Planta Med 1997; 63(5): 419-424
DOI: 10.1055/s-2006-957725
Papers
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Stimulative Effects of Saponin from Kikyo-to, a Japanese Herbal Medicine, on Pancreatic Exocrine Secretion of Conscious Rats

Ichiro Arai1 , Yasuhiro Komatsu1 , Yasuaki Hirai2 , Kazushi Shingu2 , Yoshiteru Ida2 , Hisashi Yamaura3 , Toshinori Yamamoto4 , Yukio Kuroiwa4 , Katsumi Sasaki5 , Susumu Taguchi5
  • 1Central Research Laboratories, Tsumura & Co., 3586 Yoshiwara, Ami-machi, Inashiki-gun, Ibaraki 300-11, Japan
  • 2Department of Pharmacognosy and Phytochemistry, School of Pharamceutical Science, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142, Japan
  • 3Institute of Oriental Medicine, Tokyo Women's Medical College, 8-1 Kawada-cho, Shinjyuku-ku, Tokyo 162, Japan
  • 4Department of Clinical Pharmacy, School of Pharmaceutical Science, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142, Japan
  • 5Second Department of Internal Medicine, School of Medicine, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142, Japan
Further Information

Publication History

1996

1997

Publication Date:
04 January 2007 (online)

Abstract

Our previous report stated that kikyo-to, a Japanese herbal medicine, consisting of the roots of Platycodon grandiflorum and Glycyrrhiza sp., stimulates the pancreatic exocrine secretion of conscious rats. The present study focused on the effective components of kikyo-to and the mechanism of stimuli to pancreatic secretion of rats. When 10 to 100 mg of platycodin D, a saponin from the root of Platycodon grandiflorum, was intragastrically administered, the pancreatic secretion of rats was stimulated. At the same time, the plasma CCK concentration increased. On the other hand, the stimulative effects of glycyrrhizin, a saponin from the root of Glycyrrhiza sp. were weak compared to platycodin D. The effects of 10 mg/kg of platycodin D on pancreatic secretion were inhibited by loxiglumide (50 mg/kg, i.g.), a CCK receptor antagonist. In contrast, the suppressive effect of atropine (300 µg/kg/h, i.v.) on pancreatic secretion was reduced by administering 10 mg/kg of platycodin D. In addition, up to 1 mM of platycodin D did not inhibit the trypsin activities in vitro. In conclusion, kikyo-to serves to stimulate pancreatic exocrine secretion mainly because platycodin D causes gastrointestinal hormones, particularly, CCK to be released from the duodenum.

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