• 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

一氧化氮与氧气在生物膜疏水内部的加速反应。

Accelerated reaction of nitric oxide with O2 within the hydrophobic interior of biological membranes.

作者信息

Liu X, Miller M J, Joshi M S, Thomas D D, Lancaster J R

机构信息

Department of Pediatrics, Louisiana State University Medical Center, 1901 Perdido Street, New Orleans, LA 70112, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2175-9. doi: 10.1073/pnas.95.5.2175.

DOI:10.1073/pnas.95.5.2175
PMID:9482858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC19287/
Abstract

We demonstrate herein dramatic acceleration of aqueous nitric oxide (NO) reaction with O2 within the hydrophobic region of either phospholipid or biological membranes or detergent micelles and demonstrate that the presence of a distinct hydrophobic phase is required. Per unit volume, at low amounts of hydrophobic phase, the reaction of NO with O2 within the membranes is approximately 300 times more rapid than in the surrounding aqueous medium. In tissue, even though the membrane represents only 3% of the total volume, we calculate that 90% of NO reaction with O2 will occur there. We conclude that biological membranes and other tissue hydrophobic compartments are important sites for disappearance of NO and for formation of NO-derived reactive species and that attenuation of these potentially damaging reactions is an important protective action of lipid-soluble antioxidants such as vitamin E.

摘要

我们在此证明,在磷脂或生物膜或去污剂胶束的疏水区域内,一氧化氮(NO)与O2的水相反应显著加速,并证明需要存在独特的疏水相。每单位体积,在少量疏水相的情况下,膜内NO与O2的反应速度比周围水相介质中快约300倍。在组织中,尽管膜仅占总体积的3%,但我们计算出90%的NO与O2的反应将在那里发生。我们得出结论,生物膜和其他组织疏水隔室是NO消失和形成NO衍生活性物种的重要部位,而减弱这些潜在的损伤反应是维生素E等脂溶性抗氧化剂的重要保护作用。

相似文献

1
Accelerated reaction of nitric oxide with O2 within the hydrophobic interior of biological membranes.一氧化氮与氧气在生物膜疏水内部的加速反应。
Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2175-9. doi: 10.1073/pnas.95.5.2175.
2
Acceleration of nitric oxide autoxidation and nitrosation by membranes.膜对一氧化氮自氧化和亚硝化作用的加速
IUBMB Life. 2007 Apr-May;59(4-5):243-8. doi: 10.1080/15216540701311147.
3
Diffusion of nitric oxide and oxygen in lipoproteins and membranes studied by pyrene fluorescence quenching.通过芘荧光猝灭研究一氧化氮和氧气在脂蛋白和膜中的扩散。
Free Radic Biol Med. 2018 Nov 20;128:137-143. doi: 10.1016/j.freeradbiomed.2018.04.553. Epub 2018 Apr 16.
4
Micellar catalysis for oxidation of nitric oxide (NO) in the multi-phase systems in vivo.
FEBS Lett. 1999 Jun 18;453(1-2):229-35. doi: 10.1016/s0014-5793(99)00578-5.
5
Membrane "lens" effect: focusing the formation of reactive nitrogen oxides from the *NO/O2 reaction.膜“透镜”效应:聚焦由NO/O₂反应生成活性氮氧化物的过程。
Chem Res Toxicol. 2007 Apr;20(4):709-14. doi: 10.1021/tx700010h. Epub 2007 Mar 28.
6
Modulation of protein function in membrane mimetics: Characterization of P. denitrificans cNOR in nanodiscs or liposomes.在膜类似物中调节蛋白质功能:在纳米盘或脂质体中对 P. denitrificans cNOR 的表征。
Biochim Biophys Acta Biomembr. 2017 Oct;1859(10):1951-1961. doi: 10.1016/j.bbamem.2017.06.017. Epub 2017 Jun 28.
7
Direct measurement of nitric oxide and oxygen partitioning into liposomes and low density lipoprotein.一氧化氮和氧气在脂质体与低密度脂蛋白中的分配的直接测量。
J Biol Chem. 2005 Mar 11;280(10):8850-4. doi: 10.1074/jbc.M413699200. Epub 2005 Jan 4.
8
Diffusion and Transport of Reactive Species Across Cell Membranes.活性物质在细胞膜内的扩散和传输。
Adv Exp Med Biol. 2019;1127:3-19. doi: 10.1007/978-3-030-11488-6_1.
9
Nitric oxide regulation of superoxide and peroxynitrite-dependent lipid peroxidation. Formation of novel nitrogen-containing oxidized lipid derivatives.一氧化氮对超氧化物和过氧亚硝酸盐依赖性脂质过氧化的调节。新型含氮氧化脂质衍生物的形成。
J Biol Chem. 1994 Oct 21;269(42):26066-75.
10
Fatty acid transduction of nitric oxide signaling. Nitrolinoleic acid is a hydrophobically stabilized nitric oxide donor.一氧化氮信号的脂肪酸转导。硝基油酸是一种疏水稳定的一氧化氮供体。
J Biol Chem. 2005 May 13;280(19):19289-97. doi: 10.1074/jbc.M414689200. Epub 2005 Mar 11.

引用本文的文献

1
Nitric oxide promotes cysteine N-degron proteolysis through control of oxygen availability.一氧化氮通过控制氧的可利用性促进半胱氨酸N-端规则途径的蛋白质水解。
Proc Natl Acad Sci U S A. 2025 Aug 26;122(34):e2501796122. doi: 10.1073/pnas.2501796122. Epub 2025 Aug 19.
2
The chemical biology of dinitrogen trioxide.三氧化二氮的化学生物学
Redox Biochem Chem. 2024 Jun;8. doi: 10.1016/j.rbc.2024.100026. Epub 2024 May 9.
3
NOS2 and COX-2 Co-Expression Promotes Cancer Progression: A Potential Target for Developing Agents to Prevent or Treat Highly Aggressive Breast Cancer.NOS2 和 COX-2 的共表达促进癌症进展:开发预防或治疗高度侵袭性乳腺癌的药物的潜在靶点。
Int J Mol Sci. 2024 Jun 1;25(11):6103. doi: 10.3390/ijms25116103.
4
Red light mediates the exocytosis of vasodilatory vesicles from cultured endothelial cells: a cellular, and ex vivo murine model.红光介导培养的内皮细胞中血管舒张囊泡的胞吐作用:一种细胞和离体的鼠模型。
Photochem Photobiol Sci. 2024 Feb;23(2):355-364. doi: 10.1007/s43630-023-00522-1. Epub 2024 Jan 26.
5
Nitroproteomics is instrumental for stratification and targeted treatments of astrocytoma patients: expert recommendations for advanced 3PM approach with improved individual outcomes.硝基蛋白质组学有助于星形细胞瘤患者的分层和靶向治疗:关于采用改进的个体预后的先进3PM方法的专家建议。
EPMA J. 2023 Dec 6;14(4):673-696. doi: 10.1007/s13167-023-00348-y. eCollection 2023 Dec.
6
The Chemical Biology of NO that Regulates Oncogenic Signaling and Metabolism: NOS2 and Its Role in Inflammatory Disease.调节致癌信号和代谢的 NO 的化学生物学:NOS2 及其在炎症性疾病中的作用。
Crit Rev Oncog. 2023;28(1):27-45. doi: 10.1615/CritRevOncog.2023047302.
7
Regulation of Ras Signaling by S-Nitrosylation.S-亚硝基化对Ras信号传导的调控
Antioxidants (Basel). 2023 Aug 4;12(8):1562. doi: 10.3390/antiox12081562.
8
Molecular oxygen as a probe molecule in EPR spin-labeling studies of membrane structure and dynamics.分子氧作为膜结构与动力学的电子顺磁共振自旋标记研究中的探针分子。
Oxygen (Basel). 2022 Sep;2(3):295-316. doi: 10.3390/oxygen2030021. Epub 2022 Aug 4.
9
NO and Heme Proteins: Cross-Talk between Heme and Cysteine Residues.一氧化氮与血红素蛋白:血红素与半胱氨酸残基之间的相互作用
Antioxidants (Basel). 2023 Jan 30;12(2):321. doi: 10.3390/antiox12020321.
10
Roles and current applications of S-nitrosoglutathione in anti-infective biomaterials.S-亚硝基谷胱甘肽在抗感染生物材料中的作用及当前应用
Mater Today Bio. 2022 Sep 6;16:100419. doi: 10.1016/j.mtbio.2022.100419. eCollection 2022 Dec.

本文引用的文献

1
Mechanisms of nitrogen dioxide reactions: initiation of lipid peroxidation and the production of nitrous Acid.二氧化氮反应机制:脂质过氧化的引发和亚硝酸的生成。
Science. 1981 Oct 23;214(4519):435-7. doi: 10.1126/science.214.4519.435.
2
A tutorial on the diffusibility and reactivity of free nitric oxide.关于游离一氧化氮的扩散性和反应性的教程。
Nitric Oxide. 1997 Feb;1(1):18-30. doi: 10.1006/niox.1996.0112.
3
Peroxynitrite-induced apoptosis in human intestinal epithelial cells is attenuated by mesalamine.美沙拉嗪可减轻过氧亚硝酸盐诱导的人肠上皮细胞凋亡。
Gastroenterology. 1997 Nov;113(5):1480-8. doi: 10.1053/gast.1997.v113.pm9352850.
4
DNA damage and genotoxicity by nitric oxide.
Methods Enzymol. 1996;269:230-43. doi: 10.1016/s0076-6879(96)69025-9.
5
Quantitation of nitrate and nitrite in extracellular fluids.
Methods Enzymol. 1996;268:237-46. doi: 10.1016/s0076-6879(96)68026-4.
6
The reaction between nitric oxide and alpha-tocopherol: a reappraisal.
Biochem Biophys Res Commun. 1996 Jul 25;224(3):696-702. doi: 10.1006/bbrc.1996.1086.
7
Rapid reduction of nitric oxide by mitochondria, and reversible inhibition of mitochondrial respiration by nitric oxide.线粒体对一氧化氮的快速还原作用,以及一氧化氮对线粒体呼吸的可逆抑制作用。
Biochem J. 1996 Apr 1;315 ( Pt 1)(Pt 1):295-9. doi: 10.1042/bj3150295.
8
Acceleration of peroxynitrite oxidations by carbon dioxide.二氧化碳对过氧亚硝酸盐氧化反应的加速作用。
Arch Biochem Biophys. 1996 Mar 15;327(2):335-43. doi: 10.1006/abbi.1996.0131.
9
Autoxidation kinetics of aqueous nitric oxide.一氧化氮水溶液的自氧化动力学
FEBS Lett. 1993 Jul 12;326(1-3):1-3. doi: 10.1016/0014-5793(93)81748-o.
10
Diffusion of nitric oxide in the aorta wall monitored in situ by porphyrinic microsensors.通过卟啉微传感器原位监测一氧化氮在主动脉壁中的扩散。
Biochem Biophys Res Commun. 1993 Jun 30;193(3):1076-82. doi: 10.1006/bbrc.1993.1735.