• 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

肺表面活性物质的代谢与更新

Metabolism and turnover of lung surfactant.

作者信息

Wright J R, Clements J A

出版信息

Am Rev Respir Dis. 1987 Aug;136(2):426-44. doi: 10.1164/ajrccm/136.2.426.

DOI:10.1164/ajrccm/136.2.426
PMID:3304047
Abstract

Despite the grave difficulties that beset researchers who are trying to isolate and characterize the various intracellular and extracellular forms of lung surfactant; despite the serious ambiguities of interpretation of experimental data caused by the multicomponent nature of the surfactant; despite the inaccessibility for diagnostic purposes of this material, which functions deep in the lungs; despite the fact that incisive methods of protein chemistry and molecular biology have only recently been brought to bear on lung surfactant; despite all these problems, our knowledge and understanding of lung surfactant are rapidly increasing. We know now that it is a dynamic system with many parts, and that the reserves of these are normally not large and are recycled. We believe that tight metabolic control must exist to maintain these reserves, and we already have experimental techniques to raise or lower the reserves. Heroic methods of surfactant substitution are now being tested in patients whose deficiency or risk thereof is sufficiently desperate, and the results of these clinical trials, if they are carefully documented with lung function data, will add a new dimension to our knowledge of surfactant dynamics. We may expect in the future that more subtle alterations in surfactant function will become detectable and more sophisticated methods to manipulate the system will be invented. Essential to these will be a deeper understanding of surfactant forms, pathways, kinetics, and controls. Fortunately, research on surfactant structure, metabolism, and turnover intrigues many investigators. They, we may hope, will soon provide the necessary information.

摘要

尽管试图分离和鉴定肺表面活性物质各种细胞内和细胞外形式的研究人员面临着重重困难;尽管由于表面活性物质的多组分性质导致实验数据的解释存在严重模糊性;尽管这种在肺部深处发挥作用的物质因诊断目的难以获取;尽管蛋白质化学和分子生物学的精确方法直到最近才应用于肺表面活性物质研究;尽管存在所有这些问题,我们对肺表面活性物质的认识和理解仍在迅速增加。我们现在知道它是一个由许多部分组成的动态系统,而且这些部分的储备通常不大且会循环利用。我们相信必须存在严格的代谢控制来维持这些储备,并且我们已经有了提高或降低储备的实验技术。目前正在对那些表面活性物质缺乏或有足够高缺乏风险的患者进行大胆的表面活性物质替代方法测试,如果这些临床试验结果能与肺功能数据仔细记录在一起,将为我们对表面活性物质动力学的认识增添新的维度。我们可以期待未来能够检测到表面活性物质功能更细微的变化,并且会发明出更复杂的方法来操控这个系统。对这些而言,更深入地了解表面活性物质的形式、途径、动力学和调控至关重要。幸运的是,关于表面活性物质结构、代谢和更新的研究引起了许多研究者的兴趣。我们希望他们很快能提供必要的信息。

相似文献

1
Metabolism and turnover of lung surfactant.肺表面活性物质的代谢与更新
Am Rev Respir Dis. 1987 Aug;136(2):426-44. doi: 10.1164/ajrccm/136.2.426.
2
Alterations of surfactant lipid turnover in silicosis: evidence of a role for surfactant-associated protein A (SP-A).矽肺中表面活性剂脂质周转的改变:表面活性剂相关蛋白A(SP-A)作用的证据。
Int J Exp Pathol. 1995 Aug;76(4):287-98.
3
[Lipids in the lungs and alveolar surfactant in anaphylactic shock].[过敏性休克时肺中的脂质与肺泡表面活性物质]
Fiziol Zh (1978). 1990 Jan-Feb;36(1):87-90.
4
Surfactant protein A accumulating in the alveoli of patients with pulmonary alveolar proteinosis: oligomeric structure and interaction with lipids.表面活性物质蛋白A在肺泡蛋白沉积症患者肺泡中的蓄积:寡聚体结构及其与脂质的相互作用。
Am J Respir Cell Mol Biol. 1996 Jun;14(6):608-19. doi: 10.1165/ajrcmb.14.6.8652189.
5
Protein-lipid interactions and surface activity in the pulmonary surfactant system.肺表面活性物质系统中的蛋白质-脂质相互作用及表面活性
Chem Phys Lipids. 2006 Jun;141(1-2):105-18. doi: 10.1016/j.chemphyslip.2006.02.017. Epub 2006 Mar 20.
6
The alveolar type II cells as a model for investigating the metabolism of surfactant phospholipids.作为研究表面活性物质磷脂代谢模型的Ⅱ型肺泡细胞。
Eur Respir J Suppl. 1989 Mar;3:10s-12s.
7
Alterations of the composition and metabolism of pulmonary surfactant phospholipids induced by experimental peritonitis in rats.实验性腹膜炎诱导大鼠肺表面活性物质磷脂成分及代谢的改变。
Chem Biol Interact. 2007 Aug 30;169(2):73-9. doi: 10.1016/j.cbi.2007.05.005. Epub 2007 May 24.
8
Distribution of surfactant protein A in rat lung.表面活性蛋白A在大鼠肺中的分布。
Am J Respir Cell Mol Biol. 1994 Oct;11(4):405-15. doi: 10.1165/ajrcmb.11.4.7917309.
9
[Biochemical and clinical aspects of pulmonary surfactant proteins].[肺表面活性物质蛋白的生化及临床方面]
Nihon Kyobu Shikkan Gakkai Zasshi. 1992 Dec;30 Suppl:5-14.
10
Pulmonary surfactant metabolism.肺表面活性物质代谢
Clin Chest Med. 1989 Mar;10(1):83-93.

引用本文的文献

1
Prolonged in vitro anti-bacterial, anti-inflammatory, and surfactant-promoting effects of volatile anesthetics.挥发性麻醉剂的体外抗菌、抗炎和促进表面活性剂作用的延长效应。
BMC Pulm Med. 2025 Sep 9;25(1):425. doi: 10.1186/s12890-025-03849-w.
2
Lung lipids associated with smoking and ECIG use in a cross-sectional study and clinical trial.一项横断面研究和临床试验中与吸烟及电子烟使用相关的肺脂质
Respir Res. 2025 May 20;26(1):193. doi: 10.1186/s12931-025-03267-w.
3
Transcriptomic Plasticity of Human Alveolar Macrophages Revealed by Single-Cell RNA Sequencing Following Drug Exposure: Implications for Therapeutic Development.
药物暴露后单细胞RNA测序揭示的人肺泡巨噬细胞转录组可塑性:对治疗开发的启示
Int J Mol Sci. 2025 May 7;26(9):4439. doi: 10.3390/ijms26094439.
4
Pseudomonas aeruginosa acyl-CoA dehydrogenases and structure-guided inversion of their substrate specificity.铜绿假单胞菌酰基辅酶A脱氢酶及其底物特异性的结构导向反转
Nat Commun. 2025 Mar 8;16(1):2334. doi: 10.1038/s41467-025-57532-z.
5
Choline metabolism modulates cyclic-di-GMP signaling and virulence of Pseudomonas aeruginosa in a macrophage infection model.胆碱代谢在巨噬细胞感染模型中调节铜绿假单胞菌的环二鸟苷信号传导及毒力。
BMC Infect Dis. 2024 Dec 27;24(1):1466. doi: 10.1186/s12879-024-10375-3.
6
After the Storm: Regeneration, Repair, and Reestablishment of Homeostasis Between the Alveolar Epithelium and Innate Immune System Following Viral Lung Injury.《风暴过后:病毒性肺损伤后肺泡上皮细胞和固有免疫系统之间的再生、修复和内稳态的重建》
Annu Rev Pathol. 2023 Jan 24;18:337-359. doi: 10.1146/annurev-pathmechdis-031621-024344. Epub 2022 Oct 21.
7
Mechanistic Understanding of Lung Inflammation: Recent Advances and Emerging Techniques.肺部炎症的机制性理解:最新进展与新兴技术
J Inflamm Res. 2022 Jun 15;15:3501-3546. doi: 10.2147/JIR.S282695. eCollection 2022.
8
Pulmonary surfactant protein B carried by HDL predicts incident CVD in patients with type 1 diabetes.高密度脂蛋白携带的肺表面活性物质蛋白B可预测1型糖尿病患者发生心血管疾病的风险。
J Lipid Res. 2022 Apr;63(4):100196. doi: 10.1016/j.jlr.2022.100196. Epub 2022 Mar 14.
9
mTORC1 is a mechanosensor that regulates surfactant function and lung compliance during ventilator-induced lung injury.mTORC1 是一种机械感受器,可调节呼吸机诱导性肺损伤期间的表面活性剂功能和肺顺应性。
JCI Insight. 2021 Jul 22;6(14):e137708. doi: 10.1172/jci.insight.137708.
10
Alcohol-induced lipid dysregulation impairs glycolytic responses to LPS in alveolar macrophages.酒精引起的脂质失调会损害肺泡巨噬细胞对 LPS 的糖酵解反应。
Alcohol. 2020 Mar;83:57-65. doi: 10.1016/j.alcohol.2019.08.009. Epub 2019 Sep 6.