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The inhibition of postprandial glycemic response by CMPE in normal rats after glucose (A) and sucrose (B) challenge (n = 5). The fasted rats were orally administrated with vehicle solutions, 100 mg/kg gliclazide, 20 mg/kg acarbose or 150 (CMPE-150), 300 (CMPE-300) or 600 (CMPE-600) mg/kg CMPE. * p < 0.05, ** p < 0.01 vs. vehicle control.
