-dependent manner as measured by MTT assay and fluorescent microscope. The antiproliferative effect by CJGPT treatment in A549 cells was associated with morphological changes such as membrane shrinking and cell rounding up. CJGPT treatment resulted in an up-regulation of cyclin-dependent kinase inhibitor p21 (WAFl/CIPl) in a p53-independent fashion. We found that CJGPT treatment decreased the levels of cyclooxygenase (COX)-2 and inducible nitric oxide synthease (iNOS) expression without significant changes in the expression of COX-1 , which was correlated with a decrease in prostaglandin E2 (PGE2) synthesis. Conclusion: These findings suggested that CJGPT-induced inhibition of human lung carcinoma A549 cell growth was connected with the induction of apoptotic cell death and the results provided important new insights into the possible molecular mechanisms of the anti-cancer activity of CJGPT.

The Chloroform Fraction of Carpinus tschonoskii Leaves Inhibits the Production of Inflammatory Mediators in HaCaT Keratinocytes and RAW264.7 Macrophages

  • Kang, Gyeoung-Jin;Kang, Na-Jin;Han, Sang-Chul;Koo, Dong-Hwan;Kang, Hee-Kyoung;Yoo, Byoung-Sam;Yoo, Eun-Sook
    • Toxicological Research
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    • 제28권4호
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    • pp.255-262
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    • 2012
  • Inflammation is the immune system's response to infection and injury-related disorders, and is related to pro-inflammatory factors (NO, $PGE_2$, cytokines, etc.) produced by inflammatory cells. Atopic dermatitis (AD) is a representative inflammatory skin disease that is characterized by increasing serum levels of inflammatory chemokines, including macrophage-derived chemokine (MDC). Carpinus tschonoskii is a member of the genus Carpinus. We investigated the anti-inflammatory activity of C. tschonoskii by studying the effects of various solvent fractions prepared from its leaves on inflammatory mediators in HaCaT and RAW264.7 cells. We found that the chloroform fraction of C. tschonoskii inhibited MDC at both the protein and mRNA levels in HaCaT cells, acting via the inhibition of STAT1 in the IFN-${\gamma}$ signaling pathway. In addition, the chloroform fraction significantly suppressed the expression of inflammatory factors induced by lipopolysaccharide stimulation, except COX-2 and TNF-${\alpha}$. These results suggest that the chloroform fraction of C. tschonoskii leaves may include a component with potential anti-inflammatory activity.

증숙 오미자의 항산화, 항염증 및 간보호 효과 비교 연구 (Antioxidant, Antiinflammation and Hepatoprotective activity of Schizandrae Fructus processed with differenciated steaming number)

  • 추병길;정기훈;서영배;노성수
    • 대한본초학회지
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    • 제28권2호
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    • pp.83-92
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    • 2013
  • Objectives : We investigated differances of physiological functionalities in the steamed Schisandrae Fructus. Methods : The samples were extracts of dryed schisandrae fructus without steaming process (S0), extracts of schisandrae fructus with three times steamed (S3), extracts of schisandrae fructus with five times steamed (S5) and extracts of schisandrae fructus with seven times steamed (S7). We analyzed contents of schisandrin, gomisin, total polyphenol and flavonoid and antioxidant activities. We researched antiinflammation effects for Raw264.7 cells. To evaluate liver protective activity, we measured AST, ALT and gamma-GTP in serum of alcoholic mice. Results : As the steaming number of schisandrae fructus increase, the contents of schisandrin and gomisin were more increased. The contents of total polyphenol of S5 and S7 were significantly increased compared to that of S0. DPPH free radical scavenging activities of S5 and S7 were significantly increased compared to that of S0, ABST radical scavenging activities of S3 and S5 were significantly increased compared to that of S0 in vitro. The NO production of all sample was significantly decreased compared to control, PGE2 release of S3, S5 and S7 were significantly decreased compared to control. IL-$1{\beta}$ release of S5 and S7 were significantly decreased. AST, ALT and gamma-GTP of S3, S5 and S7 were significantly decreased compared to control. Conclusions : We think that extracts of schisandrae fructus with steaming process may have more potential efficacy than a schisandrae fructus without steaming process.

Anti-inflammatory and antioxidant activities of Sargassum horneri extract in RAW264.7 macrophages

  • Kim, Min Ju;Jo, Hee Geun;Ramakrishna, Chilakala;Lee, Seung-Jae;Lee, Dong-Sung;Cheong, Sun Hee
    • 운동영양학회지
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    • 제25권4호
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    • pp.45-53
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    • 2021
  • [Purpose] In this study, we investigated whether a 70% ethanolic (EtOH) extract of Sargassum horneri had antioxidant and anti-inflammatory effects in lipopolysaccharide (LPS)-stimulated macrophage-like RAW 264.7 cells. [Methods] The proximate composition, fatty acids, amino acids, and dietary fiber of S. horneri, various biologically active compounds, and antioxidant activity were analyzed. [Results] The DPPH and ABTS free radical scavenging activities, as well as the reduction power, of the S. horneri extract used here were significantly increased in a concentration-dependent manner. This indicates that S. horneri contains bioactive compounds, such as phenols and flavonoids, that have excellent antioxidant activity. The cellular viability and metabolic activity results confirmed that the extract had no discernible toxicity at concentrations up to 100 ㎍/mL. The levels of nitrites and cytokines (PGE2, TNF-α and IL-6), which mediate pro-inflammatory effect, were significantly inhibited by treatment with either 50 or 100 ㎍/mL S. horneri extract, whereas that of IL-1β was significantly inhibited by treatment with 100 ㎍/mL of the extract. Similarly, the expression of iNOS and COX-2 proteins also decreased according to 50 or 100 ㎍/mL extract concentrations. NF-κB binding to DNA was also significantly inhibited by treatment with 100 ㎍/mL of extract. [Conclusion] These results suggest that 70% EtOH extracts of S. horneri can relieve inflammation caused by disease or high intensity exercise.

Electroacupuncture Treatment for Primary Dysmenorrhea: A Review of Randomized Controlled Trials

  • Jeon, Myung Kyu;Park, Jae Eun;Lee, Min Cheol;Kim, Hyeon Jin;Ahn, Jae Young;Shin, Na Young;Nam, Hye Jin;Chae, Go Eun;Jo, Hye Jeong;Kim, Hyun Woo;Lee, Young Jin;Koh, Arha;Kim, Woo Young
    • Journal of Acupuncture Research
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    • 제39권3호
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    • pp.182-189
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    • 2022
  • To evaluate the effectiveness of electroacupuncture treatment for primary dysmenorrhea (PD), a literature review of a randomized controlled trials (RCTs) was performed where electroacupuncture was used as a treatment intervention in patients diagnosed with PD. Relevant clinical studies (N = 226) were retrieved from multiple databases according to the study inclusion/exclusion criteria, and interventions and outcomes were analyzed. As a result of the review, there were 6 RCTs which met the criteria. In all 4 studies that measured pain indicators (visual analog scales), electroacupuncture showed significantly positive changes. In addition, positive changes were observed in most indicators (MMDQ, PGF2a, PGE2, 6-keto PGF1, TXB2, clinical efficacy score, uterine arterial blood flow parameters, and blood viscosity). 2 studies showed that electroacupuncture had a stronger therapeutic effect than NSAIDs. No major side effects were reported. Electroacupuncture may be an effective and safe treatment for PD however, further RCTs are required.

RAW 264.7 세포에 대한 NF-κ B와 MAPK 활성 억제를 통한 개다래 열매 에탄올 추출물의 항염증 효과 (Anti-inflammatory Effects of Actinidia Polygama Ethanol Extract in through the Regulated NF-κ B and MAPKs Activation in LPS Stimulated RAW 264.7 Cells)

  • 박충무;윤현서
    • 대한통합의학회지
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    • 제11권2호
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    • pp.119-128
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    • 2023
  • Purpose : The fruit of Actinidia polygama has been used in oriental medicine for the treatment of gout, rheumatoid arthritis, and inflammation. Though A. polygama exhibited anti-inflammatory activity in RAW 264.7 cells and carrageenan-induced rat paw edema, the exact mechanism for anti-inflammation was not evaluated yet. In this study, the anti-inflammatory mechanisms of A. polygama ethanol extract (APEE) in lipopolysaccharide (LPS) stimulated RAW 264.7 cells. Methods : WST-1 assay was applied to analyze the cytotoxic effect of APEE in RAW 264.7 cells. The productions of nitric oxide (NO) and prostaglandin (PG) E2 were analyzed by the Griess reaction and enzyme immunoassay (EIA) assay, respectively. In addition, protein expressions for inducible NO synthase (iNOS) and cyclooxygenase (COX)-2 were measured by Western blot analysis. The activated status of an inflammatory transcription factor, NF-κ B, and its upstream signaling molecules, mitogen-activated protein kinases (MAPKs), was also evaluated by Western blot analysis. Results : As a result, APEE treatment did not exhibit any cytotoxicity until the concentration of 200 ㎍/㎖. APEE treatment significantly inhibited NO and PGE2 productions as well as their enzymes, iNOS and COX-2 in a dose-dependent manner. The inflammatory transcription factor, NF-κ B, was also attenuated by APEE treatment. In addition, the phosphorylated status of MAPKs such as extracellular regulated kinase (ERK), c-jun NH2 kinase (JNK), and p38, were significantly diminished by APEE treatment in LPS stimulated RAW 264.7 cells. Conclusion : Consequently, APEE treatment significantly attenuated the production of inflammatory mediators and their enzyme expressions in LPS-stimulated RAW 264.7 cells. The inflammatory transcription factor, NF-κ B, and upstream signaling molecules, MAPKs, were also significantly attenuated by APEE treatment in LPS-activated RAW 264.7 cells. These results indicate that APEE might be a candidate to be utilized as a promising candidate for the treatment of inflammatory disorders.

도라지 잎 에탄올 추출물의 주요 성분 분석 및 마우스 대식세포와 인체 폐암세포에서 항염효과 (Analysis of Major Constituents of an Ethanol Extract of Platycodon Grandiflorum Leaves and Protective Effects on Inflammation in Murine Macrophage and Human Lung Carcinoma Cells)

  • 이정민;배병준;최지림;정영신
    • 한국식품영양학회지
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    • 제37권2호
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    • pp.110-122
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    • 2024
  • This study investigated major constituents and anti-inflammatory effects of an ethanol extract of Platycodon grandiflorum leaves. Through HPLC analysis, chlorogenic acid and luteolin-7-O-glucoside were identified as predominant constituents in the ethanol extract. Their anti-inflammatory effects were evaluated using murine macrophage (RAW 264.7 cells) and human lung carcinoma cells (NCI-H292 & A549). The ethanol extract significantly (p<0.01) inhibited the production of nitrite, interleukin-6 (IL-6), and prostaglandin E2 (PGE2) induced by lipopolysaccharide (LPS) in RAW 264.7 cells. Furthermore, the ethanol extract suppressed the expression of cyclooxygenase-2 (COX-2) and inducible NO synthase (iNOS) proteins in RAW 264.7 cells stimulated with LPS. In NCI-H292 and A549 cells, treatment with the ethanol extract significantly (p<0.05) decreased levels of pro-inflammatory cytokines IL-6 and IL-8 induced by IL-1β. The phosphorylation of ERK rather than JNK in the mitogen-activated protein kinase signaling pathway was observed to be a more important mediator in the down-regulation of pro-inflammatory cytokines in NCI-H292 cells. These findings suggest that the ethanol extract of Platycodon grandiflorum leaves containing luteolin-7-O-glucoside exhibits promising anti-inflammatory properties.

분만후 젖소에 있어서 $PGF_2a+PGF_2a+CIDR$ Program 적용에 의한 발정유기시 BCS의 영향 (Effect of $PGF_2a+PGF_2a+CIDR$ Program on Estrous Response in Holstein with Varying BCS in Early Postpartum)

  • 백광수;박성재;박수봉;김현섭;이현준;이왕식;전병순;안병석;김재기;정경용;손준규
    • 한국수정란이식학회지
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    • 제20권3호
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    • pp.279-287
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    • 2005
  • 본 연구는 젖소에 있어서 분만후 난소 활동의 재개 및 분만후 40일째 BCS가 $PGE_2a+PGE_2a+CIDR$ (PPC) program 적용에 미치는 영향을 구명하기 위하여 2002년부터 2003년까지 2년간에 걸쳐 축산연구소 및 천안 소재 전문 경영체 젖소농 장에서 사육중인 홀스타인 착유우를 대상으로 분만 후 난소 활동의 재개를 조사하기 위한 착유우21두 및 분만후 40일째 BCS가 PPC program 적용에 미치는 영향을 구명하기 위한 착유우 40두를 공시하여 수행한 결과 다음과 같은 성적을 얻었다. 1 분만후 처음으로 유즙중의 progesterone농도가 1.0ng/mL 이상을 나타내는 비율은 10${\~}$30일이 $42.9\%$, 31${\~}$50일이 $19.1\%$였고 분만 후 50일까지 1.0ng/mL 이상을 나타내지 않은 경우가 $38.1\%$였다. 2. 분만후 40일째부터 PPC program을 투입한 결과 1차 및 2차 $PGF_2a$ 처리에 대한 발정반응은 각각 $47.5\%$$52.4\%$였고, $PGF_2a+PGF_2a$ (PP) program투입에 의해 40두중 30두($75\%$)가 발정 반응을 나타내었다. PP program 투입에 의해 발정 반응을 나타내지 않은 10두에 대한 CIDR 처리의 발정 반응은 $50\%$를 나타내었다. 분만후 40일째에 PPC program 을 적용한 결과 40두중 35두가 발정 반응 ($87.5\%$)을 나타내었다. 3. 1차 및 2차 $PGF_2a$ 처리에 따른 발정 반응은 BCS 2.50 이하의 경우 13두중 8두($61.5\%$), BCS 2.75${\~}$3.50의 경우 27두중 22두($81.5\%$)로 2.75${\~}$3.50의 경우가 2.50 이하의 경우에 비하여 높은 발정반응을 나타내었다. 4. 2차 $PGF_2a$ 처리후 발정 반응을 나타내지 않은 개체에 대하여 CIDR을 처리한 결과, BCS 2.50이하의 경우 5두중 2두에서 발정 반응($40.0\%$)을 나타내었고 BCS 2.75${\~}$3.50의 경우 5 두중 4두에서 발정 반응($80\%$)을 나타내었다. 5. 분만후 40일째부터 PPC program을 적용하여 발정 반응을 검토한 결과 BCS 2.50 이하의 경우 13두중 10두가 발정 반응($76.9\%$)을 나타내었고 BCS 2.75${\~}$3.5의 경우 27두중 26두가 발정 반응($96.3\%$)을 나타내어 2.75${\~}$3.5의 경우가 2.50 이하의 경우에 비하여 높은 발정반응을 나타내었다.

인도메타신투여가 개의 하악두에서 COX-2와 IGF-I의 발현과 분포에 미치는 영향 (The effects of indomethacin on distribution and expression of COX-2 and IGF-I in the mandibular condyle of growing dogs)

  • 남종현;이기수;강윤구
    • 대한치과교정학회지
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    • 제35권5호
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    • pp.351-360
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    • 2005
  • 이 연구는 $PGE_2$ 생합성 억제제인 인도메타신의 투여 시 성장기 개의 하악두 연골에 나타나는 cyclooxygenase-2 (GOX-2)와 insulin-like growth factor 1(IGF-1)의 발현과 분포를 관찰하여 인도메타신이 하악두 연골 성장에 미치는 영향을 규명하기 위하여 시행하였다 생후 12- 3주된 잡견 8마리를 4군으로 구분하였다 통상적 복용량인 인도메타신 2mg/Kg/day을 각각 7일과 14일간 투여한 군 과량인 8mg/Kg/day을 14일간 투여한 군과 무처치군인 대조군으로 구분하였으며. 하악두를 연구대상으로 하였다. 연구대상 하악두는 $5{\mu}m$ 두께의 절편을 만들어, H-E 중염색, COX-2 면역염색 IGF-1 면역염색을 시행하여 광학 현미경으로 검경하였으며, tartrate resistant acid phosphatase(TRAP) 염색 후 파연골세포의 수를 측정하여 다음과 같은 결과를 얻었다. 인도메타신은 하악두 연골의 증식대에서 COX-2와 IGF-1의 발현과 분포를 억제시켰으며, 인도메타신의 투여기간에 비례해서 파연골세포 수는 유의성 있게 감소하였다 (p<0.01) IGF-1의 발현과 분포는 인도메타신의 투여 양과 기간에 비례하여 억제되었다 이상의 결과에 의하면 인도메타신의 투여는 하악두 연골에서 COX-2와 IGF-1의 발현과 분포를 억제하고 파연골세포의 수를 감소시켜 하악두 성장을 억제할 가능성이 있음을 시사한다.