Skip to main content
Gut logoLink to Gut
. 1985 Jun;26(6):579–585. doi: 10.1136/gut.26.6.579

Intestinal permeability to 51Cr-EDTA in rats with experimentally induced enteropathy.

I Bjarnason, P Smethurst, A J Levi, T J Peters
PMCID: PMC1432753  PMID: 3924747

Abstract

Intestinal permeability has been investigated in the normal rat by measuring the five hour urine excretion of 51Cr-EDTA after intragastric administration. Twelve control animals excreted 2.06% +/- 0.22 (mean +/- SE) of the administered dose. Prolonged intestinal transit times with atropine had no significant effect on the apparent permeability with a urine excretion 2.31% +/- 0.36. The concomitant administration of a hypertonic, but rapidly absorbed glycerol solution, was accompanied by increased urinary excretion (3.05% +/- 0.33) while the administration of a poorly absorbed sugar, lactulose, significantly decreased the apparent permeability (urine excretion 0.61% +/- 0.14) showing that passive intestinal permeability estimations are affected by test dose composition. Enteropathy was induced by ethanol, cetrimide, or methotrexate and each was associated with increased permeability, with urine excretions of 4.19% +/- 0.47, 4.20% +/- 0.66 and 3.97% +/- 0.49 respectively. It is thus suggested that the normal rat mucosa is maximally resistant to the absorption of foreign compounds such as 51Cr-EDTA and intestinal damage will disrupt this barrier.

Full text

PDF
579

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ahrens F. A., Aronson A. L. A comparative study of the toxic effects of calcium and chromium chelates of ethylenediaminetetraacetate in the dog. Toxicol Appl Pharmacol. 1971 Jan;18(1):10–25. doi: 10.1016/0041-008x(71)90310-3. [DOI] [PubMed] [Google Scholar]
  2. Altmann G. G. Changes in the mucosa of the small intestine following methotrexate administration or abdominal x-irradiation. Am J Anat. 1974 Jun;140(2):263–279. doi: 10.1002/aja.1001400210. [DOI] [PubMed] [Google Scholar]
  3. Aronson A. L., Rogerson K. M. Effect of calcium and chromium chelates of ethylenediaminetetraacetate on intestinal permeability and collagen metabolism in the rat. Toxicol Appl Pharmacol. 1972 Apr;21(4):440–453. doi: 10.1016/0041-008x(72)90002-6. [DOI] [PubMed] [Google Scholar]
  4. Atherton D. J. Allergy and atopic eczema II. Clin Exp Dermatol. 1981 May;6(3):317–325. doi: 10.1111/j.1365-2230.1981.tb02311.x. [DOI] [PubMed] [Google Scholar]
  5. Barona E., Pirola R. C., Leiber C. S. Small intestinal damage and changes in cell population produced by ethanol ingestion in the rat. Gastroenterology. 1974 Feb;66(2):226–234. [PubMed] [Google Scholar]
  6. Bjarnason I., O'Morain C., Levi A. J., Peters T. J. Absorption of 51chromium-labeled ethylenediaminetetraacetate in inflammatory bowel disease. Gastroenterology. 1983 Aug;85(2):318–322. [PubMed] [Google Scholar]
  7. Bjarnason I., Peters T. J. In vitro determination of small intestinal permeability: demonstration of a persistent defect in patients with coeliac disease. Gut. 1984 Feb;25(2):145–150. doi: 10.1136/gut.25.2.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Bjarnason I., Peters T. J., Veall N. A persistent defect in intestinal permeability in coeliac disease demonstrated by a 51Cr-labelled EDTA absorption test. Lancet. 1983 Feb 12;1(8320):323–325. doi: 10.1016/s0140-6736(83)91628-8. [DOI] [PubMed] [Google Scholar]
  9. Brightman M. W., Hori M., Rapoport S. I., Reese T. S., Westergaard E. Osmotic opening of tight junctions in cerebral endothelium. J Comp Neurol. 1973 Dec 15;152(4):317–325. doi: 10.1002/cne.901520402. [DOI] [PubMed] [Google Scholar]
  10. Cobden I., Rothwell J., Axon A. T. Passive permeability in experimental intestinal damage in rats. Clin Sci (Lond) 1981 Jan;60(1):115–118. doi: 10.1042/cs0600115. [DOI] [PubMed] [Google Scholar]
  11. Cornell R., Walker W. A., Isselbacher K. J. Small intestinal absorption of horseradish peroxidase. A cytochemical study. Lab Invest. 1971 Jul;25(1):42–48. [PubMed] [Google Scholar]
  12. Cronquist A. G., Mackenzie J., Smith T. A high resolution bulk-sample counter with variable geometry. Int J Appl Radiat Isot. 1975 Feb;26(2):89–91. doi: 10.1016/0020-708x(75)90108-8. [DOI] [PubMed] [Google Scholar]
  13. Dobson A., Sellers A. F., Gatewood V. H. Dependence of Cr-EDTA absorption from the rumen on luminal osmotic pressure. Am J Physiol. 1976 Nov;231(5 Pt 1):1595–1600. doi: 10.1152/ajplegacy.1976.231.5.1595. [DOI] [PubMed] [Google Scholar]
  14. Draper L. R., Gyure L. A., Hall J. G., Robertson D. Effect of alcohol on the integrity of the intestinal epithelium. Gut. 1983 May;24(5):399–404. doi: 10.1136/gut.24.5.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ecknauer R., Buck B., Breitig D. An experimental model for measuring intestinal permeability. Digestion. 1983;26(1):24–32. doi: 10.1159/000198865. [DOI] [PubMed] [Google Scholar]
  16. Fiasse R., Lurhuma A. Z., Cambiaso C. L., Masson P. L., Dive C. Circulating immune complexes and disease activity in Crohn's disease. Gut. 1978 Jul;19(7):611–617. doi: 10.1136/gut.19.7.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Fordtran J. S., Rector F. C., Jr, Ewton M. F., Soter N., Kinney J. Permeability characteristics of the human small intestine. J Clin Invest. 1965 Dec;44(12):1935–1944. doi: 10.1172/JCI105299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Franz T. J., Galey W. R., Van Bruggen J. T. Further observations on asymmetrical solute movement across membranes. J Gen Physiol. 1968 Jan;51(1):1–12. doi: 10.1085/jgp.51.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Jackson P. G., Lessof M. H., Baker R. W., Ferrett J., MacDonald D. M. Intestinal permeability in patients with eczema and food allergy. Lancet. 1981 Jun 13;1(8233):1285–1286. doi: 10.1016/s0140-6736(81)92459-4. [DOI] [PubMed] [Google Scholar]
  20. Jewell D. P., Maclennan I. C., Truelove S. C. Circulating immune complexes in ulcerative colitis and Crohn's disease. Gut. 1972 Oct;13(10):839–840. [PubMed] [Google Scholar]
  21. Jeynes B. J., Altmann G. G. Light and scanning electron microscopic observations of the effects of sublethal doses of methotrexate on the rat small intestine. Anat Rec. 1978 May;191(1):1–17. doi: 10.1002/ar.1091910102. [DOI] [PubMed] [Google Scholar]
  22. Laker M. F., Menzies I. S. Increase in human intestinal permeability following ingestion of hypertonic solutions. J Physiol. 1977 Mar;265(3):881–894. doi: 10.1113/jphysiol.1977.sp011750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Lynn K. L., Shenkin A., Marshall R. D. Factors affecting excretion of human urinary Tamm-Horsfall glycoprotein. Clin Sci (Lond) 1982 Jan;62(1):21–26. doi: 10.1042/cs0620021. [DOI] [PubMed] [Google Scholar]
  24. MacSween R. N. Alcohol and cancer. Br Med Bull. 1982 Jan;38(1):31–33. doi: 10.1093/oxfordjournals.bmb.a071729. [DOI] [PubMed] [Google Scholar]
  25. Menzies I. S., Laker M. F., Pounder R., Bull J., Heyer S., Wheeler P. G., Creamer B. Abnormal intestinal permeability to sugars in villous atrophy. Lancet. 1979 Nov 24;2(8152):1107–1109. doi: 10.1016/s0140-6736(79)92507-8. [DOI] [PubMed] [Google Scholar]
  26. NISSIM J. A. Reduction of intestinal absorption by a synthetic chemical. Nature. 1960 Jan 23;185:222–224. doi: 10.1038/185222a0. [DOI] [PubMed] [Google Scholar]
  27. Robinson G. M., Orrego H., Israel Y., Devenyi P., Kapur B. M. Low-molecular-weight polyethylene glycol as a probe of gastrointestinal permeability after alcohol ingestion. Dig Dis Sci. 1981 Nov;26(11):971–977. doi: 10.1007/BF01314757. [DOI] [PubMed] [Google Scholar]
  28. Sandhu J. S., Fraser D. R. Assessment of intestinal permeability in the experimental rat with [3H]cellobiotol and [14C]mannitol. Clin Sci (Lond) 1982 Sep;63(3):311–316. doi: 10.1042/cs0630311. [DOI] [PubMed] [Google Scholar]
  29. Slavin G., Sowter C., Robertson K., McDermott S., Paton K. Measurement in jejunal biopsies by computer-aided microscopy. J Clin Pathol. 1980 Mar;33(3):254–261. doi: 10.1136/jcp.33.3.254. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Sundqvist T., Lindström F., Magnusson K. E., Sköldstam L., Stjernström I., Tagesson C. Influence of fasting on intestinal permeability and disease activity in patients with rheumatoid arthritis. Scand J Rheumatol. 1982;11(1):33–38. doi: 10.3109/03009748209098111. [DOI] [PubMed] [Google Scholar]
  31. TIDBALL C. S. MAGNESIUM AND CALCIUM AS REGULATORS OF INTESTINAL PERMEABILITY. Am J Physiol. 1964 Jan;206:243–246. doi: 10.1152/ajplegacy.1964.206.1.243. [DOI] [PubMed] [Google Scholar]
  32. Ussing H. H. Anomalous transport of electrolytes and sucrose through the isolated frog skin induced by hypertonicity of the outside bathing solution. Ann N Y Acad Sci. 1966 Jul 14;137(2):543–555. doi: 10.1111/j.1749-6632.1966.tb50180.x. [DOI] [PubMed] [Google Scholar]
  33. WARREN S., SOMMERS S. C. Pathology of regional ileitis and ulcerative colitis. J Am Med Assoc. 1954 Jan 16;154(3):189–193. doi: 10.1001/jama.1954.02940370001001. [DOI] [PubMed] [Google Scholar]
  34. Walker W. A. Antigen absorption from the small intestine and gastrointestinal disease. Pediatr Clin North Am. 1975 Nov;22(4):731–746. doi: 10.1016/s0031-3955(16)33204-7. [DOI] [PubMed] [Google Scholar]
  35. Walker W. A., Isselbacher K. J. Uptake and transport of macromolecules by the intestine. Possible role in clinical disorders. Gastroenterology. 1974 Sep;67(3):531–550. [PubMed] [Google Scholar]
  36. Wands J. R., LaMont J. T., Mann E., Isselbacher K. J. Arthritis associated with intestinal-bypass procedure for morbid obesity. Complement activation and characterization of circulating cryoproteins. N Engl J Med. 1976 Jan 15;294(3):121–124. doi: 10.1056/NEJM197601152940301. [DOI] [PubMed] [Google Scholar]
  37. Wheeler P. G., Menzies I. S., Creamer B. Effect of hyperosmolar stimuli and coeliac disease on the permeability of the human gastrointestinal tract. Clin Sci Mol Med. 1978 May;54(5):495–501. doi: 10.1042/cs0540495. [DOI] [PubMed] [Google Scholar]
  38. Wilson F. A., Hoyumpa A. M., Jr Ethanol and small intestinal transport. Gastroenterology. 1979 Feb;76(2):388–403. [PubMed] [Google Scholar]
  39. Worthington B. S., Meserole L., Syrotuck J. A. Effect of daily ethanol ingestion on intestinal permeability to macromolecules. Am J Dig Dis. 1978 Jan;23(1):23–32. doi: 10.1007/BF01072571. [DOI] [PubMed] [Google Scholar]

Articles from Gut are provided here courtesy of BMJ Publishing Group

RESOURCES