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哇巴因诱导大鼠肥大细胞反应增强。蛋白质磷酸化和细胞内pH的调节作用。

Ouabain-induced enhancement of rat mast cells response. Modulation by protein phosphorylation and intracellular pH.

作者信息

Lago J, Alfonso A, Vieytes M R, Botana L M

机构信息

Departamento de Farmacología, Facultad de Veterinaria, 27002, Lugo, Spain.

出版信息

Cell Signal. 2001 Jul;13(7):515-24. doi: 10.1016/s0898-6568(01)00169-3.

Abstract

The digitalic glicoside ouabain induces potentiation of rat mast cell histamine release in response to several stimuli, which is mediated by Na+/Ca2+ exchanger. In this work, we studied the effect of ouabain on cytosolic calcium, intracellular pH and histamine release with Ca2+ ionophore A23187 in conditions designed to maximize ouabain-induced potentiation of rat mast cells response. The effect of protein kinase C (PKC), cAMP and phosphatase inhibition was also tested. Ouabain induced an enhancement in histamine release, cytosolic calcium and intracellular pH. The adenylate cyclase activator forskolin reduced the effect of ouabain on histamine release and intracellular pH, but enhanced the effect on cytosolic calcium. PKC activator PMA enhanced the effect of ouabain on histamine release and cytosolic calcium, without affecting intracellular pH. A PKC inhibitor, GF-109203X, reduced ouabain-induced enhancement of histamine release and intracellular pH, but increased the enhancement on cytosolic calcium. Finally, inhibition of protein phosphatases 1 and 2A with okadaic acid, increased the effect of ouabain on histamine release and intracellular pH, but reduced cytosolic calcium in presence of ouabain. This result suggest that ouabain-induced potentiation of rat mast cell histamine release with A23187 is modulated by kinases, and this modulation may be carried out by changes in intracellular alkalinization. However, the mechanism underlying cellular alkalinization remains to be elucidated.

摘要

洋地黄毒苷可诱导大鼠肥大细胞在多种刺激下组胺释放增强,这一过程由钠/钙交换体介导。在本研究中,我们在旨在使洋地黄毒苷诱导的大鼠肥大细胞反应增强最大化的条件下,研究了洋地黄毒苷对胞质钙、细胞内pH值以及组胺释放的影响,同时还测试了蛋白激酶C(PKC)、环磷酸腺苷(cAMP)和磷酸酶抑制的作用。洋地黄毒苷可增强组胺释放、胞质钙和细胞内pH值。腺苷酸环化酶激活剂福斯可林可降低洋地黄毒苷对组胺释放和细胞内pH值的影响,但增强了对胞质钙的影响。PKC激活剂佛波酯增强了洋地黄毒苷对组胺释放和胞质钙的影响,而不影响细胞内pH值。PKC抑制剂GF-109203X可降低洋地黄毒苷诱导的组胺释放增强和细胞内pH值升高,但增加了对胞质钙的增强作用。最后,用冈田酸抑制蛋白磷酸酶1和2A,增加了洋地黄毒苷对组胺释放和细胞内pH值的影响,但在存在洋地黄毒苷的情况下降低了胞质钙。该结果表明,洋地黄毒苷诱导的大鼠肥大细胞在A23187刺激下组胺释放增强受激酶调节,这种调节可能通过细胞内碱化的变化来实现。然而,细胞碱化的潜在机制仍有待阐明。

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