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炎症和趋化因子诱导的兔血清趋化因子灭活剂活性升高

Elevation of serum chemotactic factor inactivator activity in rabbits induced by inflammation and chemotactic factor.

作者信息

Hupp J R, Despins A W, McCormick J R, Armstrong G, Kreutzer D L

出版信息

Am J Pathol. 1982 Dec;109(3):277-82.

Abstract

Inflammatory mediators such as the vasoactive and chemotactic factors, which are formed during the activation of serum complement, are extremely potent biologic peptides and are thought to be under the rigid control of specific serum-derived regulators or inactivators, including the anaphylatoxin inactivator (AI) and the chemotactic factor inactivator (CFI). Our understanding of the biologic importance and implication of these regulators in inflammatory reactions is primarily based on in vitro observations, and there is only limited data on their in vivo importance. Previously, alterations in CFI and AI levels were detected in chronic inflammatory disease states, but no data on their activity or role during acute inflammatory reactions have been demonstrated. Here we demonstrate the elevation of serum CFI activity during acute inflammatory reactions in rabbits. Specifically, inflammatory reactions were induced in rabbits by intraperitoneal injections of 0.1% oyster glycogen. Rabbit serum CFI levels rose rapidly over the first 4 hours after glycogen injection, reaching levels 4-8 times higher than the preglycogen serum CFI levels. Additional studies demonstrated that acute elevations of serum CFI levels could also be induced in rabbits by intravenous infusion of activated rabbit serum or C5-derived chemotactic factors. Infusion of saline, albumin, or the synthetic chemotactic peptide f-Met-Leu-Phe did not cause elevation of the serum CFI levels in rabbits. Thus, we take these data to support our hypothesis that 1) CFI is a "hyperacute phase reactant" that is elevated during inflammatory reactions, and 2) that this elevation of serum CFI activity is probably triggered by the appearance of specific C5-derived chemotactic factors within the vasculature. These studies not only provide exciting new insights into the regulatory mechanisms involved in acute inflammatory reactions but suggest that novel approaches to antiinflammatory therapy may be forthcoming.

摘要

炎症介质,如血管活性和趋化因子,是在血清补体激活过程中形成的,它们是极具活性的生物肽,被认为受到特定血清衍生调节剂或灭活剂的严格控制,包括过敏毒素灭活剂(AI)和趋化因子灭活剂(CFI)。我们对这些调节剂在炎症反应中的生物学重要性和意义的理解主要基于体外观察,而关于它们在体内重要性的数据有限。此前,在慢性炎症疾病状态下检测到CFI和AI水平的变化,但尚未证明它们在急性炎症反应中的活性或作用的数据。在这里,我们证明了兔急性炎症反应期间血清CFI活性的升高。具体而言,通过腹腔注射0.1%的牡蛎糖原在兔中诱导炎症反应。糖原注射后的前4小时内,兔血清CFI水平迅速升高,达到比注射糖原前血清CFI水平高4 - 8倍的水平。进一步的研究表明,静脉输注活化的兔血清或C5衍生的趋化因子也可在兔中诱导血清CFI水平的急性升高。输注生理盐水、白蛋白或合成趋化肽f - Met - Leu - Phe不会导致兔血清CFI水平升高。因此,我们利用这些数据支持我们的假设,即1)CFI是一种“超急性期反应物”,在炎症反应期间升高;2)血清CFI活性的这种升高可能是由血管系统中特定的C5衍生趋化因子的出现所触发。这些研究不仅为急性炎症反应所涉及的调节机制提供了令人兴奋的新见解,而且表明可能会出现新的抗炎治疗方法。

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