Traditional Chinese formula, lubricating gut pill, improves loperamide-induced rat constipation involved in enhance of Cl- secretion across distal colonic epithelium

J Ethnopharmacol. 2010 Jul 20;130(2):347-53. doi: 10.1016/j.jep.2010.05.018. Epub 2010 May 19.

Abstract

Aim of the study: Lubricating gut pill (LGP), a traditional Chinese formula, was widely used for the treatment of chronic constipation, especially in the elderly, in China. However, it is unclear whether LGP-induced laxative and/or lubricating effect is involved in water and electrolytes transport in distal colonic epithelium.

Materials and methods: The present study was designed to evaluate the effect of LGP on Cl(-) secretion across rat distal colonic epithelium mounted in Ussing chambers, and on a rat constipation model induced by loperamide, respectively.

Results: Application of LGP in the apical side elicited a sustained increase in short circuit current (I(SC)) response in a concentration-dependent manner. Evidence that LGP-stimulated I(SC) was due to Cl(-) secretion is based on inhibition of current by (a) a Na(+)-K(+)-2Cl(-) cotransporter inhibitor bumetanide, (b) removal of Cl(-) ions in bath solution, and (c) the cystic fibrosis transmembrane conductance regulator (CFTR) Cl(-) channel blocker DPC, suggesting that a apical cAMP-dependent Cl(-) channel was activated. LGP-stimulated I(SC) was also strongly inhibited by pretreatment with clotrimazole, indicating that the basolateral K(+) channel was also involved in maintaining this cAMP-dependent Cl(-) secretion. Pretreatment of tissues with indomethacin, but not atropine, tetrodotoxin or hexamethonium, inhibited LGP-induced response. In a rat constipation model, oral administration with LGP was significantly restored number of fecal pellets, water content and mucus secretion compared with loperamide-treated group alone.

Conclusions: LGP enhances Cl(-) secretion that is mostly mediated through the release of cyclooxygenase metabolites, by which provided an osmotic force for the subsequent laxative action observed in the rat constipation model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chlorides / metabolism*
  • Cholinergic Antagonists / pharmacology
  • Colon / drug effects*
  • Colon / metabolism
  • Constipation / chemically induced
  • Constipation / drug therapy*
  • Constipation / physiopathology
  • Cyclic AMP / metabolism
  • Cyclooxygenase Inhibitors / pharmacology
  • Cystic Fibrosis Transmembrane Conductance Regulator / antagonists & inhibitors
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism
  • Defecation / drug effects
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Drugs, Chinese Herbal / pharmacology*
  • Intestinal Mucosa / drug effects*
  • Intestinal Mucosa / metabolism
  • Intestinal Secretions / metabolism*
  • Laxatives / pharmacology*
  • Loperamide
  • Male
  • Medicine, Chinese Traditional
  • Membrane Potentials
  • Osmosis
  • Potassium Channel Blockers / pharmacology
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Rats
  • Rats, Wistar
  • Sodium Potassium Chloride Symporter Inhibitors / pharmacology

Substances

  • Chlorides
  • Cholinergic Antagonists
  • Cyclooxygenase Inhibitors
  • Drugs, Chinese Herbal
  • Laxatives
  • Potassium Channel Blockers
  • Sodium Potassium Chloride Symporter Inhibitors
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Loperamide
  • Cyclic AMP
  • Prostaglandin-Endoperoxide Synthases