Müller P, Dammann H G, Simon B, Kommerell B
Leber Magen Darm. 1987 Feb;17(1):50-4.
Prostaglandin-E analogues inhibit gastric acid secretion after oral administration. Therefore, these drugs are tested in clinical trials and one of them--Misoprostol--has recently been registered. With regard to healing rate of peptic ulcers and improvement of clinical signs and symptoms the prostaglandin analogues are superior to placebo but only equally effective or even slightly inferior to H2-receptor blockers. Side effects such as diarrhea or uterotropic actions will probably limit their broad application. The exact therapeutic effectiveness of prostaglandin analogues in treatment of peptic ulcer remains to be evaluated in greater detail. The substituted benzimidazole omeprazole is the first drug which exerts a long lasting and almost complete suppressive effect on gastric acid secretion in humans. This unique inhibition leads to a significant and more rapid healing rate of duodenal ulcers compared to treatment with H2-blockers. Additionally, peptic ulcers resistant to H2-blocker therapy can be treated effectively with omeprazole. In spite of these promising results the exact therapeutic effectiveness of this drug requires further evaluation.
前列腺素 E 类似物口服给药后可抑制胃酸分泌。因此,这些药物正在进行临床试验,其中一种——米索前列醇——最近已获注册。就消化性溃疡的愈合率以及临床体征和症状的改善而言,前列腺素类似物优于安慰剂,但仅与 H2 受体阻滞剂疗效相当,甚至略逊一筹。腹泻或促子宫收缩等副作用可能会限制其广泛应用。前列腺素类似物在治疗消化性溃疡方面的确切治疗效果仍有待更详细地评估。取代苯并咪唑类药物奥美拉唑是第一种对人体胃酸分泌产生持久且几乎完全抑制作用的药物。与 H2 受体阻滞剂治疗相比,这种独特的抑制作用可使十二指肠溃疡的愈合速度显著加快且更为迅速。此外,对 H2 受体阻滞剂治疗耐药的消化性溃疡可用奥美拉唑有效治疗。尽管取得了这些令人鼓舞的结果,但该药物的确切治疗效果仍需进一步评估。