Tetrahydrobiopterin regulates cyclic GMP-dependent electrogenic Cl- secretion in mouse ileum in vitro

J Physiol. 1997 Sep 1;503 ( Pt 2)(Pt 2):347-52. doi: 10.1111/j.1469-7793.1997.347bh.x.

Abstract

1. Basal electrogenic Cl- secretion, measured as the short-circuit current (Isc), was variable in ileum removed from tetrahydrobiopterin (BH4)-deficient hph-1 mice and wild-type controls in vitro, although values were not significantly different. 2. The basal nitrite release and mucosal cyclic guanosine 3',5'-monophosphate (cyclic GMP) production were similar in control and BH4-deficient ileum. 3. Mucosally added Escherichia coli heat-stable toxin (STa, 55 ng ml-1) increased the nitrite release, cyclic GMP levels and the Isc in control ileum, but its secretory actions were reduced in BH4-deficient ileum. 4. L-Arginine (1 mM) increased the nitrite release, cyclic GMP production and the Isc in control ileum, but the actions were reduced in BH4-deficient ileum. 5. Serosal carbachol (1 mM) stimulated maximum short-circuit currents of similar magnitude in both control and BH4-deficient ileum, whilst nitrite release and cyclic GMP production were minimal. 6. E. coli STa and L-arginine increased electrogenic Cl- secretion across intact mouse ileum in vitro by releasing nitric oxide and elevating mucosal cyclic GMP. The inhibition of these processes in the hph-1 mouse ileum suggests that BH4 may be a target for the modulation of electrogenic transport, and highlight the complexity of the interactions between nitric oxide and cyclic GMP in the gut.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Antioxidants / pharmacology*
  • Arginine / pharmacology
  • Biopterins / analogs & derivatives*
  • Biopterins / metabolism
  • Biopterins / pharmacology
  • Carbachol / pharmacology
  • Chloride Channels / drug effects
  • Chloride Channels / metabolism*
  • Cholinergic Agonists / pharmacology
  • Cyclic GMP / metabolism
  • Cyclic GMP / physiology*
  • Ileum / drug effects
  • Ileum / metabolism*
  • In Vitro Techniques
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism
  • Lipopolysaccharides / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Muscle, Smooth / drug effects
  • Muscle, Smooth / metabolism*
  • Nitric Oxide / metabolism
  • Nitrites / metabolism
  • Time Factors

Substances

  • Antioxidants
  • Chloride Channels
  • Cholinergic Agonists
  • Lipopolysaccharides
  • Nitrites
  • Biopterins
  • Nitric Oxide
  • Carbachol
  • Arginine
  • sapropterin
  • Cyclic GMP