Field J, Hurley J V, McCallum N E
J Pathol. 1977 Jan;121(1):51-8. doi: 10.1002/path.1711210108.
A study has been made in rats of the relative rates of escape of plasma protein, measured by accumulation of Evans Blue, and of the large marker particle, HgS, into uninjured small bowel and into an area of intradermal injection of histamine. The rate of escape of Evans Blue, per unit mass of tissue, into small bowel and into an area of histamine-stimulated skin were found to be almost the same, but leakage of HgS into the bowel was only about 1/10 of leakage of the same tracer into a site of intradermal histamine injection. If it be assumed, as is generally accepted, that all the protein that leaks from histamine-stimulated vessels does so via gaps in vascular endothelium that are large enough to allow escape of large marker particles like HgS, these findings show that only a small fraction of the protein that leaks into normal intestinal mucosa can escape via gaps, and that most of the leakage must occur by a route not permeable to particles of HgS. The findings give no indication of the nature of the alternative route for escape of protein.
通过伊文思蓝的蓄积来测定血浆蛋白的逸出相对速率,并对大鼠进行了一项研究,该研究还测定了大标记颗粒硫化汞进入未受损小肠以及组胺皮内注射区域的情况。每单位质量组织中,伊文思蓝进入小肠和组胺刺激皮肤区域的逸出速率几乎相同,但硫化汞进入小肠的渗漏量仅为同一示踪剂进入组胺皮内注射部位渗漏量的约1/10。如果像通常所认为的那样,假设从组胺刺激血管中漏出的所有蛋白质都是通过血管内皮中的间隙漏出的,这些间隙大到足以使像硫化汞这样的大标记颗粒逸出,那么这些发现表明,漏入正常肠黏膜的蛋白质中只有一小部分能通过间隙逸出,而且大部分渗漏必定是通过一条对硫化汞颗粒不可渗透的途径发生的。这些发现并未表明蛋白质逸出的替代途径的性质。