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在大鼠离体心肌暴露于模拟缺血条件下时,对细胞质钙浓度变化进行连续荧光测定评估。

Continuous fluorimetric assessment of the changes in cytoplasmic calcium concentration during exposure of rat isolated myocardium to conditions of simulated ischaemia.

作者信息

Northover B J

机构信息

Department of Pharmacology, School of Pharmacy, Leicester Polytechnic.

出版信息

Br J Pharmacol. 1990 Jul;100(3):477-82. doi: 10.1111/j.1476-5381.1990.tb15832.x.

Abstract
  1. The cytoplasmic calcium concentration ([Ca]c) of rat isolated atrial myocardium was assessed with the dye indo-1. Dye-loaded atria were superfused with physiological salt solution and excited with radiation at 360 nm, while epifluorescence emissions were collected simultaneously at 400 nm and 500 nm. The ratio of these emissions was used as a measure of [Ca]c. 2. Dye-loaded atria showed a phasic rise and fall in [Ca]c with each applied electrical pacing stimulus. The amplitudes of systolic increments in tension and [Ca]c were augmented by the presence of isoprenaline. 3. Atria superfused with a solution the composition of which resembled that found extracellularly in regions of ischaemia rapidly lost systolic increments in tension and [Ca]c, while end-diastolic [Ca]c and tension gradually rose. 4. The presence of lactate (20 mM) or flufenamate (5 microM) in the superfusate during simulated ischaemia aggravated the rises in both end-diastolic tension and end-diastolic [Ca]c. Inclusion in the superfusate of sulphinpyrazone (50 microM) or glucose (20 mM) protected against some of the deleterious effects of lactate seen during simulated ischaemia.
摘要
  1. 用indo-1染料评估大鼠离体心房肌细胞质钙浓度([Ca]c)。将负载染料的心房用生理盐溶液灌流,并用360nm的辐射激发,同时在400nm和500nm处收集落射荧光发射。这些发射的比率用作[Ca]c的度量。2. 负载染料的心房在每次施加电起搏刺激时,[Ca]c呈现出阶段性的上升和下降。异丙肾上腺素的存在增强了张力和[Ca]c收缩期增量的幅度。3. 用一种成分类似于在缺血区域细胞外发现的溶液灌流心房,张力和[Ca]c的收缩期增量迅速丧失,而舒张末期[Ca]c和张力逐渐升高。4. 在模拟缺血期间,灌流液中存在乳酸(20mM)或氟灭酸(5μM)会加重舒张末期张力和舒张末期[Ca]c的升高。灌流液中加入磺吡酮(50μM)或葡萄糖(20mM)可防止模拟缺血期间所见乳酸的一些有害影响。

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Cytosolic calcium transients from the beating mammalian heart.来自跳动的哺乳动物心脏的胞质钙瞬变。
Proc Natl Acad Sci U S A. 1987 Nov;84(21):7793-7. doi: 10.1073/pnas.84.21.7793.

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