• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Inhibition of tissue damage by the arachidonate lipoxygenase inhibitor BW755C.花生四烯酸脂氧合酶抑制剂BW755C对组织损伤的抑制作用。
Proc Natl Acad Sci U S A. 1984 May;81(9):2890-2. doi: 10.1073/pnas.81.9.2890.
2
The effects of BW755C and other anti-inflammatory drugs on eicosanoid concentrations and leukocyte accumulation in experimentally-induced acute inflammation.BW755C及其他抗炎药物对实验性诱导急性炎症中类花生酸浓度和白细胞聚集的影响。
J Pharm Pharmacol. 1983 Dec;35(12):808-13. doi: 10.1111/j.2042-7158.1983.tb02901.x.
3
Inflammatory properties of lipoxygenase products and the effects of indomethacin and BW755C on prostaglandin production, leukocyte migration, and plasma exudation in rabbit skin.脂氧合酶产物的炎症特性以及消炎痛和BW755C对兔皮肤中前列腺素生成、白细胞迁移和血浆渗出的影响。
Adv Prostaglandin Thromboxane Leukot Res. 1982;9:331-9.
4
Leukotriene synthesis by human gastrointestinal tissues.人胃肠道组织的白三烯合成
Biochim Biophys Acta. 1986 Sep 12;878(2):184-93. doi: 10.1016/0005-2760(86)90145-1.
5
Leukocyte recruitment in the subcutaneous sponge implant model of acute inflammation in the rat is not mediated by leukotriene B1.在大鼠急性炎症的皮下海绵植入模型中,白细胞募集并非由白三烯B1介导。
Biochem Pharmacol. 1986 May 15;35(10):1709-17. doi: 10.1016/0006-2952(86)90328-x.
6
Inhibition of arachidonic acid cyclo-oxygenase and lipoxygenase activities of leukocytes by indomethacin and compound BW755C.吲哚美辛和化合物BW755C对白细胞花生四烯酸环氧化酶和脂氧化酶活性的抑制作用。
Agents Actions. 1980 Dec;10(6):553-5. doi: 10.1007/BF02024164.
7
Differential effects of putative lipoxygenase inhibitors on arachidonic acid metabolism in cell-free and intact cell preparations.假定的脂氧合酶抑制剂对无细胞和完整细胞制剂中花生四烯酸代谢的不同影响。
Inflammation. 1984 Jun;8(2):143-55. doi: 10.1007/BF00916090.
8
Inhibition of mononuclear leukocyte accumulation by the arachidonic acid lipoxygenase inhibitor BW755C.花生四烯酸脂氧合酶抑制剂BW755C对单核白细胞聚集的抑制作用。
Adv Prostaglandin Thromboxane Leukot Res. 1983;12:19-23.
9
Eicosanoid synthesis inhibition and renal allograft function during acute rejection.急性排斥反应期间类花生酸合成抑制与肾移植功能
Transplantation. 1988 May;45(5):902-7. doi: 10.1097/00007890-198805000-00012.
10
Relationship of glucocorticoid suppression of arachidonic acid metabolism to alteration of neutrophil function.糖皮质激素对花生四烯酸代谢的抑制作用与中性粒细胞功能改变的关系。
J Leukoc Biol. 1987 Feb;41(2):156-64. doi: 10.1002/jlb.41.2.156.

引用本文的文献

1
Novel Applications of NSAIDs: Insight and Future Perspectives in Cardiovascular, Neurodegenerative, Diabetes and Cancer Disease Therapy.非甾体抗炎药的新应用:心血管、神经退行性、糖尿病和癌症疾病治疗的新视角和未来展望。
Int J Mol Sci. 2021 Jun 21;22(12):6637. doi: 10.3390/ijms22126637.
2
Therapeutic role of dual inhibitors of 5-LOX and COX, selective and non-selective non-steroidal anti-inflammatory drugs.5-脂氧合酶(5-LOX)与环氧化酶(COX)双重抑制剂、选择性及非选择性非甾体抗炎药的治疗作用
Ann Rheum Dis. 2003 Jun;62(6):501-9. doi: 10.1136/ard.62.6.501.
3
Macrolide antibiotics as antiinflammatory agents: roxithromycin in an unexpected role.大环内酯类抗生素作为抗炎剂:罗红霉素的意外作用。
Agents Actions. 1993 Jan;38(1-2):85-90. doi: 10.1007/BF02027218.
4
Leukotrienes in disease. Implications for drug development.疾病中的白三烯。对药物开发的启示。
Drugs. 1985 Jul;30(1):1-5. doi: 10.2165/00003495-198530010-00001.
5
Antagonism of leukotriene receptors and administration of a 5-lipoxygenase inhibitor do not affect hypoxic vasoconstriction.白三烯受体拮抗剂和5-脂氧合酶抑制剂的给药不影响缺氧性血管收缩。
Lung. 1989;167(3):187-98. doi: 10.1007/BF02714947.
6
Pharmacological investigation of acute cellular accumulation in immunological air pouch inflammation.免疫性气囊炎症中急性细胞蓄积的药理学研究。
Agents Actions. 1989 Aug;28(1-2):73-7. doi: 10.1007/BF02022983.
7
The effects of drugs on leucocyte changes following the injection of antigen into the peritoneal cavities of actively sensitised rats.药物对向主动致敏大鼠腹腔内注射抗原后白细胞变化的影响。
Agents Actions. 1986 Mar;17(5-6):498-505. doi: 10.1007/BF01965521.
8
Anti-inflammatory pharmacology and mechanism of the orally active capsaicin analogs, NE-19550 and NE-28345.口服活性辣椒素类似物NE-19550和NE-28345的抗炎药理学及作用机制
Agents Actions. 1990 Nov;31(3-4):329-40. doi: 10.1007/BF01997628.

本文引用的文献

1
The human PMN leukocyte chemotactic activity of complex hydroxy-eicosatetraenoic acids (HETEs).复合羟基二十碳四烯酸(HETEs)的人中性粒细胞趋化活性。
J Immunol. 1980 Oct;125(4):1789-91.
2
The effects of non-steroid anti-inflammatory drugs on leukocyte migration in carrageenin-induced inflammation.非甾体抗炎药对角叉菜胶诱导的炎症中白细胞迁移的影响。
Eur J Pharmacol. 1980 Aug 22;66(1):81-6. doi: 10.1016/0014-2999(80)90297-6.
3
A phospholipase A2 inhibitory protein in rabbit neutrophils induced by glucocorticoids.糖皮质激素诱导的兔中性粒细胞中的一种磷脂酶A2抑制蛋白。
Proc Natl Acad Sci U S A. 1980 May;77(5):2533-6. doi: 10.1073/pnas.77.5.2533.
4
Macrocortin: a polypeptide causing the anti-phospholipase effect of glucocorticoids.巨皮质素:一种引起糖皮质激素抗磷脂酶作用的多肽。
Nature. 1980 Sep 11;287(5778):147-9. doi: 10.1038/287147a0.
5
The salvage of ischaemic myocardium by BW755C in anaesthetised dogs.BW755C对麻醉犬缺血心肌的挽救作用。
Prostaglandins. 1982 Aug;24(2):255-66. doi: 10.1016/0090-6980(82)90151-4.
6
Inhibition of arachidonic acid cyclo-oxygenase and lipoxygenase activities of leukocytes by indomethacin and compound BW755C.吲哚美辛和化合物BW755C对白细胞花生四烯酸环氧化酶和脂氧化酶活性的抑制作用。
Agents Actions. 1980 Dec;10(6):553-5. doi: 10.1007/BF02024164.
7
Effect of BW755C in an occlusion-reperfusion model of ischemic myocardial injury.BW755C在缺血性心肌损伤的闭塞-再灌注模型中的作用。
Am Heart J. 1983 Jul;106(1 Pt 1):8-13. doi: 10.1016/0002-8703(83)90431-3.
8
The release of leukotriene B4 during experimental inflammation.实验性炎症过程中白三烯B4的释放。
Biochem Pharmacol. 1983 Apr 15;32(8):1353-9. doi: 10.1016/0006-2952(83)90446-x.
9
Leukotrienes: mediators of immediate hypersensitivity reactions and inflammation.白三烯:速发型超敏反应和炎症的介质。
Science. 1983 May 6;220(4597):568-75. doi: 10.1126/science.6301011.
10
Lipoxygenation of arachidonic acid as a source of polymorphonuclear leukocyte chemotactic factors in synovial fluid and tissue in rheumatoid arthritis and spondyloarthritis.类风湿关节炎和脊柱关节炎中,花生四烯酸的脂氧化作为滑膜液和组织中多形核白细胞趋化因子的来源。
J Clin Invest. 1980 Nov;66(5):1166-70. doi: 10.1172/JCI109947.

花生四烯酸脂氧合酶抑制剂BW755C对组织损伤的抑制作用。

Inhibition of tissue damage by the arachidonate lipoxygenase inhibitor BW755C.

作者信息

Higgs G A, Mugridge K G, Moncada S, Vane J R

出版信息

Proc Natl Acad Sci U S A. 1984 May;81(9):2890-2. doi: 10.1073/pnas.81.9.2890.

DOI:10.1073/pnas.81.9.2890
PMID:6326150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC345178/
Abstract

The effects of three anti-inflammatory drugs, which interfere with arachidonic acid transformation by three different enzymes, have been compared by using a simple model of tissue damage and foreign body rejection. In groups of control rats, subcutaneously implanted polyester sponges were rejected after a mean of 12 days. Indomethacin, which selectively inhibits prostaglandin synthesis, did not significantly change time to rejection but BW755C (3-amino-1-[m-(trifluoromethyl) phenyl]-2-pyrazoline), which is a dual inhibitor of prostaglandin and leukotriene synthesis, prolonged time to rejection to a mean of 22 days. The anti-inflammatory steroid dexamethasone, which reduces arachidonic acid metabolism by stimulating the formation of a phospholipase inhibitor, prolonged time to sponge rejection as BW755C did. Treatment with BW755C or dexamethasone was also accompanied by a reduction in total leukocyte numbers in inflammatory exudates collected at 1-14 days, whereas indomethacin increased leukocyte migration on days 1 and 2 and had no effect at later times. These results suggest that the inhibition of the leukotriene-forming lipoxygenase suppresses leukocyte activation and that this leads to a reduced rate of tissue damage in experimental inflammation.

摘要

通过使用组织损伤和异物排斥的简单模型,比较了三种抗炎药物的效果,这三种药物通过三种不同的酶干扰花生四烯酸的转化。在对照组大鼠中,皮下植入的聚酯海绵平均在12天后被排斥。选择性抑制前列腺素合成的吲哚美辛并没有显著改变排斥时间,但BW755C(3-氨基-1-[间-(三氟甲基)苯基]-2-吡唑啉),一种前列腺素和白三烯合成的双重抑制剂,将排斥时间延长至平均22天。抗炎类固醇地塞米松通过刺激磷脂酶抑制剂的形成来减少花生四烯酸代谢,与BW755C一样延长了海绵排斥时间。用BW755C或地塞米松治疗还伴随着在1 - 14天收集的炎性渗出物中白细胞总数的减少,而吲哚美辛在第1天和第2天增加了白细胞迁移,在后期没有影响。这些结果表明,对白三烯形成的脂氧合酶的抑制抑制了白细胞的激活,并且这导致实验性炎症中组织损伤的速率降低。