Mg2+ transport in sheep rumen epithelium: evidence for an electrodiffusiveuptake mechanism

Citation
M. Schweigel et al., Mg2+ transport in sheep rumen epithelium: evidence for an electrodiffusiveuptake mechanism, AM J P-GAST, 277(5), 1999, pp. G976-G982
Citations number
35
Categorie Soggetti
da verificare
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
ISSN journal
01931857 → ACNP
Volume
277
Issue
5
Year of publication
1999
Pages
G976 - G982
Database
ISI
SICI code
0193-1857(199911)277:5<G976:MTISRE>2.0.ZU;2-7
Abstract
The potential difference (PD)-dependent component of transcellular Mg2+ upt ake in sheep rumen epithelium was studied. Unidirectional Mg-28(2+) fluxes were measured at various transepithelial PD values, and the unidirectional mucosal-to-serosal Mg-28(2+) flux (J(ms)(Mg)) was correlated with the PD ac ross the apical membrane (PDa) determined by mucosal impalement with microe lectrodes. PDa was found to be -54 +/- 5 mV, and J(ms)(Mg) was 65.9 +/- 13. 8 nmol.cm(-2).h(-1) under short-circuit conditions. Hyperpolarization of th e ruminal epithelium (blood-side positive) depolarized PDa and, mast notice ably, decreased J(ms)(Mg). Further experiments were performed with cultured ruminal epithelial cells (REC). With the aid of the fluorescence probe mag -fura 2, we measured the intracellular free Mg2+ concentration (Mg2+](i)) o f isolated REC under basal conditions at various extracellular Mg2+ concent rations ([Mg2+](e)) and after alterations of the transmembrane voltage. Bas al [Mg2+](i) was 0.54 +/- 0.08 mM. REC suspended in media with [Mg2+](i) be tween 0.5 and 7.5 mM showed an increase in [Mg2+](i) that was dependent on [Mg2+](i) and that exhibited a saturable component (Michaelis-Menten consta nt = 1.2 mM; maximum [Mg2+](i) = 1.26 mM). Membrane depolarization with hig h extracellular K+ (40, 80, or 140 mM K+) and the K+ channel blocker quinid ine (50 and 100 mu M) resulted in a decrease in [Mg2+](i). On the other han d, hyperpolarizatian created by K+ diffusion (intracellular K+ concentratio n > extracellular K+ concentration) in the presence of valinomycin induced a 15% increase in [Mg2+](i). None of the manipulations had any effect on in tracellular Ca2+ concentration and intracellular pH. The results support th e assumption that the membrane potential acts as a principal driving force for Mg2+ entry in REC and suggest that the pathway for this electrodiffusiv e Mg2+ uptake across the luminal membrane is a channel or a carrier.