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α1-肾上腺素能刺激后肝细胞中游离胞质Ca2+的变化。对负载喹啉-2的肝细胞的研究。

Changes in free cytosolic Ca2+ in hepatocytes following alpha 1-adrenergic stimulation. Studies on Quin-2-loaded hepatocytes.

作者信息

Charest R, Blackmore P F, Berthon B, Exton J H

出版信息

J Biol Chem. 1983 Jul 25;258(14):8769-73.

PMID:6134732
Abstract

The Ca2+ selective fluorescent indicator, Quin-2, was employed to monitor continuously the concentration of free cytosolic Ca2+ [ Ca2+ ]i in isolated rat hepatocytes. Epinephrine (10(-6) M) and phenylephrine (10(-5) M), acting via alpha 1-adrenergic receptors, increases [ Ca2+ ]i from a basal concentration of approximately 0.2 microM to approximately 0.6 microM. This increase in [ Ca2+ ]i is evident as early as 1 to 1.5 s, the earliest time so far reported for any hepatic alpha 1-adrenergic event. Vasopressin (10(-8) M), after a lag which is 2 to 3 s longer, increases [ Ca2+ ]i to the same extent and at the same rate as the alpha 1-adrenergic agonists. Glucagon (10(-8) M) also increases [ Ca2+ ]i but at a significantly slower rate and only after a lag of about 10 s. All of these agents also induce an increase in the fluorescence of control cells. This Quin-2 independent fluorescence, which is due to an increased reduction of pyridine nucleotides, must be corrected for before the maximum change in [ Ca2+ ]i can be calculated but is sufficiently slow so as not to contribute to the initial rate of increase in the Quin-2-dependent fluorescence.

摘要

采用钙离子选择性荧光指示剂喹啉-2,连续监测分离的大鼠肝细胞中游离胞质钙离子浓度[Ca²⁺]i。通过α₁-肾上腺素能受体起作用的肾上腺素(10⁻⁶ M)和去氧肾上腺素(10⁻⁵ M),可使[Ca²⁺]i从约0.2微摩尔的基础浓度增加到约0.6微摩尔。[Ca²⁺]i的这种增加早在1至1.5秒时就很明显,这是迄今为止报道的任何肝脏α₁-肾上腺素能事件的最早时间。血管加压素(10⁻⁸ M)在延迟2至3秒后,以与α₁-肾上腺素能激动剂相同的程度和速率增加[Ca²⁺]i。胰高血糖素(10⁻⁸ M)也会增加[Ca²⁺]i,但速率明显较慢,且仅在约10秒的延迟后才出现。所有这些药物还会诱导对照细胞的荧光增加。这种与喹啉-2无关的荧光是由于吡啶核苷酸还原增加所致,在计算[Ca²⁺]i的最大变化之前必须对其进行校正,但它足够缓慢,不会影响喹啉-2依赖性荧光的初始增加速率。

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