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. Author manuscript; available in PMC: 2019 Jan 1.
Published in final edited form as: Exp Physiol. 2017 Nov 2;103(1):40–57. doi: 10.1113/EP086367

Fig. 1.

Fig. 1

The effect of replacing extracellular chloride, [Cl]o with gluconate on slow wave activity recorded from mouse jejunal smooth muscle layer. Replacement of [Cl]o by gluconate significantly altered slow wave properties in a concentration dependent manner (see Fig. 2). A1, A2-C, Representative traces of intracellular recording made in [Cl]o/[gluconate]o: 13.3/120 mM (A1, A2); 39.9/93.4 mM (B); and 120/13.3 mM (C), respectively. Control [Cl]o was 134 mM. In 5 out of 9 experiments, slow waves were abolished (A1). In the remaining 4 experiments, small amplitude residual slow wave activity was observed (A2). The horizontal bar over each trace indicates the perfusion period of low [Cl]o solution. Expanded time scales are shown at the bottom of A1, A2, B, and C with different time points before and after the low [Cl]o perfusion.