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在腺苷介导的平滑肌舒张过程中,由水母发光蛋白监测细胞内钙离子。

Cellular Ca2+ monitored by aequorin in adenosine-mediated smooth muscle relaxation.

作者信息

Bradley A B, Morgan K G

出版信息

Am J Physiol. 1985 Jan;248(1 Pt 2):H109-17. doi: 10.1152/ajpheart.1985.248.1.H109.

Abstract

We studied the effect of adenosine on cytoplasmic ionized calcium-force relationships in vascular smooth muscle (VSM) and determined the dose dependence of the observed effects. The bioluminescent protein aequorin was used as an index of cytoplasmic ionized calcium and was chemically loaded into ferret portal vein strips. The VSM strips were contracted with 33 mM potassium (K+), 5 X 10(-6) M phenylephrine (PE), or electrical stimulation. Force and aequorin light, i.e., cytoplasmic ionized calcium, were simultaneously recorded. Adenosine pretreatment (3.7 X 10(-6) M) reduced both force and light responses in contractures with K+, PE, or electrical stimulation. In contrast, the addition of adenosine during PE or K+ contractions decreased force without a change in light. Dose-response curves for the effects of adenosine on K+ contractures indicated that at low doses adenosine decreases force and cytoplasmic ionized calcium but that at high concentrations (greater than 3.7 X 10(-6) M) adenosine increases light and apparently relaxes VSM by desensitizing the myofilaments to cytoplasmic ionized calcium.

摘要

我们研究了腺苷对血管平滑肌(VSM)细胞质游离钙离子与张力关系的影响,并确定了所观察到的效应的剂量依赖性。生物发光蛋白水母发光蛋白被用作细胞质游离钙离子的指标,并通过化学方法加载到雪貂门静脉条中。VSM条用33 mM钾(K+)、5×10^(-6) M去氧肾上腺素(PE)或电刺激使其收缩。同时记录张力和水母发光蛋白的光,即细胞质游离钙离子。腺苷预处理(3.7×10^(-6) M)可降低K+、PE或电刺激引起的挛缩中的张力和光反应。相反,在PE或K+收缩过程中添加腺苷可降低张力,而光无变化。腺苷对K+挛缩效应的剂量反应曲线表明,低剂量时腺苷降低张力和细胞质游离钙离子,但高浓度(大于3.7×10^(-6) M)时腺苷增加光,并通过使肌丝对细胞质游离钙离子脱敏而明显松弛VSM。

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