PubMed Health⌕ Search

Biomedical subjects

I J Douglas

Publications and source records attributed to I J Douglas.

2 recordsLinked to original sources
PubMed1996

Regulatory volume increase in rat lacrimal gland acinar cells.

The volume of acinar cells isolated from rat lacrimal glands was measured during hypertonic shock. Cells shrank in hypertonic solutions, but a regulatory volume increase (RVI) was only observed under certain conditions. In HEPES-buffered solutions at 37 degrees C, an RVI was observed. This was inhibited by 20 microM bumetanide, an inhibitor of Na(+)-K(+)-2Cl- cotransport. RVI did not occur in HEPES-buffered solutions at 20 degrees C suggesting that Na(+)-K(+)-2Cl- cotransport is inactive at this temperature. In HCO3- buffered solutions however, an RVI was observed at 20 degrees C. In these conditions, the RVI was inhibited by 500 microM 4,4'-diisothiocyanatodihydrostilbene-2,2'-disulfonic acid (H2-DIDS) and 10 microM 5-(N-methyl-N-isobutyl)-amiloride (MIBA) indicating the involvement of Cl(-)-HCO3- exchange and Na(+) -H+ exchange respectively. RVI was also supported by a mixture of neutral amino acids, and by the nonmetabolizable amino acids 5 mM alpha-(methylamino)isobutyric acid (MeAIB) and 5 mM alpha-aminoisobutyric acid (AIB). These data suggest that the accumulation of amino acids, possibly by the system A Na(+)-coupled amino acid cotransporter, contributes to RVI in these cells. In conclusion, rat lacrimal gland acinar cells are capable of undergoing RVI following shrinkage by hypertonic shock.

Amino Acids↗
PubMed1994

Ca(2+)-activated K+ channels are involved in regulatory volume decrease in acinar cells isolated from the rat lacrimal gland.

The volumes of acinar cells isolated from rat lacrimal gland were measured on computer by video-imaging. Cells were found to swell on exposure to hypotonic solutions; they subsequently exhibited a regulatory volume decrease (RVD). RVD was inhibited in the absence of extracellular Ca2+, and by the K+ channel blocker tetraethylammonium chloride (2 mM TEA+). The possible involvement of K+ channels in RVD was further investigated in cell-attached patches. Exposing the cells to a hypotonic solution activated channels with a conductance of 141 +/- 6 pS (n = 11). These channels were partially blocked by 0.5 mM TEA+, and channel activation was not observed in the absence of extracellular Ca2+. Experiments in the inside-out patch configuration demonstrated that the channels activated by hypotonic stress were "maxi" Ca(2+)-activated K+ channels. It is concluded that the opening of these channels plays an important role in RVD, by facilitating K+ loss from the cell.

Animals↗