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Altered polyamine biosynthesis with aging after massive proximal small bowel resection in rat

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Abstract

We examined the effect of aging on polyamine biosynthesis in the small intestine. Two groups of male Wistar rats (young; 10-week-old,n=40; old; 24-month-old,n=40) underwent either a jejunal transection and reanastomosis or 90% proximal small bowel resection. The rats were sacrificed on the 1st, 2nd, 4th, and 7th postoperative day (POD). The mucosa was submitted for histological examination, weighed, and assayed for protein, DNA, RNA, and polyamine content. Ornithine decarboxylase (ODC) activity was measured and ODC mRNA in the mucosa was determined by Northern blot analysis. Compared with the values for wet weight and protein content in old rats, young rats showed significantly higher values for wet weight on the 1st and 2nd POD, and for protein content on the 1st POD, but there were no differences between young and old rats after the 4th POD. The values for ODC activity and ODC mRNA were significantly lower in old rats than in young rats on the 1st POD, but there were no differences between young and old rats after the 2nd POD. The value for putrescine in old rats was significantly lower on the 2nd POD, but was significantly higher on the 4th POD than that in young rats. The present study showed that, in old rats, the residual intestine after small bowel resection preserved sufficient adaptive capacity, but that the adaptive response was decreased. The findings in this study also suggest that a decrease in ODC mRNA expression is involved in the decreased adaptive response that occurs with aging.

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References

  1. Weser E, Hernandez MH. Studies of small bowel adaptation after intestinal resection in the rat. Gastroenterology 1971;60:69–75.

    CAS  PubMed  Google Scholar 

  2. Dowling RH. Small bowel adaptation and its regulation. Scand J Gastroenterol 1982;74:[Suppl]:53–74.

    CAS  Google Scholar 

  3. Bristol JB, Williamson RCN, Chir M. Postoperative adaptation of the small intestine. World J Surg 1985;9:825–832.

    Article  CAS  PubMed  Google Scholar 

  4. Wilson HD, Miller T, Ogesen B, et al. Adaptation of the duodenum and ileum of the rat to mid-gut resection: Enzyme activity and trace metal status. Am J Clin Nutr 1986;43:185–193.

    CAS  PubMed  Google Scholar 

  5. Heby O. Role of polyamines in the control of cell proliferation and differentiation. Differentiation 1981;19:1–20.

    CAS  PubMed  Google Scholar 

  6. Pegg AE, McCann PP. Polyamine metabolism and function. Am J Physiol;1982;243:C212-C221.

    CAS  PubMed  Google Scholar 

  7. Tabor CW, Tabor H. Polyamines. Annu Rev Biochem 1984; 53:749–790.

    Article  CAS  PubMed  Google Scholar 

  8. Seiler N. Polyamine metabolism. Digestion 1990;46[Suppl 2]:319–330.

    CAS  PubMed  Google Scholar 

  9. Dowling RH. Polyamines in intestinal adaptation and disease. Digestion 1990;46[Suppl 2]:331–344.

    CAS  PubMed  Google Scholar 

  10. Bamba T, Vaja S, Murphy GM, et al. Role of polyamines in the early adaptive response to jejunectomy in the rat: Effect of DFMO on the ileal villus and crypt axis. Digestion 1990;46[Suppl 2]: 410–423.

    CAS  PubMed  Google Scholar 

  11. Luk GD, Marton LJ, Baylin SB. Ornithine decarboxylase is important in intestinal mucosal maturation and recovery from injury in rats. Science 1980;210:195–198.

    CAS  Google Scholar 

  12. Luk GD, Baylin SB. Polyamines and intestinal growth—increased polyamine biosynthesis after jejunectomy. Am J Physiol 1983; 245:G656–660.

    CAS  PubMed  Google Scholar 

  13. Luk GD, Baylin SB. Inhibition of intestinal epithelial DNA synthesis and adaptive hyperplasia after jejunectomy in the rat by suppression of polyamine biosynthesis. J Clin Invest 1984;74:698–704.

    CAS  PubMed  Google Scholar 

  14. Rountree DB, Ulshen MH, Selub S, et al. Nutrient-independent increases in proglucagon and ornithine decarboxylase messenger RNAs after jejunoileal resection. Gastroenterology 1992;103:462–468.

    CAS  PubMed  Google Scholar 

  15. Poston GJ, Saydjari R, Lawrence J, et al. The effect of age on small bowel adaptation and growth after proximal enterectomy. J Gerontol 1990;45:B220-B225.

    CAS  PubMed  Google Scholar 

  16. Holt PR, Luk GD. Aging and intestinal polyamine metabolism in the rat. Exp Gerontol 1990;25:173–181.

    Article  CAS  PubMed  Google Scholar 

  17. Yoshinaga K, Ishizuka J, Evers BM, et al. Age-related changes in polyamine biosynthesis after fasting and refeeding. Exp Gerontol 1993;28:565–572.

    Article  CAS  PubMed  Google Scholar 

  18. Holt PR, Pascal RP, Kotler DP, et al. Effect of aging upon small intestinal structure in the Fischer rat. J Gerontol 1984;39:642–647.

    CAS  PubMed  Google Scholar 

  19. Holt PR, Tierney AR, Kolter DP. Delayed enzyme expression: A defect of aging rat gut. Gastroenterology 1985;89:1026–1034.

    CAS  PubMed  Google Scholar 

  20. Holt PR, Kotler DP. Adaptive changes of intestinal enzymes to nutritional intake in the aging rat. Gastroenterology 1987;93:295–300.

    CAS  PubMed  Google Scholar 

  21. Holt PR, Yeh KY, Kotler DP. Altered controls of proliferation in proximal small intestine of the senescent rat. Proc Natl Acad Sci USA 1988;85:2771–2775.

    CAS  PubMed  Google Scholar 

  22. Holt PR, Yeh KY. Small intestinal crypt cell proliferation rates are increased in senescent rats. J Gerontol 1988;44:B9-B14.

    Google Scholar 

  23. Lowry OH, Rosebrough NJ, Fart AL, et al. Problem measurement with the Folin-phenol reagent. J Biol Chem 1951;193:265–275.

    CAS  PubMed  Google Scholar 

  24. Andersen KJ, Skagen DW. Fluorometric determination of DNA in fixed tissue using ethidium bromide. Anal Biochem 1977; 83:703–708.

    Article  CAS  PubMed  Google Scholar 

  25. Chomczynski P, Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 1987;162:156–159.

    Article  CAS  PubMed  Google Scholar 

  26. Kanamoto R, Boyle SM, Oka T, et al. Molecular mechanisms of the synergistic induction of ornithine decarboxylase by asparagine and glucagon in primary cultured hepatocytes. J Biol Chem 1987;262(30):14801–14805.

    CAS  PubMed  Google Scholar 

  27. Tso JY, Sun XH, Kao T, et al. Isolation and characterization of rat and human glyceraldehyde-3-phosphate dehydrogenase cDNAs: Genomic complexity and molecular evolution of the gene. Nucleic Acid Res 1985;13:2485–2502.

    CAS  PubMed  Google Scholar 

  28. Arlow FL, Colarian J, Calzada R, et al. Differential activation of ornithine decarboxylase and tyrosine kinase in the rectal mucosa of patients with hyperplastic and adenomatous polyps. Gastroenterology 1991;100:1528–1532.

    PubMed  Google Scholar 

  29. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248–254.

    Article  CAS  PubMed  Google Scholar 

  30. Murakami Y, Nishiyama M, Hayashi S. Involvement of antizyme in stabilization of ornithine decarboxylase caused by inhibitors of polyamine synthesis. Eur J Biochem 1989;180:181–184.

    Article  CAS  PubMed  Google Scholar 

  31. Wen L, Huang JK, Blackshear PJ. Rat ornithine decarboxylase gene. J Biol Chem 1989;264:9016–9021.

    CAS  PubMed  Google Scholar 

  32. Koruda MJ, Rolandelli RH, Settle RG, et al. Small bowel disaccharidase activity in the rat as affect by intestinal resection and pectin feeding. Am J Clin Nutr 1988;47:448–453.

    CAS  PubMed  Google Scholar 

  33. Yoshinaga K, Ishizuka J, Townsend CM, et al. Age-related changes in duodenal adaptation after distal small bowel resection in rat. Dig Dis Sci 1993;38:410–416.

    Article  CAS  PubMed  Google Scholar 

  34. Katz A, Kahana C. Transcriptional activation of mammalian ornithine decarboxylase activity. Mol Cell Biol 1987;7:2641–2643.

    CAS  PubMed  Google Scholar 

  35. Seidel ER, Ginty DD. Apparent post-transcriptional modification of ornithine decarboxylase accounts for its induction in IEC-6 cells in culture. Digestion 1990;46[Suppl 2]:383–389.

    CAS  PubMed  Google Scholar 

  36. Chung DH, Evers BM, Townsend CM, et al. Burn-induced transcriptional regulation of small intestinal ornithine decarboxylase. Am J Surg 1992;163:157–163.

    Article  CAS  PubMed  Google Scholar 

  37. Seidel ER, Haddox MK, Johnson LR. Ileal mucosal growth during intraluminal infusion of ethylamine or putrescine. Am J Physiol 1985;246:G434-G438.

    Google Scholar 

  38. Wang JY, McCormack SA, Viar MJ, et al. Stimulation of proximal small intestinal mucosal growth by luminal polyamines. Am J Physiol 1991;261:G504-G511.

    CAS  PubMed  Google Scholar 

  39. Lentze MJ. Intestinal adaptation in short-bowel syndrome. Eur J Pediatr 1989;148:294–299.

    Article  CAS  PubMed  Google Scholar 

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Sakamoto, K., Fujiyama, Y. & Bamba, T. Altered polyamine biosynthesis with aging after massive proximal small bowel resection in rat. J Gastroenterol 31, 338–346 (1996). https://doi.org/10.1007/BF02355022

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