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. 2009 Aug 5;297(4):F904–F915. doi: 10.1152/ajprenal.90685.2008

Fig. 2.

Fig. 2.

Effect of luminal (L) H89 (10 μM) on basal and flow-stimulated net cation transport in isolated perfused rabbit CCDs. A: JNa increased in untreated control (C) tubules as the luminal flow rate was increased from ∼1 to 5 nl·min−1·mm−1. H89 added to the luminal solution had no effect on flow-stimulated JNa. JNa in 2 tubules perfused with H89 and luminal IBX (10.5 and 17.8 pmol·min−1·mm−1) was similar to that measured in control CCDs and those perfused with H89 alone at a flow rate of ∼1 nl·min−1·mm−1. B: JK increased ∼3-fold in response to a 5-fold increase in luminal flow rate in control CCDs. Addition of H89 to the luminal solution increased JK in CCDs perfused at a flow rate of 1 nl·min−1·mm−1; a subsequent increase in flow rate augmented JK only slightly. JK in 2 tubules perfused with H89 and luminal IBX (−8.5 and −9.7 pmol·min−1·mm−1) was similar to that measured in control CCDs perfused at a flow rate of ∼1 nl·min−1·mm−1. Values are means ± SE. For each protocol, n is indicated in results. *P < 0.05 compared with Jx at 1 nl·min−1·mm−1 in same tubules. #P < 0.05 compared with Jx in control tubules studied at same flow rate.