首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Suramin antagonizes responses to P2-purinoceptor agonists and purinergic nerve stimulation in the guinea-pig urinary bladder and taenia coli.
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Suramin antagonizes responses to P2-purinoceptor agonists and purinergic nerve stimulation in the guinea-pig urinary bladder and taenia coli.

机译:苏拉明可拮抗豚鼠膀胱和带中对P2-嘌呤受体激动剂和嘌呤能神经刺激的反应。

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摘要

1. Suramin, an inhibitor of several types of ATPase, was investigated for its ability to antagonize responses mediated via P2X-purinoceptors in the guinea-pig urinary bladder and P2Y-purinoceptors in the guinea-pig taenia coli. 2. In isolated strips of bladder detrusor muscle, suramin (100 microM-1 mM) caused a non-competitive antagonism of responses to alpha, beta-methylene ATP with an estimated pA2 of approximately 4.7, and inhibited responses to stimulation of the intramural purinergic nerves, with a similar pA2 value. At a concentration of 10 microM, suramin had little effect, but at a concentration of 1 microM, suramin potentiated responses to alpha,beta-methylene ATP, and potentiated responses to electrical stimulation of intramural purinergic nerves. 3. In isolated strips of taenia coli, in which a standard tone had been induced by carbachol (100 nM), suramin at 100 microM and 1 mM significantly antagonized relaxant responses to ATP (at an EC50 concentration) with an estimated pA2 of 5.0 +/- 0.82 and relaxant responses to electrical stimulation of the intramural non-adrenergic, non-cholinergic inhibitory nerves, either single pulses or trains of 8 Hz for 10 s, with estimated pA2 values of 4.9 +/- 0.93 and 4.6 +/- 1.01, respectively. Suramin had no significant effect at 1 or 10 microM. 4. Suramin, at any of the concentrations tested, did not affect contractile responses to histamine (10 microM) or carbachol (10 microM) in the bladder detrusor preparations. In the taenia coli, suramin did not affect either the relaxant responses to noradrenaline (at an EC50 concentration) or the contractile responses to carbachol (100 nM).(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.研究了苏拉明(Suramin),它是几种类型的ATPase的抑制剂,具有拮抗豚鼠膀胱中P2X-嘌呤受体和豚鼠带中P2Y-嘌呤受体介导的应答的能力。 2.在孤立的膀胱逼尿肌条中,苏拉明(100 microM-1 mM)引起对α,β-亚甲基ATP的反应的非竞争性拮抗作用,估计pA2约为4.7,并抑制了对壁内嘌呤能刺激的反应神经,具有类似的pA2值。在浓度为10 microM时,苏拉明几乎没有作用,但是在浓度为1 microM时,苏拉明增强了对α,β-亚甲基ATP的反应,并增强了对壁内嘌呤能神经的电刺激的反应。 3.在分离的条带状条带中,卡巴胆碱(100 nM)诱导了标准音调,100 microM和1 mM的苏拉明显着拮抗对ATP的松弛反应(在EC50浓度下),估计pA2为5.0 + /-0.82和电刺激壁内非肾上腺素,非胆碱能抑制性神经的松弛反应,单脉冲或以8 Hz的频率持续10 s,pA2值估计为4.9 +/- 0.93和4.6 +/- 1.01 , 分别。苏拉明在1或10 microM时无明显作用。 4.在任何测试浓度下,苏拉明均不影响膀胱逼尿肌制剂中对组胺(10 microM)或卡巴胆碱(10 microM)的收缩反应。在Taenia大肠杆菌中,苏拉明既不影响对去甲肾上腺素的松弛反应(在EC50浓度下),也不对对卡巴胆碱(100 nM)的收缩反应产生影响(摘要截断为250字)。

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