Tache Y, Gunion M
Life Sci. 1985 Jul 15;37(2):115-23. doi: 10.1016/0024-3205(85)90414-x.
Bombesin or gastrin releasing peptide injected into the lateral, third, or fourth ventricle, or into the cisterna magna, inhibited gastric acid secretion induced by a wide variety of gastric acid stimulants in several animal models. Studies of bombesin microinfusion into specific hypothalamic nuclei of intact rats, or injection into the cisterna magna of midbrain transected rats, indicated that the peptide can trigger inhibition of gastric acid secretion from both forebrain and hindbrain structures. The neural pathways mediating bombesin action required the integrity of the cervical spinal cord; the vagus did not play an important role. Spantide, a substance P and bombesin receptor antagonist, was not useful in studying the physiological role of bombesin. This was due both to its inability to reverse the central action of bombesin on gastric secretion, and to its in vivo toxicity.
向侧脑室、第三脑室或第四脑室,或向小脑延髓池注射蛙皮素或胃泌素释放肽,可在多种动物模型中抑制由多种胃酸刺激物诱导的胃酸分泌。对完整大鼠特定下丘脑核微量注射蛙皮素,或对中脑横断大鼠的小脑延髓池注射蛙皮素的研究表明,该肽可触发前脑和后脑结构对胃酸分泌的抑制。介导蛙皮素作用的神经通路需要颈脊髓的完整性;迷走神经未发挥重要作用。P物质和蛙皮素受体拮抗剂spantide在研究蛙皮素的生理作用方面并无用处。这既是因为它无法逆转蛙皮素对胃分泌的中枢作用,也是因为其体内毒性。