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Effect of herbal medicine Saiko-Keishi-to (TJ-10) on rat spontaneous chronic pancreatitis

Comparison with other herbal medicines

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Summary

Background. In an attempt to obtain evidence of the beneficial effects of TJ-10, we investigated the gene expression of PAP, an acute phase protein specific for pancreatitis in rat spontaneous chronic pancreatitis.

Methods. Four-wk-old male WBN/Kob rats were fed with MB-3 pellet diet containing herbal medicine. There were two administration groups for each drug: the prophylactic group administered from 4–12 wk, and the therapeutic group administered from 12–20 wk. Untreated control rats were fed with MB-3 alone. Histopathologic changes and PAP gene expressions were analyzed at 12 and 20 wk.

Results. In the prophylactic group, TJ-10-treated WBN/Kob rats showed no evidence of pancreatitis, and there was the amelioration of pancreatitis in the pancreata of the rats treated with other herbal medicines except TJ-24 at 12 wk. PAP mRNA was not expressed in the TJ-10-treated rats, and PAP gene expression was suppressed in rats treated with other drugs except TJ-107. In the therapeutic group, the amelioration of pancreatitis was seen only in TJ-10-treated rats, but PAP gene expression was significantly suppressed in the rats treated with all herbal medicines tested, compared with that in untreated control rats.

Conclusion. An herbal medicine Saiko-keishi-to (TJ-10) delayed the onset of chronic pancreatitis in the WBN/Kob rat, and suppressed the pancreatitis-associated protein (PAP) gene expression more significantly than other herbal medicines.

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References

  1. Lankisch PG and Banks PA. Chronic pancreatitis: pathology, in Pancreatitis (Lankisch PG and Banks PA, eds.), Springer-Verlag, Berlin 1998; pp. 215–218.

    Google Scholar 

  2. Mori Y, Yokoyama J, Nishimura M, Serizawa O, Ikeda Y. Effect of camostat on pancreatic impairment in WBN/Kob rats. Biomed Res 1989; 10(Suppl 1): 157–166.

    CAS  Google Scholar 

  3. Otsuki M, Tani S, Okabayashi Y, Fuji M, Nakamura T, Fujisawa T, Itoh H. Beneficial effects of the synthetic trypsin inhibitor camostate in cerulein-induced acute pancreatitis in rats. Dig Dis Sci 1990; 35: 242–250.

    Article  PubMed  CAS  Google Scholar 

  4. Sugiyama M, Kobori O, Atomi Y, Wada N, Kuroda A, Muto T. Effect of oral administration of protease inhibitor on pancreatic exocrine function in WBN/Kob rats with chronic pancreatitis. Pancreas 1996; 13: 71–79.

    Article  PubMed  CAS  Google Scholar 

  5. Nakata K, Hosono Y, Hosono H, Sakaguchi H, Hosono S. The treatment with Kampo medicine for chronic pancreatitis. Jpn J Orient Med 1986; 36: 25–43 (in Japanese with English abstract).

    Google Scholar 

  6. Wakasugi H. Kampo treatment of chronic pancreatitis. J Clin Exp Med 1993; 67: 824–829 (in Japanese).

    Google Scholar 

  7. Su S-B, Motoo Y, Xie M-J, Sakai J, Taga H, Sawabu N. Expression of pancreatitis-associated protein (PAP) in spontaneous chronic pancreatitis in the WBN/Kob rat: effect of herbal medicine Saiko-keishi-to (TJ-10). Pancreas 1999; 19: 239–247.

    Article  PubMed  CAS  Google Scholar 

  8. Ohashi K, Kim JH, Hara H, Aso R, Akimoto T, Narama K. WBN/Kob rats, a new spontaneously occurring model of chronic pancreatitis. Int J Pancreatol 1990; 6: 231–247.

    PubMed  CAS  Google Scholar 

  9. Arai I, Hasegawa M, Mase A, Kitani T, Komatsu Y, Yamaura H, et al. Development of pancreatic dysfunction and pathohistology in WBN/Kob rats using special breeding diet. Jpn J Appl Physiol 1997; 27: 373–380.

    Google Scholar 

  10. Itoh T, Teraoka H. Cloning and tissue-specific expression of cDNAs for the human and mouse homologues of rat pancreatitis-associated protein (PAP). Biochem Biophys Acta 1993; 1172: 184–186.

    PubMed  CAS  Google Scholar 

  11. Keim V, Iovanna JL, Dagorn J-C. The acute phase reaction of the exocrine pancreas: gene expression and synthesis of pancreatitis-associated proteins. Digestion 1994; 55: 65–72.

    Article  PubMed  CAS  Google Scholar 

  12. Iovanna JL, Keim V, Nordback I, et al. Serum levels of pancreatitis-associated protein as indicators of the course of acute pancreatitis. Gastroenterology 1994; 106: 728–734.

    PubMed  CAS  Google Scholar 

  13. Motoo Y, Satomura Y, Mouri I, et al. Serum levels of pancreatitis-associated protein in digestive diseases with special reference to gastrointestinal cancers. Dig Dis Sci 1999; 44: 1142–1147.

    Article  PubMed  CAS  Google Scholar 

  14. Sparmann G, Merkord J, Jaschke A, et al. Pancreatic fibrosis in experimental pancreatitis induced by dibutyltin dichloride. Gastroenterology 1997; 112: 1664–1672.

    Article  PubMed  CAS  Google Scholar 

  15. Kataoka K, Sasaki T, Yorizumi H, Sakagami J, Kashima K. Pathophysiologic studies of experimental chronic pancreatitis in rats induced by injection of zein-oleic acid-linoleic acid solution into the pancreatic duct. Pancreas 1998; 16: 289–299.

    Article  PubMed  CAS  Google Scholar 

  16. Yamamoto M, Kumagai A, Yamamura Y. Structure and actions of saikosaponins isolated from Bupleurum falcatum L. I. Anti-inflammatory action of saikosaponins. Arzneimittelforschung 1975; 25: 1021–1023.

    PubMed  CAS  Google Scholar 

  17. Zhou ZC, Wang GZ, Ma JL. The anti-allergic inflammation action of saikosaponins. J Tradit Chin Med 1983; 3: 103–112.

    PubMed  CAS  Google Scholar 

  18. Shiratori K, Watanabe S, Takeuchi T. Effect of licorice extract (Fm 100) on release of secretin and exocrine pancreatic secretion in humans. Pancreas 1986; 1: 483–487.

    Article  PubMed  CAS  Google Scholar 

  19. Takahashi S, Yoshikawa T, Naito Y, Minamiyama Y, Tanigawa T, Kondo M. Antioxidant properties of anti-ulcer Kampo medicines. Free Radic Res Commun 1993; 19(Suppl 1): S101-S108.

    PubMed  Google Scholar 

  20. Kim YH, Park KH, Rho HM. Transcriptional activation of the Cu, Zn-superoxide dismutase gene through the AP2 site by ginsenoside Rb2 extracted from a medicinal plant, Panax ginseng. J Biol Chem 1996; 271: 24,539–24,543.

    CAS  Google Scholar 

  21. Fan ZH, Isobe K, Kiuchi K, Nakashima I. Enhancement of nitric oxide production from activated macrophages by a purifued form of ginsenoside (Rg1). Am J Chin Med 1995; 23: 279–287.

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Yoshiharu Motoo.

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Motoo, Y., Su, SB., Xie, MJ. et al. Effect of herbal medicine Saiko-Keishi-to (TJ-10) on rat spontaneous chronic pancreatitis. International Journal of Pancreatology 27, 123–129 (2000). https://doi.org/10.1385/IJGC:27:2:123

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  • DOI: https://doi.org/10.1385/IJGC:27:2:123

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