Lebedev N N, Rakhimov Z S
Biull Eksp Biol Med. 1982 Jul;94(7):28-31.
Chronic experiments on 9 dogs with gastric fistulas (with preliminary selective vagotomy in 5) were made to examine the action of morphine on periodic gastric motility (PGM). Morphine was injected subcutaneously at rest, selecting the minimal threshold vomitive dose (TVD) that provoked a series of contractions with a single vomiting attack, and the maximal dose that produced only an extra period of contractions. Clear-cut differences were discovered in the dogs' sensitivity to morphine (the groups with high and low sensitivity, the TVD 35 and 110 micrograms/kg on the average, respectively). Three consecutive stages were defined on the part of PGM in the response to morphine injection. After vagal denervation the sensitivity to morphine (as evaluated from the TVD magnitude) remained unchanged, the second stage (the alternating accelerated cycles) was lost, while the third stage involved continuous contractions. It is inferred that the primary reaction to morphine occurs as a result of eliminating the central inhibitory effects on PGM, the second stage is effected according to the mechanism of the enterogastric reflex, whereas the third stage reflects complete loss of the central and peripheral inhibitory mechanisms that regulate PGM.
对9只患有胃瘘的狗(其中5只预先进行了选择性迷走神经切断术)进行了慢性实验,以研究吗啡对周期性胃动力(PGM)的作用。在狗安静时皮下注射吗啡,选择能引发一系列收缩并伴有单次呕吐发作的最小阈值呕吐剂量(TVD),以及仅产生额外一段收缩的最大剂量。发现狗对吗啡的敏感性存在明显差异(分为高敏组和低敏组,平均TVD分别为35和110微克/千克)。PGM对吗啡注射的反应可分为连续三个阶段。迷走神经去支配后,对吗啡的敏感性(根据TVD大小评估)保持不变,第二阶段(交替加速周期)消失,而第三阶段则出现持续收缩。据推断,对吗啡的主要反应是由于消除了对PGM的中枢抑制作用而产生的,第二阶段是通过肠胃反射机制实现的,而第三阶段则反映了调节PGM的中枢和外周抑制机制的完全丧失。