Surgery Today

, Volume 22, Issue 4, pp 339–345 | Cite as

The proliferative kinetics of somatostatin-producing cells in the rat antral mucosa after truncal vagotomy

  • Hiroshi Shimoda
  • Shigeo Yokoyama
  • Iwao Nakayama
  • Tetsuo Hadama
  • Yuzo Uchida
Original Articles

Abstract

The kinetics of somatostatin-producing cells (D-cells) in the rat antral mucosa after truncal vagotomy were studied using double immunostaining for bromodeoxyuridine (BrdU) and somatostatin. Both the concentration of somatostatin and D-cell density in the antral mucosa demonstrated a significant increase on the 3rd day after truncal vagotomy. With the single labeling of BrdU, a few D-cells showed positive immunostaining for BrdU throughout the experimental period in both vagotomized and sham operated rats. With cumulative labeling, the BrdU labeled cells demonstrated a linear increase in an identical number for each experimental time-point in both groups. The labeling index of BrdU in the D-cells increased significantly, beginning on the 3rd day and attaining a maximum level of 41.8% on the 10th day, in the vagotomized group after cumulative labeling. In this group, however, the density of D-cells with no immunoreactive BrdU also increased quickly on the 3rd day with cumulative labeling. The present study indicates that the most important factor involving D-cell hyperplasia observed after truncal vagotomy is the activation of pre-existing D-cells to synthesize and release hormones, together with the rapid replication of progenitor cells and their maturation to D-cells.

Key Words

somatostatin-producing cell truncal vagotomy BrdU immunohistochemistry 

References

  1. 1.
    Delince P, Willems G, De Graef J (1978) Antral gastrin cell proliferation after vagotomy in rats. Digestion 18:27–34Google Scholar
  2. 2.
    Miyagami H, Watanabe Y, Sawada Y, Kato K, Shiono K, Kondo K, Kidokoro K (1977) Ultrastructures of G cells and the mechanism of gastrin release before and after selective vagotomy with pyloroplasty. Arch Histol Jpn 40:51–62Google Scholar
  3. 3.
    Alumets J, El Munshid HA, Håkanson R, Hedenbro J, Liedberg G, Oscarson J, Rehfeld JF, Sundler F, Vallgren S (1980) Gastrin cell proliferation after chronic stimulation: Effect of vagal denervation or gastric surgery in the rat. J Physiol 298:557–569Google Scholar
  4. 4.
    Murakami S, Nakayama I, Uchida Y (1988) Alteration of gastrin-producing cells in rat antral mucosa after truncal vagotomy. Acta Pathol Jpn 38:841–852Google Scholar
  5. 5.
    Shimoda H, Murakami S, Nakayama I, Uchida Y (1990) Dynamics of gastrin-producing cells in the rat after truncal vagotomy. Evaluation by double immunostaining for bromodeoxyuridine and little gastrin. Acta Pathol Jpn 40:469–475Google Scholar
  6. 6.
    Mulholland MW, Bonsack M, Delaney JP (1985) Proliferation of gastric endocrine cells after vagotomy in the rat. Endocrinology 117:1578–1584Google Scholar
  7. 7.
    Nomiyama S, Nishioka B, Ishii T, Nakamura K, Fujita Y, Majima S (1982) Effects of vagotomy on gastric G and D cell population in rat (in Japanese with English abstract). Nippon Shokakibyo Gakkai Zassi (Jpn J Gastroenterol) 79:1073–1083Google Scholar
  8. 8.
    Wada D, Tamura T, Fukumoto T, Yamamoto M, Morimoto H, Ando M, Miyamoto H, Komi N (1984) Experimental study on antral gastrin cell and somatostatin cell population with special reference to serum gastrin level after selective proximal vagotomy (in Japanese with English abstract). Shikoku Igaku Zassi (Shikoku M J) 40:293–297Google Scholar
  9. 9.
    Nomiyama S, Takeda Y, Sasaki Y, Nakamura K, Nishioka B, Fujita Y, Majima S, Inokuchi H, Yoshikawa M, Kawai K, Takeuchi Y (1984) Effect of selective proximal vagotomy on gastric G-, D-and EC-cell density in dog (in Japanese with English abstract). Skokakibyo Gakkai Zassi (Jpn J Gastroenterol) 81:1159–1164.Google Scholar
  10. 10.
    Holle GE, Buck E, Pradayrol L, Wünsch E, Holle F (1985) Behavior of somatostatin-immunoreactive cells in the gastric mucosa before and after selective proximal vagotomy and pyloroplasty in treatment of gastric and duodenal ulcers. Gastroenterology 89:736–745Google Scholar
  11. 11.
    Taniyama K, Mandai K, Hata J, Tahara E, Hirata K, Sumii K, Kajiyama G (1984) Serum gastrin level and gastric endocrine cells after vagotomy in rats (in Japanese). In: Miyoshi A, Abe K, Ito Z, Kanno T, Fujita T, Matsuo Y, Yanaihara N, (eds) Shokakan horumon (Proceedings of the Third Gut Hormone Conference), vol. 4. Igaku Tosho Shuppan, Tokyo, pp 87–94Google Scholar
  12. 12.
    Jaffe BM, Clendinnen BG, Clarke RJ, Williams JA (1974) Effect of selective and proximal gastric vagotomy on serum gastrin. Gastroenterology 66:944–953Google Scholar
  13. 13.
    Stadil F, Rehfeld JF (1974) Gastrin response to insulin after selective, highly selective, and truncal vagotomy. Gastroenterology 66:7–15Google Scholar
  14. 14.
    Dunn DH, Decanini C, Bonsack ME, Eisenberg MM, Delaney JP (1979) Gastrin cell populations after highly selective vagotomy in the dog. Am J Surg 137:111–115Google Scholar
  15. 15.
    Lezoche E, Vagni V, Baisi G (1978) Serum gastrin levels after truncal and highly selective vagotomy. Acta Gastroenterol Belg 41:468–471Google Scholar
  16. 16.
    Yoshinaka M, Inokuchi H, Kawai K (1984) Effect of truncal vagotomy on antral G-cell kinetics in hamsters (in Japanese). In: Miyoshi A, Abe K, Ito Z, Kanno T, Fujita T, Matsuo Y, Yanaihara N, (eds) Shokakan horumon (Proceeding of the Third Gut Hormone Conference), vol. 4. Igaku Tosho Shuppan, Tokyo, pp 81–86Google Scholar
  17. 17.
    Morstyn G, Hsu S-M, Kinsella T, Gratzner H, Russo A, Mitchell JB (1983) Bromodeoxyuridine in tumors and chromosomes detected with a monoclonal antibody. J Clin Invest 72:1844–1850Google Scholar
  18. 18.
    Tada T, Kodama T, Watanabe S, Sato Y, Shimosato Y (1986) Immunohistochemical cell kinetic study of human lung cancer by using monoclonal antibody to bromodeoxyuridine. Jpn J Clin Oncol 16:129–135Google Scholar
  19. 19.
    Schutte B, Reynders MMJ, Bosman FT, Blijham GH (1987) Studies with anti-bromodeoxyuridine antibodies: II. Simultaneous immunocytochemical detection of antigen expression and DNA synthesis by in vivo labeling of mouse intestinal mucosa. J Histochem Cytochem 35:371–374Google Scholar
  20. 20.
    Gratzner HG (1982) Monoclonal antibody to 5-bromo- and 5-iododeoxyuridine: A new reagent for detection of DNA replication. Science 218:474–475Google Scholar
  21. 21.
    Schutte B, Reynders MMJ, Bosman FT, Blijham GH (1987) Effect of tissue fixation on anti-bromodeoxyuridine immunohistochemistry. J Histochem Cytochem 35:1343–1345Google Scholar
  22. 22.
    Fukushima T (1982) The establishment of radioimmunoassay for somatostatin and its clinical applications (in Japanese with English abstract). Hiroshima Daigaku Igaku Zassi (Hiroshima M J) 30:167–185Google Scholar
  23. 23.
    Guesdon JL, Ternynck T, Avrameas S (1979) The use of avidinbiotin interaction in immunoenzymatic techniques. J Histochem Cytochem 27:1131–1139Google Scholar
  24. 24.
    Takahashi T, Shimazu H, Yamagishi T, Tani M (1979) G-cell population in antral mucosa of the dog. Dig Dis Sci 24:921–925Google Scholar
  25. 25.
    Alumets J, Ekelund M, El Munshid HA, Håkanson R, Lóren I, Sundler F (1979) Topography of somatostatin cells in the stomach of the rat: Possible functional significance. Cell Tissue Res 202:177–188Google Scholar
  26. 26.
    Fujimoto S, Hattori T, Kimoto K, Yamashita S, Fujita S, Kawai K (1980) Tritiated thymidine autoradiographic study on origin and renewal of gastrin cells in antral area of hamsters. Gastroenterology 79:785–791Google Scholar

Copyright information

© Springer-Verlag 1992

Authors and Affiliations

  • Hiroshi Shimoda
    • 1
  • Shigeo Yokoyama
    • 2
  • Iwao Nakayama
    • 2
  • Tetsuo Hadama
    • 1
  • Yuzo Uchida
    • 1
  1. 1.The Second Department of SurgeryMedical College of OitaOitaJapan
  2. 2.The First Department of PathologyMedical College of OitaOitaJapan

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