Caldara R, Ferrari C, Romussi M, Grimaldi M G
Arzneimittelforschung. 1980;30(9):1610-1.
The effects of oral administration of the anti-inflammatory drug, (Z)-5-fluoro-2-methyl-1-[p-(methylsulfinyl)-benzylidene]-indene-3-acetic acid (sulindac, Clinoril) 400 mg/d for 8 days, on basal and submaximal (3 micrograms/kg b.2. i.m.) and maximal (6 micrograms/kg b.w.) pentagastrin-stimulated gastric acid secretion as well as on serum gastrin concentration have been evaluated in female patients affected with osteoarthrosis. No significant changes in either gastric acid or gastrin secretion were induced by the treatment. Serum gastrin levels were also unaltered after acute administration of 200 mg sulindac. These results confirm and extend previous observations suggesting that the drug does not exert major actions on the stomach.
在骨关节炎女性患者中,评估了口服抗炎药(Z)-5-氟-2-甲基-1-[对-(甲基亚磺酰基)-亚苄基]-茚-3-乙酸(舒林酸,奇诺力)400mg/d,连续8天,对基础胃酸分泌、次最大剂量(3μg/kg体重,肌肉注射)和最大剂量(6μg/kg体重)五肽胃泌素刺激的胃酸分泌以及血清胃泌素浓度的影响。该治疗未引起胃酸或胃泌素分泌的显著变化。急性给予200mg舒林酸后,血清胃泌素水平也未改变。这些结果证实并扩展了先前的观察结果,表明该药物对胃没有主要作用。