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首页> 外文期刊>American Journal of Physiology >Modeling serotonin uptake in the lung shows endothelial transporters dominate over cleft permeation
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Modeling serotonin uptake in the lung shows endothelial transporters dominate over cleft permeation

机译:对肺中5-羟色胺摄取的建模显示内皮细胞转运在裂缝渗透中起主导作用

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摘要

A fourregion (capillary plasma, endothelium, interstitial fluid, cell) multipath model was configured to describe the kinetics of blood-tissue exchange for small solutes in the lung, accounting for regional flow heterogeneity, permeation of cell membranes and through interendothelial clefts, and intracellular reactions. Serotonin uptake data from the Multiple indicator dilution 'bolus sweep' experiments of Rickaby and coworkers (Rickaby DA, Linehan JH, Bronikowski TA, Dawson CA. J Appl Physiol 51: 405-414, 1981; Rickaby DA, Dawson CA, and Linehan JH. J Appl Physiol 56: 1170-1177, 1984) and Malcorps et al. (Malcorps CM, Dawson CA, Linehan JH, Bronikowski TA, Rickaby DA, Herman AG, Will JA. J Appl Physiol 57: 720-730, 1984) were analyzed to distinguish facilitated transport into the endothelial cells (EC) and the inhibition of tracer transport by nontracer serotonin in the bolus of injectate from the free uninhibited permeation through the clefts into the interstitial fluid space. The permeability-surface area products (PS) for serotonin via the inter-EC clefts were ~0.3 ml·g-1·min-1, low compared with the transportermediated maximum PS of 13 ml·g-1·min-1 (with Km = ~0.3 μM and Vmax = ~4 nmol·g-1·min-1). The estimates of serotonin PS values for EC transporters from their multiple data sets were similar and were influenced only modestly by accounting for the cleft permeability in parallel. The cleft PS estimates in these Ringer-perfused lungs are less than half of those for anesthetized dogs (Yipintsoi T. Circ Res 39: 523-531, 1976) with normal hematocrits, but are compatible with passive noncarrier-mediated transport observed later in the same laboratory (Dawson CA, Linehan JH, Rickaby DA, Bronikowski TA. Ann Biomed Eng 15: 217-227, 1987; Peeters FAM, Bronikowski TA, Dawson CA, Linehan JH, Bult H, Herman AG. J Appl Physiol 66: 2328-2337, 1989) The identification and quantitation of the cleft pathway conductance from these studies affirms the importance of the cleft permeation.
机译:配置了一个四区域(毛细管血浆,内皮,间质液,细胞)多径模型来描述肺中小溶质的血液-组织交换动力学,从而说明了局部血流的异质性,细胞膜的渗透以及通过内皮间裂和细胞内的渗透反应。来自Rickaby及其同事的多指示剂稀释``推注清除''实验中血清素的摄取数据(Rickaby DA,Linehan JH,Bronikowski TA,Dawson CA.J Appl Physiol 51:405-414,1981; Rickaby DA,Dawson CA和Linehan JH J Appl Physiol 56:1170-1177,1984)和Malcorps等人。 (Malcorps CM,Dawson CA,Linehan JH,Bronikowski TA,Rickaby DA,Herman AG,Will JA.J Appl Physiol 57:720-730,1984)进行了分析,以区分便利转运到内皮细胞(EC)和抑制示踪剂通过非示踪剂5-羟色胺在大剂量注射液中从游离的不受抑制的渗透物通过裂隙进入间隙液体空间。通过EC缝隙传播的血清素渗透性表面积积(PS)为〜0.3 ml·g-1·min-1,低于转运蛋白介导的最大PS值13 ml·g-1·min-1( Km =〜0.3μM,Vmax =〜4 nmol·g-1·min-1。 EC转运蛋白从其多个数据集获得的血清素PS值估算值相似,并且仅通过并行考虑裂缝渗透性而仅受到中等程度的影响。这些林格灌注肺中的裂隙PS估计值不到血细胞比容正常的麻醉犬的一半(Yipintsoi T. Circ Res 39:523-531,1976),但与后来在实验中观察到的被动非携带者介导的转运相容。同一实验室(Dawson CA,Linehan JH,Rickaby DA,Bronikowski TA。Ann Biomed Eng 15:217-227,1987; Peeters FAM,Bronikowski TA,Dawson CA,Linehan JH,Bult H,Herman AG.J Appl Physiol 66:2328 -2337,1989)通过这些研究对裂隙通路电导的鉴定和定量证实了裂隙渗透的重要性。

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