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Effects of Alisma canaliculatum Extract in Pacemaker Potential of Intestinal Interstitial cells of Cajal in mice

생쥐 소장 및 대장 카할세포의 자발적 탈분극에서 택사의 효과에 관한 비교연구

  • Kwon, Hyo Eun (Division of Longevity and Biofunctional Medicine School of Korean Medicine, Pusan National University) ;
  • Park, Dong Suk (Division of Longevity and Biofunctional Medicine School of Korean Medicine, Pusan National University) ;
  • Kim, Jeong Nam (Division of Longevity and Biofunctional Medicine School of Korean Medicine, Pusan National University) ;
  • Kim, Byung Joo (Division of Longevity and Biofunctional Medicine School of Korean Medicine, Pusan National University)
  • 권효은 (부산대학교 한의학전문대학원 양생기능의학교실) ;
  • 박동석 (부산대학교 한의학전문대학원 양생기능의학교실) ;
  • 김정남 (부산대학교 한의학전문대학원 양생기능의학교실) ;
  • 김병주 (부산대학교 한의학전문대학원 양생기능의학교실)
  • Received : 2022.03.02
  • Accepted : 2022.05.11
  • Published : 2022.05.31

Abstract

Objectives : The purpose of this study was to examine the effects of Alisma canaliculatum Extract (ACE) on pacemaker potentials of small and large intestinal interstitial Cells of Cajal (ICC) in mice. Methods : We used enzymatic digestions to dissociate the ICC in the small and large intestine in mice. The whole-cell patch-clamp method was used to record pacemaker potentials in ICC. Results : 1. The ICC generated the pacemaker potentials in small intestine in mice. ACE (0.1-1mg/ml) induced membrane depolarization and decreased frequency with concentration-dependent manners. 2. Pretreatment with a Ca2+ free solution, Na+ 5 mM solution or 2-APB, a nonselective cation channel blocker, stopped the small intestinal ICC pacemaker potentials. In the case of Ca2+-free solution, Na+ 5 mM solution or 2-APB, ACE had no effects on the membrane depolarizations in small intestinal ICC. 3. The ICC generated the pacemaker potentials in large intestine in mice. Membrane depolarization appears regularly in the small intestine, but irregularly in the large intestine. ACE induced membrane depolarization (0.1-1mg/ml) and increased frequency (0.1-0.5mg/ml). 4. Pretreatment with a Ca2+ free solution, Na+ 5 mM solution or 2-APB, stopped the large intestinal ICC pacemaker potentials. In the case of Ca2+-free solution, Na+ 5 mM solution or 2-APB, ACE depolarized the membrane depolarizations in large intestinal ICC. 5. In mice, intestinal transit rate (ITR) values were dose-dependently decreased by the intragastric administration of ACE. Conclusions : These results suggest that ACE can regulate the pacemaker activity of ICC and the reaction by ACE is different from the small and large intestinal ICC, and the control of the intestinal motion by ACE may be caused by many complex processes.

Keywords

Acknowledgement

이 논문은 부산대학교 기본연구지원사업 (2년)에 의하여 연구되었다.

References

  1. Kim BJ, Lim HH, Yang DK, Jun JY, Chang IY, Park CS, et al. Melastatin-type transient receptor potential channel 7 is required for intestinal pacemaking activity. Gastroenterology. 2005;129:1504-1517. https://doi.org/10.1053/j.gastro.2005.08.016
  2. Zhu MH, Sung TS, O'Driscoll K, Koh SD, Sanders KM. Intracellular Ca(2+) release from endoplasmic reticulum regulates slow wave currents and pacemaker activity of interstitial cells of Cajal. Am J Physiol Cell Physiol. 2015;308:C608-C620. https://doi.org/10.1152/ajpcell.00360.2014
  3. Sanders KM, Ward SM, Koh SD. Interstitial cells: regulators of smooth muscle function. Physiol Rev. 2014;94:859-907. https://doi.org/10.1152/physrev.00037.2013
  4. Vanderwinden JM, Rumessen JJ. Interstitial cells of cajal in human gut and gastrointestinal disease. Microsc Res Tech. 1999;47:344-360. https://doi.org/10.1002/(SICI)1097-0029(19991201)47:5<344::AID-JEMT6>3.0.CO;2-1
  5. Vandercappellen J, Van Damme J, Struyf S. The role of CXC chemokines and their receptors in cancer. Cancer Lett. 2008;267:226-244. https://doi.org/10.1016/j.canlet.2008.04.050
  6. Mikamo H, Kawazoe K, Izumi K, Sato Y, Tamaya T. Effects of crude herbal ingredients on intrauterine infection in a rat model. Curr Ther Res. 1998;59:122-127. https://doi.org/10.1016/S0011-393X(98)85007-8
  7. Huang YT, Huang DM, Chueh SC, Teng CM, Guh JH. Alisol B acetate, a triterpene from Alismatis rhizoma, induces Bax nuclear translocation and apoptosis in human hormone-resistant prostate cancer PC-3 cells. Cancer Lett. 2006;231:270-278. https://doi.org/10.1016/j.canlet.2005.02.011
  8. Jang MK, Han YR, Nam JS, Han CW, Kim BJ, Jeong HS, et al. Protective Effects of Alisma orientale Extract against Hepatic Steatosis via Inhibition of Endoplasmic Reticulum Stress. Int J Mol Sci. 2015;16:26151-26165. https://doi.org/10.3390/ijms161125944
  9. Kim KJ, Leutou AS, JT, Choi SW, Kim SH, Yee ST, et al. The Inhibitory Effect of Alisol A 24-Acetate from Alisma canaliculatum on Osteoclastogenesis. Int J Endocrinol. 2015;2015:132436.
  10. Hwang YH, Kang KY, Lee SJ, Nam SJ, Son YJ, Yee ST. The Protective Effects of Alisol A 24-Acetate from Alisma canaliculatum on Ovariectomy Induced Bone Loss in Vivo. Molecules. 2016;21:74. https://doi.org/10.3390/molecules21010074
  11. Choi J, Ahn SS, Lim Y, Lee YH, Shin SY. Inhibitory Effect of Alisma canaliculatum Ethanolic Extract on NF-κB-Dependent CXCR3 and CXCL10 Expression in TNFα-Exposed MDA-MB-231 Breast Cancer Cells. Int J Mol Sci. 2018;19:2607. https://doi.org/10.3390/ijms19092607
  12. Yuan H, Ma Q, Ye L, Piao G. The Traditional Medicine and Modern Medicine from Natural Products. Molecules. 2016;21:559. https://doi.org/10.3390/molecules21050559
  13. Sanders KM, Koh SD, Ro S, Ward SM. Regulation of gastrointestinal motility-insights from smooth muscle biology. Nat Rev Gastroenterol Hepatol. 2012;9:633-645. https://doi.org/10.1038/nrgastro.2012.168
  14. Hirst GD, Bramich NJ, Teramoto N, Suzuki H, Edwards FR. Regenerative component of slow waves in the Guinea-pig gastric antrum involves a delayed increase in [Ca(2+)](i) and Cl(-) channels. J Physiol. 2002;540:907-919. https://doi.org/10.1111/j.1469-7793.2002.00907.x
  15. Hwang SJ, Blair PJ, Britton FC, O'Driscoll KE, Hennig G, Bayguinov YR, et al. Expression of anoctamin 1/TMEM16A by interstitial cells of Cajal is fundamental for slow wave activity in gastrointestinal muscles. J Physiol. 2009;587:4887-4904. https://doi.org/10.1113/jphysiol.2009.176198
  16. Maeda H, Yamagata A, Nishikawa S, Yoshinaga K, Kobayashi S, Nishi K, et al. Requirement of c-kit for development of intestinal pacemaker system. Development. 1992;116:369-753. https://doi.org/10.1242/dev.116.2.369
  17. Torihashi S, Ward SM, Nishikawa S, Nishi K, Kobayashi S, Sanders KM. c-kit-dependent development of interstitial cells and electrical activity in the murine gastrointestinal tract. Cell Tissue Res. 1995;280:97-111. https://doi.org/10.1007/BF00304515
  18. Sung SK, Kim SJ, Ahn TS, Hong NR, Park HS, Kwon YK, et al. Effects of Dangkwisoo-san, a traditional herbal medicine for treating pain and blood stagnation, on the pacemaker activities of cultured interstitial cells of Cajal. Mol Med Rep. 2015;12:6370-6376. https://doi.org/10.3892/mmr.2015.4203