Changes of Somatostatin-Immunoreactive Cells on the Stomach of Ovariectomized Rats

  • Chang, Jeong-Hyun (Department of Clinical Laboratory Science, Daegu Haany University)
  • Published : 2009.03.31

Abstract

The changes on the regional distributions and frequencies of somatostatin-immunoreactive (IR) cells in the fundus and pylorus of the stomach of osteoporotic Sprague-Dawley rats induced by ovariectomy were studied by immunohistochemical methods. The experimental animals were divided into two groups, one for non-ovariectomized group (Sham) and the other for ovariectomized group (OVX). Samples were collected from the fundus and pylorus regions at the 10 th week after ovariectomy or sham-operation. Somatostatin-IR cells were observed in both regions of the stomach regardless of ovariectomy. Most of these IR cells in the mucosa of the fundus or pylorus were generally spherical or spindle in shape (open type cell) while cells found in the gastric gland regions were round in shape (close type cell). Significantly lower number (P<0.01) of somatostatin-IR cells were detected in OVX as compared with Sham in the fundus and pylorus. In the present study, the density of somatostatin in the stomach was markedly decreased. Therefore, these changes in density of somatostatin-IR cells detected in this study may support the speculation that the development of gastrointestinal symptoms in osteoporosis such as impairments of calcium and some lipids, frequently encountered in patients with postmenopausal osteoporosis because the changes in gastrointestinal endocrine density would reflect the change in the capacity of producing these hormones and regulating gut motility and digestion.

Keywords

References

  1. Bell FR. The relevance of the new knowledge of gastrointestinal hormones to veterinary science. Vet Sci Commun. 1979. 2: 305-314. https://doi.org/10.1007/BF02291460
  2. Brazeau P, Vale W, Burgus RN, Ling M, Butcher J, Rivier R. Guillemin. Hypothalamic polypeptide that inhibits the secretion of immunoreactive pituitary growth hormone. Science 1973. 179: 77-79. https://doi.org/10.1126/science.179.4068.77
  3. El-Salhy M. The nature and implication of intestinal endocrine cell changes in celiac disease. Histol Histopathol. 1998. 13: 1069-1075.
  4. El-Salhy M, Sitohy B. Abnormal gastrointestinal endocrine cells in patients with diabetes type I: relationship to gastric emptying and myoelectrical activity. Scand J Gastroenterol. 2001. 36: 1162-1169. https://doi.org/10.1080/00365520152584789
  5. Guyton AC. Secretory functions of the alimentary tract. In: Guyton, A.C. (ed.) Textbook of medical physiology. WB Saunders, Philadelphia. 1988. 801-815.
  6. Kalu DN. The ovariectomized rat model of postmenopausal bone loss. Bone Miner Res. 1991. 15: 175-191. https://doi.org/10.1016/0169-6009(91)90124-I
  7. Kalu DN, Chen C. Ovariectomized murine model of postmenopausal calcium malabsorption. J Bone Miner Res. 1999. 14: 593-601. https://doi.org/10.1359/jbmr.1999.14.4.593
  8. Kitamura N, Yamada J, Calingasan NY, Yamashita T. Immunocytochemical distribution of endocrine cells in the gastrointestinal tract of the horse. J Equine Vet. 1984. 16: 103-107. https://doi.org/10.1111/j.2042-3306.1984.tb01870.x
  9. Ku SK, Lee HS, Lee JH. An immunohistochemical study of the gastrointestinal endocrine cells in the C57BL/6 mice. Anat Histol Embryol. 2003. 32: 21-28. https://doi.org/10.1046/j.1439-0264.2003.00433.x
  10. Ku SK, Lee HS, Lee JH. Changes of gastrointestinal argyrophil endocrine cells in the osteoporotic SD rats induced by ovariectomy. J Vet Sci. 2004a. 5: 183-188.
  11. Ku SK, Lee HS, Lee JH. A histochemical study of argentaffin endocrine cells in the gastrointestinal tract of ovariectomized rats. Korean J Vet Res. 2004b. 44: 171-177.
  12. Ku SK, Lee HS, Lee JH. An immunohistochemical study of chromogranin A and Sp-1 immunoreactive cells in the gastrointestinal tract of ovariectomized rats. J Vet Sci. 2005. 6: 191-196.
  13. Loest HB, Noh SK, Koo SI. Green tea extract inhibits the lymphatic absorption of cholesterol and alpha-tocopherol in ovariectomized rats. J Nutr. 2002. 132: 1282-1288. https://doi.org/10.1093/jn/132.6.1282
  14. Lucini C, De Girolamo P, Coppola L, Paino G, Castaldo L. Postnatal development of intestinal endocrine cell populations in the water buffalo. J Anat. 1999. 195: 439-446.
  15. Mitamura R, Hara H, Aoyama Y, Chiji H. Supplemental feeding of difructose anhydride III restores calcium absorption impaired by ovariectomy in rats. J Nutr. 2002. 132: 3387-3393.
  16. O'Toole K, Fenoglio-Preiser C, Pushparaj N. Endocrine changes associated with the human aging process: III. Effect of age on the number of calcitonin immunoreactive cells in the thyroid gland. Hum Pathol. 1985. 16: 991-1000. https://doi.org/10.1016/S0046-8177(85)80276-8
  17. Penissi A, Mariani L, Souto M, Guzman J, Piezzi R. Changes in gastroduodenal 5-hydroxytryptamine-containing cells induced by dehydroleucodine. Cells Tissues Organs 2000. 166: 259 -266. https://doi.org/10.1159/000016739
  18. Queiroz DM, Mendes EN, Rocha GA, Moura SM, Esende LM, Barbosa AJ, Coelho LG, Passos MC, Castro LP, Oliveira CA. Effect of Helicobacter pylori eradication on antral gastrinand somatostatin-immunoreactive cell density and gastrin and somatostatin concentrations. Scand J Gastroenterol. 1993. 28: 858-864. https://doi.org/10.3109/00365529309103125
  19. Riggs BL. Endocrine causes of age-related bone loss and osteoporosis. Novartis Found Symp. 2002. 242: 247-259.
  20. Solcia E, Capella C, Vassallo G, Buffa R. Endocrine cells of the gastric mucosa. Int Rev Cytol. 1975. 42: 223-286. https://doi.org/10.1016/S0074-7696(08)60982-1
  21. Spangeus A, Forsgren S, El-Salhy M. Effect of diabetic state on co-localization of substance P and serotonin in the gut in animal models. Histol Histopathol. 2001. 16: 393-398.
  22. Sternberger LA. The unlabeled antibody peroxidase-antiperoxidase (PAP) method. In: Sternberger LA. (ed.) Immunocytochemistry. John Wiley, New York. 1979. 104-169.
  23. Thomas T. Leptin: a potential mediator for protective effects of fat mass on bone tissue. Joint Bone Spine 2003. 70: 18-21. https://doi.org/10.1016/S1297-319X(02)00005-2
  24. Yamaguchi K, Yada M, Tsuji T, Kuramoto M, Uemura D. Suppressive effect of norzoanthamine hydrochloride on experimental osteoporosis in ovariectomized mice. Biol Pharm Bull. 1999. 22: 920-924. https://doi.org/10.1248/bpb.22.920
  25. Zhao R, Wang Y, Chen T. Somatostatin and its secretory cells in tumor surrounding mucosa in colorectal cancer patients and its significance. Zhonghua Wai Ke Za Zhi. 1997. 35: 268-270.