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. 1977 Oct;18(10):805–813. doi: 10.1136/gut.18.10.805

Effects of long chain fatty acids on solute absorption: perfusion studies in the human jejunum.

H V Ammon, P J Thomas, S F Phillips
PMCID: PMC1411680  PMID: 590838

Abstract

Perfusion studies were performed in healthy volunteers to test the hypothesis that net fluid secretion induced by fatty acids is accompanied by parallel reduction in solute transport. Ricinoleic acid provoked a marked net secretion of fluid and concomitantly inhibited the absorption of all solutes tested; these included glucose, xylose, L-leucine, L-lysine, Folic acid, and 2-mono-olein. Oleic acid also reduced net fluid and solute transport, but was less potent in reducing solute absorption than was ricinoleic acid. When fluid secretion was induced osmotically with mannitol, glucose and xylose absorption was not affected. The mechanism for this generalised effect of fatty acids on solute absorption is uncertain, possibly nonspecific, and might be related to mucosal damage and altered mucosal permeability induced by these agents.

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Selected References

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

  1. Alvarado F. D-xylose active transport in the hamster small intestine. Biochim Biophys Acta. 1966 Feb 7;112(2):292–306. doi: 10.1016/0926-6585(66)90328-1. [DOI] [PubMed] [Google Scholar]
  2. Ammon H. V., Phillips S. F. Inhibition of ileal water absorption by intraluminal fatty acids. Influence of chain length, hydroxylation, and conjugation of fatty acids. J Clin Invest. 1974 Jan;53(1):205–210. doi: 10.1172/JCI107539. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ammon H. V., Thomas P. J., Phillips S. F. Effects of oleic and ricinoleic acids on net jejunal water and electrolyte movement. Perfusion studies in man. J Clin Invest. 1974 Feb;53(2):374–379. doi: 10.1172/JCI107569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Binder H. J., Filburn C., Volpe B. T. Bile salt alteration of colonic electrolyte transport: role of cyclic adenosine monophosphate. Gastroenterology. 1975 Mar;68(3):503–508. [PubMed] [Google Scholar]
  5. Bright-Asare P., Binder H. J. Stimulation of colonic secretion of water and electrolytes by hydroxy fatty acids. Gastroenterology. 1973 Jan;64(1):81–88. [PubMed] [Google Scholar]
  6. Burke V., Gracey M., Thomas J., Malajczuk A. Inhibition of intestinal amino acid absorption by unconjugated bile salt in vivo. Aust N Z J Med. 1975 Oct;5(5):430–432. doi: 10.1111/j.1445-5994.1975.tb03051.x. [DOI] [PubMed] [Google Scholar]
  7. Carpenter C. C., Sack R. B., Feeley J. C., Steenberg R. W. Site and characteristics of electrolyte loss and effect of intraluminal glucose in experimental canine cholera. J Clin Invest. 1968 May;47(5):1210–1220. doi: 10.1172/JCI105810. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cline W. S., Lorenzsonn V., Benz L., Bass P., Olsen W. A. The effects of sodium ricinoleate on small intestinal function and structure. J Clin Invest. 1976 Aug;58(2):380–390. doi: 10.1172/JCI108482. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. DAWSON A. M., ISSELBACHER K. J. Studies on lipid metabolism in the small intestine with observations on the role of bile salts. J Clin Invest. 1960 May;39:730–740. doi: 10.1172/JCI104090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dietschy J. M. Effects of bile salts on intermediate metabolism of the intestinal mucosa. Fed Proc. 1967 Nov-Dec;26(6):1589–1598. [PubMed] [Google Scholar]
  11. Dietschy J. M., Sallee V. L., Wilson F. A. Unstirred water layers and absorption across the intestinal mucosa. Gastroenterology. 1971 Dec;61(6):932–934. [PubMed] [Google Scholar]
  12. Field M: Intestinal secretion: effect of cyclic AMP and its role in cholera. N Engl J Med. 1971 May 20;284(20):1137–1144. doi: 10.1056/NEJM197105202842008. [DOI] [PubMed] [Google Scholar]
  13. Forth W., Rummel W., Glasner H. Zur resorptionshemmenden Wirkung von Gallensäuren. Naunyn Schmiedebergs Arch Pharmakol Exp Pathol. 1966;254(4):364–380. [PubMed] [Google Scholar]
  14. Gaginella T. S., Phillips S. F. Ricinoleic acid (castor oil) alters intestinal surface structure. A scanning electronmiscroscopic study. Mayo Clin Proc. 1976 Jan;51(1):6–12. [PubMed] [Google Scholar]
  15. Goodwin J. F. Method for simultaneous direct estimation of glucose and xylose in serum. Clin Chem. 1970 Feb;16(2):85–91. [PubMed] [Google Scholar]
  16. HOFMANN A. F., BORGSTROEM B. THE INTRALUMINAL PHASE OF FAT DIGESTION IN MAN: THE LIPID CONTENT OF THE MICELLAR AND OIL PHASES OF INTESTINAL CONTENT OBTAINED DURING FAT DIGESTION AND ABSORPTION. J Clin Invest. 1964 Feb;43:247–257. doi: 10.1172/JCI104909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. HOFMANN A. F. THE FUNCTION OF BILE SALTS IN FAT ABSORPTION. THE SOLVENT PROPERTIES OF DILUTE MICELLAR SOLUTIONS OF CONJUGATED BILE SALTS. Biochem J. 1963 Oct;89:57–68. doi: 10.1042/bj0890057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hajjar J. J., Khuri R. N., Bikhazi A. B. Effect of bile salts on amino acid transport by rabbit intestine. Am J Physiol. 1975 Aug;229(2):518–523. doi: 10.1152/ajplegacy.1975.229.2.518. [DOI] [PubMed] [Google Scholar]
  19. Kameda H., Abei T., Nasrallah S., Iber F. L. Functional and histological injury to intestinal mucosa produced by hypertonicity. Am J Physiol. 1968 May;214(5):1090–1095. doi: 10.1152/ajplegacy.1968.214.5.1090. [DOI] [PubMed] [Google Scholar]
  20. Krag E., Phillips S. F. Active and passive bile acid absorption in man. Perfusion studies of the ileum and jejunum. J Clin Invest. 1974 Jun;53(6):1686–1694. doi: 10.1172/JCI107720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. LARSEN P. R., ROSS J. E., TAPLEY D. F. TRANSPORT OF NEUTRAL, DIBASIC AND N-METHYL-SUBSTITUTED AMINO ACIDS BY RAT INTESTINE. Biochim Biophys Acta. 1964 Nov 29;88:570–577. doi: 10.1016/0926-6577(64)90100-7. [DOI] [PubMed] [Google Scholar]
  22. Lenormand Y., Rautureau M., Mary J. Y., Rambaud J. C. Absorption intestinale de la vitamine D3, de l'acide linoléique et du cholestérol à partir de solutions micellaires: étude chez l'homme normal par la méthode de perfusion "in situ". Biol Gastroenterol (Paris) 1975 Jul-Aug;8(3):207–221. [PubMed] [Google Scholar]
  23. Levitt D. G., Hakim A. A., Lifson N. Evaluation of components of transport of sugars by dog jejunum in vivo. Am J Physiol. 1969 Sep;217(3):777–783. doi: 10.1152/ajplegacy.1969.217.3.777. [DOI] [PubMed] [Google Scholar]
  24. Matuchansky C., Bernier J. J. Effect of prostaglandin E 1 on glucose, water, and electrolyte absorption in the human jejunum. Gastroenterology. 1973 Jun;64(6):1111–1118. [PubMed] [Google Scholar]
  25. Nasrallah S. M., Coburn W. M., Jr, Iber F. L. The effect of hypertonic mannitol on the intestine of man. Johns Hopkins Med J. 1968 Sep;123(3):134–137. [PubMed] [Google Scholar]
  26. Porter H. P., Saunders D. R. Isolation of the aqueous phase of human intestinal contents during the digestion of a fatty meal. Gastroenterology. 1971 Jun;60(6):997–1007. [PubMed] [Google Scholar]
  27. REYNELL P. C., SPRAY G. H. Chemical gastroenteritis in the rat. Gastroenterology. 1958 May;34(5):867–873. [PubMed] [Google Scholar]
  28. Riddell W. M., Jordan P. H., Jr Enhancement of glucose absorption by oleic acid. Proc Soc Exp Biol Med. 1966 Aug-Sep;122(4):1204–1208. doi: 10.3181/00379727-122-31361. [DOI] [PubMed] [Google Scholar]
  29. Russell R. I., Allan J. G., Gerskowitch V. P., Cochran K. M. The effect of conjugated and unconjugated bile acids on water and electrolyte absorption in the human jejunum. Clin Sci Mol Med. 1973 Sep;45(3):301–311. doi: 10.1042/cs0450301. [DOI] [PubMed] [Google Scholar]
  30. Serebro H. A., Bayless T. M., Hendrix T. R., Iber F. L., McGonagle T. Absorption of d-glucose by the rabbit jejunum during cholera toxin-induced diarrhoea. Nature. 1968 Mar 30;217(5135):1272–1273. doi: 10.1038/2171272a0. [DOI] [PubMed] [Google Scholar]
  31. Sladen G. E., Harries J. T. Studies on the effects of unconjugated dihydroxy bile salts on rat small intestinal function in vivo. Biochim Biophys Acta. 1972 Nov 2;288(2):443–456. doi: 10.1016/0005-2736(72)90265-9. [DOI] [PubMed] [Google Scholar]
  32. Taketa K., Pogell B. M. The effect of palmityl coenzyme A on glucose 6-phosphate dehydrogenase and other enzymes. J Biol Chem. 1966 Feb 10;241(3):720–726. [PubMed] [Google Scholar]
  33. Teem M. V., Phillips S. F. Perfusion of the hamster jejunum with conjugated and unconjugated bile acids: inhibition of water absorption and effects on morphology. Gastroenterology. 1972 Feb;62(2):261–267. [PubMed] [Google Scholar]
  34. Wingate D. L., Krag E., Mekhjian H. S., Phillips S. F. Relationships between ion and water movement in the human jejunum, ileum and colon during perfusion with bile acids. Clin Sci Mol Med. 1973 Nov;45(5):593–606. doi: 10.1042/cs0450593. [DOI] [PubMed] [Google Scholar]
  35. Wingate D. L., Phillips S. F., Hofmann A. F. Effect of glycine-conjugated bile acids with and without lecithin on water and glucose absorption in perfused human jejunum. J Clin Invest. 1973 May;52(5):1230–1236. doi: 10.1172/JCI107290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Wingate D. L., Sandberg R. J., Phillips S. F. A comparison of stable and 14 C-labelled polyethylene glycol as volume indicators in the human jejunum. Gut. 1972 Oct;13(10):812–815. doi: 10.1136/gut.13.10.812. [DOI] [PMC free article] [PubMed] [Google Scholar]

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