Kaplita P V, Waters D H, Triggle D J
Eur J Pharmacol. 1982 Apr 8;79(1-2):43-51. doi: 10.1016/0014-2999(82)90573-8.
The responses of the guinea-pig ileum myenteric plexus-longitudinal muscle preparation to gamma-aminobutyric acid (GABA) and several analogs were examined in direct and electrically stimulated preparations. GABA, muscimol and 3-aminopropane sulfonic acid (3-APS), but not baclofen, produced a transient, concentration-dependent contraction followed by relaxation. These responses were antagonized by atropine, tetrodotoxin, bicuculline methiodide and picrotoxin. Responses to GABA and 3-APS exhibited a marked tachyphylaxis. GABA and baclofen, but not muscimol or 3-APS, exerted a relaxant effect on contractions induced by supramaximal field stimulation in the longitudinal muscle. These responses were insensitive to bicuculline, bicuculline methiodide and picrotoxin, and were unaffected by other pharmacological agents including adrenergic, cholinergic and histamine antagonists. The results suggest that GABA and its analogs act at a population of excitatory receptors mediating the release of acetylcholine from enteric neurons, and at a population of inhibitory receptors which inhibit the stimulated release of acetylcholine.
在直接和电刺激的豚鼠回肠肌间神经丛 - 纵肌标本中,检测了γ-氨基丁酸(GABA)及其几种类似物的反应。GABA、蝇蕈醇和3-氨基丙烷磺酸(3-APS)可产生短暂的、浓度依赖性的收缩,随后松弛,但巴氯芬无此作用。这些反应可被阿托品、河豚毒素、荷包牡丹碱甲碘化物和印防己毒素拮抗。对GABA和3-APS的反应表现出明显的快速耐受性。GABA和巴氯芬,但不是蝇蕈醇或3-APS,对纵肌中由超强电场刺激诱导的收缩具有松弛作用。这些反应对荷包牡丹碱、荷包牡丹碱甲碘化物和印防己毒素不敏感,并且不受包括肾上腺素能、胆碱能和组胺拮抗剂在内的其他药理剂的影响。结果表明,GABA及其类似物作用于介导肠神经元释放乙酰胆碱的一群兴奋性受体,以及抑制乙酰胆碱刺激释放的一群抑制性受体。