西姆瓦斯塔丁在体内抑制了内毒素诱导的组织因子
Sabine Steiner1, Walter S Speidl, Johannes Pleiner
1Second Department of Medicine, Division of Angiology, Medical University of Vienna,Vienna, Austria.
Circulation
|April 13, 2005
概括
在内毒性病期间,西姆瓦斯塔丁可降低炎症和单细胞组织因子 (TF) 表达. 这种他类药物治疗对健康人群的血小板激活没有影响.
科学领域:
- 药理学 药理学是指药理学的学科.
- 免疫学 免疫学 免疫学
- 心血管医学 心血管医学
背景情况:
- 类他类药物除了降脂之外,还具有抗炎性质.
- 实验室研究表明,他类药物抑制了脂聚糖 (LPS) 诱导的单细胞组织因子 (TF) 表达.
- 这项研究调查了在实验性内毒症中对炎症和血凝剂反应的他类药物的影响.
研究的目的:
- 评估simvastatin对LPS的炎症和血凝剂反应的体内影响.
- 评估simvastatin对单细胞TF表达和相关炎症标志物的影响.
- 为了确定simvastatin是否会在内毒性病期间影响血小板激活.
主要方法:
- 这是一项双盲,安慰剂控制的研究,涉及20名健康男性,随机分配给simvastatin或安慰剂4天.
- 静脉注射LPS后进行血hsCRP,MCP-1,sCD40L,sCD40和F1.2.2.的测量.
- 通过全血流细胞计评估的单细胞TF表达和单细胞-血小板聚合物.
主要成果:
- 西姆瓦斯塔丁显著抑制了LPS诱导的hsCRP和MCP-1的增加.
- 在LPS挑战后,他类药物治疗减弱了单细胞TF表达的增加.
- 西姆瓦斯塔丁显著降低了内毒素诱导的前热血素碎片F1.2.2.的形成.
- 输入LPS并没有改变单细胞 - 血小板聚合物的形成或血sCD40/sCD40L水平.
结论:
- 辛巴斯塔丁在体内有效抑制对内毒素的炎症反应.
- 在实验性内毒症期间,西姆瓦斯塔丁减弱单细胞组织因子表达.
- 在这个模型中,静止剂的使用没有影响血小板激活.
相关概念视频
Destabilization of Microtubules
The destabilization of microtubules can occur during different stages of the microtubule lifecycle, such as nucleation or elongation. It can take place at either end of the microtubule or in the microtubule lattices as a whole. The lifespan of individual microtubules within a cell varies according to the cell type and stage of the cell cycle. During interphase, the lifespan of the microtubule is about 30 minutes, while during cell division, it is about 15 minutes. In axonal microtubules of...
TGF - β Signaling Pathway
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors are of three kinds RI, RII, and RIII. The RI...
Combined Effects of Drugs: Antagonism
The combined effects of drugs can result in various interactions, of which an important type is antagonism. Antagonism is a mechanism where one drug inhibits or counteracts the effects of another drug. Antagonism can occur through various means, including receptor binding, allosteric modulation, functional interaction, chemical reactions, and pharmacokinetic processes.
The most common type is receptor antagonism, where one drug acts as an antagonist to block the effects of another drug by...
The most common type is receptor antagonism, where one drug acts as an antagonist to block the effects of another drug by...
Desensitization and Tachyphylaxis
Tachyphylaxis is described as a rapid decrease in response to a drug after repeated or continuous administration of the same drug dose. It is a phenomenon where the body becomes less responsive to a particular substance or intervention over time, requiring higher doses or stronger interventions to achieve the same effect. It results from adaptive changes in the body's receptors, signaling pathways, or physiological processes that occur in response to prolonged exposure to a stimulus.
Several...
Several...
Nondepolarizing (Competitive) Neuromuscular Blockers: Mechanism of Action
Nondepolarizing neuromuscular blockers induce paralysis by competitively blocking nicotinic acetylcholine receptors at the muscle end plate. Examples include pancuronium, mivacurium, vecuronium, and rocuronium. These quaternary ammonium derivatives are administered intravenously, are poorly absorbed, and are excreted via the kidneys.
Competitive antagonists prevent acetylcholine from binding to its receptor, inhibiting membrane depolarization. Without conformational changes or intrinsic...
Competitive antagonists prevent acetylcholine from binding to its receptor, inhibiting membrane depolarization. Without conformational changes or intrinsic...
Depolarizing Blockers: Mechanism of Action
Depolarizing blockers act on skeletal muscle fibers' membranes and induce their depolarization. Most depolarizing blockers have two quaternary N+ atoms that bind the nicotinic acetylcholine receptors and cause neuromuscular blockade within minutes.
Succinylcholine is the most commonly used depolarizing blocker. Chemically, it constitutes two molecules of acetylcholine joined together by an acetate methyl group. They act on the receptors in the same way as acetylcholine. Because succinylcholine...
Succinylcholine is the most commonly used depolarizing blocker. Chemically, it constitutes two molecules of acetylcholine joined together by an acetate methyl group. They act on the receptors in the same way as acetylcholine. Because succinylcholine...


