Alkaline pH, membrane potential, and magnesium cations are negative modulators of purine nucleotide inhibition of H+ and Cl- transport through the uncoupling protein of brown adipose tissue mitochondria

J Bioenerg Biomembr. 1988 Oct;20(5):603-22. doi: 10.1007/BF00768922.

Abstract

Modulators of purine nucleotide (PN) inhibition of H+ and Cl- transport mediated by the uncoupling protein (UP) of brown adipose tissue (BAT) mitochondria were studied: Alkalinization strongly diminishes GDP inhibition of H+ transport (delta log IC50 = -delta pHout), while more intensive inhibition of Cl- transport is only slightly altered. Higher delta psi decreases GDP inhibition of H+ transport. Mg2+, but not palmitoyl-CoA, decreases PN inhibitory ability. Simulations of conditions similar to those found in BAT cells in the resting state and in the thermogenic state showed that three factors act in concert: pH, Mg2+, and free fatty acids (FFA): (a) with endogenous FFA present and 2 mM ATP and 0.5 mM AMP (pH 7.1), H+ transport was inhibited by 95% in the absence of Mg2+, while by 60% with Mg2+; (b) 0.5 mM ATP and 1 mM AMP, H+ transport was inhibited by 40% without Mg2+ and by 30% with Mg2+. State b thus represents a model thermogenic state, while state a represents a resting state. However, the latter state in vivo must be accomplished either by combustion or FFA or by elimination of Mg2+ to attain a total inhibition of H+ transport (cf. a). The model of UP possessing two independent channels, an H+ channel and a Cl- channel, controlled from a single PN-binding site is supported by independent kinetics by different pH dependence of H+ and Cl- transport, and by a lower sensitivity of H+ transport to PN inhibition.

MeSH terms

  • Adipose Tissue, Brown / drug effects
  • Adipose Tissue, Brown / metabolism*
  • Animals
  • Carrier Proteins*
  • Chlorides / metabolism
  • Cricetinae
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Ion Channels / drug effects
  • Ion Channels / metabolism
  • Magnesium / pharmacology
  • Membrane Potentials
  • Membrane Proteins / metabolism*
  • Mesocricetus
  • Mitochondria / metabolism
  • Mitochondrial Proteins
  • Palmitoyl Coenzyme A / pharmacology
  • Purine Nucleotides / pharmacology
  • Uncoupling Protein 1
  • Valinomycin / pharmacology

Substances

  • Carrier Proteins
  • Chlorides
  • Ion Channels
  • Membrane Proteins
  • Mitochondrial Proteins
  • Purine Nucleotides
  • Uncoupling Protein 1
  • Palmitoyl Coenzyme A
  • Valinomycin
  • Magnesium