Koop H, Schwarting H, Knorr-Marin A, Willhardt C, Möser T, Arnold R
Klin Wochenschr. 1987 Feb 16;65(4):169-73. doi: 10.1007/BF01728228.
The influence of a 4-week treatment with the substituted benzimidazole omeprazole (20 mg daily) or placebo on gastric endocrine function was tested in healthy male volunteers. Compared with placebo-treated subjects basal serum gastrin levels were slightly but significantly increased after treatment with omeprazole from 10 to 22 pg/ml (medians; P less than 0.05) but returned to pretreatment values after 2 weeks recovery (9 pg/ml). Antral gastrin tissue concentration increased and was still elevated after recovery; however, antral gastrin concentrations also increased in placebo controls, and increments immediately after cessation of omeprazole treatment (2.58 micrograms/g; median) were not significantly over control values (1.92 micrograms/g; P greater than 0.1). Postprandial gastrin release, basal and food-stimulated insulin release, antral somatostatin concentration, and volume densities of antral G and D cells were unaffected. It is concluded that, due to incomplete inhibition of gastric acid secretion at the omeprazole dose studied, only slight effects on the endocrine stomach are to be expected after 4 weeks of administration of omeprazole.
在健康男性志愿者中测试了用取代苯并咪唑奥美拉唑(每日20毫克)或安慰剂进行4周治疗对胃内分泌功能的影响。与接受安慰剂治疗的受试者相比,用奥美拉唑治疗后基础血清胃泌素水平略有但显著升高,从10 pg/ml升至22 pg/ml(中位数;P<0.05),但在2周恢复期后恢复到治疗前水平(9 pg/ml)。胃窦胃泌素组织浓度增加,恢复后仍升高;然而,安慰剂对照组的胃窦胃泌素浓度也增加,奥美拉唑治疗停止后立即增加(2.58微克/克;中位数)并不显著高于对照值(1.92微克/克;P>0.1)。餐后胃泌素释放、基础和食物刺激的胰岛素释放、胃窦生长抑素浓度以及胃窦G细胞和D细胞的体积密度均未受影响。得出的结论是,由于在所研究的奥美拉唑剂量下胃酸分泌的抑制不完全,预计在服用奥美拉唑4周后对胃内分泌的影响很小。