Poli E, Coruzzi G, Bertaccini G
Institute of Pharmacology, University of Parma, Ospedale Maggiore, Italy.
Agents Actions. 1990 Apr;30(1-2):191-4. doi: 10.1007/BF01969035.
The effects of the histamine H2-receptor antagonists ranitidine and famotidine on acetylcholine release have been studied in the guinea pig myenteric plexus longitudinal muscle preparation incubated with [3H]-choline. Ranitidine (3 x 10(-5)-3 x 10(-4) M) dose-dependently increased the resting release of acetylcholine and that evoked by electrical stimulation. The effect was present only in strips perfused with 10(-5) M physostigmine. The effect of ranitidine was inhibited by tetrodotoxin and hexamethonium. Famotidine (10(-5)-3 x 10(-4) M) was totally ineffective in modifying both the resting release and that evoked by field stimulation. Ranitidine did not antagonize the inhibitory effect of oxotremorine, which specifically activates negative feedback mechanisms via presynaptic muscarinic receptors.
在豚鼠肠肌丛纵肌标本中,用[³H] - 胆碱孵育后,研究了组胺H2受体拮抗剂雷尼替丁和法莫替丁对乙酰胆碱释放的影响。雷尼替丁(3×10⁻⁵ - 3×10⁻⁴M)剂量依赖性地增加乙酰胆碱的静息释放以及电刺激诱发的释放。该效应仅在灌注10⁻⁵M毒扁豆碱的肠肌条中出现。雷尼替丁的效应被河豚毒素和六甲铵抑制。法莫替丁(10⁻⁵ - 3×10⁻⁴M)对改变静息释放和场刺激诱发的释放均完全无效。雷尼替丁不拮抗震颤素的抑制作用,震颤素通过突触前毒蕈碱受体特异性激活负反馈机制。