Aas P, Tansø R, Fonnum F
Norwegian Defence Research Establishment, Division for Environmental Toxicology, Kjeller.
Eur J Pharmacol. 1989 May 2;164(1):93-102. doi: 10.1016/0014-2999(89)90235-5.
The bronchial smooth muscle of the rat was examined for contractile responses to excitatory amino acids. The nerve-mediated contraction induced by electrical field stimulation was enhanced by exogenous L-glutamate (L-Glu). The apparent affinity (ED50) of L-Glu was 3.5 +/- 0.1 mM. Both tetrodotoxin and hemicholinium-3 completely abolished the electrical field-induced contraction and therefore the potentiation by L-Glu, which indicates that L-Glu has a prejunctional effect. Concentrations of L-Glu higher than 22 mM inhibited the electrical field-induced contractions and enhanced the tonus of the smooth muscle by postjunctional stimulation. The ED50 of exogenous ACh was not altered by L-Glu. High concentrations (62 mM) of L-Glu increased the intrinsic activity (alpha) of ACh, indicating a postjunctional potentiation of ACh-induced contractions. L-Glu did not inhibit the activity of acetylcholinesterase, therefore the postjunctional potentiation was not due to ACh accumulation. Inhibition of the electrical field-induced contraction was seen with high concentrations of D-Glu, L-aspartate (L-Asp), L-alpha-amino adipate and ibotenate. Neither glutamate diethyl ester nor 2-amino-5-phosphonovalerate had any inhibitory effects on the L-Glu- and L-Asp-induced alterations of the electrical field-stimulated contraction or on the L-Glu-enhanced tonus of the bronchial smooth muscle. Kainate, N-methyl-D-aspartate, quisqualate and N-acetyl-aspartyl-glutamate had only minor transient potentiating effects on the electrical field-induced contraction. The results provide evidence for a L-Glu receptor in rat bronchi that has a different specificity for glutamate agonists and antagonists than the L-Glu receptor described in the CNS. The receptor seems to be located prejunctionally and enhances nerve-mediated responses and thereby stimulates the bronchial smooth muscle to contract. The possible involvement of this type of receptor in the 'Chinese restaurant syndrome' is discussed.
研究了大鼠支气管平滑肌对兴奋性氨基酸的收缩反应。电场刺激诱导的神经介导收缩可被外源性L-谷氨酸(L-Glu)增强。L-Glu的表观亲和力(ED50)为3.5±0.1 mM。河豚毒素和3-羟基-4-吡啶基三甲基氯化铵完全消除了电场诱导的收缩以及L-Glu的增强作用,这表明L-Glu具有突触前效应。高于22 mM的L-Glu浓度通过突触后刺激抑制电场诱导的收缩并增强平滑肌张力。L-Glu不会改变外源性乙酰胆碱(ACh)的ED50。高浓度(62 mM)的L-Glu增加了ACh的内在活性(α),表明ACh诱导收缩存在突触后增强作用。L-Glu不会抑制乙酰胆碱酯酶的活性,因此突触后增强作用并非由于ACh积累所致。高浓度的D-谷氨酸、L-天冬氨酸(L-Asp)、L-α-氨基己二酸和鹅膏蕈氨酸可抑制电场诱导的收缩。谷氨酸二乙酯和2-氨基-5-磷酸戊酸对L-Glu和L-Asp诱导的电场刺激收缩变化或L-Glu增强的支气管平滑肌张力均无抑制作用。 kainate、N-甲基-D-天冬氨酸、quisqualate和N-乙酰-天冬氨酰-谷氨酸对电场诱导的收缩仅有轻微的短暂增强作用。结果为大鼠支气管中存在一种L-Glu受体提供了证据,该受体对谷氨酸激动剂和拮抗剂的特异性与中枢神经系统中描述的L-Glu受体不同。该受体似乎位于突触前,增强神经介导的反应,从而刺激支气管平滑肌收缩。讨论了这类受体可能与“中餐馆综合征”的关系。