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. 1980 May;65(5):1174–1181. doi: 10.1172/JCI109772

Circadian Rhythm of Intestinal Sucrase Activity in Rats

MECHANISM OF ENZYME CHANGE

Mark A Kaufman 1,2, Helen A Korsmo 1,2, Ward A Olsen 1,2
PMCID: PMC371451  PMID: 7364944

Abstract

Past investigation has revealed that the circadian rhythm of intestinal sucrase activity in rats is primarily cued by the time of feeding. We examined the mechanism of the circadian rhythm by methods involving quantitative immunoprecipitation of sucrase-isomaltase protein and study of decay of radioactively labeled protein. Rats were placed on a controlled feeding regimen (1000-1500 h) and then sacrificed at 3-h intervals over a 24-h period. Immunotitration experiments indicated that the circadian rhythm was the result of changes in the absolute amount of sucrase-isomaltase protein present and not of changes in the enzyme's catalytic efficiency.

To study the mechanism of this circadian variation in sucrase-isomaltase mass, [14C]sodium carbonate was injected and, after maximum incorporation into brush border protein, the rats were sacrified at 3-h intervals. Sucrase-isomaltase protein was isolated by immunoprecipitation, and the decrease in total disintegrations per minute over time was used to study degradation of the protein. Enzyme degradation was not constant but exhibited a clear circadian rhythm. The period of increasing enzyme mass was characterized by virtual cessation of enzyme degradation (t½ of 38 h), and the period of declining enzyme mass by rapid degradation (t½ of 6 h or less). We found similar changes in enzyme degradation in fasted animals, demonstrating that the changes were not the result of decreased isotope reutilization during feeding. We found no evidence of a circadian rhythm in [14C]leucine incorporation into the protein, suggesting that enzyme synthesis was constant.

These results indicate that the circadian rhythm of sucrase activity represents changes in the total amount of enzyme protein that are, at least in large part, secondary to changes in the enzyme's degradation rate.

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Selected References

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

  1. Alpers D. H., Seetharam B. Pathophysiology of diseases involving intestinal brush-border proteins. N Engl J Med. 1977 May 5;296(18):1047–1050. doi: 10.1056/NEJM197705052961808. [DOI] [PubMed] [Google Scholar]
  2. Alpers D. H., Tedesco F. J. The possible role of pancreatic proteases in the turnover of intestinal brush border proteins. Biochim Biophys Acta. 1975 Aug 5;401(1):28–40. doi: 10.1016/0005-2736(75)90338-7. [DOI] [PubMed] [Google Scholar]
  3. Arvanitakis C., Olsen W. A. Intestinal mucosal disaccharidases in chronic pancreatitis. Am J Dig Dis. 1974 May;19(5):417–421. doi: 10.1007/BF01255605. [DOI] [PubMed] [Google Scholar]
  4. Chee P. Y., Dahl J. L. Measurement of protein turnover in rat brain. J Neurochem. 1978 Jun;30(6):1485–1493. doi: 10.1111/j.1471-4159.1978.tb10482.x. [DOI] [PubMed] [Google Scholar]
  5. DAHLQVIST A., THOMSON D. L. The digestion and absorption of sucrose by the intact rat. J Physiol. 1963 Jul;167:193–209. doi: 10.1113/jphysiol.1963.sp007141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dahlqvist A. Assay of intestinal disaccharidases. Anal Biochem. 1968 Jan;22(1):99–107. doi: 10.1016/0003-2697(68)90263-7. [DOI] [PubMed] [Google Scholar]
  7. Deren J. J., Broitman S. A., Zamcheck N. Effect of diet upon intestinal disaccharidases and disaccharide absorption. J Clin Invest. 1967 Feb;46(2):186–195. doi: 10.1172/JCI105521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Götze H., Adelson J. W., Hadorn H. B., Portmann R., Troesch V. Hormone-elicited enzyme release by the small intestinal wall. Gut. 1972 Jun;13(6):471–476. doi: 10.1136/gut.13.6.471. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Herzfeld A., Raper S. M. Enzymes of ornithine metabolism in adult and developing rat intestine. Biochim Biophys Acta. 1976 May 28;428(3):600–610. doi: 10.1016/0304-4165(76)90188-4. [DOI] [PubMed] [Google Scholar]
  10. Kolínská J., Kraml J. Separation and characterization of sucrose-isomaltase and of glucoamylase of rat intestine. Biochim Biophys Acta. 1972 Sep 19;284(1):235–247. doi: 10.1016/0005-2744(72)90062-9. [DOI] [PubMed] [Google Scholar]
  11. Kwong W. K., Seetharam B., Alpers D. H. Effect of exchange exocrine pancreatic insufficiency on small intestine in the mouse. Gastroenterology. 1978 Jun;74(6):1277–1282. [PubMed] [Google Scholar]
  12. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  13. Millward D. J. Protein turnover in skeletal muscle. I. The measurement of rates of synthesis and catabolism of skeletal muscle protein using (14C)Na2CO3 to label protein. Clin Sci. 1970 Nov;39(5):577–590. doi: 10.1042/cs0390577. [DOI] [PubMed] [Google Scholar]
  14. Millward D. J. Protein turnover in skeletal muscle. II. The effect of starvation and a protein-free diet on the synthesis and catabolism of skeletal muscle proteins in comparison to liver. Clin Sci. 1970 Nov;39(5):591–603. doi: 10.1042/cs0390591. [DOI] [PubMed] [Google Scholar]
  15. Nishida T., Saito M., Suda M. Parallel between circadian rhythms of intestinal disaccharidases and foot intake of rats under constant lighting conditions. Gastroenterology. 1978 Feb;74(2 Pt 1):224–227. [PubMed] [Google Scholar]
  16. OUCHTERLONY O. Diffusion-in-gel methods for immunological analysis. Prog Allergy. 1958;5:1–78. [PubMed] [Google Scholar]
  17. Olsen W. A., Korsmo H. The intestinal brush border membrane in diabetes. Studies of sucrase-isomaltase metabolism in rats with streptozotocin diabetes. J Clin Invest. 1977 Jul;60(1):181–188. doi: 10.1172/JCI108755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. PORTEOUS J. W., CLARK B. THE ISOLATION AND CHARACTERIZATION OF SUBCELLULAR COMPONENTS OF THE EPITHELIAL CELLS OF RABBIT SMALL INTESTINE. Biochem J. 1965 Jul;96:159–171. doi: 10.1042/bj0960159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Poole B. The kinetics of disappearance of labeled leucine from the free leucine pool of rat liver and its effect on the apparent turnover of catalase and other hepatic proteins. J Biol Chem. 1971 Nov;246(21):6587–6591. [PubMed] [Google Scholar]
  20. Quaroni A., Gershon-Quaroni E., Semenza G. Tryptic digestion of native small-intestinal sucrase - isomaltase complex: isolation of the sucrase subunit. Eur J Biochem. 1975 Apr 1;52(3):481–486. doi: 10.1111/j.1432-1033.1975.tb04017.x. [DOI] [PubMed] [Google Scholar]
  21. Rosensweig N. S., Herman R. H. Control of jejunal sucrase and maltase activity by dietary sucrose or fructose in man. A model for the study of enzyme regulation in man. J Clin Invest. 1968 Oct;47(10):2253–2262. doi: 10.1172/JCI105910. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Rosenweig N. S., Herman R. H. Time response of jejunal sucrase and maltase activity to a high sucrose diet in normal man. Gastroenterology. 1969 Mar;56(3):500–505. [PubMed] [Google Scholar]
  23. SCHIMKE R. T., SWEENEY E. W., BERLIN C. M. THE ROLES OF SYNTHESIS AND DEGRADATION IN THE CONTROL OF RAT LIVER TRYPTOPHAN PYRROLASE. J Biol Chem. 1965 Jan;240:322–331. [PubMed] [Google Scholar]
  24. SIEKEVITZ P. Uptake of radioactive alanine in vitro into the proteins of rat liver fractions. J Biol Chem. 1952 Apr;195(2):549–565. [PubMed] [Google Scholar]
  25. STEIN W. H., MOORE S. The free amino acids of human blood plasma. J Biol Chem. 1954 Dec;211(2):915–926. [PubMed] [Google Scholar]
  26. SWICK R. W., HANDA D. T. The distribution of fixed carbon in amino acids. J Biol Chem. 1956 Feb;218(2):577–585. [PubMed] [Google Scholar]
  27. Saito M. Daily rhythmic changes in brush border enzymes of the small intestine and kidney in rat. Biochim Biophys Acta. 1972 Nov 24;286(1):212–215. doi: 10.1016/0304-4165(72)90108-0. [DOI] [PubMed] [Google Scholar]
  28. Stevenson N. R., Ferrigni F., Parnicky K., Day S., Fierstein J. S. Effect of changes in feeding schedule on the diurnal rhythms and daily activity levels of intestinal brush border enzymes and transport systems. Biochim Biophys Acta. 1975 Sep 16;406(1):131–145. doi: 10.1016/0005-2736(75)90048-6. [DOI] [PubMed] [Google Scholar]
  29. Stevenson N. R., Fierstein J. S. Circadian rhythms of intestinal sucrase and glucose transport: cued by time of feeding. Am J Physiol. 1976 Mar;230(3):731–735. doi: 10.1152/ajplegacy.1976.230.3.731. [DOI] [PubMed] [Google Scholar]
  30. Swick R. W., Ip M. M. Measurement of protein turnover in rat liver with (14C)carbonate. Protein turnover during liver regeneration. J Biol Chem. 1974 Nov 10;249(21):6836–6841. [PubMed] [Google Scholar]

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