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白细胞介素-1对离体牛肠系膜淋巴管液体泵吸功能的抑制作用:与前列腺素E2的相互作用

Suppression of fluid pumping in isolated bovine mesenteric lymphatics by interleukin-1: interaction with prostaglandin E2.

作者信息

Hanley C A, Elias R M, Movat H Z, Johnston M G

机构信息

Department of Pathology, University of Toronto, Ontario, Canada.

出版信息

Microvasc Res. 1989 Mar;37(2):218-29. doi: 10.1016/0026-2862(89)90039-3.

Abstract

In addition to local physiological forces, the modulation of lymphatic pumping by chemical mediators may play an important role in the regulation of extravascular water in inflammation and shock. Since Interleukin-1 (IL-1) appears to be of major importance in the host's response to infection by mediating many inflammatory events, we thought it important to determine if this cytokine could affect the lymphatic circulation and in particular to ask whether IL-1 was capable of altering lymphatic pumping in response to changes in transmural pressure. Bovine lymphatic segments (6 to 8 cm in length) were cannulated at both ends and suspended in an organ bath preparation. The vessels were provided with Krebs solution from a reservoir. With no net driving pressure, a transmural pressure applied to the ducts elicited contractile activity and fluid pumping with increases in pumping up to 8 cm H2O and reductions in flow above this level of distension. Human recombinant IL-1 alpha (10(-7) to 10(-9) M) administered into the lumina of the vessels depressed pumping activity approximately 5-30% at transmural pressures between 2 and 16 cm H2O. With limited supplies, we could only assess the effects of human recombinant IL-1 beta at 10(-8) M. However, it was more potent than IL-1 alpha, inhibiting pumping at all transmural pressures with maximum suppression in the range of 70% at peak flows. The ability of IL-1 to induce prostaglandin synthesis may be one of its most important biologic functions. It is likely therefore that IL-1 and PGE2 are closely linked and are probably present together in inflammatory lesions. With this in mind, we investigated the effects of PGE2 alone and in combination with IL-1 alpha. PGE2 by itself reduced pumping at concentrations between 10(-6) and 10(-9) M. When mixed with IL-1 alpha (both agents at a final concentration of 10(-9) M), the mixture had a marked inhibitory effect on flow, reducing pumping 50 to 70% at peak flows. The effect of the mixture of IL-1 alpha and PGE2 compared with the two agents administered separately was greater than the predicted additive effect at transmural pressures above 6 cm H2O. At lower transmural pressures, however, the level of real inhibition was less than the predicted additive effect.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

除了局部生理力量外,化学介质对淋巴泵的调节在炎症和休克状态下血管外水分的调节中可能起重要作用。由于白细胞介素-1(IL-1)似乎在宿主对感染的反应中通过介导许多炎症事件而具有重要意义,我们认为确定这种细胞因子是否会影响淋巴循环很重要,特别是要探究IL-1是否能够响应跨壁压力的变化而改变淋巴泵功能。取牛的淋巴节段(长度为6至8厘米),两端插管并悬吊于器官浴槽制备装置中。通过储液器向血管提供 Krebs 溶液。在没有净驱动压力的情况下,对导管施加跨壁压力会引发收缩活动和液体泵出,泵出量增加至8厘米水柱,超过此扩张水平时流量会减少。将人重组IL-1α(10⁻⁷至10⁻⁹M)注入血管腔内,在2至16厘米水柱的跨壁压力下,泵出活性降低约5 - 30%。由于供应有限,我们只能评估10⁻⁸M的人重组IL-1β的作用。然而,它比IL-1α更有效,在所有跨壁压力下均抑制泵出,在峰值流量时最大抑制范围为70%。IL-1诱导前列腺素合成的能力可能是其最重要的生物学功能之一。因此,IL-1和前列腺素E2(PGE2)可能密切相关,并且可能共同存在于炎症病变中。考虑到这一点,我们研究了单独的PGE2以及与IL-1α联合使用的效果。PGE2自身在浓度为10⁻⁶至10⁻⁹M时会降低泵出。当与IL-1α混合(两种试剂的终浓度均为10⁻⁹M)时,混合物对流量有明显的抑制作用,在峰值流量时泵出减少50%至70%。与分别给予这两种试剂相比,IL-1α和PGE2的混合物在跨壁压力高于6厘米水柱时的作用大于预测的相加效应。然而,在较低的跨壁压力下,实际抑制水平低于预测的相加效应。(摘要截短至400字)

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