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Phorbol-ester-induced alterations of free calcium ion transients in single rat hepatocytes.

机译:佛波酯诱导的单只大鼠肝细胞中游离钙离子瞬变的变化。

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摘要

The effect of the phorbol esters phorbol 12-myristate 13-acetate (TPA) and phorbol 12,13-dibutyrate (PDB) on changes in free Ca2+ concentration ([Ca2+]i) in single rat hepatocytes, microinjected with the photoprotein aequorin, were investigated. [Arg8]vasopressin and phenylephrine induced a series of repetitive [Ca2+]i transients. Phorbol esters inhibited the alpha 1-adrenoceptor-induced response; sub-nanomolar concentrations decreased the transient frequency, and higher concentrations abolished the transients. The inhibitory effect of PDB was readily reversible. Phorbol esters were less effective in decreasing the frequency of [Arg8]-vasopressin-induced transients, and the inhibition could be overcome by high [Arg8]vasopressin concentrations.
机译:佛波醇酯佛波醇12-肉豆蔻酸酯13-乙酸酯(TPA)和佛波醇12,13-二丁酸酯(PDB)对显微注射光蛋白水母发光蛋白的单只大鼠肝细胞中游离Ca2 +浓度([Ca2 +] i)的影响。调查。 [Arg8]加压素和去氧肾上腺素诱导了一系列重复的[Ca2 +] i瞬变。佛波酯可抑制α1肾上腺素受体诱导的反应。亚纳摩尔浓度降低了瞬态频率,较高的浓度消除了瞬态。 PDB的抑制作用易于逆转。佛波酯在降低[Arg8]-加压素诱导的瞬变频率方面效果较差,并且可以通过高[Arg8]-加压素浓度来克服这种抑制作用。

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