Suppr超能文献

在孤立肢体灌注期间全身性肿瘤坏死因子(TNF)渗漏后可溶性TNF受体的脱落动力学。与脓毒性休克病理生理学的相关性。

Shedding kinetics of soluble tumor necrosis factor (TNF) receptors after systemic TNF leaking during isolated limb perfusion. Relevance to the pathophysiology of septic shock.

作者信息

Aderka D, Sorkine P, Abu-Abid S, Lev D, Setton A, Cope A P, Wallach D, Klausner J

机构信息

Department of Oncology, Tel-Aviv Medical Center, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv 64239, Israel.

出版信息

J Clin Invest. 1998 Feb 1;101(3):650-9. doi: 10.1172/JCI694.

Abstract

We examined the kinetics of shedding of the soluble TNF receptors (TNF-Rs) in response to TNF leakage during isolated limb perfusion procedures and correlated them to the resulting hemodynamic effects. Shedding of the TNF-Rs started 7 min after TNF leakage into the systemic circulation. Three waves of shedding were observed peaking at 1, 8-12, and 48-72 h both in vivo and in cell cultures. The soluble receptors prolonged the half-life of TNF in the systemic circulation to 2.5-6 h. Excess shedding of the p75 compared with p55 TNF-Rs was noted during the first wave. The amount and speed of shedding of the p75 TNF-Rs were proportional to the serum TNF levels (P < 0.001). A maximal shedding capacity was attained only during the first wave of shedding, at TNF concentrations of approximately 1.5 ng/ml. Above this level, the linearity between TNF and its soluble receptors was lost. TNF-induced hypotension coincided with the initial imbalance between the concentrations of TNF and its soluble receptors. Despite the spontaneous correction of this imbalance at 8-12 h, the hemodynamic and biochemical alterations persisted and were further aggravated at 18 h, suggesting that other factors induced earlier by TNF are responsible for the perpetuation of the hemodynamic instability. This study may provide the basis for a more physiological therapeutic approach to TNF neutralization in septic shock patients.

摘要

我们研究了在离体肢体灌注过程中,可溶性肿瘤坏死因子受体(TNF-Rs)因TNF泄漏而产生的脱落动力学,并将其与由此产生的血流动力学效应相关联。TNF-Rs的脱落于TNF泄漏至体循环后7分钟开始。在体内和细胞培养中均观察到三波脱落高峰,分别出现在1、8 - 12和48 - 72小时。可溶性受体将TNF在体循环中的半衰期延长至2.5 - 6小时。在第一波脱落过程中,与p55 TNF-Rs相比,p75的脱落过量。p75 TNF-Rs的脱落量和速度与血清TNF水平成正比(P < 0.001)。仅在第一波脱落期间,当TNF浓度约为1.5 ng/ml时达到最大脱落能力。高于此水平,TNF与其可溶性受体之间的线性关系丧失。TNF诱导的低血压与TNF及其可溶性受体浓度的初始失衡同时出现。尽管这种失衡在8 - 12小时时自发纠正,但血流动力学和生化改变持续存在,并在18小时时进一步加重,这表明TNF早期诱导的其他因素是血流动力学不稳定持续存在的原因。本研究可能为脓毒症休克患者TNF中和的更生理性治疗方法提供依据。

相似文献

引用本文的文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验