Caldara R, Ferrari C, Barbieri C, Romussi M, Rampini P, Telloli P
Eur J Clin Pharmacol. 1980 Jan;17(1):13-8. doi: 10.1007/BF00561671.
The effects of acute oral administration of the antiserotoninergic drugs methysergide (3 mg) and metergoline (4 mg) on basal, submaximal (0.6 micrograms/kg i. m.) and maximal (6 micrograms/kg) pentagastrin-stimulated gastric acid secretion, as well as on basal and food-induced gastrin release, have been evaluated in healthy volunteers. Methysergide significantly increased basal and submaximal pentagastrin-stimulated gastric acid secretion, and metergoline significantly inhibited gastric acidity in all experiments. Basal and stimulated serum gastrin concentrations were not modified by either drug. The effect of methysergide on gastric acid secretion was opposed to that of serotonin and was probably dependent on its antiserotoninergic action, but the decrease in gastric acidity caused by metergoline is not easily explained. Although the effect is similar to that of a dopamine infusion, it does not depend on dopamine infusion, it does not depend on dopamine receptor stimulation, since it was not influenced by pretreatment with metoclopramide. It is suggested that it might be due to the weak anticholinergic and/or antihistaminic properties of metergoline.
已在健康志愿者中评估了急性口服抗血清素能药物麦角新碱(3毫克)和米替戈林(4毫克)对基础胃酸分泌、次最大剂量(0.6微克/千克,肌肉注射)和最大剂量(6微克/千克)五肽胃泌素刺激的胃酸分泌的影响,以及对基础胃泌素释放和食物诱导的胃泌素释放的影响。在所有实验中,麦角新碱显著增加基础胃酸分泌和次最大剂量五肽胃泌素刺激的胃酸分泌,而米替戈林显著抑制胃酸分泌。两种药物均未改变基础和刺激后的血清胃泌素浓度。麦角新碱对胃酸分泌的作用与血清素的作用相反,可能依赖于其抗血清素能作用,但米替戈林引起的胃酸分泌减少不易解释。虽然其作用类似于多巴胺输注的作用,但它不依赖于多巴胺输注,也不依赖于多巴胺受体刺激,因为它不受甲氧氯普胺预处理的影响。有人认为这可能是由于米替戈林的弱抗胆碱能和/或抗组胺特性所致。