USE OF MQAE FOR MEASUREMENT OF INTRACELLULAR [CL-] IN CULTURED AORTICSMOOTH-MUSCLE CELLS

A novel fluorescent indicator, N-[ethoxycarbonylmethyl]-6-methoxy-quin olinium bromide (MQAE), was used to measure intracellular chloride con centration ([Cl-](i)) in primary cultures of rat aortic smooth muscle cells (VSMC). The hydrolytic and fluorescent properties of the dye wer e characterized. The intracellular Stern-Volmer constant was calculate d to be 25 M(-1). Cl- efflux curves were characteristic of saturation- type kinetics, with an apparent Michaelis-Menten constant value of 11 +/- 4.8 (SD) mM, a maximum velocity of 0.038 +/- 0.021 mM/s, and a hal f time (t(1/2)) of 9.0 +/- 3.7 min. The average efflux rate in the fir st 10 min (0.023 +/- 0.004 mM/s) was reduced in the presence of either 130 mu M '-diisothiocyanato-dihydrostilbene-2,2'-disulfonic acid (H2D IDS) (0.014 +/- 0.006, P = 0.02) or 40 mu M furosemide (0.017 +/- 0.00 4, P = 0.04). Restoration of physiological extracellular chloride conc entration (Cl-](o)) after zero Cl- resulted in net Cl- influx with a t (1/2) of 3.6 +/- 1.0 min. The initial Cl- influx rate was reduced afte r exposure to furosemide, from 0.069 +/- 0.006 to 0.046 +/- 0.008 mM/s , P < 0.002, and was reduced after exposure to H2DIDS from 0.102 +/- 0 .013 to 0.033 +/- 0.003 mM/s, P < 0.001. Furosemide reduced the steady -state [Cl-](i) from 31.6 +/- 3.2 to 26.1 +/- 2.4 mM, P < 0.01, wherea s H2DIDS had little effect on [Cl-](i). Our results demonstrate that M QAE can be used to measure [Cl-](i) in primary cultures of VSMC.