Segmental heterogeneity of electrogenic secretions in human ascending colon and rectum

Int J Colorectal Dis. 2006 May;21(4):357-64. doi: 10.1007/s00384-005-0034-0. Epub 2005 Sep 13.

Abstract

Aims: We have attempted to ascertain putative segmental differences in the secretory responses of the human ascending colon and rectum.

Methods: From the mucosal biopsy samples of two segments, the short-circuit current (I(sc)) and tissue resistance (R(te)) were compared under control conditions, as well as after the induction of secretion, using a modified Ussing chamber. We also performed semiquantitative reverse transcriptase-polymerase chain reaction (RT-PCR) to detect and quantify transport proteins.

Results: The spontaneous I(sc) in the ascending colon was found to be greater than that in the rectum (P<0.01), whereas isobutylmethylxanthine/forskolin and carbachol (CCh) induced a greater rise in I(sc) in the rectum than in the ascending colon (P<0.05). When coupled with indomethacin pretreatment, the increase in Delta I(sc) after the addition of CCh and forskolin was significant as compared to that observed without pretreatment (P<0.05). However, in the rectum, the secretory response to CCh and forskolin was abolished to a significant degree by indomethacin (P<0.05). Moreover, these indomethacin-induced changes were reversed by the addition of PGE2. Upon semiquantitative RT-PCR analysis, the amounts of cystic fibrosis transmembrane regulator, KCNQ1, and CLCA1 mRNAs were not found to be different between the two segments.

Conclusion: There was a clear segmental heterogeneity with regard to electrogenic secretion in the human colon, and this difference can be explained by differences in the ascending colon and rectum.

MeSH terms

  • 1-Methyl-3-isobutylxanthine / pharmacokinetics
  • Carbachol / pharmacokinetics
  • Chloride Channels / genetics
  • Chloride Channels / metabolism
  • Colforsin / pharmacokinetics
  • Colon / metabolism*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism
  • Dinoprostone / pharmacokinetics
  • Electrophoresis, Agar Gel
  • Electrophysiology*
  • Humans
  • Intestinal Mucosa / metabolism
  • Ion Transport
  • KCNQ1 Potassium Channel / genetics
  • KCNQ1 Potassium Channel / metabolism
  • RNA, Messenger / metabolism
  • Rectum / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • CLCA1 protein, human
  • Chloride Channels
  • KCNQ1 Potassium Channel
  • KCNQ1 protein, human
  • RNA, Messenger
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Colforsin
  • Carbachol
  • Dinoprostone
  • 1-Methyl-3-isobutylxanthine