Feldman M, Richardson C T, Peterson W L, Walsh J H, Fordtran J S
N Engl J Med. 1977 Dec 29;297(26):1427-30. doi: 10.1056/NEJM197712292972603.
We evaluated the widely held notion that anticholinergic drugs must be used in near toxic doses to inhibit gastric acid secretion effectively. Nine patients with duodenal ulcer were studied after a low dose (15 mg) and after a near toxic dose (averaging 48 mg) of the anticholinergic, propantheline. Mean (+/- S.E.) inhibition of food-stimulated acid secretion was identical with the two doses of propantheline: 29 +/- 10 and 29 +/- 11 per cent, respectively. In addition, when 15 mg of propantheline was combined with the histamine H2-receptor antagonist, cimetidine, acid secretion was suppressed to a greater degree than with either drug alone. A low dose of propantheline is as effective as a near toxic dose in suppressing food-stimulated acid secretion and augments the inhibitory effect of cimetidine.
我们对一种广泛持有的观念进行了评估,即抗胆碱能药物必须使用接近中毒剂量才能有效抑制胃酸分泌。对9名十二指肠溃疡患者在给予低剂量(15毫克)和接近中毒剂量(平均48毫克)的抗胆碱能药物丙胺太林后进行了研究。两种剂量的丙胺太林对食物刺激的胃酸分泌的平均(±标准误)抑制作用相同:分别为29±10%和29±11%。此外,当15毫克丙胺太林与组胺H2受体拮抗剂西咪替丁合用时,胃酸分泌的抑制程度比单独使用任何一种药物时都更大。低剂量的丙胺太林在抑制食物刺激的胃酸分泌方面与接近中毒剂量一样有效,并且增强了西咪替丁的抑制作用。