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拮抗剂与嘌呤能神经假说:2,2'-吡啶异吲哚啉甲苯磺酸盐(PIT),一种P2Y受体的变构调节剂。对25年进展的回顾。

Antagonists and the purinergic nerve hypothesis: 2, 2'-pyridylisatogen tosylate (PIT), an allosteric modulator of P2Y receptors. A retrospective on a quarter century of progress.

作者信息

Spedding M, Menton K, Markham A, Weetman D F

机构信息

Institut de Recherches Internationales Servier, 192 Avenue Charles de Gaulle, 92200, Neuilly sur Seine, France.

出版信息

J Auton Nerv Syst. 2000 Jul 3;81(1-3):225-7. doi: 10.1016/s0165-1838(00)00142-9.

Abstract

2,2'-Pyridylisatogen tosylate (PIT) is a selective antagonist of P2Y responses in smooth muscle and does not antagonise the effects of adenosine. Responses to purinergic nerve stimulation are resistant to PIT. PIT is an allosteric modulator of responses to ATP in recombinant P2Y(1) receptors expressed in Xenopus oocytes with potentiation of ATP at low concentrations (0.1-10 microM) and antagonism at higher ones (>10 microM). A radioligand binding profile showed that PIT did not interact with any other receptors, with the exception of low affinity for the adenosine A(1) receptor (pK(i), 5.3). The compound recognises purine sites and then may cause irreversible binding to sulfhydryl groups following prolonged incubation or high concentrations. PIT is a potent spin trapper.

摘要

2,2'-吡啶异吲哚啉对甲苯磺酸盐(PIT)是平滑肌中P2Y反应的选择性拮抗剂,且不拮抗腺苷的作用。对嘌呤能神经刺激的反应对PIT具有抗性。PIT是非洲爪蟾卵母细胞中表达的重组P2Y(1)受体对ATP反应的变构调节剂,在低浓度(0.1 - 10微摩尔)时增强ATP的作用,在较高浓度(>10微摩尔)时产生拮抗作用。放射性配体结合图谱显示,PIT除了对腺苷A(1)受体具有低亲和力(pK(i),5.3)外,不与任何其他受体相互作用。该化合物识别嘌呤位点,长时间孵育或高浓度时可能导致与巯基的不可逆结合。PIT是一种有效的自旋捕获剂。

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