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CCK1 receptor antagonist SR27897 (1 mg kg−1) or VIP receptor antagonist VIP6–28 (100 nmol kg−1) was injected i.v. at t = 0 min. PA1 (1 μm)-induced HCO3− secretion was not affected by SR27897 (A) or VIP6–28 (B). Each data point represents the mean ± SEM (n = 6 rats). *P < 0.05 vs. pH 7.0 Krebs group.
