• 제목/요약/키워드: Gout

검색결과 167건 처리시간 0.022초

인삼잎의 수용성 분획의 생리활성 (Biological Activities of the Water Soluble Fraction from the Overground Part of Panax ginseng)

  • 한덕룡
    • 고려인삼학회:학술대회논문집
    • /
    • 고려인삼학회 1988년도 학술대회지
    • /
    • pp.139-140
    • /
    • 1988
  • 인삼잎의 수용성 분획에서 플라보노이드와 다당류를 확인하였다. 플라보노이드 분획은 xanthine oxidase 활성을 억제하였고, 다당류 분획은 세망내피계의 macrophage 기능을 촉진하였다.

  • PDF

능이버섯의 항고혈압 활성과 항통풍 활성 (Antihypertensive Activity and Anti-gout Activity of Mushroom Sarcodon aspratus)

  • 강민구;;이종석;서건식;이종수
    • 한국균학회지
    • /
    • 제39권1호
    • /
    • pp.53-56
    • /
    • 2011
  • 야생 능이버섯에 함유되어 있는 생리 기능성 물질들을 탐색, 분리하여 이들을 고부가가치의 건강식품 소재로 활용하고자 덕유산 일대에서 채집한 능이버섯의 물 추출물은 제조하여 몇 가지 생리 기능성을 측정하였다. 능이버섯 자실체의 물 추출물은 항고혈압성 엔지오텐신 전환효소(ACE) 저해 활성과 항통풍성 xanthine 산화효소(XOD) 저해활성이 각각 74.3%와 59.6%로 우수하였다. 그러나 tyrosinase 저해 활성과 항산화 활성, SOD 유사활성 등은 매우 낮거나 없었다. 능이버섯 자실체중의 ACE 저해활성은 자실체 분말의 물현탁액을 $30^{\circ}C$에서 24시간, XOD 저해물질은 $50^{\circ}C$에서 24시간 진탕 시켰을 때 가장 높았다. 이들 두 가지 생리활성 물질을 함유한 능이버섯 물 추출물은 앞으로 건강식품이나 대체 의약 소재 개발에 매우 유용하게 활용 할 것으로 사료된다.

한약재 열수추출물의 항산화 활성 및 Xanthine Oxidase 저해 활성 (Antioxidant and Xanthine Oxidase Inhibitory Activities of Hot Water Extracts of Medicinal Herbs)

  • 신유진;황정만;이승철
    • 한국식품영양과학회지
    • /
    • 제42권10호
    • /
    • pp.1712-1716
    • /
    • 2013
  • 통풍 증상을 개선하고 예방 및 치료에 효과를 확인하여 이를 일상생활에 지장을 주지 않고 장기간 쉽게 복용하기에 적합한 식품 소재를 발굴하기 위하여 한의학 및 식품 관련 서적에서 통풍 개선 및 치료 효과가 있어 널리 사용되고 있는 29가지 식용 가능 한약재를 선별하였다. 각 한약재의 열수추출액의 총 페놀 함량, DPPH 라디칼 소거능, ABTS 라디칼 소거능, xanthine oxidase 저해능을 측정한 결과, 황금추출액이 가장 높은 활성을 나타내었다. 이상의 결과는 황금추출액을 주 소재로 하여 항산화능과 통증 개선에 유용한 식품 개발에 활용될 수 있을 것으로 기대된다.

The Anti-Inflammatory Effects of Bee Venom in Monosodium Urate Crystal-Induced THP-1 Cells

  • Sang-Yeup Chae;Dongmin Lee;Min-Jung Ko;Seungeun Lee;Jaeho Song;Jinkyung Park;Sinwoo Park;Yeon-Cheol Park;Foo Young Cho
    • Journal of Acupuncture Research
    • /
    • 제40권4호
    • /
    • pp.368-376
    • /
    • 2023
  • Background: Although bee venom (BV) has clinical benefits in osteoarthritis and rheumatoid arthritis, it has not been tested as treatment for gouty arthritis. Moreover, in vitro, BV has been proven to exhibit anti-inflammatory and positive effects on osteoarthritis, but only limited evidence can confirm its beneficial effects on gout. Thus, this study aims to assess the anti-inflammatory effects of BV on monosodium urate (MSU)-induced THP-1 monocytes. Methods: THP-1 monocytes were differentiated into mature macrophages using phorbol 12-myristate 13-acetate (PMA) and pretreated for 6 hours with BV and a Caspase-1 inhibitor in a physiologically achievable range of concentrations (BV, 0.1-1 ㎍/mL; Caspase-1 inhibitor, 1-10 μM), followed by MSU crystal stimulation for 24 hours. The secretions of interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), IL-6, IL-8, cyclooxygenase-2 (COX-2), prostaglandin E2 (PGE2), and nitric oxide (NO) were increased in the MSU crystal-stimulated THP-1 cells. Results: Caspase-1 inhibitors suppressed the production of all mediators in a dose-dependent manner. BV worked on equal terms with Caspase-1 inhibitors and showed more satisfactory effects on TNF-α, PGE2, COX-2, and inducible nitric oxide synthase (iNOS). Moreover, the western blot analysis revealed that BV regulated the transcriptional levels of these mediators via the suppression of extracellular signal-regulated kinase (ERK) pathway activation. Conclusion: The results of the present study clearly suggest that BV inhibits MSU-induced inflammation in vitro, suggesting a possible role for BV in gout treatment.

RAW 264.7 대식세포에서 마늘 유래 황 함유 화합물에 의한 요산 유도 inflammasome 활성화의 억제는 ROS 생성 차단과 연관성이 있음 (Suppression of Monosodium Urate-induced NLRP3 Inflammasome Activation by Garlic-derived Sulfur-containing Phytochemicals is Associated with Blocking ROS Generation in RAW 264.7 Macrophages)

  • 김민영;최영현
    • 생명과학회지
    • /
    • 제33권4호
    • /
    • pp.349-356
    • /
    • 2023
  • 만성 염증성 관절염 질환인 통풍은 고요산혈증을 특징으로 하며 NLRP3 inflammasome의 활성화에 따른 IL-1β와 같은 염증성 cytokine 방출과 연관된 MSU에 대한 염증 반응에 의해 유발될 수 있다. 마늘에 함유된 황 함유 화합물은 다양한 질병에 대한 잠재적인 유익한 약리학적 효능을 가지지만, NLRP3 inflammasome 활성화와 연관된 통풍 억제에 대한 효능은 현재까지 입증되지 않았다. 본 연구에서는 대표적인 마늘 유래 황화합물인 DADS와 DATS가 MSU에 의한 NLRP3 inflammasome 활성을 억제할 수 있는지를 조사하였다. 본 연구의 결과에 의하면, 비세포 독성 조건에서 DADS와 DATS는 LPS가 전처리된 RAW 264.7 대식세포에서 MSU에 대한 반응으로 증가된 NO의 생성과 IL-1β 유리를 유의적으로 차단하였다. DADS와 DATS는 또한 증가된 NLRP3, ASC, caspase-1 p20 및 IL-1β의 발현을 감소시켰으며, 이는 MSU로 유도된 LRP3 inflammasome 활성화가 DADS와 DATS에 의해 억제되었음을 의미한다. 아울러, DADS와 DATS는 NLRP3 inflammasome 활성화에 상위 신호로 작용하는 산화적 스트레스를 차단했으며 ROS 생성을 제거한다는 사실에서 입증되었다. 결론적으로, 본 연구의 결과는 DADS와 DATS가 ROS/NLRP3 경로를 억제하여 inflammasome 활성화를 차단함으로서 NLRP3 의존성 통풍성 관절염 치료를 위한 잠재력이 우수함을 의미한다.

3D-QSAR Studies on 2-(indol-5-yl)thiazole Derivatives as Xanthine Oxidase (XO) Inhibitors

  • Nagarajan, Santhosh Kumar;Madhavan, Thirumurthy
    • 통합자연과학논문집
    • /
    • 제8권4호
    • /
    • pp.258-266
    • /
    • 2015
  • Xanthine Oxidase is an enzyme, which oxidizes hypoxanthine to xanthine, and xanthine to uric acid. It is widely distributed throughout various organs including the liver, gut, lung, kidney, heart, brain and plasma. It is involved in gout pathogenesis. In this study, we have performed Comparative Molecular Field Analysis (CoMFA) on a series of 2-(indol-5-yl) thiazole derivatives as xanthine oxidase (XO) inhibitors to identify the structural variations with their inhibitory activities. Ligand based CoMFA models were generated based on atom-by-atom matching alignment. In atom-by-atom matching, the bioactive conformation of highly active molecule 11 was generated using systematic search. Compounds were aligned using the bioactive conformation and it is used for model generation. Different CoMFA models were generated using different alignments and the best model yielded a cross-validated $q^2$ of 0.698 with five components and non-cross-validated correlation coefficient ($r^2$) of 0.992 with Fisher value as 236.431, and an estimated standard error of 0.068. The predictive ability of the best CoMFA models was found to be $r^2_{pred}$0.653. The CoMFA study revealed that the $R_3$ position of the structure is important in influencing the biological activity of the inhibitors. Electro positive groups and bulkier substituents in this position enhance the biological activity.

Familial Juvenile Hyperuricemic Nephropathy 2례 (Two cases of Familial Juvenile Hyperuricemic Nephropathy)

  • 박진호;최보화;이소영;유은실;박영서
    • Childhood Kidney Diseases
    • /
    • 제1권2호
    • /
    • pp.183-188
    • /
    • 1997
  • Familial juvenile hyperuricemic nephropathy is an autosomal dominant disease characterized by progressive renal disease and hyperuricemia or gout, affecting young people of either sex equally. There are two biochemical markers of this disorder. The first is hyperuricemia disproportionate to the degree of renal dysfunction; the second is a grossly reduced clearance of uric acid relative to creatinine, dispropotionate to age, sex and degree of renal failure. We experienced 2 family members with hyperuricemia. One family member, a 13-year-old girl who had suffered from tophaceous gout and chronic renal failure. Her younger brother also had hyperuricemia and moderately reduced renal function. Their urinary excretion fractions of uric acid($FE_{uric\;acid}$) were reduced and renal biopsy specimens showed interstitial fibrosis with tubular atrophy and interstitial urate crystal deposition. We have treated these two patients with allopurinol but we have done renal transplantation because she progressed to end stage renal disease at 16 year old age.

  • PDF

대황목단탕(大黃牧丹湯)의 요산지표 개선효과와 관련 유전자 탐색 (Effects of Daihwangmudan-tang on Urate Lowering and Detection of Relevant Genes)

  • 김중배;지규용;엄현섭
    • 동의생리병리학회지
    • /
    • 제19권6호
    • /
    • pp.1534-1540
    • /
    • 2005
  • In order to testify the urate lowering effects of Daihwangmudan-tang(DMT), ICR mice were injected monosodium urate into the abdominal cavity and then DMT was administered on 2 and 4 days after Injection. Uric acid and triglyceride were measured as hematological indices of gout, and some genes related with this change were identified by ACP based GeneFishing PCR method and direct sequencing. From this experiment, DMT highly decreased the blood levels of uric acid and significantly suppressed and lowered the acute increment of triglyceride level. There were 11 differentially expressed genes(DEG) having relations with positive actions of DMT, and 4 major genes in the middle of DEGs were sequenced; Mfap 2, jagged 2, Hsd17b7, DkkI-1, These genes were supposed that several mechanisms through interleukin 1 and T-cell anergy, LDL cholesterol metabolism, wnt pathway would be related with the anti-inflammation effect against gout.

Comparative Molecular Similarity Index Analysis on 2-(indol-5-yl)thiazolederivatives as Xanthine Oxidase(XO)inhibitors

  • Nagarajan, Santhosh Kumar;Madhavan, Thirumurthy
    • 통합자연과학논문집
    • /
    • 제9권3호
    • /
    • pp.190-198
    • /
    • 2016
  • Xanthine Oxidase is an enzyme, which oxidizes hypoxanthine to xanthine, and xanthine to uric acid. It is widely distributed throughout various organsincluding the liver, gut, lung, kidney, heart, brain and plasma. It is involved in gout pathogenesis. In this study, we have performed Comparative Molecular Field Analysis (CoMSIA) on a series of 2-(indol-5-yl) thiazole derivatives as xanthine oxidase (XO) inhibitors to identify the structural variations with their inhibitory activities. Ligand based CoMSIA models were generated based on atom-by-atom matching alignment. In atom-by-atom matching, the bioactive conformation of highly active molecule 11 was generated using systematic search. Compounds were aligned using the bioactive conformation and it is used for model generation. Different CoMSIA models were generated using different alignments and the best model yielded across-validated $q^2$ of 0.698 with five components and non-cross-validated correlation coefficient ($r^2$) of 0.992 with Fisher value as 236.431, and an estimated standard error of 0.068. The predictive ability of the best CoMSIA models was found to be $r{^2}_{pred}$ 0.653. The study revealed the important structural features required for the biological activity of the inhibitors and could provide useful for the designing of novel and potent drugs for the inhibition of Xanthine oxidase.