Ca(2+)-dependent nonspecific permeability of the inner membrane of liver mitochondria in the guinea fowl (Numida meleagris)

J Bioenerg Biomembr. 2015 Jun;47(3):235-42. doi: 10.1007/s10863-015-9606-z. Epub 2015 Feb 18.

Abstract

This comparative study presents the results of the induction of Ca(2+)-dependent nonspecific permeability of the inner membrane (pore opening) of rat and guinea fowl liver mitochondria by mechanisms that are both sensitive and insensitive to cyclosporin A (CsA). It was established that energized rat and guinea fowl liver mitochondria incubated with 1 mM of inorganic phosphate (Pi) are capable of swelling upon addition of at least 125 and 875 nmol of CaCl2 per 1 mg protein, respectively. Under these conditions, the Ca(2+) release from the mitochondria of these animals and a drop in Δψ are observed. All of these processes are inhibited by 1 μM of CsA. FCCP, causing organelle de-energization, induces pore opening in rat and guinea fowl liver mitochondria upon addition of 45 и 625 nmol of CaCl2 per 1 mg protein, respectively. These results suggest the existence of a CsA-sensitive mechanism for the induction of Ca(2+)-dependent pores in guinea fowl liver mitochondria, which has been reported in rat liver mitochondria. However, guinea fowl liver mitochondria have a significantly greater resistance to Ca(2+) as a pore inducer compared to rat liver mitochondria. It was found that the addition of α,ω-hexadecanedioic acid (HDA) to rat and guinea fowl liver mitochondria incubated with CsA and loaded with Ca(2+) causes organelle swelling and Ca(2+) release from the matrix. It is assumed that in contrast to the CsA-sensitive pore, the CsA-insensitive pore induced by HDA in the inner membrane of guinea fowl liver mitochondria, as well as in rat liver mitochondria, is lipid in nature.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium Chloride / metabolism
  • Cell Respiration / physiology*
  • Cyclosporine / pharmacology*
  • Galliformes / metabolism*
  • Liver / metabolism*
  • Male
  • Mitochondrial Membranes / metabolism*
  • Mitochondrial Swelling / drug effects
  • Oxygen Consumption / physiology
  • Palmitic Acids / pharmacology
  • Permeability / drug effects
  • Phosphates / metabolism
  • Phosphorylation
  • Rats
  • Species Specificity

Substances

  • Palmitic Acids
  • Phosphates
  • hexadecanedioic acid
  • Cyclosporine
  • Calcium Chloride
  • Calcium