The Effect of External Divalent Cations on Intestinal Pacemaking Activity

  • Kim, Byung-Joo (Department of Physiology and Biophysics, Seoul National University College of Medicine) ;
  • Kim, Ki-Whan (Department of Physiology and Biophysics, Seoul National University College of Medicine)
  • Published : 2005.08.21

Abstract

Electrical rhythmicity in the gastrointestinal (GI) muscles is generated by pacemaker cells, known as interstitial cells of Cajal (ICC). In the present study, we investigated the effect of external divalent cations on pacemaking activity in cultured ICC from murine small intestine by using whole-cell patch clamp techniques. ICC generated pacemaker currents under a voltage clamp or electrical pacemaker potentials under a current clamp, and showed a mean amplitude of $-500{\pm}50$ pA or $30{\pm}1$ mV and the frequency of $18{\pm}2$ cycles/min. Treatments of the cells with external 0 mM $Ca^{2+}$ stopped pacemaking activity of ICC. In the presence of 2 mM $Ca^{2+}$, 0 mM external $Mg^{2+}$ depolarized the resting membrane potential, and there was no change in the frequency of pacemaking activity. However, 10 mM external $Mg^{2+}$ decreased the frequency of pacemaking activity ($6.75{\pm}1$ cycles/min, n=5). We replaced external 2 mM $Ca^{2+}$ with equimolar $Ba^{2+}$, $Mn^{2+}$ and $Sr^{2+}$, and they all developed inward current in the sequence of $Ba^{2+}$>$Mn^{2+}$>$Sr^{2+}$. Also the frequency of the pacemaking activity was stopped or irregulated. We investigated the effect of 10 mM $Ba^{2+}$, $Mn^{2+}$ and $Sr^{2+}$ on pacemaking activity of ICC in the presence of external 0 mM $Mg^{2+}$, and found that 10 mM $Ba^{2+}$ and $Mn^{2+}$ induced large inward current and stopped the pacemaking activity of ICC (n=5). Interestingly, 10 mM $Sr^{2+}$ induced small inward current and potentiated the amplitude of pacemaking activity of ICC (n=5). These results indicate that extracellular $Ca^{2+}$ and $Mg^{2+}$ are requisite for the pacemaking activity of ICC.

Keywords

References

  1. Dickens EJ, Hirst GD, Tomita T. Identification of rhythmically active cells in guinea-pig stomach. J Physiol 514: 515-531, 1999 https://doi.org/10.1111/j.1469-7793.1999.515ae.x
  2. Furuzono S, Nakayama S, Imaizumi Y. Purinergic modulation of pacemaker $Ca^{2+}$ activity in interstitial cells of Cajal. Neuropharmacology 48: 264-273, 2005 https://doi.org/10.1016/j.neuropharm.2004.10.007
  3. Goto K, Matsuoka S, Noma A. Two types of spontaneous depolarizations in the interstitial cells freshly prepared from the murine small intestine. J Physiol 559: 411-422, 2004 https://doi.org/10.1113/jphysiol.2004.063875
  4. Horowitz B, Ward SM, Sanders KM. Cellular and molecular basis for electrical rhythmicity in gastrointestinal muscles. Annu Rev Physiol 61: 19-43, 1999 https://doi.org/10.1146/annurev.physiol.61.1.19
  5. Huizinga JD, Thuneberg L, Kluppel M, Malysz J, Mikkelsen HB, Bernstein A. W/kit gene required for intestinal pacemaker activity. Nature 373: 347-349, 1995. https://doi.org/10.1038/373347a0
  6. Jun JY, Choi S, Chang IY, Yoon CK, Jeong HG, Kong ID, So I, Kim KW, You HJ. Deoxycholic acid inhibits pacemaker currents by activating ATP-dependent $K^{+}$ channels through prostaglandin E2 in interstitial cells of Cajal from the murine small intestine. Br J Pharmacol 144: 242-251, 2005 https://doi.org/10.1038/sj.bjp.0706074
  7. Jun JY, Choi S, Yeum CH, Chang IY, You HJ, Park CK, Kim MY, Kong ID, Kim MJ, Lee KP, So I, Kim KW. Substance P induces inward current and regulates pacemaker currents through tachykinin NK1 receptor in cultured interstitial cells of Cajal of murine small intestine. Eur J Pharmacol 495: 35-42, 2004 https://doi.org/10.1016/j.ejphar.2004.05.022
  8. Koh SD, Jun JY, Kim TW, Sanders KM. A Ca2+-inhibited nonselective cation conductance contributes to pacemaker currents in mouse interstitial cell of Cajal. J Physiol 540: 803-814, 2002 https://doi.org/10.1113/jphysiol.2001.014639
  9. Koh SD, Sanders KM, Ward SM. Spontaneous electrical rhythmicity in cultured interstitial cells of Cajal from the murine small intestine. J Physiol 513: 203-213, 1998 https://doi.org/10.1111/j.1469-7793.1998.203by.x
  10. Langton P, Ward SM, Carl A, Norell A, Sanders KM. Spontaneous electrical activity of interstitial cells of Cajal isolated from canine proximal colon. Proc Natl Acad Sci USA 86: 7280-7284, 1989 https://doi.org/10.1073/pnas.86.18.7280
  11. Liu HN, Ohya S, Furuzono S, Wang J, Imaizumi Y, Nakayama S. Co-contribution of IP3R and $Ca^{2+}$ influx pathways to pacemaker $Ca^{2+}$ activity in stomach ICC. J Biol Rhythms 20: 15-26, 2005 https://doi.org/10.1177/0748730404269572
  12. Liu HN, Ohya S, Wang J, Imaizumi Y, Nakayama S. Involvement of ryanodine receptors in pacemaker $Ca^{2+}$ oscillation in murine gastric ICC. Biochem Biophys Res Commun 328: 640-646, 2005 https://doi.org/10.1016/j.bbrc.2005.01.029
  13. Ozaki H, Blondfield DP, Stevens RJ, Publicover NG, Sanders KM. Simultaneous measurement of membrane potential, cytosolic calcium and muscle tension in smooth muscle tissue. Am J Physiol 260: C917-C925, 1991 https://doi.org/10.1152/ajpcell.1991.260.5.C917
  14. Sanders KM. Ionic mechanisms of electrical rhythmicity in gastrointestinal smooth muscles. Annu Rev Physiol 54: 439-453, 1992 https://doi.org/10.1146/annurev.ph.54.030192.002255
  15. Sanders KM. A case for interstitial cells of Cajal as pacemakers and mediators of neurotransmission in the gastrointestinal tract. Gastroenterology 111: 492-515, 1996 https://doi.org/10.1053/gast.1996.v111.pm8690216
  16. Strege PR, Bernard CE, Ou Y, Gibbons SJ, Farrugia G. Effect of mibefradil on sodium and calcium currents. Am J Physiol Gastrointest Liver Physiol 289: G249-G253, 2005 https://doi.org/10.1152/ajpgi.00022.2005
  17. Suzuki H, Takano H, Yamamoto Y, Komuro T, Saito M, Kato K, Mikoshiba K. Properties of gastric smooth muscles obtained from mice which lack inositol trisphosphate receptor. J Physiol 525: 105-111, 2000 https://doi.org/10.1111/j.1469-7793.2000.00105.x
  18. Szurszewski JH. Electrical basis for gastrointestinal motility. In: Johnson LR ed, Physiology of the Gastrointestinal Tract. 2nd ed. Raven Press, New York, p 383-422, 1987
  19. Thomsen L, Robinson TL, Lee JC, Farraway LA, Hughes MJ, Andrews DW, Huizinga JD. Interstitial cells of Cajal generate a rhythmic pacemaker current. Nat Med 4: 848-851, 1998 https://doi.org/10.1038/nm0798-848
  20. Tomita T. Electrical activity (spikes and slow waves) in gastrointestinal smooth muscle. In: Bulbring E, Brading AF, Jones AW, Tomita A ed, Smooth Muscle: An Assessment of Current Knowledge. University of Texas Press, Austin, TX, USA, p 127-156, 1981
  21. Torihashi S, Ward SM, Nishikawa SI, Nishi K, Kobayashi S, Sanders KM. c-Kit-dependent development of interstitial cells and electrical activity in the murine gastrointestinal tract. Cell Tissue Res 280: 97-111, 1995
  22. Vanhelden DF, Imtiaz MS, Nurgaliyeva K, Von Derweid P, Dosen PJ. Role of calcium stores and membrane voltage in the generation of slow wave action potentials in guinea pig gastric pylorus. J Physiol 524: 245-265, 2000 https://doi.org/10.1111/j.1469-7793.2000.00245.x
  23. Ward SM, Burns AJ, Torihashi S, Sanders KM. Mutation of the proto-oncogene c-kit blocks development of interstitial cells and electrical rhythmicity in murine intestine. J Physiol 480: 91-97, 1994
  24. Ward SM, Ordog T, Koh SD, Baker SA, Jun JY, Amberg G, Monaghan K, Sanders KM. Pacemaking in interstitial cells of Cajal depends upon calcium handling by endoplasmic reticulum and mitochondria. J Physiol 525: 355-361, 2000 https://doi.org/10.1111/j.1469-7793.2000.t01-1-00355.x