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重组人肿瘤坏死因子降低小鼠血清铁水平。

Recombinant human tumor necrosis factor depresses serum iron in mice.

作者信息

Tanaka T, Araki E, Nitta K, Tateno M

机构信息

Pharmacology Division, National Cancer Center Research Institute and Hospital, Tokyo, Japan.

出版信息

J Biol Response Mod. 1987 Oct;6(5):484-8.

PMID:3681344
Abstract

Recently many findings about the physiological and biochemical functions of recombinant human tumor necrosis factor (rHu-TNF) have been reported. In the present study, the effect of rHu-TNF on serum iron in C3H/HeN and C57BL/6 mice was determined. Blood samples were obtained before intravenous injection of rHu-TNF, and also at various times after the injection. Results from five experiments showed that the serum iron was depressed between 1/3 to 1/5 of that of untreated mice 4 to 24 h after injection of 5 or 10 micrograms of rHu-TNF. The low level persisted for 33 h, rebounded at 48 to 72 h, and returned to normal by 96 h after the injection. Serum iron was determined by the colorimetric method using the sensitive reagent, ferrozine (3-(2-pyridyl)-5,6-bis(4-sulfophenyl)-1,2,4-triazine. We believe that this is the first report of depression of serum iron in mice by intravenous injection of rHu-TNF. The physiological role of repressed serum iron in the in vivo response to TNF remains to be established.

摘要

最近,关于重组人肿瘤坏死因子(rHu-TNF)生理生化功能的许多研究结果已被报道。在本研究中,测定了rHu-TNF对C3H/HeN和C57BL/6小鼠血清铁的影响。在静脉注射rHu-TNF之前以及注射后的不同时间采集血样。五个实验的结果表明,注射5或10微克rHu-TNF后4至24小时,血清铁水平降至未处理小鼠的1/3至1/5。低水平持续33小时,在48至72小时反弹,并在注射后96小时恢复正常。血清铁采用比色法,使用灵敏试剂亚铁嗪(3-(2-吡啶基)-5,6-双(4-磺基苯基)-1,2,4-三嗪)进行测定。我们认为,这是首次关于静脉注射rHu-TNF导致小鼠血清铁降低的报道。血清铁降低在体内对TNF反应中的生理作用仍有待确定。

相似文献

1
Recombinant human tumor necrosis factor depresses serum iron in mice.重组人肿瘤坏死因子降低小鼠血清铁水平。
J Biol Response Mod. 1987 Oct;6(5):484-8.
2
Recombinant human tumor necrosis factor causes long-lasting and prostaglandin-mediated fever, with little tolerance, in rabbits.重组人肿瘤坏死因子可使兔子产生持续时间长且由前列腺素介导的发热,几乎没有耐受性。
J Pharmacol Exp Ther. 1988 Apr;245(1):336-41.
3
Tumor necrosis factor depresses gut absorptive function.肿瘤坏死因子会抑制肠道吸收功能。
Circ Shock. 1993 Apr;39(4):279-84.
4
Induction of hypoferremia and modulation of macrophage iron metabolism by tumor necrosis factor.肿瘤坏死因子诱导低铁血症并调节巨噬细胞铁代谢
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5
Evaluation of the significance of elevated levels of systemic and localized tumor necrosis factor in different animal models of inflammation.
J Lab Clin Med. 1994 Dec;124(6):813-20.
6
Tumor necrosis factor-alpha potentiates RhoA-mediated monocyte transmigratory activity in vivo at a picomolar level.肿瘤坏死因子-α在皮摩尔水平增强体内RhoA介导的单核细胞迁移活性。
Arterioscler Thromb Vasc Biol. 2009 Dec;29(12):2138-45. doi: 10.1161/ATVBAHA.109.195735. Epub 2009 Sep 10.
7
Trophoblastic cell lines generated from tumour necrosis factor receptor-deficient mice reveal specific functions for the two tumour necrosis factor receptors.从肿瘤坏死因子受体缺陷小鼠产生的滋养层细胞系揭示了两种肿瘤坏死因子受体的特定功能。
Placenta. 1999 Mar-Apr;20(2-3):213-22. doi: 10.1053/plac.1998.0356.
8
[Damaging action of human recombinant TNF on tumor vessels as an aspect of its anti-neoplastic action against Meth A sarcoma in mice].[人重组肿瘤坏死因子对肿瘤血管的损伤作用,作为其对小鼠Meth A肉瘤抗肿瘤作用的一个方面]
Gan To Kagaku Ryoho. 1987 Jan;14(1):91-9.
9
Tumor necrosis factor alpha-induced leukocyte adhesion in normal and tumor vessels: effect of tumor type, transplantation site, and host strain.肿瘤坏死因子α诱导正常及肿瘤血管中的白细胞黏附:肿瘤类型、移植部位和宿主品系的影响
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10
Tumor necrosis factor-alpha modulates survival, proliferation, and neuronal differentiation in neonatal subventricular zone cell cultures.肿瘤坏死因子-α调节新生脑室下区细胞培养物中的细胞存活、增殖和神经元分化。
Stem Cells. 2008 Sep;26(9):2361-71. doi: 10.1634/stemcells.2007-0914. Epub 2008 Jun 26.

引用本文的文献

1
Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating plasma tumor necrosis factor-alpha and macrophage migration inhibitory factor concentrations in African children.铁蛋白(SLC40A1)Q248H 突变与非洲儿童循环血浆肿瘤坏死因子-α和巨噬细胞移动抑制因子浓度降低相关。
Clin Chim Acta. 2010 Sep 6;411(17-18):1248-52. doi: 10.1016/j.cca.2010.04.031. Epub 2010 May 10.
2
Repression of repulsive guidance molecule C during inflammation is independent of Hfe and involves tumor necrosis factor-alpha.炎症期间排斥导向分子C的抑制与遗传性血色素沉着症蛋白(Hfe)无关,且涉及肿瘤坏死因子-α 。
Am J Pathol. 2007 Feb;170(2):497-504. doi: 10.2353/ajpath.2007.060437.
3
Tumour necrosis factor alpha causes hypoferraemia and reduced intestinal iron absorption in mice.
肿瘤坏死因子α导致小鼠低铁血症并降低肠道铁吸收。
Biochem J. 2006 Jul 1;397(1):61-7. doi: 10.1042/BJ20060215.
4
Tumor necrosis factor alpha (TNFalpha) promotes growth of virulent Mycobacterium tuberculosis in human monocytes iron-mediated growth suppression is correlated with decreased release of TNFalpha from iron-treated infected monocytes.肿瘤坏死因子α(TNFα)促进毒力结核分枝杆菌在人单核细胞中的生长,铁介导的生长抑制与铁处理的受感染单核细胞中TNFα释放减少相关。
J Clin Invest. 1997 May 15;99(10):2518-29. doi: 10.1172/JCI119436.
5
Regulation of transferrin receptor expression and ferritin content in human mononuclear phagocytes. Coordinate upregulation by iron transferrin and downregulation by interferon gamma.人单核吞噬细胞中转铁蛋白受体表达和铁蛋白含量的调节。铁转铁蛋白协同上调,γ干扰素下调。
J Clin Invest. 1993 Mar;91(3):969-76. doi: 10.1172/JCI116318.
6
Lactoferrin can protect mice against a lethal dose of Escherichia coli in experimental infection in vivo.乳铁蛋白在体内实验性感染中可保护小鼠免受致死剂量大肠杆菌的侵害。
Br J Exp Pathol. 1989 Dec;70(6):697-704.