Babulová A, Nosálová V, Bauer V, Buran L
Institute of Experimental Pharmacology, Slovak Academy of Sciences, Bratislava, Czechoslovakia.
Agents Actions. 1988 Apr;23(3-4):286-8. doi: 10.1007/BF02142566.
The action of pentacaine, a new prospective antiulcer drug with gastric cytoprotective activity, on gastric acid secretion was analysed and compared with the action of other antisecretory drugs. The drugs were given orally or intraduodenally to Wistar rats after pylorus ligation. The gastric acid secretion was studied under basal or stimulated (histamine, pentagastrin, carbachol) conditions. Oral administration of pentacaine, oxethazaine and procaine, in contrast to atropine, had no influence either under basal or stimulated conditions. However, intraduodenal administration of pentacaine significantly suppressed both the basal and stimulated gastric secretion. The present study suggests that the mechanism of antisecretory activity of pentacaine differs from that of anticholinergic and antihistaminergic drugs.
对一种具有胃细胞保护活性的新型潜在抗溃疡药物喷他卡因对胃酸分泌的作用进行了分析,并与其他抗分泌药物的作用进行了比较。在幽门结扎后,将这些药物口服或十二指肠内给予Wistar大鼠。在基础或刺激(组胺、五肽胃泌素、卡巴胆碱)条件下研究胃酸分泌。与阿托品不同,口服喷他卡因、奥昔卡因和普鲁卡因在基础或刺激条件下均无影响。然而,十二指肠内给予喷他卡因可显著抑制基础和刺激状态下的胃分泌。本研究表明,喷他卡因的抗分泌活性机制与抗胆碱能和抗组胺药物不同。