Gibert A J, Hersey S J
J Cell Physiol. 1984 May;119(2):220-6. doi: 10.1002/jcp.1041190212.
Gastric glands were isolated from rabbit stomach and pepsinogen secretion was measured after stimulation with isoproterenol, forskolin, 8-bromo cyclic adenosine monophosphate (8-bromo cAMP), cholecystokinin octapeptide (CCK-OP), carbachol, and hyperosmolar medium. The responses to these stimuli in medium containing 143 mM Na+ and 5.4 mM K+ (normal medium) were compared with responses to the same stimuli in media containing either 0 Na+ and 5.4 mM K+, or 143 mM Na+ and O K+. In addition, the effects of ouabain and furosemide on secretion elicited by these stimuli were determined. Medium containing 0 Na+ inhibited all stimuli. Medium containing 0 K+ inhibited the action of 8-bromo cAMP and stimuli postulated to be mediated by cAMP. Ouabain inhibited the same stimuli as O K+ medium, and, in addition, inhibited the response to hyperosmolar medium. However, ouabain enhanced the response to CCK-OP. Furosemide inhibited the response to hyperosmolar medium but had no effect on the action of any secretagogue employed. Intraglandular [Na+] increased and [K+] decreased after exposure to K+-free medium or ouabain. cAMP content of the glands was assayed after stimulation with both isoproterenol and hyperosmolar medium. Isoproterenol and hyperosmolar medium significantly increased cAMP levels. The results are discussed in relation to possible involvement of ion transport or intracellular ion concentration in the secretory process.
从兔胃中分离出胃腺,在用异丙肾上腺素、福斯高林、8-溴环磷酸腺苷(8-溴 cAMP)、八肽胆囊收缩素(CCK-OP)、卡巴胆碱和高渗培养基刺激后,测量胃蛋白酶原的分泌。将在含有 143 mM Na⁺和 5.4 mM K⁺的培养基(正常培养基)中对这些刺激的反应,与在含有 0 Na⁺和 5.4 mM K⁺或 143 mM Na⁺和 0 K⁺的培养基中对相同刺激的反应进行比较。此外,还测定了哇巴因和呋塞米对这些刺激引起的分泌的影响。含有 0 Na⁺的培养基抑制所有刺激。含有 0 K⁺的培养基抑制 8-溴 cAMP 的作用以及假定由 cAMP 介导的刺激。哇巴因抑制与 0 K⁺培养基相同的刺激,此外,还抑制对高渗培养基的反应。然而,哇巴因增强了对 CCK-OP 的反应。呋塞米抑制对高渗培养基的反应,但对所使用的任何促分泌剂的作用均无影响。暴露于无钾培养基或哇巴因后,腺体内[Na⁺]升高而[K⁺]降低。在用异丙肾上腺素和高渗培养基刺激后,测定腺体的 cAMP 含量。异丙肾上腺素和高渗培养基显著提高了 cAMP 水平。结合离子转运或细胞内离子浓度在分泌过程中可能的参与情况对结果进行了讨论。