• 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

新型合成蛋白酶抑制剂FUT-175对(NZB×NZW)F1小鼠狼疮性肾炎发展的影响。

Effect of FUT-175, a new synthetic protease inhibitor, on the development of lupus nephritis in (NZB x NZW) F1 mice.

作者信息

Ikehara S, Shimamura K, Aoyama T, Fujii S, Hamashima Y

出版信息

Immunology. 1985 Aug;55(4):595-600.

PMID:4018844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1453784/
Abstract

FUT-175 (6-amidino-2-naphthyl p-guanidinobenzoate dimethanesulphonate), a new synthetic protease inhibitor, was administrated to (NZB x NZB) F1 mice in order to examine its influence on the development of autoimmune diseases. A dose (400 mg/kg of body weight) of FUT-175 has both prophylactic and curative effects on the development of lupus nephritis: mice showed a significantly low percentage of proteinuria, a marked decrease in BUN levels, and the lowest degree of glomerular damages. Dexamethasone had almost the same effect as FUT-175 (400 mg/kg), but it was slightly less effective than FUT-175. These results suggest that the administration of FUT-175 may become a viable strategy for the treatment of human autoimmune diseases.

摘要

FUT - 175(6 - 脒基 - 2 - 萘基对 - 胍基苯甲酸盐二甲磺酸盐),一种新型合成蛋白酶抑制剂,被给予(新西兰黑鼠×新西兰黑鼠)F1代小鼠,以研究其对自身免疫性疾病发展的影响。FUT - 175剂量为400毫克/千克体重时,对狼疮性肾炎的发展具有预防和治疗作用:小鼠蛋白尿百分比显著降低,血尿素氮水平明显下降,肾小球损伤程度最低。地塞米松与FUT - 175(400毫克/千克)效果几乎相同,但稍逊于FUT - 175。这些结果表明,给予FUT - 175可能成为治疗人类自身免疫性疾病的可行策略。

相似文献

1
Effect of FUT-175, a new synthetic protease inhibitor, on the development of lupus nephritis in (NZB x NZW) F1 mice.新型合成蛋白酶抑制剂FUT-175对(NZB×NZW)F1小鼠狼疮性肾炎发展的影响。
Immunology. 1985 Aug;55(4):595-600.
2
Successful treatment of autoimmunity in (NZB X NZW)F1 mice with cyclosporin and (Nva2)-cyclosporin: II. Reduction of glomerulonephritis.用环孢素和(Nva2)-环孢素成功治疗(NZB×NZW)F1小鼠自身免疫:II. 肾小球肾炎的减轻
Clin Exp Immunol. 1986 May;64(2):234-42.
3
Successful treatment of autoimmunity in (NZB X NZW)F1 mice with cyclosporin and (Nva2)-cyclosporin: I. Reduction of autoantibodies.用环孢素和(Nva2)-环孢素成功治疗(NZB×NZW)F1小鼠的自身免疫:I.自身抗体的减少。
Clin Exp Immunol. 1986 May;64(2):225-33.
4
Effects of LS-2616 administration upon the autoimmune disease of (NZB x NZW) F1 hybrid mice.给予LS-2616对(NZB×NZW)F1杂交小鼠自身免疫性疾病的影响。
Immunology. 1986 Dec;59(4):589-94.
5
Interleukin-6 exacerbates glomerulonephritis in (NZB x NZW)F1 mice.白细胞介素-6会加剧(新西兰黑鼠×新西兰白鼠)F1代小鼠的肾小球肾炎。
Am J Pathol. 1994 May;144(5):927-37.
6
The effect of 6-amidino-2-naphtyl-4-guanidinobenzoate dimethane sulfonate (FUT-175) on experimental glomerulonephritis in mice.二甲基磺酸6-脒基-2-萘基-4-胍基苯甲酸酯(FUT-175)对小鼠实验性肾小球肾炎的影响。
Jpn J Pharmacol. 1984 May;35(1):55-60. doi: 10.1254/jjp.35.55.
7
Treatment of lupus-prone NZB/NZW F1 mice with recombinant soluble Fc gamma receptor II (CD32).用重组可溶性Fcγ受体II(CD32)治疗易患狼疮的NZB/NZW F1小鼠。
Ann Rheum Dis. 2008 Feb;67(2):154-61. doi: 10.1136/ard.2006.068981. Epub 2007 Jun 8.
8
Suppressive oligodeoxynucleotides delay the onset of glomerulonephritis and prolong survival in lupus-prone NZB x NZW mice.抑制性寡脱氧核苷酸可延缓狼疮易感的新西兰黑鼠与新西兰白鼠杂交小鼠肾小球肾炎的发病并延长其生存期。
Arthritis Rheum. 2005 Feb;52(2):651-8. doi: 10.1002/art.20810.
9
Azathioprine administration to NZB X NZW hybrid mice with lupus nephritis: beneficial effect complicated by development of malignant lymphomas.给患有狼疮性肾炎的NZB×NZW杂交小鼠施用硫唑嘌呤:有益效果因恶性淋巴瘤的发生而变得复杂。
N Z Med J. 1973 Oct 10;79(500):290-5.
10
Inhibitory effect of FUT-175 on complement activation and its application for glomerulonephritis with hypocomplementemia.FUT-175对补体激活的抑制作用及其在低补体血症性肾小球肾炎中的应用。
Nihon Jinzo Gakkai Shi. 1993 Apr;35(4):393-7.

引用本文的文献

1
Protective effects of nafamostat mesilate on liver injury induced by lipopolysaccharide in rats: possible involvement of CD14 and TLR-4 downregulation on Kupffer cells.甲磺酸萘莫司他对大鼠脂多糖诱导的肝损伤的保护作用:可能与库普弗细胞上CD14和TLR-4下调有关。
Dig Dis Sci. 2006 Nov;51(11):2007-12. doi: 10.1007/s10620-006-9141-1. Epub 2006 Oct 28.
2
Effect of oral camostat mesilate on hematuria and/or proteinuria in children.口服甲磺酸卡莫司他对儿童血尿和/或蛋白尿的影响。
Pediatr Nephrol. 2004 Mar;19(3):313-6. doi: 10.1007/s00467-003-1377-9. Epub 2004 Jan 23.
3
The treatment of immune glomerular disease.免疫性肾小球疾病的治疗
Springer Semin Immunopathol. 1987;9(4):417-29. doi: 10.1007/BF00197218.
4
Amelioration of immune complex-mediated glomerulonephritis by synthetic protease inhibitors.合成蛋白酶抑制剂对免疫复合物介导的肾小球肾炎的改善作用
Am J Pathol. 1987 Jun;127(3):499-506.
5
Autoimmune kidney disease in MRL/Mp-lpr/lpr mice inhibited by OK-432, a streptococcal preparation.链球菌制剂OK-432可抑制MRL/Mp-lpr/lpr小鼠的自身免疫性肾病。
Clin Exp Immunol. 1989 Oct;78(1):102-7.

本文引用的文献

1
Long term administration of cyclophosphamide in MRL/1 mice. I. The effects on the development of immunological abnormalities and lupus nephritis.环磷酰胺对MRL/1小鼠的长期给药。I. 对免疫异常和狼疮性肾炎发展的影响。
Clin Exp Immunol. 1984 Feb;55(2):333-9.
2
New synthetic inhibitor to the alternative complement pathway.新型替代补体途径合成抑制剂。
Immunology. 1983 Aug;49(4):685-91.
3
Pharmacological studies of FUT-175, nafamstat mesilate. I. Inhibition of protease activity in in vitro and in vivo experiments.甲磺纳法莫司他(FUT-175)的药理学研究。I. 体内外实验中对蛋白酶活性的抑制作用
Jpn J Pharmacol. 1984 Jul;35(3):203-27. doi: 10.1254/jjp.35.203.
4
Marked reduction of DNA antibody production and glomerulopathy in thymulin (FTS-Zn) or cyclosporin A treated (NZB X NZW) F1 mice.在胸腺素(FTS-Zn)或环孢素A处理的(新西兰黑鼠×新西兰白鼠)F1代小鼠中,DNA抗体产生和肾小球病变显著减少。
Clin Exp Immunol. 1983 Nov;54(2):359-65.
5
New synthetic inhibitors of C1r, C1 esterase, thrombin, plasmin, kallikrein and trypsin.C1r、C1酯酶、凝血酶、纤溶酶、激肽释放酶和胰蛋白酶的新型合成抑制剂。
Biochim Biophys Acta. 1981 Oct 13;661(2):342-5. doi: 10.1016/0005-2744(81)90023-1.
6
Inhibition of various immunological reactions in vivo by a new synthetic complement inhibitor.一种新型合成补体抑制剂对体内各种免疫反应的抑制作用。
Int Arch Allergy Appl Immunol. 1982;69(3):262-7. doi: 10.1159/000233181.
7
Etiopathogenesis of murine SLE.小鼠系统性红斑狼疮的病因发病机制。
Immunol Rev. 1981;55:179-216. doi: 10.1111/j.1600-065x.1981.tb00343.x.
8
The effect of complement depletion by cobra venom factor on delayed hypersensitivity reactions.眼镜蛇毒因子对补体的消耗对迟发型超敏反应的影响。
Proc Soc Exp Biol Med. 1971 Dec;138(3):1041-3. doi: 10.3181/00379727-138-36046.
9
Depletion of plasma complement in vivo by a protein of cobra venom: its effect on various immunologic reactions.眼镜蛇毒蛋白在体内对血浆补体的消耗:其对各种免疫反应的影响。
J Immunol. 1970 Jul;105(1):55-69.
10
Suppression of contact hypersensitivity and acute inflammation by anti-complement serum.抗补体血清对接触性超敏反应和急性炎症的抑制作用。
Nature. 1968 Jul 13;219(5150):192-3. doi: 10.1038/219192a0.