Chetty N, Coupar I M, Chess-Williams R, Kerr K P
Department of Pharmaceutical Biology, Victorian College of Pharmacy, Monash University, Parkville, Victoria 3052, Australia.
Naunyn Schmiedebergs Arch Pharmacol. 2007 Aug;375(6):359-68. doi: 10.1007/s00210-007-0173-7. Epub 2007 Jul 3.
The aim of this study was to demonstrate the presence of 5-HT(3) receptors in the mouse bladder and to determine their location. Bladder strips from female mice were set up in gassed Krebs-Henseleit solution at 37 degrees C and contractions recorded in response to electrical field stimulation (8 Hz, 60 V, 0.5-ms pulse duration) applied for 2 s every 50 s. The potentiating effects of 5-hydroxytryptamine (5-HT) were recorded (in the presence of 1-microM methysergide and 1-microM GR125487 to isolate the 5-HT(3) receptor response), and contractions were expressed as a percentage of the response to 0.1-M KCl. Responses to (5-HT) were also obtained in the presence of the 5-HT(3) receptor antagonist, ondansetron. RT-PCR was used to detect the expression of the 5-HT(3A) and 5-HT(3B) subunit transcripts of the mouse 5-HT(3) receptor. 5-HT and 5-HT(3) receptor agonists caused concentration-dependent increases in the force of neurogenic contractions without affecting the baseline tone. The rank order of potency was: meta-chloro-phenylbiguanide (m-CPB) = 5-HT > 2-methyl-5-HT (2m5-HT) = 1-phenylbiguanide (1-PBG). The respective pEC(50) values were: 6.42 +/- 0.2 = 5.95 +/- 0.19 > 5.35 +/- 0.12 = 5.14 +/- 0.13. m-CPB acted as a full agonist (E (max) = 40.65 +/- 3.81% KCl), but both 2m5-HT and 1-PBG acted as lower potency partial agonists. Ondansetron (30, 100, 300 nM) caused concentration-related rightward displacements to the concentration-effect curve to 5-HT. Nonlinear regression analysis of the effect of the ondansetron concentrations on the pEC(50) values produced a pK(B) value of 8.29 +/- 0.22. Desensitization of sensory nerves to the contractile effect of capsaicin (10 microM for 60 min) did not alter the ability of 5-HT to potentiate neurogenic contractions. 5-HT (3 microM) inhibited contractions induced by direct muscle stimulation (lignocaine, 300 microM and 10-ms pulse width). m-CPB also caused the same effect with a pIC(50) of 6.62 +/- 0.10 and an E (max) of 48.03 +/- 2.25%. The concentration-response curve to m-CPB was shifted rightwards by ondansetron (1 microM) giving an apparent pK(B) value of 8.15 +/- 0.33. mRNA for both the 5-HT(3A) and 5-HT(3B) receptor subunits was detected in the detrusor as well as the mucosa with a greater relative expression of the 5-HT(3A) subunit in both layers. This study demonstrates that 5-HT mediates enhanced neurogenic contractions of the mouse bladder muscle by an action at 5-HT(3) receptors located prejunctionally on nonsensory nerve elements. Additionally, an inhibitory postjunctional population of the 5-HT(3) receptor was identified. The presence of the 5-HT(3) receptor was confirmed by the expression of both 5-HT(3A) and 5-HT(3B) receptor subunits of the 5-HT(3) receptor.
本研究的目的是证实5-羟色胺(5-HT)3受体在小鼠膀胱中的存在并确定其位置。将雌性小鼠的膀胱条置于37℃的通有气体的克雷布斯 - 亨斯莱特溶液中,记录对每隔50秒施加2秒的电场刺激(8Hz,60V,0.5毫秒脉冲持续时间)的收缩反应。记录5-羟色胺(5-HT)的增强作用(在存在1μM麦角酰二乙胺和1μM GR125487以分离5-HT3受体反应的情况下),收缩反应以对0.1M氯化钾反应的百分比表示。在5-HT3受体拮抗剂昂丹司琼存在的情况下也获得了对(5-HT)的反应。采用逆转录聚合酶链反应(RT-PCR)检测小鼠5-HT3受体的5-HT3A和5-HT3B亚基转录本的表达。5-HT和5-HT3受体激动剂引起神经源性收缩力的浓度依赖性增加,而不影响基线张力。效价顺序为:间氯苯双胍(m-CPB)= 5-HT> 2-甲基-5-HT(2m5-HT)= 1-苯基双胍(1-PBG)。各自的pEC50值为:6.42±0.2 = 5.95±0.19> 5.35±0.12 = 5.14±0.13。m-CPB作为完全激动剂(E(max)= 40.65±3.81%KCl),但2m5-HT和1-PBG均作为效价较低的部分激动剂。昂丹司琼(30、100、300 nM)使5-HT的浓度 - 效应曲线产生浓度相关的右移。对昂丹司琼浓度对pEC50值影响的非线性回归分析得出pK(B)值为8.29±0.22。感觉神经对辣椒素(10μM,60分钟)收缩作用的脱敏并未改变5-HT增强神经源性收缩的能力。5-HT(3μM)抑制直接肌肉刺激(利多卡因,300μM和10毫秒脉冲宽度)诱导的收缩。m-CPB也产生相同的作用。pIC50为6.62±0.10,E(max)为48.03±2.25%。昂丹司琼(1μM)使m-CPB的浓度 - 反应曲线右移,表观pK(B)值为