Stilbene disulfonate blockade of colonic secretory Cl- channels in planar lipid bilayers

Am J Physiol. 1989 Apr;256(4 Pt 1):C902-12. doi: 10.1152/ajpcell.1989.256.4.C902.

Abstract

We studied blockade by 4,4'-dinitrostilbene-2,2'-disulfonic acid (DNDS) of a secretory Cl- channel from colonic enterocyte plasma membrane vesicles incorporated into planar lipid bilayer membranes. Except for intermittent long-lived closed periods (100 ms to several min), the control channel open probability (Po) was greater than 90%. DNDS, added to the cis or vesicle-containing side, which corresponds to the outer membrane side of the channel, caused a dramatic increase in the number of current transitions from the open-to-closed state. DNDS caused a concentration-dependent decrease in Po with a maximum inhibition of 95 +/- 2.0% and a half-maximal inhibitory concentration of 3.3 +/- 1.4 microM. DNDS added to the trans side of the channel had no effect on either the single-channel conductance or kinetic behavior of the channel. Kinetic analysis revealed that DNDS blockade from the cis side could be explained by a linear, closed-open-blocked, kinetic scheme. The estimated DNDS block rate constants were kon = 3.2 X 10(7) M-1.s-1 and koff = 52 s-1, yielding an equilibrium dissociation constant (KD) of 2.1 +/- 0.38 microM, similar to the Ki for inhibition of Po. The effects of DNDS were fully reversible after perfusion of the cis compartment with DNDS-free solution. In contrast, the covalently reactive 4,4'-diisothiocyano-substituted stilbene disulfonate caused an irreversible blockade of the Cl- channel.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chloride Channels
  • Chlorides / physiology*
  • Colon / drug effects
  • Colon / physiology*
  • Electric Conductivity
  • Epithelium / physiology
  • Female
  • Kinetics
  • Lipid Bilayers / metabolism*
  • Membrane Proteins / physiology*
  • Rats
  • Rats, Inbred Strains
  • Stilbenes / pharmacology*

Substances

  • Chloride Channels
  • Chlorides
  • Lipid Bilayers
  • Membrane Proteins
  • Stilbenes
  • 4,4'-dinitro-2,2'-stilbenedisulfonic acid