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三磷酸腺苷(ATP)仅在大型背根神经节神经元中诱导三磷酸肌醇(IP3)敏感的钙库释放钙离子。

ATP induces Ca2+ release from IP3-sensitive Ca2+ stores exclusively in large DRG neurones.

作者信息

Svichar N, Shmigol A, Verkhratsky A, Kostyuk P

机构信息

Bogomoletz Institute of Physiology, Kiev, Ukraine.

出版信息

Neuroreport. 1997 May 6;8(7):1555-9. doi: 10.1097/00001756-199705060-00002.

Abstract

PURINORECEPTOR-MEDIATED intracellular Ca2+ release was studied in freshly isolated adult mouse dorsal root ganglia (DRG) neurones. The cytoplasmic Ca2+ concentration ([Ca2+]i) was measured using indo-1-based microfluorimetry. The application of 100 microM ATP in Ca(2+)-free solution triggered an increase in [Ca2+]i in 93% of large DRG neurones but in no small ones. The ATP-induced [Ca2+]i transients in large neurones were inhibited by cells incubation with thapsigargin or by intracellular dialysis with heparin-containing solution. The ATP-triggered increase in [Ca2+]i was not mimicked by adenosine and was blocked by suramin, suggesting the involvement of metabotropic (PZY) purinoreceptors. We conclude that large (proprioceptive) DRG neurones express PZY purinoreceptors linked to the inositol 1,4,5-triphosphate-Ca2+ intracellular signal transduction cascade, whereas small (nociceptive) DRG neurones are devoid of such a mechanism.

摘要

在新鲜分离的成年小鼠背根神经节(DRG)神经元中研究了嘌呤受体介导的细胞内Ca2+释放。使用基于indo-1的显微荧光测定法测量细胞质Ca2+浓度([Ca2+]i)。在无Ca(2+)溶液中施加100 microM ATP可使93%的大型DRG神经元中的[Ca2+]i增加,但小型DRG神经元中则无此现象。大型神经元中ATP诱导的[Ca2+]i瞬变可通过用毒胡萝卜素孵育细胞或用含肝素的溶液进行细胞内透析来抑制。ATP引发的[Ca2+]i增加不能被腺苷模拟,且被苏拉明阻断,这表明代谢型(PZY)嘌呤受体参与其中。我们得出结论,大型(本体感觉)DRG神经元表达与肌醇1,4,5-三磷酸-Ca2+细胞内信号转导级联相关的PZY嘌呤受体,而小型(伤害性感受)DRG神经元则缺乏这种机制。

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