F. Muller et al., Role of Na+/H+ exchange and HCO3- transport in pH(i) recovery from intracellular acid load in cultured epithelial cells of sheep rumen, J COMP PH B, 170(4), 2000, pp. 337-343
Citations number
33
Categorie Soggetti
Animal Sciences",Physiology
Journal title
JOURNAL OF COMPARATIVE PHYSIOLOGY B-BIOCHEMICAL SYSTEMIC AND ENVIRONMENTALPHYSIOLOGY
This study sought to investigate effects of short-chain fatty acids and CO2
on intracellular pH (pH(i)) and mechanisms that mediate pHi recovery from
intracellular acidification ill cultured ruminal epithelial cells of sheep.
pH(i) was studied by spectrofluorometry using the DH-sensitive fluorescent
indicator 2',7'-bis (carboxyethyl)-5(6')-carboxyfluorescein acetoxymethyl
ester (BCECF/AM). The resting pH(i) in N-2-hydroxy-ethylpiperazine-N'-2-eth
anesulfonic acid (HEPES)-buffered solution was 7.37 +/- 0.03. in HEPES-buff
ered solution, a NH4+/NH3-prepulse (20 mM) or addition of butyrate (30 mM)
led to a rapid intracellular acidification (P < 0.05). Addition of 5-(N-eth
yl-N-isopropyl)amiloride (EIPA; 10 mu M) or HOE-694 (200 mu M) inhibited pH
(i) recovery from an NH4+/NH3-induced acid load by 58% and 70%, respectivel
y. pH(i) recovery from acidification by butyrate was reduced by 62% and 69%
in the presence of EIPA (10 mu M) and HOE-694 (200 mu M), respectively. Ch
anging from HEPES(20 mM) to CO2/HCO3--buffered (5%/20 mM) solution caused a
rapid decrease of pH(i) (P < 0.01), followed by an effective counter-regul
ation. 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid (DIDS; 100 mu M)
blocked the pH(i) recovery by 88%. The results indicate that intracellular
acidification by butyrate and CO2 is effectively counter-regulated by an Na
+/H+ exchanger and by DIDS-sensitive, HCO3--dependent mechanism(s). Conside
ring the large amount of intraruminal weak acids in vivo, both mechanisms a
re of major importance for maintaining the pH(i) homeostasis of ruminal epi
thelial cells.