Luzzi S, Spagnesi S, Franchi-Micheli S, Rosi E, Ciuffi M, Zilletti L
Arch Int Pharmacodyn Ther. 1986 Jan;279(1):29-39.
Both GABA-receptors and benzodiazepine receptors have recently been described in the ileum. In this work we tested whether an interaction between diazepam and GABA-A- or GABA-B-mediated effects took place in guinea-pig ileum longitudinal muscle. We found that diazepam dose-dependently (10(-9) M-10(-6) M) potentiates the contractions caused by the activation of GABA-A receptor while it is ineffective at the same doses on GABA-B- mediated effects (relaxation and inhibition of twitch response). The drug "per se" does not affect the ileum. Diazepam potentiation is specific since this drug does not potentiate contractions caused by acetylcholine (10(-8) M), 5-HT (10(-7) M), histamine (10(-7) M), and electrical stimulation. Diazepam potentiating effect was not evident in the presence of bicuculline (10(-5) M) or hyoscine (2 X 10(-7) M). Ro 15-1788 (10(-5)M) and beta CCE (10(-5)M) antagonized diazepam potentiation of GABA contraction, while PK 11195 (10(-5) M) was ineffective. We conclude that diazepam modulates the effects evoked by stimulation of peripheral GABA-A receptors, while it is ineffective on GABA-B mediated effects.
最近在回肠中发现了γ-氨基丁酸(GABA)受体和苯二氮䓬受体。在本研究中,我们检测了地西泮与GABA-A或GABA-B介导的效应之间是否存在相互作用,实验对象为豚鼠回肠纵肌。我们发现,地西泮(剂量范围为10⁻⁹M - 10⁻⁶M)呈剂量依赖性增强激活GABA-A受体所引起的收缩,而相同剂量下对GABA-B介导的效应(舒张和抑制抽搐反应)无效。该药物本身对回肠无影响。地西泮的增强作用具有特异性,因为该药物不会增强由乙酰胆碱(10⁻⁸M)、5-羟色胺(5-HT,10⁻⁷M)、组胺(10⁻⁷M)和电刺激所引起的收缩。在存在荷包牡丹碱(10⁻⁵M)或东莨菪碱(2×10⁻⁷M)的情况下,地西泮的增强作用不明显。Ro 15 - 1788(10⁻⁵M)和β-CCE(10⁻⁵M)可拮抗地西泮对GABA收缩的增强作用,而PK 11195(10⁻⁵M)则无效。我们得出结论,地西泮可调节外周GABA-A受体刺激所诱发的效应,而对GABA-B介导的效应无效。