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低温时钙相关效应在能量代谢中的重要性:膜通道拮抗剂对大鼠肝脏能量代谢的影响。

The importance of calcium-related effects on energetics at hypothermia: effects of membrane-channel antagonists on energy metabolism of rat liver.

作者信息

Churchill T A, Green C J, Fuller B J

机构信息

University Department of Surgery, Royal Free Hospital School of Medicine, London, United Kingdom.

出版信息

Cryobiology. 1995 Oct;32(5):477-86. doi: 10.1006/cryo.1995.1047.

Abstract

During normothermic metabolism, the active pumping of Ca2+ across the cell membrane, mitochondria, and specialized sequestration organelles accounts for a large proportion of total energy expenditure in the cell. This study was designed to determine the effects of Ca2+ channel antagonists (chlorpromazine, verapamil, nifedipine, prenylamine, and nisoldipine) on energy metabolism and levels of glycolytic substrate (glucose) and anaerobic endproduct (lactate) during cold ischemia in rat livers. We hypothesized that if the passive channels were blocked during cold ischemia, then the ATP requirement of active ion pumping would be reduced and ATP levels and energy charge ratios would remain higher throughout the ischemic period; thus, viability of the liver would also be increased after prolonged ischemia. The most positive effect on energy metabolism was observed in the chlorpromazine-treated livers, followed by verapamil treatment. In the chlorpromazine treatment, total adenylate (TA) contents were 0.5-1.0 mumol/g (P < 0.05) higher than the sham group for most of the 24-h time course. Energy charge (EC) ratios were 0.05-0.07 higher than the sham values up to 4-10 h ischemia. Verapamil treatment was less effective, but still exhibited positive effects on TA levels at several time points (20 min, 10 h, and 24 h) throughout the entire 24-h period. In both of these groups, TA values by 24 h ischemia were similar to levels at 10 h in the sham group (3.1 mumol/g), thus showing a considerable effect in maintaining adenylate levels. Despite similar pharmacological antagonist activities, ATP levels in the nifedipine, prenylamine, and nisoldipine treatment groups were 1.0-1.5 mumol/g (P < 0.05) less than the corresponding sham group (without Ca2+ antagonists) over the first 1 h ischemia. The decreases in high energy adenylate levels were reflected in lower EC ratios in these three groups; values were 0.06-0.17 (P < 0.05) lower than corresponding sham values. Finally, it was an unexpected finding that the sham injection (0.5 mg/kg ethanol+PEG400) resulted in the sustained elevation of ATP, total adenylates, and EC values over the first h; EC ratios remained at initial (t = 0) values (EC = 0.71 +/- 0.01) up to 1 h.

摘要

在正常体温代谢过程中,钙离子(Ca2+)跨细胞膜、线粒体及特殊隔离细胞器的主动转运消耗了细胞总能量的很大一部分。本研究旨在确定钙离子通道拮抗剂(氯丙嗪、维拉帕米、硝苯地平、普尼拉明和尼索地平)对大鼠肝脏冷缺血期间能量代谢、糖酵解底物(葡萄糖)水平及无氧代谢终产物(乳酸)水平的影响。我们推测,若在冷缺血期间阻断被动通道,那么主动离子转运所需的三磷酸腺苷(ATP)将会减少,且在整个缺血期ATP水平及能荷比将维持在较高水平;因此,长时间缺血后肝脏的存活率也会提高。氯丙嗪处理的肝脏对能量代谢的影响最为显著,其次是维拉帕米处理的肝脏。在氯丙嗪处理组中,在24小时的大部分时间里,总腺苷酸(TA)含量比假手术组高0.5 - 1.0微摩尔/克(P < 0.05)。在缺血4 - 10小时期间,能荷(EC)比高于假手术组0.05 - 0.07。维拉帕米处理效果稍差,但在整个24小时期间的几个时间点(20分钟、10小时和24小时)对TA水平仍有积极影响。在这两组中,缺血24小时时的TA值与假手术组10小时时的水平(3.1微摩尔/克)相似,从而显示出在维持腺苷酸水平方面有显著效果。尽管硝苯地平、普尼拉明和尼索地平具有相似的药理拮抗活性,但在缺血的最初1小时内,这三组的ATP水平比相应的假手术组(未使用钙离子拮抗剂)低1.0 - 1.5微摩尔/克(P < 0.05)。这三组中高能腺苷酸水平的降低反映在较低的能荷比上;其值比相应的假手术组低0.06 - 0.17(P < 0.05)。最后,一个意外的发现是,假注射(0.5毫克/千克乙醇 + 聚乙二醇400)导致在最初1小时内ATP、总腺苷酸和能荷值持续升高;能荷比在1小时内一直维持在初始(t = 0)值(EC = 0.71 ± 0.01)。

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