Baumert J E, Cataland S, Tetirick C E, Pace W G, Mazzaferri E L
J Clin Endocrinol Metab. 1978 Mar;46(3):473-6. doi: 10.1210/jcem-46-3-473.
The effect of atropine on meal-stimulated gastric inhibitory polypeptide (GIP) and gastrin release was studied in 5 purebred foxhounds and compared with control studies done in the same animals given a meal without atropine, peak incremental serum gastrin occurred between 5 and 15 min after the meal whereas the greatest increment in serum GIP occurred 60 min postcibal. Atropine had no effect on basal concentrations of gastrin or GIP. However, when atropine was given before feeding serum gastrin concentrations from 75 to 120 min postcibal were significantly higher (P less than 0.04) than after the meal alone. The normal meal-stimulated rise in serum GIP was almost completely inhibited by atropine. We conclude that: 1) the rise in serum gastrin adter a meal preceeds the rise in serum GIP; 2) atropine potentiates the late gastrin response while suppressing the increase in serum GIP after a meal; and 3) the mechanism by which atropine potentiates gastrin release may be related to its suppressive effects on intestinal inhibitors of gastrin secretion, such as GIP.
研究了阿托品对5只纯种猎狐犬进食刺激后胃抑制性多肽(GIP)和胃泌素释放的影响,并与在同一动物身上给予无阿托品的进食进行的对照研究相比较。进食后5至15分钟出现血清胃泌素峰值增量,而血清GIP的最大增量出现在进食后60分钟。阿托品对胃泌素或GIP的基础浓度无影响。然而,在喂食前给予阿托品时,进食后75至120分钟的血清胃泌素浓度显著高于仅进食后(P小于0.04)。正常进食刺激引起的血清GIP升高几乎完全被阿托品抑制。我们得出结论:1)进食后血清胃泌素升高先于血清GIP升高;2)阿托品增强胃泌素的晚期反应,同时抑制进食后血清GIP的增加;3)阿托品增强胃泌素释放的机制可能与其对胃泌素分泌的肠道抑制剂(如GIP)的抑制作用有关。