Takeda Y, Krause J E
Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO 63110.
Eur J Pharmacol. 1989 Feb 28;161(2-3):267-71. doi: 10.1016/0014-2999(89)90858-3.
The effects of gamma-preprotachykinin-(72-92)-peptide amide [gamma-PPT-(72-92)-NH2] on salivation in the rat were investigated and were compared with salivation responses elicited by a variety of other tachykinin and related peptides. On intravenous injection or continuous infusion, gamma-PPT-(72-92)-NH2, a naturally occurring N-terminally extended derivative of neurokinin A (NKA), potently stimulated salivation. The rank order of potency of peptides that stimulated salivation was: NPK greater than gamma-PPT-(72-92)-NH2 greater than substance P greater than NKA = Asp-Ala-NKA. Moreover, gamma-PPT-(72-92)-NH2, like NPK, potentiated the effects of substance P on salivary secretion. These results indicate that the actions of gamma-PPT-(72-92)-NH2 may be pharmacologically or physiologically relevant in the actions of tachykinin peptides.
研究了γ-前速激肽-(72 - 92)-肽酰胺[γ-PPT-(72 - 92)-NH2]对大鼠唾液分泌的影响,并将其与多种其他速激肽及相关肽引发的唾液分泌反应进行了比较。静脉注射或持续输注时,γ-PPT-(72 - 92)-NH2(一种天然存在的神经激肽A(NKA)N端延伸衍生物)能有效刺激唾液分泌。刺激唾液分泌的肽的效价顺序为:神经肽K大于γ-PPT-(72 - 92)-NH2大于P物质大于神经激肽A = 天冬酰胺-丙氨酸-神经激肽A。此外,γ-PPT-(72 - 92)-NH2与神经肽K一样,能增强P物质对唾液分泌的作用。这些结果表明,γ-PPT-(72 - 92)-NH2的作用在速激肽肽类的作用中可能具有药理学或生理学相关性。