Hirschowitz B I, Gibson R, Wright L, Hutchison G
Am J Physiol. 1976 Jan;230(1):105-9. doi: 10.1152/ajplegacy.1976.230.1.105.
By the use of small doses of atropine (0.2-10 mug/kg-h) the kinetics of atropine antagonism to the gastric stimuli Urecholine and pentagastrin could be defined in intact dogs and in dogs after fundic vagotomy. Though pentagastrin was a much less effective stimulus after vagotomy, atropine had very similar effects on the pentagastrin response before and after vagotomy. Stimulation of both acid and pepsin by Urecholine remained unchanged by vagotomy but was uncompetitively inhibited by atropine in the intact dog, suggesting irreversible binding of atropine to gastric cholinergic receptors. After vagotomy, however, atropine inhibited Urecholine competitively, suggesting that atropine was now bound reversibly to cholinergic receptors. These changes are analogous to those occurring in muscle after denervation and suggest the growth of new cholinergic receptors with changed characteristics after denervation of the stomach.
通过使用小剂量阿托品(0.2 - 10微克/千克·小时),可以在完整的狗以及胃底迷走神经切断术后的狗身上确定阿托品对胃刺激剂乌拉胆碱和五肽胃泌素的拮抗动力学。尽管迷走神经切断术后五肽胃泌素作为刺激剂的效果要差得多,但阿托品对迷走神经切断术前和术后的五肽胃泌素反应具有非常相似的作用。乌拉胆碱对胃酸和胃蛋白酶的刺激在迷走神经切断术后保持不变,但在完整的狗中被阿托品非竞争性抑制,这表明阿托品与胃胆碱能受体发生不可逆结合。然而,迷走神经切断术后,阿托品竞争性抑制乌拉胆碱,这表明阿托品现在与胆碱能受体可逆性结合。这些变化类似于去神经后肌肉中发生的变化,表明胃去神经后出现了具有改变特征的新胆碱能受体。