Galligan J J, North R A
Department of Pharmacology and Toxicology, Michigan State University, East Lansing 48824.
J Auton Nerv Syst. 1991 Jan;32(1):1-11. doi: 10.1016/0165-1838(91)90229-v.
The expression of mu opioid, alpha 2 and 5-hydroxytryptamine1A (5-HT1A) receptors on guinea-pig myenteric neurons was determined using receptor selective agonists during intracellular recordings in vitro. Agonists known to hyperpolarize myenteric neurons by increasing potassium conductance were tested: noradrenaline and UK 14304 (alpha 2 agonists); 5-HT, 8-hydroxydipropylaminotetralin, 5-carboxamidotryptamine (5-HT1A agonists); normorphine, [Met5]-enkephalin and D-Ala2-Phe4, Gly-ol5 enkephalin (mu agonists). The alpha 2 agonists hyperpolarized 46/67 AH cells; mu agonists hyperpolarized 11/66 AH cells and 5-HT1A agonists inhibited 28/57 AH cells. Hyperpolarizations to both alpha 2 and mu agonists were observed in 11/59 AH cells; hyperpolarizations to both alpha 2 and 5-HT1A agonists were observed in 23/49 AH cells. Hyperpolarizations mediated at alpha 2 receptors were observed in 11/54 S neurons and mu agonists hyperpolarized 17/45 S cells. alpha 2 and mu receptors were localized together on 10/43 S cells tested with receptor selective agonists. 5-HT1A-mediated hyperpolarizations were not observed in 36 S cells. Presynaptic inhibition of fast excitatory post-synaptic potentials (fast e.p.s.p.s., S neurons) was observed in all cells tested with alpha 2 agonists (n = 32); in 14/23 cells tested with 5-HT1A agonists and in 8/22 cells tested with mu agonists. Both alpha 2 and 5-HT1A agonists inhibited fast e.p.s.p.s in 15/23 cells, while alpha 2 and mu agonists both inhibited the fast e.p.s.p. in 8/21 cells. Inhibition of fast e.p.s.p.s by mu and 5-HT1A agonists occurred together in 2/19 cells. Slow non-cholinergic e.p.s.p.s were inhibited by alpha 2 agonists in 19/19 cells and by 5-HT1A agonists in 19/21 cells. alpha 2- and 5-HT1A-mediated inhibition of slow e.p.s.p.s occurred together in 12/14 cells. These data allow AH neurons to be divided into two groups: those expressing alpha 2 and 5-HT1A receptors and those expressing alpha 2 and mu receptors. alpha 2 and mu receptors coexist on S neurons which do not express 5-HT1A receptors. Terminals that release acetylcholine express either alpha 2 and mu or alpha 2 and 5-HT1A receptors, consistent with the idea that they are provided by AH cells. Terminals that release mediators of the slow e.p.s.p. express primarily alpha 2 and 5-HT1A receptors.
在体外细胞内记录过程中,使用受体选择性激动剂测定豚鼠肌间神经元上μ阿片受体、α2和5-羟色胺1A(5-HT1A)受体的表达。测试了已知通过增加钾电导使肌间神经元超极化的激动剂:去甲肾上腺素和UK 14304(α2激动剂);5-羟色胺、8-羟基二丙基氨基四氢萘、5-羧酰胺色胺(5-HT1A激动剂);去甲吗啡、[Met5]-脑啡肽和D-Ala2-Phe4,Gly-ol5脑啡肽(μ激动剂)。α2激动剂使67个AH细胞中的46个超极化;μ激动剂使66个AH细胞中的11个超极化,5-HT1A激动剂抑制57个AH细胞中的28个。在59个AH细胞中的11个中观察到对α2和μ激动剂均有超极化反应;在49个AH细胞中的23个中观察到对α2和5-HT1A激动剂均有超极化反应。在54个S神经元中的11个中观察到由α2受体介导的超极化,μ激动剂使45个S细胞中的17个超极化。在用受体选择性激动剂测试的43个S细胞中的10个上,α2和μ受体共定位。在36个S细胞中未观察到5-HT1A介导的超极化。在用α2激动剂测试的所有细胞(n = 32)中均观察到对快速兴奋性突触后电位(快速e.p.s.p.s.,S神经元)的突触前抑制;在用5-HT1A激动剂测试的23个细胞中的14个以及在用μ激动剂测试的22个细胞中的8个中观察到。α2和5-HT1A激动剂在23个细胞中的15个中均抑制快速e.p.s.p.s,而α2和μ激动剂在21个细胞中的8个中均抑制快速e.p.s.p.。μ和5-HT1A激动剂对快速e.p.s.p.s的抑制在19个细胞中的2个中同时出现。慢非胆碱能e.p.s.p.s在19个细胞中的19个中被α2激动剂抑制,在21个细胞中的19个中被5-HT1A激动剂抑制。α2和5-HT1A介导的对慢e.p.s.p.s的抑制在14个细胞中的12个中同时出现。这些数据可将AH神经元分为两组:表达α2和5-HT1A受体组以及表达α2和μ受体组。α2和μ受体在不表达5-HT1A受体的S神经元上共存。释放乙酰胆碱的终末表达α2和μ或α2和5-HT1A受体,这与它们由AH细胞提供的观点一致。释放慢e.p.s.p.介质的终末主要表达α2和5-HT1A受体。