Wiig H, Kaysen G A, al-Bander H A, De Carlo M, Sibley L, Renkin E M
Department of Human Physiology, University of California, Davis 95616.
Am J Physiol. 1994 Jan;266(1 Pt 2):H212-9. doi: 10.1152/ajpheart.1994.266.1.H212.
Interstitial exclusion, defined as the fraction of interstitial fluid volume inaccessible to a solute, was evaluated for immunoglobulin G (IgG) in selected tissues of rats by a method previously applied to serum albumin (29). IgG distribution volumes were also measured for intestine. 125I-labeled rat IgG was infused for 5 or 7 days (n = 4 rats each) with an implanted osmotic pump (Alzet). At the termination of infusion, the rat was anesthetized, nephrectomized, and injected with 51Cr-labeled EDTA (4 h) to label total extracellular fluid volume and 131I-labeled bovine IgG (5 min) to label plasma volume. Samples of skin, muscle, and tendon were assayed for total and extractable tracer activity. Interstitial fluid from these tissues was sampled postmortem with nylon wicks for assay of 125I-labeled IgG and endogenous albumin and IgG. Exclusion of IgG was calculated from the difference between extravascular 125I-labeled IgG and 51Cr-labeled EDTA distribution volumes. In contrast to our previous experience with tracer albumin, 125I-labeled IgG was not fully extractable from minced skin, muscle, or tendon by isotonic saline; only 71-83% was recovered under conditions that eluted 92-96% of tracer albumin and 94-99% of tracer EDTA. We conclude that approximately 20% of extravascular 125I-labeled IgG in these tissues is sequestered or bound in the interstitium. Calculation of IgG fractional exclusion from extractable tracer yielded the following values (means +/- SE, n = 8 rats): leg muscles 0.37 +/- 0.09, leg skin 0.44 +/- 0.03, back skin 0.36 +/- 0.04, tail skin 0.40 +/- 0.08, and tail tendon 0.55 +/- 0.04.(ABSTRACT TRUNCATED AT 250 WORDS)
间质排除定义为溶质无法进入的间质液体积分数,通过先前应用于血清白蛋白的方法(29)对大鼠选定组织中的免疫球蛋白G(IgG)进行评估。还测量了肠道的IgG分布容积。用植入式渗透泵(Alzet)输注125I标记的大鼠IgG 5天或7天(每组4只大鼠)。输注结束时,将大鼠麻醉、切除肾脏,并注射51Cr标记的EDTA(4小时)以标记总细胞外液体积,注射131I标记的牛IgG(5分钟)以标记血浆体积。对皮肤、肌肉和肌腱样本进行总示踪剂活性和可提取示踪剂活性检测。这些组织的间质液在死后用尼龙芯取样,用于检测125I标记的IgG以及内源性白蛋白和IgG。根据血管外125I标记的IgG与51Cr标记的EDTA分布容积之间的差异计算IgG的排除率。与我们先前对示踪白蛋白的经验不同,等渗盐水无法从切碎的皮肤、肌肉或肌腱中完全提取125I标记的IgG;在洗脱92 - 96%的示踪白蛋白和94 - 99%的示踪EDTA的条件下,仅回收了71 - 83%。我们得出结论,这些组织中约20%的血管外125I标记的IgG被隔离或结合在间质中。从可提取示踪剂计算的IgG分数排除率得出以下值(平均值±标准误,n = 8只大鼠):腿部肌肉0.37 ± 0.09,腿部皮肤0.44 ± 0.03,背部皮肤0.36 ± 0.04,尾部皮肤0.40 ± 0.08,尾部肌腱0.55 ± 0.04。(摘要截断于250字)